Ichem6e Answers

Answers to self-tests and exercises
Please note that just the final numerical

solutions and short-answer solutions are
supplied. For full worked solutions, please
refer to the Solutions Manual by Alen
Hadzovic (9780198701712).
102.5 nm,
1.7
1.524 10 nm , 656.3 nm
1.8
CHAPTER 1
Self-tests
1
S1.1
779967m , 1.28 10 m or 1280 nm.
S1.2
3d set of orbitals, 5 orbitals
S1.3
S1.4
3p
S1.5
The s electron already present in Li repels the

incoming electron more strongly than the p
electron already present in B repels the
incoming p electron, because the incoming p
electron goes into a new orbital.
S1.6
Ni :[Ar]3d 8 4s 2 , Ni 2+ :[Ar]3d 8
S1.7
Period 4, Group 2, s block
S1.8
Generally, going down a group the atomic

radius increases and the first ionization energy
generally decreases.
S1.9
Group 14.
S1.10
The electron-gain
unfavourable
S1.11
Na+
process
1.2
for
is
12
12
1
12
1
12
1
7 1
1.0974 10 m
2

1
7 1
1.0288 10 m
2
4
1
6 1
9.7547 10 m
2
3
1
6 1
8.2305 10 m
2
2
1.9
For a given value of n, the angular momentum

quantum number l can assume all integer
values from 0 to n 1.
1.10
n2 (e.g., n2 = 1 for n = 1, n2 = 4 for n = 2, etc.)
ml
Orbital
designation
2
3
1
2
2p
3d
4
4
0
3
+1, 0, 1
+2, +1,
, 2
0
+3, +2,
, 3
Number
of
orbitals
3
5
4s
4f
1
7
1.12
When n = 5, l = 3 (for the f orbitals) and ml =

3,2,1,0,1,2,3, which represent the seven
orbitals that complete the 5f subshell. The 5f
orbitals represent the start of the actinoids,
starting with Th and ending with Lr.
1.13
Comparing the plots for 1s (Figure 1.10) and

2s (Figure 1.12) orbitals, the radial
distribution function for a 1s orbital has a
single maximum, and that for a 2s orbital has
two maxima and a minimum (at r = 2ao/Z for
hydrogenic 2s orbitals). The presence of the
node at r = 2a0/Z for R(2s) requires the
presence of the two maxima and the minimum
in the 2s radial distribution function. The
absence of a radial node for R(2p) requires
that the 2p radial distribution function has
only a single maximum.
E(He+)/E(Be3+) = Z2(He+)/Z2(Be3+) = 22/42 =

0.25
(a) At nucleus
(b) Exactly at Bohr radius, a0
(c) 3+ 5a 0
1.3
E(H, n = 1) E(H, n = 6) = 13.6 eV 0.378

eV = 13.2 eV.
1.4
0.544eV , The discrepancy is due to the

shielding effect
1.5
1.11
Exercises
1.1
1.937 1018 J
1.6
14.0eV , 4.16 eV
1
To accompany Inorganic Chemistry, Sixth Edition by Weller, Overton, Rourke, and Armstrong
ANSWERS TO SELF-TESTS AND EXERCISES
1.14
1.15
Each 4p orbital has one nodal plane; the total

number of nodes is 3
1.21
The first ionization energies of strontium,

barium, and radium are 5.69, 5.21, and 5.28
eV. Radium has a higher first ionization
energy because it has such a large Zeff due to
the insertion of the lanthanides.
1.22
Both the first and the second ionization

processes remove electrons from the 4s orbital
of these atoms, with the exception of Cr. In
general, the 4s electrons are poorly shielded
by the 3d electrons, so Zeff(4s) increases from
left to right and I2 also increases from left to
right.
1.23
(a) [He]2s22p2
1.16
(b) [He]2s22p5
dxy Function: xyR (r ) Label: xy
(c) [Ar]4s2
(d) [Ar]3d10
(e) [Xe]4f145d106s26p3
(f) [Xe]4f145d106s2
1.24
d x 2 y 2 Function:
(a) [Ar]3d14s2
(b) [Ar]3d2
1 2
x y 2 R(r ) Label: x2 y2
2
(c) [Ar]3d5
(d) [Ar]3d4
(e) [Ar]3d6
(f) [Ar] or [Ar]3d0
1.17
The 1s electrons shield the positive charge

from the 2s electrons, which are further out
from the nucleus than the 1s electrons.
Consequently, the 2s electrons feel less
positive charge than the 1s electrons for
beryllium.
1.18
1.70, 2.05, 2.40, 2.75, 3.10, 3.45, 3.80
1.19
The higher value of I2 for Cr relative to Mn is

a consequence of the special stability of halffilled subshell configurations and the higher
Zeff of a 3d electron vs. a 4s electron.
1.20
Both of these atoms have an electron

configuration that ends with 4s2: Ca is [Ar]4s2
and Zn is [Ar]3d104s2. An atom of zinc has 30
protons in its nucleus and an atom of calcium
has 20, so clearly zinc has a higher nuclear
charge than calcium. However it is effective
nuclear charge (Zeff) that directly affects the
ionization energy of an atom. Since I(Zn) >
I(Ca), it would seem that Zeff(Zn) > Zeff(Ca).
1.25
(a) [Xe]4f145d46s2
(b) [Kr]4d6
(c) [Xe]4f6
(d) [Xe]4f7
(e) [Ar] or [Ar]3d0
(f) [Kr]4d2
1.26
(a) S
(b) Sr
(c) V
(d) Tc
(e) In
(f) Sm
1.27
See Figure 1.22 and the inside front cover of

the book.
1.28
In general, I1, Ae, and all increase from left

to right across period 3. The cause of the
general increase across the period is the

gradual increase in Zeff, which itself is caused
by the incomplete shielding of electrons of a
given value of n by electrons with the same n.
2
(b)
(c)
1.29
2s and 2p
1.30
One 2s and three 2p
(d)
CHAPTER 2
(e)
Self-tests
S2.1
2.2
2.3
S2.2
(a) Angular
(a) Bent
(b) Tetrahedral
(b) Tetrahedral
(c) Tetrahedral
(c) Trigonal bipyramidal

S2.3
S2.4
2.4
(a) Linear
(a) Trigonal-planar
(b) Bent
(b) Trigonal-pyramidal
(a) 2, 1, 0
(c) Square-pyramidal
(b) 1g22u23g21u42g4
1g22u23g21u42g44u1
S2.5
1222321424
S2.6
[2-2+4+2] = 3
S2.7
Bond length (shortest to longest): CN, C=N,

and CN; Bond strength (strongest to
weakest): CN > C=N > CN.
S2.8
24 kJ mol
S2.9
(a) +1/2
2.5
(a) Octahedral
(b) T-shaped
(c) Square pyrimidal
2.6
(a) T-shaped
(b) Square planar
(c) Linear
(b) +5
2.7
ICl6
(c) 6
2.8
Tetrahedral and octahedral
(d) +3
2.9
(a) 176 pm
(b) 217 pm
(c) 221 pm
Exercises
2.10
2.1
(a)
The single bond covalent radii decrease if we

move horizontally from left to right in the
periodic table. The atomic radii decrease
while the Zeff increases in the same direction.
As a consequence of these two trends, the

valence electrons are held tighter and closer to
the atomic nucleus. This means that, as we
move from left to right, the distance between
two non-metallic atoms has to decrease in
order for the covalent bond to be formed. This
results in a shorter internuclear separation
and as a consequence smaller covalent radii in
the same direction.
As we go down a group the valence electrons
are found in the atomic orbitals of higher
principal quantum number. There are more
core electrons between the valence electrons
and the nucleus that shield the valence
electrons from the influence of the nucleus.
As a consequence, the valence electrons are
further away from the nucleus. This means
that when a covalent bond is formed, two
atomic nuclei are further apart as we go down
the group and the covalent radii increase.
(b) Ionic
(c) Ionic
2.19
(b) sp3
(c) sp3d or spd3
(d) sp3d2
2.20
2.12
(c) 0
(d) 2
(a) 1g21u2
2(Si-O) (Si=O) = 2(466 kJ) (640 kJ) =

292 kJ
..
Therefore two single bonds will always be

better enthalpically than one double bond.
u
2s - 2s
If N2 were to exist as N4 molecules with the

P4 structure, then two NN triple bonds would
be traded for six NN single bonds, which are
weak. The net enthalpy change can be
estimated to be 2(945 kJ) 6(163 kJ) = 912
kJ.
The net enthalpy change for 2P2 P4 can be
estimated to be 2(481 kJ) 6(201 kJ) = 244
kJ.
(b) 1g21u21u2
..
2p - 2p
(c) 1g21u21u42g1
2.13
483 kJ
2.14
The atoms that obey the octet rule are O in

BeO, F in NF, and O in O2.
2.15
(a) 0 kJ
..
2p - 2p
(b) 205 kJ
2.16
(a) 1
(b) 1
2.21
2.11
(a) sp2
(d) 1g21u22g21u41g3
(a) +4
..
(b) +3
(c) +6
(d) +5
(e) +5
2p - 2p
2.17
AD < BD < AC < AB
2.18
(a) Covalent
2.22
The configuration of C22 would be 1g21u2

1u4 2u2. The bond order would be [22+4+2] = 3. So C22 has a triple bond. The
configuration for the neutral C2 would be
1g21u2 1u4. The bond order would be [22+4] = 2.

2.23
See figure 2.18. The bond order would be

[2-2+4] = 2.
2.24
See figure 2.22.
2.25
(a) The 5p and 5s of I, and the 4p and 4s of Br

(b) [2+22+44] = 1
2.26
Probably not stable in isolation; unstable in solution.
(a) (1/2)((2 + 4 + 2) (2 + 2)) = 2

2.31
(b) (1/2)((2 + 4 + 2) (2 + 4)) = 1

(c) (1/2)((2 + 2 +4) 2) = 3
2.27
(a) Bond order increases from 2 to 2.5; bond

in O2+ becomes shorter
(b) N2 has a weaker and longer bond than N2
(c) Increase the bond order from 2.5 to 3,
making the bond in NO+ stronger
2.28
The line at about 15.2 eV corresponds to

excitation of the electrons from 3 molecular
orbital (the HOMO of CO). The group of four
peaks between 17 and about 17.8 eV
correspond to the excitation of 1 electrons,
and finally the last peak (highest in energy)
corresponds to the excitation of 2 electrons.
he UV photoelectron spectrum of SO should
have one more line at even lower energies
corresponding to the ionization from 2
degenerate set of molecular orbitals.
2.29
Four atomic orbitals can yield

independent linear combinations
2.32
3/3 = 1
2.33
More S character
2.34
Your molecular orbital diagram for the N2

molecule should look like the one shown on
Figure 2.18, whereas the diagrams for O2 and
NO should be similar to those shown on
Figures 2.12 and 2.22 respectively. The
variation in bond lengths can be attributed to
the differences in bond orders.
2.35
(a) Hypothetical example of (4c,2e) bonding;

not likely to exist.
four
(b) It is electron precise. It could very well

exist.
2.30
CHAPTER 3
Self-tests
S3.1
P- type lattice of chloride anions with caesium

cation in cubic hole.
S3.20
n-type, p-type
S3.2
Exercises
3.1
a b c and = 90, = 90, = 90
3.2
S3.3
(a) 52%
(b) 68%
S3.4
rh = ((3/2)1/2 1) r = 0.225 r
S3.5
Each unit cell contains eight tetrahedral holes,

each inside the unit cell. As outlined in
Example 3.5, the ccp unit cell has four
identical spheres. Thus, the spheres-totetrahedral holes ratio in this cell is 4 : 8 or 1 :
2.
S3.6
409 pm
S3.7
401 pm
S3.8
FeCr3
S3.9
X2A3.
S3.10
The coordination of O2 is two Ti4+ and four

Ca2+ and longer distances.
S3.11
LaInO3
3.3
Points on the cell corners are (0,0,0), (1,0,0),

(0,1,0), (0,0,1), (1,1,0), (1,0,1), (0,1,1), and
(1,1,1); the fractional coordinates for the
points at the centre of each face are (,,0),
(,1,), (0,,), (,,1), (,1,), and
(1,,).
3.4
Perovskite-type structure
3.5
(c) and (f)
3.6
(a) MX
(b) M2A
3.7
K3C60
3.8
S3.12
NaCl structure, TiO2 structure
S3.13
2421 kJ mol1
S3.14
Unlikely
S3.15
MgSO4 < CaSO4 < SrSO4 < BaSO4.
S3.16
NaClO4
S3.17
(a) Frenkel defects

(b) Schottky defects
S3.18
Phosphorus and aluminium.
S3.19
The dx2-y2 and dz2 have lobes pointing along

the cell edges to the nearest neighbor metals.
3.9
6, W2C3
3.10
429 pm
3.11
Cu3Au, primitive cubic, 12 carat
3.12
Alloy
3.13
(a) 6:6 and 8:8

(b) Larger when RbCl has the caesiumchloride structure
3.14
3.15
(a) Coordination number of O atoms is two;

coordination number of Re atoms is six

185 kJ mol1,
exothermic salt.
(b) Perovskite- type structure

3.16
Cations in site A have coordination number

12, whereas those in site B have coordination
number six
3.17
CaF2
3.18
(a) MX2
(b) MX2
(c) M2X3
3.20
3.21
3.22
(a) TiO2-type
(b) CsCl-type
(c) ZnS-type
(d) NaCl- or NiAs-type
r(Mg2+) = 79.8 pm, r(Ca2+) = 102.8 pm,
r(Sr2+) = 118.8 pm, and r(Ba2+) = 138.3 pm
(a) (6,6)
(b) (6,6)
(c) (6,6)
(d) (6,6)
Each of the complex ions in this exercise
([PtCl6]2, [Ni(H2O)6]2+, [SiF6]2) is highly
symmetric and their shape can be
approximated with a sphere. For example,
K2PtCl6 has an antifluorite structure with
anions [PtCl6]2 forming a ccp array and K+
cations occupying each tetrahedral hole.
3.23
Calcite has a rhombohedral unit cell, whereas

NaCl has a cubic one. Both rhombohedral and
cubic unit cells have all three dimensions
equal (a = b = c) but they differ in the angles,
with cubic unit cell having all angles at 90
and rhombohedral all angles equal but
different from 90.
3.24
The most important terms will involve the

lattice enthalpies for the di- and the trivalent
ions. Also, the bond dissociation energy and
third electron gain enthalpy for nitrogen (N2)
will be large.
3.25
MgO: 3144 kJmol1

AlN: 7074 kJmol1
3.26
(a) 1990 kJ mol

(b) The massive second ionization energy for
K, 3051 kJ mol1
3.27
From the Born-Haber cycle for CaCl,

fH(CaCl) = +176 kJ mol1 + 589 kJ mol1 +
122 kJ mol1 355 kJ mol1 717 kJ mol1 =
showing that CaCl is an
Although CaCl has a favourable (negative)

fH, this compound does not exist and would
convert to metallic Ca and CaCl2 (2CaCl
Ca + CaCl2). This reaction is very favourable
because CaCl2 has a higher lattice enthalpy
(higher cation charge). The higher lattice
enthalpy combined with gain of I1 for Ca
(Ca+(g) + e Ca(g)) are sufficient to
compensate for I2 (Ca+(g) Ca2+(g) + e)
required to form CaCl2
M: (a) 6 and (b) 4

X: (a) -3 and (b) 2
3.19
3.28
Hexagonal ZnS
3.29
(b) Ca2+ and Hg2+
3.30
(a) 10906 kJ mol1

(b) 1888 kJ mol1
(c) 664 kJ mol1
3.31
(a) CaSeO4
(b) NaBF4
3.32
CsI < RbCl < LiF < CaO < NiO < AlN
3.33
Ba2+, Na+, Ba2+
3.34
(a) MgCO3
(b) CsI3
3.35
(a) Schottky defects

(b) Frenkel defects
3.36
In sapphire, the blue colour is due to the

electron transfer between Fe2+ and Ti4+
substituting for Al3+ in adjacent octahedral
sites in Al2O3 structure. As beryl also contains
Al3+ in octahedral sites, it is plausible that the
blue colour of aquamarine is due to the same
two dopants.
3.37
Vanadium carbide and manganese oxide
3.38
The formation of defects is normally

endothermic because as the lattice is disrupted
the enthalpy of the solid rises. However, the
term TS becomes more negative as defects
are formed because they introduce more
disorder into the lattice and the entropy rises.
As temperature is raised, this minimum in G
shifts to higher defect concentrations.
Increase in pressure would result in fewer
defects in the solid. This is because at higher
pressures, lower coordination numbers
(tighter packing) are preferred.
3.39
UO2+x
3.40
(a) p-type
(b) n-type
(c) n-type
3.41
TiO and VO have metallic properties
3.42
A semiconductor is a substance with an

electrical conductivity that decreases with
increasing temperature. It has a small,
measurable band gap. A semimetal is a solid
whose band structure has a zero density of
states and no measurable band gap.
3.43
Ag2S and CuBr: p-type

VO2: n-type
3.44
Both KC8 and C8Br should have metallic

properties.
The N atom of (H3Si)3N is trigonal planar,

whereas the N atom of (H3C)3N is trigonal
pyramidal.
S4.9
Dimethylsulfoxide (DMSO) and ammonia.
S4.10
A base
S4.11
Exercises
CHAPTER 4
Self-tests
S4.1
S4.8
4.1
See the diagram below for the outline of the

acid-base properties of main group oxides.
The elements that form basic oxides have
symbols printed in bold, those forming acidic
oxides are underlined, and those forming
amphoteric oxides are in italics.
4.2
(a) [Co(NH3)5(OH)]2+
(a) HNO3, acid. Nitrate ion, conjugate base.

H2O, base. H3O+, conjugate acid.
(b) Carbonate ion, base; hydrogen carbonate,
or bicarbonate, conjugate acid; H2O, acid;
hydroxide ion, conjugate base.
(c) Ammonia, base; NH4+, conjugate acid;
hydrogen sulphide, acid; HS, conjugate base.
S4.2
pH= 2.24
S4.3
pH=1.85
S4.4
[Na(H2O)6]+ < [Mn(H2O)6]2+ < [Ni(H2O)6]2+ <

[Sc(H2O)6]3+
S4.5
(a) 3. The actual value, given in Table 4.3, is

2.1.
(b) 8. The actual value, given in Table 4.3, is
7.4.
(c) 13. The actual value, given in Table 4.3, is
12.7.
S4.6
S4.7
H2O2 would not react with Ti(IV) since

Ti(IV) cannot be further oxidized.
(a) The acid FeCl3 forms a complex, [FeCl4],
with the base Cl.
(b) The acid I2 forms a complex,
base I.
I3,
with the
(b) SO4
(c) CH3O
(d) HPO42
(e) SiO(OH)3
4.14
(f) S2
(a) The Fe(III) complex, [Fe(OH2)6]3+, is the

stronger acid.
(b) The aluminum-aqua ion is more acidic.
4.3
(a) C5H6N+
(c) Si(OH)4 is more acidic.
(b) H2PO4
(c) OH
(d) HClO4 is a stronger acid.
(d) CH3C(OH)2
(e) HMnO4 is the stronger acid.
(e) HCo(CO)4
(f) H2SO4 is a stronger acid.
(f) HCN
4.4
[H3O+] = 1.4 10-3

pH=2.85
4.5
5.6 1010
4.6
5.6 10
4.7
Base
4.15
Cl2O7 < SO3 < CO2 < B2O3 < Al2O3 < BaO.
4.16
NH3 < CH3GeH3 < H4SiO4 < HSO4 < H3O+ <
HSO3F.
4.17
The Ag+ ion is the stronger acid.
4.18
polycation formation reduces the overall

positive charge of the species by +1 per M.
4.19
(a)
4.8
O
Cl
O
H3PO4(aq) + HPO42(aq)
Cl
H
O
2H2PO4(aq)
H
O
(b)
chloric acid
chlorous acid
CO2(aq) + CaCO3(s) + H2O(l)

+ 2HCO3
Chloric acid, the predicted pKa = 2; actual

value = 1.
Chlorous acid, the predicted pKa = 3; actual
value = 2.
4.9
(a) CO32 is of directly measurable base

strength. O2, is too strong to be studied
experimentally in water.
4.20
NO3 is of directly measurable base strength

in liquid H2SO4.
ClO4, cannot be studied in sulfuric acid.
4.10
Electron withdrawing.
4.11
The difference in pKa values can be explained

by looking at the structures of the acids in
question.
4.12
Na+ < Sr2+ < Ca2+ < Mn2+ < Fe3+ < Al3+
4.13
HClO4 > HBrO3 > H2SO4 > HNO2.
H3SO4+ + F
NH4+ + HF
NH3 + H2F+
4.21
As you go down a family in the periodic

chart, the acidy of the homologous hydrogen
compounds increases.
4.22
Fluorines high electronegativity results in

electron withdrawal from the central Si atom
making the Si very nucleophilic. This fact,
combined with the small size of F atom (little
steric hindrance at Si) makes SiF4 the
strongest Lewis acid of the four.
ClO42 and NO3 are too weak to be studied

experimentally.
(b) HSO4, not too strong to be studied
experimentally.
H2SO4 + HF
Ca2+(aq)
The order of Lewis acidity for boron halides

is due to additional electronic effects. See
Section 4.7(b) Group 13 Lewis acids in the
textbook.
10
4.23
(a) The acids in this reaction are the Lewis

acids SO3 and H+ and the base is the Lewis
base OH. This is a displacement reaction.
4.29
SiO2 + 6HF
or
(b) This is a displacement reaction. The

Lewis acid Hg2+ displaces the Lewis acid
[B12] from the Lewis base CH3.
SiO2 + 4HF
(c) This is also a displacement reaction. The

Lewis acid SnCl2 displaces the Lewis acid K+
from the Lewis base Cl.
The Brnsted reaction involves the transfer of

protons from HF molecules to O2 ions,
whereas the Lewis reaction involves complex
formation between Si(IV) centre and F ions.
(d) It is a displacement reaction. The very

strong Lewis acid SbF5 (one of the strongest
known) displaces the Lewis acid [AsF2]+ from
the Lewis base F.
4.25
(a) Boron tribromide; the acceptor orbital on

boron is involved to a greater extent in
bonding in BF3 and BCl3 than in BBr3
Al2O3 + 3H2S
Al2S3 + 3H2O
An equilibrium is established between two

hard acids, Al(III) and H+, and the bases O2
and S2:
4.31
(a) The ideal solvent properties in this case

would be weak, hard, and acidic, for example
HF.
(b) The smaller Lewis base NMe3 is the

stronger in this case.
(b) Alcohols such as methanol or ethanol

would be suitable.
(a) Less than 1.
(c) A solvent that is a hard base is suitable, for

example diethyl ether.
(d) The solvent must be a softer base than Cland have an appreciable dielectric constant,
for example acetonitrile.
(b) Greater than 1.

(c) Less than 1.
(d) Greater than 1.
4.26
2H2O + SiF4
4.30
(e) A Lewis acidbase complex formation

reaction between EtOH (the acid) and py (the
base) produces the adduct EtOHpy, which is
held together by a hydrogen bond.
4.24
2H2O + H2SiF6
4.32
An alumina surface, such as the partially

dehydroxylated one shown below, would also
provide Lewis acidic sites that could abstract
Cl:
4.33
Mercury(II) is a soft Lewis acid, and so is

found in nature only combined with soft
Lewis bases, the most common of which is
S2.
(a) CsF + BrF3 Cs+ + BrF4; in this case F

is a Lewis base whereas BrF3 is a Lewis acid.
(b) ClF3 + SbF5 ClF2+ + SbF6; again F is
a Lewis base, whereas SbF5 is Lewis acid.
(c) B(OH)3 + H2O [B(OH)3(H2O)]
[B(OH)4] + H+; the Lewis acid in this
reaction is B(OH)3, whereas the Lewis base is
H2O.
(d) B2H6 + 2PMe3 2[BH3(PMe3)]; the base
is PMe3 and the acid is B2H6.
4.27
4.28
Trimethylamine is sterically large enough to

fall out of line with the given enthalpies of
reaction.
(a) DMSO is the stronger base; the ambiguity
for DMSO is that both the oxygen atom and
sulfur atom are potential basic sites.
(b) Depending on the EA and CA values for
the Lewis acid, either base could be stronger.
Zinc(II), which exhibits borderline behaviour,

is harder and forms stable compounds (i.e.,
complexes) with hard bases such as O2,
CO32, and silicates, as well as with S2
4.34
(a) CH3CH2OH + HF
F
(b) NH3 + HF
CH3CH2OH2+ +
NH4+ + F
ANSWERS TO SELF-TESTS AND EXERCISES 11

C6H5COO + H2F+
4.49
Both a Brnsted acidbase reaction and a

Lewis acidbase reaction.
Cations such as I2+ and Se82+ should behave

like good Lewis acids while anions such as
S42 and Pb94 are good Lewis bases.
4.50
For titration of a weak base with a strong acid

we have to find a solvent other than water in
which a weak base is going to behave as
strong one and give us a sharp and easy to
detect end point. To achieve this, we have to
find solvent more acidic than water, which
can be acetic acid.
(c) C6H5COOH + HF
4.35
4.36
Very hard.
4.37
-20.0kJ/mol
4.38
The lowest solvation energy is going to be

observed for the largest cation of the group.
4.39
CO2(g)
CO2(aq)
CO2(aq) + H2O(l)
(1)
H2CO3(aq)
M2SiO4(s) + 4H2CO3(aq)
Si(OH)4(aq) + 4HCO3(aq)
4.40
4.41
(a) Fe3+(aq) + 6H2O(l)

3H3O+
(2)
2M
2+
+
(3)
Fe(OH)3(s) +
CHAPTER 5
Self-tests
(b) 0.1547 M; pH= 1.6; neglected Fe3+

containing species are Fe(OH)2+ and
Fe(OH)2+.
S5.1
2 MnO4 (aq) + 5 Zn(s) + 16 H+(aq) 5

Zn2+(aq) + 2 Mn2+(aq) + 8 H2O(l)
With increasing charge density the attraction

between M2+ cation and partially negative O
atom in H2O is increasing. For the same
reason, the acidity of these aqua acids is
increasing showing that two trends correlate
closely.
S5.2
No.
S5.3
Fe2+ will be oxidized to Fe3+ by dichromate; a

side reaction with Cl should be expected.
S5.4
+ 1.25 V
S5.5
The aqueous solution of SO42 and H+ ions

precipitates as acid rain.
S5.6
No.
S5.7
Ru(II) preferentially. 17 orders of magnitude

decreased.
S5.8
+0.223 V.
S5.9
(a) Pu(IV) disproportionates to Pu(III) and

Pu(V) in aqueous solution.
(b) Pu(V) does not disproportionate into
Pu(VI) and Pu(IV).
4.42
[AlCl2(NCCH3)4] and Cl (sol)
4.43
Equation (b) is better in explaining the

observations described in the exercise.
4.44
The borderline does agree with describing S2

as a softer base than O2.
4.45
*SO2 + Cl
*SO2Cl
*SO2Cl + SOCl2
*SOCl2 + SO2Cl
SO2Cl
SO2 + Cl
*SOCl2 + SbCl5
*SOCl2.SbCl5
*SOCl2.SbCl5
SOCl2.SbCl5 + *SO2
SOCl2.SbCl5
S5.10
SOCl2 + SbCl5
4.46
The reasons for the difference in stability are

steric.
4.47
(a) Less than 1

(b) Greater than 1
(c) Greater than 1
4.48
(a) Fe(ClO4)3
(b) Mg(NO3)2
(c) Zn(NO3)2
12
S5.11

Mn2+(aq) is the most stable species present
because it has the most negative fG.
Therefore, Mn2+(aq) will be the final product
of the redox reaction when MnO4 is used as
an oxidizing agent in aqueous acid.
S5.12
Nitrate is a stronger oxidizing agent in acidic

solution than in basic solution.
S5.13
Fe(OH)3 is not stable and Fe2+(aq) will be the

predominant species.
S5.14
2000C or above.
(ii) Fe2+ will not reduce water.

(iii) Fe2+ will reduce O2 and in doing so will
be oxidized to Fe3+.
(iv) Disproportionation will not occur.
(b) Ru2+ will not oxidize or reduce water.
Ru2+ will reduce O2 and in doing so will be
oxidized to Ru3+. Ru2+ will disproportionate in
aqueous acid to Ru3+ and metallic ruthenium.
(c) HClO2 will oxidize water, will not reduce
water. HClO2 will reduce O2 and in doing so
will be oxidized to ClO3. HClO2 will
disproportionate in aqueous acid to ClO3 and
HClO.
Exercises
5.1
(d) Br2 will not oxidize or reduce water. Br2

will not reduce O2. Br2 will not
disproportionate in aqueous acid to Br and
HBrO.
2 NO(g) + O2(g) 2 NO2(g)

+2 -2
0
+4 -2
2Mn3+(aq) + 2H2O MnO2 + Mn2+ + 4H+(aq)

+3
+1 -2
+4 -2
+2
+1
5.5
LiCoO2(s) + C(s) LiC(s) + CoO2(s)

+1 +3 -2
0
+1-1
+4 -2
Ca(s) + H2(g)
0
0
5.2
5.6
2MnO4 (aq) + 5H2SO3(aq) + H+(aq)
2Mn2+(aq) +5HSO3 (aq) + 3H2O(l)
The potential decreases as the pH increases.
CaH2(s)
+2 -1
(a) S2O82, H2O2, PbO2 or MnO4 to oxidize

Cl to Cl2.
(b) Metallic manganese, metallic zinc, or
NH3OH+.
5.7
OxH equals +445 kJ mol1
(c) The reduced form of any couple with a

reduction potential less than 0.799 V, for
example Cu2+/Cu (+0.340 V).
5.8
(a)
(d) The reduced form of any couple with a

reduction potential less than 0.535 V for
example S/H2S (+0.144 V).
5.3
The change in temperature has the opposite

effect on one or both K values for the two
complexes.
(a) 4Cr2+(aq) + O2(g)

4Cr3+(aq) + 2H2O(l)
+ 4H+(aq)
1
4
and E = E 0.059V log

4
p (O2 )[ H ]
1
p(O2 )[ H ]4
In terms of pH:
E = E
0.059 V
log
1
4
p (O2 )[ H ]
0.059 V
4
log 1 4 pH
p (O )
E = 1.65 V
(b) 4Fe2+(aq) + O2(g)
4Fe3+(aq) + 2H2O(l)
+ 4H+(aq)
+0.81 V
E = 0.46 V
(b)
(c) No reaction.
Q = 1/[H+]6 and E = E RT/eF)ln(1/[H+]6)
(d) No reaction.
(e) 2Zn(s) + O2(g) + 4H+(aq) 2Zn2+(aq)
+2H2O(l)
E = 1.99 V
A competing reaction is:
Zn(s) + 2H+(aq) Zn2+(aq) + H2(g) (E =
0.763 V).
5.4
In terms of pH:
E = E (RT/eF)ln(1/[H+]6) = E (0.059
V/6)log([H+]6) = E (0.059 V/6)6pH =
E 0.059VpH.
(a) (i) Fe2+ will not oxidize water.
5.9
(a) Cl2 is thermodynamically susceptible to

disproportionation to Cl and ClO4 when it is
dissolved in aqueous base.
5.20
The oxidation of ClO is slow, so a solution of

Cl and ClO is formed when Cl2 is dissolved
in aqueous base.
(b) Cl2 will not disproportionate. Cl2 is
thermodynamically capable of oxidizing
water.
(c) ClO3 should disproportionate, the failure
of
it
to
exhibit
any
observable
disproportionation must be due to a kinetic
barrier.
5.10
Hg2+ and Hg22+ are both oxidizing agents; not

likely to be good reducing agents; Hg22+ is not
likely to undergo disproportionation
(a)
5N2O(aq) + 2OH(aq) 2NO3(aq) +
4N2 (g) + H2O(l)
5.21
(b)
Zn(s) +
(b) +0.55 V; solid Mn2O3

I3 (aq)
Zn (aq) + 3I (aq)
2+
(c) At pH 0, 0.387 V. At pH 14, SO42 would

again predominate. HSO4 is the predominant
sulfur species at pH 6.
(c)
3I2(s) + 5ClO3 (aq) + 3H2O(l) 6IO3
(aq) + 5Cl (aq) + 6H+(aq)
5.11
5.12
5.22
Air oxidation of iron is favored in acidic

solution: lower pH values would have more
positive Ecorr. Increased levels of carbon
dioxide and water generate carbonic acid that
lowers the pH of the medium, which makes
the corrosion process more favorable.
5.23
0.1 V
5.24
Any boundary between a soluble species and

an insoluble species will change as the
concentration of the soluble species changes.
The boundaries between the two soluble
species, and between the two insoluble
species, will not depend on the choice of
[Fe2+].
5.25
Above about 1600C. This is a rather high

temperature, achievable in an electric arc
furnace.
5.26
(a) Reduction potentials that couple transfer

of both electrons and protons decrease
(become more negative) as the pH is
increased (solution becomes more basic).
0.21 V
(a) Base
(b) Acid
(c) Base
(d) Acid or base, no difference.
5.13
+1.275V
5.14
+1.392 V
(a) +0.5 to + 0.6 V; Fe(OH)3
2ClO4 (aq) + 16H+(aq) + 14e Cl2 (g)

+ 8H2O(l)
5.15
+0.387 V
5.16
+0.98 V
5.17
4.37 1010
5.18
5.7 1038
5.19
The reduction potentials become less positive.
(b)
(b)
14
S6.2
(a) D3h.
(b) Td.
S6.3
d z 2 is A1
d x 2 y 2 is A1
dxy is A2
dyz is B2
dzx is B1
(c) In basic solutions P4 can disproportionate

to PH3 and H2PO2; 7.11058
5.27
5.28
(a) 0.716 V, 207.2 kJ mol1, 2.11036

(b) 0.726 V, 70.0 kJ mol1, 1.91012
S6.4
rH =1386.1 kJ mol1
S6.5
Not polar
S6.6
Yes; we would not be able to observe

optically active H2O2 under ordinary
conditions.
S6.7
Yes
S6.8
D2h character table, which is the Ag symmetry

type.
S6.9
S6.10
A1g + B1g are Raman active. Eu is IR active.

A1
S6.11
B2g
S6.12
5s and 4dz2 have A1g symmetry; the dx2-y2 has

B1g symmetry; and 5px and 5py have Eu
symmetry.
S6.13
For trans-SF4Cl2 we will observe two IR and

three Raman stretching absorptions, whereas
for SF6 only one IR
and
two
Raman
absorptions.
S6.14
A1g + B1g + B2g + A2u + B2u + 2Eu
S6.15
A1g + Eg +T1u.
rS = -0.282 kJ K mol
rG = 1302 kJ mol
E = 2.25 V
5.29
Thallium is more stable as Tl+ in aqueous

solutions; In3+ is more stable than In+ in
aqueous solutions.
Exercises
6.1
5.30
(a)
(i) Ru2+ should be less stable than Fe2+

(ii) Expected reaction is oxidation of Fe(s) to
Fe2+ by H+
N
H
See Section 5.10.
C3
(b)
CHAPTER 6
Self-tests
S6.1
N
H
(iii) 3.7 1062

5.31
Three S4 axes.
H
H
(c) 3px and 3py orbitals are doubly degenerate.
Cl
Cl
Cl
Cl
Cl
6.8
Cl
Cl
C4
6.2
Cl
Pt
Pt
12 vibrational modes; six Raman bands: 2A1

+ 3E + E
6.9
(a) CO2? i
(a) 5
(b) 1
(b) C2H2? i.
(c) BF3? neither.
6.10
(d) SO42? three different S4.
6.3
(a) NH2Cl? Cs
(b) BF3? The E modes are active in both IR

and Raman.
6.11
px = (1/2)(1 2 + 3 3) (= T2)
(c) SiF4? Td
py = (1/2)(1 2 3 + 3) (= T2)
pz = (1/2)(1 + 2 3 3) (= T2)
(e) SiFClBrI? C1.

(f) BrF4? D4h.
6.4
7; C6H3Cl3.
6.5
(a) An infinite number of mirror planes that

pass through both lobes and include the long
axis of the orbital. In addition, the long axis is
a Cn axis, where n can be any number from 1
to .
The MOs would be constructed from SALCs

with H1s and 2s and 2p atomic orbitals on C.
6.12
(c) In addition to the symmetry elements

possessed by a p orbital: (i) a center of
symmetry, (ii) a mirror plane that is
perpendicular to the C axis, (iii) an infinite
number of C2 axes that pass through the
center of the orbital and are perpendicular to
the C axis, and (iv) an S axis.
3) (=
(b) PF5?
(axial F atoms are 4 + 5)
(1/2)(4 + 5) (= A1)
(1/2)(4 5) (= A2)
(1/3)(1 + 2 + 3) (= A1)
(1/6)(21 2 3) and (1/2)(2 3) (=
E)
CHAPTER 7
Self-tests
S7.1
(a) C3v
(a) BF3?
(1/3)(1 + 2 + 3) (= A1)
(1/6)(21 2 3) and (1/2)(2
E)
(b) Center of symmetry, three mutually

perpendicular C2 axes, three mutually
perpendicular mirror planes of symmetry, two
planes that are rotated by 45 about the z axis
from the xz plane and the yz plane.
6.7
s = (1/2)(1 + 2 + 3 + 3) (= A1)
(b) CO32? D3h

(d) HCN? Cv.
6.6
(a) SF6? None.
(a) [PtCl2(OH2)2]
(b) 2
(b) [Cr(NCS)4(NH3)2]
(c) 3px and 3py orbitals are doubly degenerate.
(c) [Rh(2N-H2NCH2CH2NH2)]3+ abbreviated

to [Rh(en)3]3+
(a) D3h.
(b) 2.
(d) [MnBr (CO)5].

(e) [RhCl(PPh3)3].
16
S7.2
The hydrate isomers and linkage isomers of

the NO2 group. Also, [Cr(ONO)(H2O)5]NO2 .
H2O.
S7.3
The NMR data indicate that isomer A is the

trans isomer. Isomer B is the cis isomer.
S7.4
7.2
(a) [CoCl(NH3)5]Cl2
(b) [Fe(OH2)6](NO3)3
(c) cis-[RuCl2(en)2]
(d) [Cr(NH3)5-OHCr(NH3)5]Cl5
Non-superimposable
S7.5
(a) Chiral
7.3
(b) Not chiral

(c) Not chiral
S7.6
(c) bis(1,2diaminoethane)ethylenediamineoxalatocobalt(
III)
Kf2 = Kf1 0.42 = 1 105 0.42 = 4.2 104

Kf3 = Kf2 0.53 = 4.2 104 0.53 = 2.23
104
Kf4 = Kf3 0.56 = 2.23 104 0.56 = 1.25
104
Kf5 = Kf4 0.53 = 1.25 104 0.53 = 6.61
103
Kf6 = Kf5 0.42 = 6.61 103 0.42 = 2.77
103
(a) cis-tetraamminedichloridochromium(III)
(b) trans-diamminetetra(Nthiocyanato)chromate(III)
7.4
(a)
(b) For a tetrahedral complex there are no

isomers for MA2B2; however, for a squareplanar complex, there are two isomers, cis and
trans.
6 = 1 105 4.2 104 2.23 104 1.25

104 6.61 103 2.77 103 = 2.14 1025
7.5
Exercises
7.1
(a) Tetracyanidonickelate(II)
2-
NC
Ni
NC
CN
CN
7.6
(a)
(b) Tetrachlorocobaltate (II)
2-
Cl
(b) The trigonal prism is rare
Co
Cl
Cl
Cl
(c) Hexaamminemanganese(II)
7.7
A monodentate ligand can bond to a metal

atom only at a single atom, a bidentate ligand
can bond through two atoms, a quadridentate
ligand can bond through four atoms.
7.8
Linkage isomers can arise with ambidentate

ligands. An example is the thiocyanide anion
NCS.
NCSM (thiocyanato-S)
(thiocyanato-N)
7.9
SCNM
[Pd(gly)2] has two isomers
(a) Bisdimethylphosphino ethane (dmpe):

bidentate, chelating ligand that could also be a
bridging ligand
(b) 2,2-Bipyridine (bpy) is a bidentate,
chelating ligand
(c) Pyrazine is a monodentate ligand. The
ligand can only bond to one metal; it can,
however, bridge two metals.
7.14
[IrCl3(PEt3)2]:
(d) Diethylenetriamine (dien) can be a

tridentate ligand, can also act as a bidentate
ligand and could be a bridging ligand.
(e) Tetraazacyclododecane ligand could be a
tetradentate, macrocyclic ligand. This ligand
could be bidentate and bridging.
7.10
[Ru(bpy)3]2+:
[CoCl2(en)(NH3)2]+:
7.11
Ionization isomers.
7.12
[CoBrClI(OH2)]
[W(CO)4(py)2]
7.13
[PdBrCl(PEt3)2] has two isomers:
7.15
Including optical isomers, 15 isomers are

possible.
7.16
(a) All octahedral tris(bidentate ligand)

complexes are chiral.
[IrHCO(PR3)2] has two isomers
18
Self-tests
(b) The five-membered chelate ring formed

by the 1,2-diaminoethane ligand is not planar,
so, strictly speaking, the complex is not
planar. It can exist as two enantiomers,
depending on the conformation of the chelate
ring.
However,
the
conformational
interconversion of the carbon backbone is
extremely rapid, so the two enantiomers
cannot be separated.
S8.1
XRD pattern for CrO2 will show identical

reflections to those of rutile TiO2 but shifted
to slightly higher diffraction angles.
S8.2
Technique would require X-ray sources of

higher intensity which are obtained using
synchrotron radiation.
S8.3
TiO2 particles absorb the ultraviolet radiation.
S8.4
Linear molecule, 4 total vibrational modes.

modes cannot be both IR and Raman active.
(a) Two different chemical shifts in 19F NMR:
one for Fa and one for Fb. The intensity of
these signals should have relative ratios 1 : 4.
The Fa resonance would be split into five
equally spaced lines by four basal F atoms
with line intensities 1 : 4 : 6 : 4 : 1 according
to Pascals triangle. The signal due to Fb
atoms will be split into a doublet by one Fa
with line intensities 1 : 1.
S8.5
(c) Not chiral; this complex has two mirror

planes.
(d) Octahedral
complex; chiral;
tris
(bidentate
ligand)
(b) The hydride resonance couples to three

nuclei that are 100% abundant and all of
which have I = . The first doublet is
observed due to the coupling between hydride
and rhodium. Since the two atoms are directly
bonded, the coupling constant is going to be
large. Then, through coupling with P atom
trans to the hydride, each line of the first
doublet is going to be split into a doublet
creating doublet of doublets. Finally, due to
the coupling to the P atom cis to the hydride,
every line of the doublet of doublets is going
to be further split into a doublet giving the
observed doublet of doublets of doublets
pattern. Since the three coupling constants are
different, the effect is to split the signal into a
doublet of doublet of doublets, thus
generating eight lines in the NMR of equal
intensity.
(e) Mirror plane through the metal; not chiral.

(f) Two mirror planes; not chrial.
7.17
isomer
7.18
7.19
7.20
The very stable square planar complex ion

[Cu(NH3)4]2+ is formed, and the addition of
the fifth NH3 ligand is very difficult. The
equilibrium for this step is actually shifted to
the left (toward reactants). This results in Kf5
< 1 with a negative log value.
S8.6
Three signals in 29Si-MASNMR of this

compound: one for SiO44 (with intensity 1)
and two for Si3O108 (with intensities 1 : 2 for
central and end Si atoms).
S8.7
14% of the naturally occurring tungsten is

183
W, which has I = . Owing to this spin, the
signal is split into two lines. This will be
superimposed on a nonsplit signal that arises
from the 86% of tungsten that does not have a
spin.
S8.8
Below 0.2 mm s1.
The values for the 1,2-diaminoethane reaction

are substantially higher, indicating more
favourable complex formation, and this can
be attributed to the chelate effect.
CHAPTER 8
S8.9
S8.10
S8.11
The energy of XAS K-edge is expected to

gradually increase with an increase in
oxidation state of sulfur from S(-II) in S2- to
S(VI) in SO42.
35
diffraction and neutron diffraction with

measurement of C-H bonds.
8.6
79
The lightest isotopomer of ClBr3 is Cl Br3

at 272 u and the heaviest is 37Cl81Br3 at 280 u.
Three other molecular masses are possible,
giving rise to a total of five peaks in the mass
spectrum. The differences in the relative
intensities of these peaks are a consequence of
the differences in the percent abundance for
each isotope.
Because the atomic masses of 5d metals are
significantly higher than the atomic masses of
3d metals, the hydrogen percentages will be
less accurate as they correspond to smaller
fractions of the overall molecular masses of
the compounds.
S8.12
Because the three elements (Mg, Al, and Si)

are next to each other in the periodic table;
thus we can expect some peak overlapping.
S8.13
2:5.
S8.14
Should see one reversible peak in the cyclic

voltamograms in this pH range.
8.7
Powder X-ray diffraction.
8.2
0.5 m 0.5 m 0.5 m; 500m 500m

500m.
8.3
Because a hydrogen atom has only one

electron it lacks suffient electron density
around the nucleus for their location to be
determined with a high accuracy. However
both Se and O have a sufficient number of
electrons for accurate determination of their
locations in the crystal structure. Hydrogen
bonding can also further reduce the accuracy.
8.4
180 pm; suitable for diffraction studies.
8.5
The X-ray analysis always underestimates

element-hydrogen bond lengths because of
very low electron density at H nucleus. This is
not an issue with neutron diffraction because
neutrons will be scattered by hydrogen
nucleus giving a very accurate location.
The CH bond is of low polarity and the
bonding pair is more equally distributed
between the two nuclei so we would expect to
see less discrepancy between X-ray
2404cm1
8.8
The smaller effective mass of the oscillator

for CN causes the molecule to have the
higher stretching frequency because they are
inversely proportional. The bond order for
NO is 2.5, and N is heavier than C, hence CO
has a higher stretching frequency than NO.
8.9
In the region of 1800 cm1; Raman.
8.10
The 19F NMR of 77SeF4 would consist of two

doublet of triplets with relative intensity 1 : 1.
The 77Se NMR would consist of triplet of
triplets.
8.11
XeF5has a pentagonal planar molecular

geometry, so all five of the F atoms are
magnetically equivalent and thus the molecule
shows a single 19F resonance. Approximately
25% of the Xe is present as 129Xe, which has I
= 1/2, and in this case the 19F resonance is
split into a doublet. The final result is a
composite: two lines each of 12.5% intensity
from the 19F coupled to the 129Xe, and one line
of 75% intensity for the remainder.
8.12
The structure is fluxional at room temperature

and the CO ligands are exchanging bridging
and terminal position sufficiently fast so that
an average signal is seen and only one peak is
observed.
8.13
If the 31P MASNMR of PCl5 shows two

resonances, one of which is similar to the one
found in the 31P MASNMR of the salt, that
means solid PCl5 contains PCl6 anions. The
second resonance must belong to some other
P-containing species in PCl5, which in this
case is the cation PCl4+.
8.14
1.94, 1.74, and 1.56
8.15
EPR
8.16
Room temperature: molecular tumbling is

fast removing effect of g-value anisotropy;
expect derivative-type spectrum, possibly
exhibiting hyperfine structure that is centred
at the average g value
Exercises
8.1
N(SiH3)3 is planar and thus N is at the center

of the molecule and does not move in the
symmetric stretch. N(CH3)3 is pyramidal and
the NC symmetric stretch involves
displacement of N.
20
Frozen solution: g-value anisotropy can be

observed, averaging from molecular tumbling
does not apply.
8.17
Below +0.2 mm s1.
8.18
Mssbauer spectroscopy
8.19
Because there is no isotope with this mass

number. Compounds that contain silver will
have two mass peaks flanking this average
mass.
8.20
Major peaks would be at 258, 230, 200, 186,

174
8.21
n=7
8.22
The complex undergoes a reversible oneelectron reduction with a reduction potential

of 0.21 V. Above 0.720 V the complex is
oxidized to a species that undergoes a further
chemical reaction, and thus is not re-reduced.
This step is not reversible.
8.23
The regular crystalline periodicity is required

for Bragg diffraction in order to have
constructive interference of the X-rays that
leads to observable peaks in the XRD pattern.
Glass, however, is a network covalent solid
with no long-range periodicity or order; as
such it will not diffract X-rays.
The
observation of X-ray diffraction pattern after
the glass sample was heated indicates that at
least a part of the sample crystallized. The
fact that the exothermic event was observed
suggests either change of phase or chemical
reaction that yielded a crystalline product.
8.24
For each mole of Co there are three moles of

acac
8.25
(a) Voltamogram would not be reversible, and

would be unsymmetrical.
(b) One peak in voltamogram with twice the
height of single peaks shown in Figure
8.53(a).
S9.3
Owing to oxygens strong tendency to form

strong double bonds, it is very unlikely that
longer-chain polyoxygen anions would exist.
Sulfur is much less likely to form bonds and
therefore more likely to generate catenated
polysulfide anions.
S9.4
It is evident from the values that as we move

down the group, steric crowding of the
fluorines is minimized.
S9.5
We would have to know the products formed

upon decomposition and thermodynamic data
for the product.
S9.6
A tetrahedral geometry; OsO4.
Exercises
9.1
(a) Ba, +2; (b) As, +5; (c) P, +5; (d) Cl, +7;
(e) Ti, +4; (f) Cr, +6
9.2
The alkaline earth metals or Group 2

elements.
9.3
Elements in Group 15.
9.4
Chromium group of Group 6.
9.5
The second ionization energy of sodium is

4562 kJ mol-1 and is responsible for the fact
that the compound does not exist.
9.6
Beyond Group 15 we see inert pair effect

influencing the favoured +3 oxidation state
for elements such as Bi and Sb and we also
find stable +5 oxidation states for the
halogens in Group 17. The inert pair effect
would manifest itself the most for Po, the
heaviest member of the Group 16.
9.7
Metallic character and ionic radii decrease

across a period and down a group. Ionization
energy increases across a period and
decreases down a group.
9.8
(a) Be
(b) C
(c) Mn
9.9
(a) Na
(b) O
9.10
(a) Saline
(b) Molecular
(c) Molecular
(d) Saline
CHAPTER 9
Self-tests
S9.1
S9.2
Cd and Pb will be found as sulfides.

Rb and Sr can be found in aluminosilicate
minerals.
Cr and Pd can be found in both oxides and
sulfides.
3+
V (aq) and/or VO
2+
(e) Metallic hydride

9.11
(e) H bonded to an oxygen atom = +1. H

bonded to the phosphorus atom? If they are
assigned an oxidation number of +1, and O =
2, then P = +1.
(a) Basic
(b) Acidic
(c) Amphoteric
(d) Acidic
(e) Amphoteric
(f) Basic
10.3
9.12
CrF2 < CrF3 < CrF6
(iii) CO(g) + H2O CO2(g) + H2 (g)
9.13
(a) MgCO3 magnesite

(b) Al2O3 bauxite
(c) PbS galena
(d) Magnetite Fe3O4
(i) CH4(g) + H2O CO(g) + 3H2(g) (1000C)

(ii) C(s) + H2O CO(g) + H2(g) (1000C)
(iv) Zn(s) + 2HCl(aq) Zn2+(aq) + 2Cl(aq) +

H2(g)
(v) NaH(s) + H2O Na+(aq) + OH(aq) + H2(g)
9.14
V (vanadium)
9.15
fH = 1397 kJ mol-1.
10.4
(a) Your result should look like Figure 10.2.

(b) Your result should reflect the data shown
in Table 10.1.
CHAPTER 10
(c) Those in Group 13 are electron-deficient,

those in Group 14 are electron-precise, and
those in Groups 15 through 17 are electronrich.
Self-tests
S10.1
CH4, the strongest Bronsted acid.

would be the best hydride donor.
S10.2
(a) Ca(s) + H2(g) CaH2(s).
GeH4
10.5
It most likely would be a gas at room

temperature. We can estimate a boiling point
of about 50C or below for H2O without Hbonding. It would be expected that ice would
be denser than water.
10.6
OHS because the electrostatic interaction

between the more positive H in H2O and a
lone electron pair on S is stronger.
10.7
(a) Barium hydride. It is a saline hydride.

(b) Silane. It is an electron-precise molecular
hydride.
(c) Ammonia. It is an electron-rich molecular
hydride.
(d) Arsine. It is also an electron-rich
molecular hydride.
(b) NH3(g) + BF3(g) H3NBF3(g).

(c) LiOH(s) + H2(g) NR.
1
S10.3
HG(Pd) = 227 kJ mol
S10.4
Et3SnH + 2 Na 2Na+ Et3Sn + H2

2Na+ Et3Sn + CH3Br MeEt3Sn + NaBr
Exercises
10.1
Hydrogen has one valence electron like the

group 1 metals and is stable as H+, especially
in aqueous media.
Hydrogen can fill its 1s orbital and make a
hydride H. The halogens are diatomic gases
just like hydrogen, but chemically it fits well
in both group 1 and group 17.
10.2
(e) Palladium hydride. It is a metallic hydride.

(f) Hydrogen iodide. It is an electron-rich
molecular hydride.
10.8
(a) Barium hydride

BaH2(s) + 2H2O(l) 2H2(g) + Ba(OH)2(s)
There are no compelling reasons for hydrogen

to be placed in group 14.
Net reaction: 2H + 2H+ 2H2

(b) Hydrogen iodide
(a) H = +1, S = 2.
(b) H = 1, K = +1.
HI + H2O I + H3O+
(c) PdH0.9
(c) H = 1, Re = +7.
(d) NH3
(d) H = +1, O = 2, S = +6.
NH3(g) + BMe3(g) H3NBMe3(g)
22
10.9
BaH2 and PdH0.9 are solids; none is a liquid;

and SiH4, NH3, AsH3, and HI are gases. Only
PdH0.9 is likely to be a good electrical
conductor.
10.10
All hydrides of the Group 1 metals have the

rock-salt structure. This means that in all
Group 1 hydrides H has a coordination
number 6 and is surrounded by cations in an
octahedral geometry. The sizes of cations
increase down the group (i.e., r(Li+) < r(Na+)
< r(K+)< r(Cs+)); as a consequence both the
sizes of octahedral holes and the apparent
radius of H will increase in the same
direction.
No clear trend for Group 2 hydrides. Whereas
CaH2 and BaH2 adopt the fluorite structure,
MgH2 has a rutile structure.
10.11
Reaction (b) will produce 100% HD and no

H2 or D2.
10.12
(CH3)3SnH, the tin compound is the most

likely to undergo radical reactions with alkyl
halides.
10.13
because it is an unsymmetrical H bond,

whereas the surface for the bifluoride ion has
a single minimum. The second difference is
that the surface for the H2O, Cl system is not
symmetric because the proton is bonded to
two different atoms whereas the surface for
bifluoride ion is symmetric.
10.18
H2 is an oxidizing agent in this case:

2Na(s) + H2(g) 2NaH(s)
H2 as a reducing agent:
2H2(g) + O2(g) 2H2O (l or g)
10.19
Overall an oxidative addition.
10.20
(a) Incorrect: some p-block hydrides are not

thermodynamically stable
(b) Incorrect: the isotope of mass number 3 is
radioactive, not of mass number 2.
B (2.04), Al (1.61), and Ga (1.81); AlH4 is

the strongest reducing agent.
(c) Incorrect: not all hydrides of Group 2 are

ionic; H is not compact and as a consequence
it does not have a well-defined radius.
(d) Incorrect: not all structures can be
predicted by VSEPR theory
(e) Incorrect: while NaBH4 is a common
reagent, it does not have greater hydridic
character (hydridicity) than a saline hydride
such as NaH.
(f) Incorrect: boron hydrides are electrondeficient because they lack the electrons
required to fill the bonding and non-bonding
molecular orbitals.
GaH4 + 4HCl(aq) GaCl4 (aq) + 4H2(g)

10.14
The period 2 hydrides, except for BeH2 and

B2H6, are all exergonic. Their period 3
homologues either are much less exergonic or
are endergonic.
Period 2 compounds tend to be weaker
Brnsted acids and stronger Brnsted bases
than their period 3 homologues.
The bond angles in period 2 hydrogen
compounds reflect a greater degree of sp3hybridization than the homologous period 3
compounds.
As a consequence of hydrogen bonding, the
boiling points of HF, H2O, and NH3 are all
higher than their respective period 3
homologues.
10.15
It is expected that it would be very difficult to

prepare a sample of BiH3. The current method
for the synthesis of bismuthine, BiH3, is by
the redistribution of methylbismuthine,
BiH2Me.
10.16
Clathrate hydrate. Clathrate hydrate consists

of cages of water molecules found in ice, all
hydrogen bonded together, each surrounding
a single krypton atom.
10.17
The first difference is that the surface for the

H2O, Cl system has a double minimum
Dihydrogen can behave both as a reducing

and oxidising agent because hydrogen can
have two oxidation states in its compounds:
+1 and 1.
10.21
2074cm1
10.22

Hydration enthalpy for Cs+ (710 kJ mol1) is
about the lattice enthalpy for CsF, and it is
expected that CsF should be more soluble
than LiF.
S11.3
We would expect that, on warming, NaO3

would decompose first and CsO3 last.
S11.4
M2CO3(s)
10.23
M2O(s) + CO2(g)
(a)
2M+(g) + CO32(g)
S11.5
2M+(g) +
O2(g) + CO2(g)
KNO3 decomposes in two steps at two

different temperatures.
KNO3(s) KNO2(s) + 1/2O2(g)
2KNO2(s) K2O(s) + 2NO2(g) + 1/2O2(g)
LiNO3 decomposes in one step.
(b) The [H He] bond should be polarized with a

partial negative charge on He and a partial positive
charge on H.
(c)
Most common solvents (such as water,

alcohols, and alike) would easily deprotonate
this species. Other surfaces would also
heterolytically cleave this species into H+ and
He.
LiNO3(s) 1/2 Li2O(s) + NO2(g) + 1/4O2(g)

S11.6
Exercises
11.1
CHAPTER 11
(a) The observed major peak in the Bragg

pattern would shift to lower two theta values
upon heating through the phase transition
according to the Bragg relation
11.2
The caesium-bearing silicate minerals are

digested with sulfuric acid and Cs and Al are
precipitated as alum. The simple sulfate,
obtained after roasting with carbon, is then
converted to chloride using anion exchange.
The isolated CsCl is then reduced with Ca or
Ba.
11.3
LiH: NaCl structure type

NaH: NaCl structure type
KH: CsCl structure type
RbH: CsCl structure type
CsH: CsCl structure type
FrH: CsCl structure type
(b) d = 2(196 + 220)/31/2 pm = 481 pm; data

are consistent with the prediction
S11.2
(a) They have one valence electron in the ns1

subshell, and relatively low first ionization
energies.
(b) They are large, electropositive metals and
have little tendency to act as Lewis acids.
Self-tests
S11.1
Two peaks in the NMR spectrum at low

temperature. Only one resonance in the NMR
at high temperature.
966.8kJ mol1 ; 713.9kJ mol1

LiF is insoluble, because the hydration
enthalpy for Li+ (956 kJ mol1) is insufficient
to compensate for the lattice enthalpy of LiF.
11.4
24

fH /(kJ
mol1)
fH
/(kJ
mol1)
LiF
625
LiCl
470
NaF
535
NaCl
411
KF
564
KCl
466
RbF
548
RbCl
458
CsF
537
CsCl
456
Your plot should look like a part of Figure
11.6. Fluoride is a hard Lewis base and will
form
strong complexes with hard Lewis
acids. The
trends reverse for the
chloride ion.
4
11.5
(a) Edta is expected to give a more stable

complex with Cs+ compared to acetate.
(b) K+ is more likely to form a complex with
the cryptate ligand C2.2.2 than Li+.
11.6
(i) A = LiOH; B = Li2O; C = none; D =

LiNH2
(ii) A = CsOH; B = CsO2; = Cs2O; D =
CsNH2
11.7
Solubility is lower if cation and anion have

similar radii.
11.8
FrI, FrBr
11.9
The difference in lattice energy between metal

carbonate and metal oxide decreases down the
group, which results in increased stability.
11.10
11.11
See Figure 11.4 and Figure 11.5. Na+ is sixcoordinate, whereas Cs+ is eight-coordinate.
The compounds have different structures
because Na+ is smaller than Cs+ resulting in a
different r+/r for the same anion.
S12.4
(i) Anhydrous BeSO4 with loss of all four

water molecules.
(ii) SrO and BeO with elimination of two
equivalents of H2O.
S12.5
MgF2 is 2945 kJ mol1l; MgBr2 is 2360 kJ

mol1 and MgI2 is 2193 kJ mol1.
Lattice enthalpies decrease with an increase in
the ionic radius of the halide anion; can
expect the increase in solubility in the same
direction.
Exercises
12.1
Be2+ has large polarizing power and a high

charge density due to its small radius. Also,
beryllium has the highest electronegativity
among Group 2 elements. Descending Group
2 the atoms of elements increase in size, they
are more electropositive
12.2
Because of the diagonal relationship between

Be and Al.
12.3
Metallic bond.
12.4
A = Ba(OH)2
B = BaCO3
C = BaC2
D = BaCl2
12.5
BeF2 adopts SiO2-like arrangement which

forms vitreous matter when melted because of
the strength of the Si-O bonds.
12.6
BeH2: 18.2%
MgH2: 7.6%
(a) Li(CH3) + LiBr
BeH2 cannot be prepared directly from the

elements
(b) Mg(C2H5)Br + LiCl

12.7
Group 1 hydroxides are more soluble than

group 2 hydroxides, and therefore have higher
OH concentrations.
CHAPTER 12
12.8
MgSeO4
Self-tests
12.9
Ra2+ could be selectively precipitated by

addition of a large anion.
12.10
Anhydrous Mg and Ca sulphates; because of

the higher affinity of Mg and Ca sulphates for
water.
12.11
ZnS-like structure; NaCl-like structure.
12.12
Covalent; ionic; ionic.
12.13
C2H5MgBr will be tetrahedral with two

molecules of solvent coordinated to the
(c) LiC6H5 + C2H6
S12.1
S12.2
S12.3
BeCl2 is covalent with a polymeric, molecular

structure; BaCl2 is ionic and likely to adopt a
CaF2-type ionic structure.
Calcium oxide and calcium peroxide are 3465
kJ mol1 and 3040 kJ mol1. Trend is
confirmed.
Close to ZnS-like structure.
magnesium. The bulky organic group in

2,4,6-(CH3)3C6H2MgBr leads to a
coordination number of two.
12.14
S13.9
(a) LiCl + (C2H5)MgCl or 2LiCl + Mg(C2H5)2
1,7-B10C2H10Li2 + 2Si(CH3)2Cl2 1,7 B10C2H10(Si(CH3)2 + 2LiCl
(b) Mg(C2H5)2 + Hg
(c) C2H5MgCl + Hg
1,2-B10C2H12
1,7-B10C2H12 (90%) +
1,12-B10C2H12 (10%)
S13.10 (a) (Me)2SAlCl3 + GaBr3 Me2SGaBr3 +

AlCl3
(b) 2 TlCl3 + H2CO + H2O 2TlCl +
CO2 + 4 H+ + 4 Cl
CHAPTER 13
Self-tests
Exercises
S13.1
4 lines of equal intensity (1 : 1 : 1 : 1).
13.1
B2O3 + 3Mg 2B + 3MgO
S13.2
B2H6 + 2R2O 2H3B OR2
13.2
(a) Covalent.
H3B OR2 + H2C=CHCH3 H2BCH2

CH2CH3 + OR2
(b) In the solid state, a layered structure. At

melting point, dimeric form, Al2Cl6, with 2c,
2e bridging bonds.
and:
(c) Electron-deficient dimer with 3c, 2e

bridging bonds.
B2H6 + 2THF 2H3B THF

13.3
H3B THF + NH4Cl H2 + H2B NH2 +
HCl
S13.3
(c) BBr3(l) + F3BN(CH3)3(s) BF3(g) +

Br3BN(CH3)3(s)
Heat
3[CH3NH3]Cl + 3BCl3
9HCl +
Cl3BNCH3
(a) Seven electron pairs per cluster structure;

arachno
BCl3
(BCl3 > BF3)
NR
13.4
Na[TlBr4]; Na+ is the cation and [TlBr4] is

the anion.
13.5
A = B2H6
B = B(OH)3
C = B2O3
13.6
No; B2H6 + 3 O2 B2O3 + 3 H2O

3 O2 2B(OH)3
13.7
(a) 3
(b) 2
13.8
(a) BH3 + 3(CH3)2C=CH2

B[CH2CH(CH3)2]3
(b) BH3 + 3CHCH B(CH=CH2)3
13.9
73,172 kJ ; Diborane is extremely toxic and
Cl3BNCH3 + 3CH3MgBr
(CH3)3B3N3(CH3)3 + 3Mg(Br, Cl)2
S13.5
BCl3 > BF3 > AlCl3

(a) BF3N(CH3)3 +
BCl3N(CH3)3 + BF3
(b) BH3CO + BBr3
(a) BCl3(g) + 3 EtOH(l) B(OEt)3(l) + 3

HCl(g)
(b) BCl3(g) + py(l) Cl3B py(s)
S13.4
H < 0
or B2H6 +
the boron containing product of combustion is

a solid, B2O3.
13.10
(b) Nido structure type.
S13.6
B5H9; the cluster is nido and is based on

closo-B6 octahedral cage.
S13.7
[B10H11 (AlCH3)]
S13.8
Closo structure (octahedral).
2BCl3 + 2Hg B2Cl4 +

2HgCl2
electron impact
B2Cl4 + 4AgF B2F4 + 4AgCl

B2F4 + C2H4 F2BH2CH2BF2
26
13.11

(a) NaBH4 + 4HCl(ether sol.) BCl3 +
NaCl(s) + 4H2(g)
(5) 2Na2[B9C2H11] + FeCl2 2NaCl +

Na2[Fe(B9C2H11)2]
(b) [HN(C2H5)3]Cl + NaBH4 H2 +

H3BN(C2H5)3 + NaCl
13.12
13.13
Closo; corresponds to the icosahedral

structure with one BH unit replaced with an
NH unit.
13.22
(a) Both of these substances have layered

structures.
In general, boron hydrides with more

hydrogen atoms are thermally unstable. We
expect B6H10 to be stable relative to B6H12.
13.14
14 skeleton electrons in total.
13.15
(a) 2B5H9(l)
9H2O(l)
12O2(g)
5B2O3(s)
(b) Graphite
unreactive.
13.23
boron
nitride
is
(a) 3 [PhNH3]Cl + 3 BCl3 Ph3N3B3Cl3 + 9

HCl
(b) 3 MeNH3+Cl + 3 BCl3 Me3N3B3Cl3 +
9 HCl
(a) Nido
(b) 12 electron pairs
Me3N3B3Cl3 + 3 LiH Me3N3B3H3 + 3 LiCl
(c) Valence electrons for B10H14 is

(103)+(141) = 44. Ten 2c-2e BH bonds,
which account for 20 of the total valence
electrons; the number of cluster electrons is
the remainder of 44-20=24.
13.17
reacts,
(c) The large HOMOLUMO gap in BN

means it is more difficult to remove an
electron from it than from the HOMO of
graphite.
(b) The boron-containing product of

combustion is a solid, B2O3; If an internal
combustion engine is used, the solid will
eventually coat the internal surfaces,
increasing friction, and will clog the exhaust
valves.
13.16
13.21
(a) Arachno-type structure

(b) Nido-type structure
13.24
B2H6 < B5H9 < B10H14
13.18
B6H12; cluster is arachno and is based on

closo-B8 structure cage.
13.25
All of the structures in the given series are

dimeric and have BHB bridges.
13.19
Tetraborane(10); arachno
13.26
(a) 11B NMR spectrum of BH3CO would

show one quartet resonance.
Pentaborane(9); nido
1,2-closo-dodecaborane(12); closo
13.20
(1) B10H14 + 2SEt2 B10H12(SEt2)2 + H2

(2) B10H12(SEt2)2 + C2H2 B10C2H12 +
2SEt2 + H2
(3) 2 B10C2H12 + 2EtO + 4EtOH 2
B9C2H12 + 2B(OEt)3 + 2H2
(4) Na[B9C2H12] + NaH Na2[B9C2H11]
+ H2
(b) The 11B NMR should show two signals in

relative intensity 1:5 both of which should be
doublets.
13.27
(a) Incorrect; only boron has some nonmetallic properties

(b) Incorrect; hardness decreases down the
group
(c) Partially correct; Lewis acidity of BX3

does increase from F to Br, it is not due to
stronger BBr bonding but the opposite.
(d) Incorrect; arachno boron hydrides are less
stable than nido-borohydrides and skeletal
electron count is n+3.
(e) Correct.
(f) Partially incorrect; layered BN and
graphite have similar structures but layered
BN has a very large HOMO-LUMO gap and
is an insulator.
CHAPTER 14
(c) Silicon tetrahalides are mild Lewis acids

whereas analogous carbon compounds are not
Lewis acidic.
14.3
14.4
The bond enthalpy of a CF bond is higher

than the bond enthalpy of a CH bond,
making CF bond more difficult to break.
Further, the combustion produces not only
CO2
but
H2O
as
well
that
is
thermodynamically a very stable compound.
14.5
(a) Cation:
Self-tests
S14.1
(a) Results in a material with a higher

conductivity.
(b) Bromine can remove electrons from the symmetry HOMOs of graphite. This also
results in a material with a higher
conductivity.
S14.2
Anion:
CO(g) + 2MnO2(s) 13CO2(g) + Mn2O3(s)

13
2Li(s) + D2 2LiD(s)
S14.4
CH3
S14.3
13
CH3
H3C
CH4: fH= 61kJ mol1

SiH4: fH= +39 kJ mol
H3C
F
Si
CO2(g) + LiD(et) Li+D13CO2(et)
Decrease in bond orderfrom 3 to 2.5; CC

bond length in C2 would be longer than in
C22.
Exercises
14.1
(b) In the structure of the anion there are two

different fluorine environments: axial and
equatorial.
(a) Incorrect; tin and lead are metallic

(b) Correct
(c) Partially correct but CS2 is softer than CO2
(d) Incorrect; zeolites are framework
alumosilicates and do contain metal cations.
14.6
(e) Correct
14.2
(a) Diamond with silicon both have

diamond-type structure which results in a
wide energy gap between filled and empty
bandsa gap that is, however, smaller for
Si(diamond) than for C(diamond). As a
consequence, C(diamond) is generally
considered an insulator, whereas Si(diamond)
is a semiconductor.
(b) Striking differences between C and the
rest of the elements of the Group 14 are the
properties and structures of the oxides.
Si
O
O
8-
8-
Si
Si
O
O
Si
O
Charge is -8
14.7
Spectrum would show a single environment

for 119Sn (I = ) nucleus in a tetrahedral
geometry, split into 13 lines.
28
14.8
Spectrum would show a doublet peak for 1H (

I = ) nucleus.
14.9
110 kJ mol1, 86 kJ mol1
14.10
A = SiCl4
B = SiRCl3
C = RSi(OH)3
D = RSiOSiR
E = SiR4
F = SiO2
14.11
14.17
Na4SiO4(aq) + 4HCl(aq) 4NaCl(aq) +

SiO2(s) + 2H2O(l)
14.18
The [SiO32]n ions in jadeite are a linear

polymer of SiO4 tetrahedra; the twodimensional aluminosilicate layers in
kaolinite represent another way of connecting
SiO4 tetrahedra.
(a) +4 is the most stable oxidation state for

the lighter elements, but +2 is the most stable
oxidation state for Pb; Pb displays the inertpair effect.
14.19
(a) 48
(b) The polyhedron at the centre has six
octagonal faces and eight smaller square
faces.
(b) Sn2+ + PbO2 + 4 H+ Sn4+ + Pb2+ + 2

H 2O
14.20
The phyllosilicates are characterised with

two-dimensional sheets composed of vertexsharing SiO4-tetrahedra; each SiO4tetrahedron is connected to three
neighbouring SiO4-tetrahedra via bridging O
atoms. These sheets are negatively charged
and held together via electrostatic interactions
with cations sandwiched between the sheets.
Because of this layered structure, both
pyrophyllite and muscovite have excellent
cleavage parallel to the layers (just like
graphite).
14.21
Glasses (many uses), activated carbon

(adsorbent), carbon fibres (can be added to
plastic to increase strength), carbon black
(pigment).
14.22
Ca2+ cations are too large for the octahedral

holes, and it is more likely that they will be
found in larger holes with coordination
number 12.
2 Sn2+ + O2 + 4 H+ 2 Sn4+ + 2 H2O.

14.12
+1.31 V; 1.08 V
14.13
Silicon:
SiO2(s) + C(s) Si(s) + CO2(g) rH < 0
(reaction takes place in an electric arc
furnace)
Germanium:
GeO2(s) + 2 H2(g) Ge(s) + 2 H2O(g)
rH < 0
or
GeO2(s) + 2CO(g) Ge(s) + 2CO2(g)
14.14
14.15
K2CO3(aq) + 2HCl(aq) 2KCl(aq) + CO2(g)

+ H2O(l)
(a) Decrease in band gap energy from carbon

(diamond) to grey tin.
(b) Increase.
See Figure 14.12 and Section 14.13.
CHAPTER 15
14.16
(a) Formed by heating graphite with

potassium vapour or by treating graphite with
a solution of potassium in liquid ammonia. It
has a layered structure of alternating sp2
carbon atoms and potassium ions and is an
example of a saline carbide.
(b) 2 ways of preparing calcium carbide, both
require temperatures 2000C. The first is
the direct reaction of the elements, and the
second is the reaction of calcium oxide with
carbon. Calcium carbide contains discrete C22
ions with carboncarbon triple bonds. This
carbide is ionic.
(c) A solution of C60, in a high boiling point
solvent (such as toluene), can be treated with
elemental potassium to form this compound.
It is also ionic, and it contains discrete K+ ions
and C603 ions.
Self-tests
S15.1
(a) Yes.
(b) Triple bond between two N atoms; means
that it is unreactive, a gas, and diamagnetic.
S15.2
Dimehylhydrazine ignites spontaneously and

produces less CO2.
S15.3
Sulphur.
S15.4
(a) Unlike NO2, the colourless NO is rapidly

oxidized by O2 in air producing NO2. N2O is
unreactive for purely kinetic reasons.
(b)
NH3 + ClO + H+ [H3NCl-O] + H+
H2NCl + H2O
(c) 2H3PO4(l) + 3CaCl2(aq)
H2NCl + NH3 H2NNH2 + HCl

Both can be thought of as redox reactions.
S15.5
There are (30.4 cm3)/(7.6 cm3) = 4 strongly

acidic OH groups per molecule.
Ca3(PO4)2(s) + 6HCl(aq)
15.9
(a)
4NH3(aq) + 7O2(g) 6H2O(g) + 4NO2(g)
High temperature
3NO2(aq) + H2O(l) 2HNO3(aq) + NO(g)
Exercises
15.1
Type of
element
N
P
As
Sb
Bi
nonmetal
nonmetal
nonmetal
metalloid
metalloid
15.2
Diatomic
gas?
yes
no
no
no
no
Achieves
maximum
oxidation state?
yes
yes
yes
yes
yes
(b)
Displays
inert pair
effect?
no
no
no
no
yes
2NO2(aq) + 2OH(aq)
NO2(aq) + NO3(aq) + H2O(l)
(c) Cold aqueous acidic solution
NO2(aq) + 2HSO3(aq) + H2O(l)
NH3OH+(aq) + 2SO42(aq)
(d) At elevated temperatures:
3NaNH2(l) + NaNO3
(a)
NaN3 + 3NaOH + NH3(g)
2Ca3(PO4)2 + 10C + 6SiO2
2NaNH2(l) + N2O NaN3 + NaOH +

NH3
P4 + 10CO + 6CaSiO3
P4 (pure) + 5O2 P4O10
15.10
P4O10 + 6H2O 4H3PO4 (pure)

(b)
P4(s) + 5O2(g) P4O10(s)

P4 is a tetrahedron
15.11
(i) Bi(III) is much more stable than Bi(V), and

(ii) P(III) and P(V) are both about equally
stable.
15.12
The rates of reactions in which nitrite ion is

reduced are increased as the pH is lowered.
Ca5(PO4)3OH + 5H2SO4
3H3PO4 (impure) + 5CaSO4 + H2O
(c) Fertilizer-grade phosphoric acid involves a
single synthetic step for a product that
requires little or no purification.
15.3
(a)
6Li(s) + N2(g) 2Li3N(s)
2Li3N(s) + 3H2O(l) 2NH3(g) + 3Li2OH(aq)

(b) N2(g) + 3H2(g) 2NH3(g)
(c) The second process is considerably
cheaper than the first, because lithium is very
expensive.
15.4
NH4NO3(s) + H2O(l) NH4+(aq) + NO3(aq)
15.5
N2 itself, with a triple bond between the two

atoms, is strikingly unreactive.
15.6
The only isolable nitrogen chloride is NCl3,

and it is thermodynamically unstable. Both
PCl3 and PCl5 are stable.
15.7
HNO2(aq) + H+(aq) NO+(aq) + H2O(l)

15.13
The rate law must be more than first order in

NO concentration. It turns out to be second
order; an equilibrium between NO and its
dimer N2O2 precedes the rate-determining
reaction with oxygen.
15.14
Ered = 0.736V
15.15
(a) Tetrahedral POCl3.
(a) Tetrahedron.
(b) A see-saw.
(c) A trigonal bipyramid.
15.8
(a) P4 + 5O2 P4O10

(b) P4O10 + 6H2O 4H3PO4
30

PCl5 + H2O POCl3 + 2HCl
S16.1
(b) 2PCl5(g) + 8H2O(l) 2H3PO4(aq) +

10HCl(aq)
The decomposition of H2O2 is also

thermodynamically favored in presence of Cl
(c) Tetrahedral.
PCl5 + AlCl3 [PCl4]+[AlCl4]
S16.2
(a) The SO3 molecule is planar and belongs to

the D3h point group.
(b) The SO3F anion is tetrahedral, but the
point group is C3v.
S16.3
S4N4 is aromatic
(d) Cyclic molecules or linear chain polymers

nPCl5 + nNH4Cl
[(N = P(Cl)2)n] + 4nHCl
15.16
15.17
P atom in POF3 is more deshielded and its

resonance will appear downfield in
comparison to the P resonance in PF3.
E = 0.839 V.
HPO32 and H2PO2 ions will be much better
reducing agents than oxidizing agents.
15.18
12 valence skeletal electrons, nido, trigonal

bipyramid.
15.19
(a) A = AsCl3
Exercises
16.1
CO2, SO3, and P2O5 are acidic, Al2O3

is amphoteric, MgO and K2O are basic.
16.2
The bond order in O2 molecule is [2 2 +2

+ 4 2] = 2, and it corresponds to the bond
length of 121 pm.
The bond order in O2+ cation is [2 2 +2 +
4 1] = 2.5, higher than in O2 molecule. This
higher bond order is reflected in a shorter
bond length of 112 pm.
The bond order for O22 is [2 2 +2 + 4 4]
= 1. Of the three dioxygen species, O22 has
the lowest bond order and the longest bond:
149 pm.
16.3
(a) +1.068 V.
(b) B = AsCl5
(c) C = AsR3
(d) D = AsH3
15.20
The
decomposition
of
H2O2
is
thermodynamically favored in presence of Br
The cis isomer gives two 19F signals and the

trans isomer gives one signal.
(b) Cr2+ is not capable of decomposing H2O2.

(c) rG = 157 kJ. For the disproportionation
of H2O2 (part (a)), rG = 103 kJ.
16.4
(a) Incorrect; this group exhibits alternation

effect.
(b) Partially correct; the ground state of O2 is
a triplet state but it does not react as an
electrophile in Diels-Alder reactions.
15.21
(c) Partially correct; while ozone is

considered a pollutant, it is very unlikely that
the ozone pollution is caused by the diffusion
of this gas from the stratosphere.
(a) A = NO2
(b) B = HNO3; C = NO
(c) D = N2O4
16.5
OHS
(e) F = NH4+
16.6
Ethylenediamine is a better solvent than

sulfur dioxide.
The species of N and P that disproportionate

are N2O4, NO, N2O, NH3OH+, H4P2O6, and P.
16.7
S2O82 > SO42 > SO32
16.8
Mn (+VII, +VI, +V, +IV, +III) will be

reduced by sulfite ions in basic solution.
16.9
(a) H5TeO6 and HSO4
(d) E= NO2
15.22
CHAPTER 16
(b) Tellurium is a larger element than sulfur

and can increase its coordination number.
Self-tests
16.10
S2O62and S2O32.
16.11
SeO32 is marginally more stable in acid

solutions.
16.12
All will be reduced as their potentials are

greater than the potential of thiosulfate.
Fluorine
F2
gas
highest (4.0)
Hardness
of halide
ion
hardest
16.13
SF4+ trigonal pyramidal, BF4 tetrahedral.
Chlorine
Cl2
gas
lower
softer
16.14
(a) SF4 + (CH3)4NF [(CH3)4N] [SF5] ; (b)

square pyramidal structure; (c) two F
environments.
Bromine
Br2
liquid
lower
softer
16.15
A = S2Cl2, B = S4N4, C = S2N2, D = K2S2O3,

E = S2O62, F = SO2.
Iodine
I2
solid
lowest
softest
16.16
(a) Expected to exhibit inorganic aromaticity.

(b) Expected to be aromatic.
(c) Not expected to be aromatic.
16.17
Electronegativity
Color
light
yellow
yellowgreen
dark
redbrown
dark
violet
For Cl:
2 Cl + 2 H2O + electricity Cl2 + H2 +
2 OH
For Br and I:
Sulfuric and selenic acids are rather similar;

telluric acid is remarkably different from
sulfuric and selenic acid.
2 X + Cl2 X2 + 2 Cl
I)
17.3
CHAPTER 17
(X = Br,
A drawing of the cell is shown in Figure 17.3.

anode: 2 Cl(aq) Cl2(g) + 2 e
cathode: 2 H2O(l) + 2 e 2 OH(aq) + H2(g)
Self-tests
S17.1
Both. SO2 is cheaper.
S17.2
2 resonances a sextet and a triplet.
S17.3
ClF3: trigonal bipyramidal shape and a

distorted T-shaped molecular geometry.
SbF5: trigonal bipyramidal geometry.
[ClF2]+: tetrahedral electron group geometry
and a bent molecular shape.
[SbF6]-: octahedral molecular shape.
S17.4
Examples include I3, IBr2, ICl2, and IF2.

The three centers contribute four electrons to
three molecular orbitals, one bonding, one
nonbonding, and one antibonding.
S17.5
(a) Br2 and BrO:

Br2 + 2OH Br + BrO + H2O
BrO + 2OH Br +
BrO3
+H2O
17.4
Since the 2u* antibonding orbital is the

LUMO for a X2 molecule, it is the orbital that
accepts the pair of electrons from a Lewis
base.
17.5
Cl2 and F2.
17.6
(a) Ammonia exhibits very strong hydrogen

bonding.
(b) The strong electron-withdrawing effect in
NF3 reduces the basicity.
I2 + 2OH I + IO + H2O
IO + 2OH I + IO3 +H2O
Exercises
17.7
17.1
unwanted reaction:
2 OH(aq) + Cl2(aq) ClO(aq) +
Cl(aq) + H2O(l)
(b) I2 and IO:
17.2
Physical
state
(a) (CN)2(aq) + 2 OH(aq) CN(aq) +

NCO(aq) + H2O(l)
(b) 2SCN(aq) + MnO2(s) + 4 H+(aq)
(SCN)2(aq) + Mn2+(aq) + 2 H2O(l)
For F:
CaF2 + H2SO4 CaSO4 + 2 HF
2 HF + 2 KF 2 K+HF2
(c) Trimethylsilyl cyanide contains an SiCN

single bond.
2 K+HF2 + electricity F2 + H2 + 2 KF
32
17.8
(a) [N(CH3)4][IF4].
17.20
Large cations stabilize large, unstable anions.
(b) Three bonding pairs and two lone pairs

on the iodine yield trigonal bipyramidal
electron geometry and T-shaped molecular
geometry.
17.21
(a) Angular shape, point group is C2v.
The shape of anion IF4 is Square planar. The

shape of cation (CH3)4N+ is Tetrahedral.
(b) One iodine atom is trigonal pyramidal; the

other iodine atom, is tetrahedral. The point
group is Cs.
(c) IF3, two. IF4, one.

17.9
SbCl5 is trigonal bipyramidal, FClO3 is

pyramidal, and [ClF6]+ is octahedral.
17.10
[ClF4]+[SbF6] .
17.11
MCl4F2, the cis isomer, 1; the trans isomer, 2.

MCl3F3, the fac isomer, 1 the mer isomer, 2.
17.22
(a) The formulas are HBrO4 and H5IO6. The

difference lies in iodines ability to expand its
coordination shell.
(b) Periodic acid is thermodynamically more
stable.
17.23
17.12
(a) IF6+,
bipyramid.
octahedral;
IF7,
(b) E = 1.201 V (see Appendix 2).
pentagonal
At pH 7, V = 0.788 V
(b) IF7 + SbF5 [IF6][SbF6]

17.13
Planar dimer (I2Cl6) with bridging Cl atoms.

The point group of I2Cl6 is D2h.
17.14
Trigonal pyramidal, Cs symmetry.
17.15
(a) Increases the acidity of BrF3.

(b) No effect on the acidity or basicity of
BrF3.
17.24
Low pH results in a kinetic promotion:

protonation of an oxo group aids oxygen
halogen bond scission.
17.25
Periodic acid. It can form a complex with a

potential reducing agent, providing for an
efficient and rapid mechanism by which the
redox reaction can occur.
17.26
(a)
Two different II bond lengths: longer central

I-I distances (290 pm) and shorter terminal I-I
distances (268 pm). The difference in bond
lengths can be explained by different bond
order. This gives us one description of I5+
structure as a hybrid of two structures.
17.17
Two resonances: a doublet and a quintet.
17.18
(a) Since SbF5 cannot be oxidized, it will not

form an explosive mixture with BrF3.
(c) 0.317V
17.27
(a) HClO, HClO2, and ClO3 are unstable with

respect to disproportionation.
(b) The rates of disproportionation are
probably HClO > HClO2 > ClO3.
17.28
(b) Methanol, being an organic compound, is

readily oxidized by strong oxidants.
(a) Ammonium perchlorate is a dangerous

compound, since the N atom of the NH4+ ion
is in its lowest oxidation state and can be
oxidized.
(b) Not an explosion hazard.
(c) Not an explosion hazard.
(c) The two will not form an explosive

mixture but will react.
(d) S2Cl2 will be oxidized to higher valent
sulfur fluorides.
17.19
0.45V
(b) 0.67V
(c) Increases the basicity of BrF3.

17.16
(a) E decreases as the pH increases.
(d) An explosion hazard, since Fe(II) can be

oxidized to Fe(III).
17.29
(a) Cr3+? Yes. (b) V3+? Yes. (c) Fe2+? Yes.

(d) Co2+? No.
17.30
A = ClF
Br3 + I2 2 IBr + Br
E = CsClF2
B = OF2
C = HF
D = SiF4
G = CaF2
17.31
17.32
18.4
(a) BrO4 is capable of oxidizing water. This

makes preparation and isolation of KBrO4
very difficult.
(b) All compounds are kinetically reasonably
stable to be isolated.
(c) IO2 ion is too unstable for its salts to be
isolated.
(d) BrO and IO are disproportionating too
rapidly to be isolated.
(a) Correct
(b) Incorrect - the two anions do not have
identical structures.
(c) Incorrect - it is the nucleophilicity of the
Cl atom in ClO that is crucial for the
oxidation mechanism.
(d) Correct.
18.5
(a) XeF4. The anion has a square-planar

geometry.
(b) Linear geometry. Isostructural with XeF2.
(c)Trigonal pyramidal geometry. Isostructural
with XeO3.
(d) Isostructural with the cation XeF+.
18.6
(a)
CHAPTER 18
(b) Speculate that would be pentagonal
bipyramid; actually capped octahedral.
Self-tests
S18.1
18.7
He22+ = 0.5, Ne22+ = 0.5.
18.8
(a) Electron pair geometry: trigonal

bipyramid. Molecular geometry: trigonal
planar.
(b) Electron pair geometry: octahedral.
Molecular geometry: t-shaped.
(c) Electron pair geometry: octahedral.
Molecular geometry: square pyramidal.
(d) Electron pair geometry: pentagonal
bipyramid. Molecular geometry: pentagonal
planar.
18.9
A = XeF2(g)
B = [XeF]+[MeBF3]
C = XeF6
D = XeO3
E = XeF4 (g).
18.10
1:3:3:1 quartet
18.11
Strong central line, two other lines

symmetrically distributed around the central
line.
2 HXeO4 (aq) + 2 OH (aq) XeO6 (aq) + Xe(g)

+ O2(g) + 2 H2O(l)
Exercises
18.1
Earths gravitational field is not strong

enough to hold light gases such as He and H2,
and they eventually diffuse away into space.
18.2
(a) Helium.
(b) Xenon.
(c) Argon.
18.3
(a) Xe and F2 at 400C, or photolyze Xe and

F2 in glass:
Xe(g) + F2(g) XeF2(s)
(b) High temperature, but have a large excess
of F2:
Xe(g) + 3 F2(g) XeF6(s)
(c)
XeF6(s) + 3 H2O(l) XeO3(s) + 6 HF(g)
CHAPTER 19
Self-tests
34
S19.1
V2O3 is more stable than VO in presence of

oxygen.
S19.2
Discrete molecular species such as Re3Cl123

or Re3Cl9(PPh3)3 are formed.
19.8
Hg22+ will not disproportionate. Rather, Hg

and Hg2+ would comproportionate to Hg22+.
19.9
Pigments should be permanent and stable.

They should also be non-toxic and have low
vapour pressure.
Exercises
19.1
Mn, MnO4Ru/Os. Within a group, the

heavier elements can achieve higher oxidation
states than first-row members.
19.2
(a) The most oxidizing state for Cr and Mo is

+6. Tungsten has no species with oxidizing
properties.
19.3
(b) For Cr, Cr(IV) and Cr(V) are susceptible

to disproportionation. Other elements do not
have species that would be expected to
disproportionate.
(a)
CHAPTER 20
Self-tests
S20.1
A high-spin d7 configuration is t25geg2. High

spin, 0.8 o.
S20.2
t2g3eg2
S20.3
If it were not for ligand field stabilization

energy (LFSE), MF2 lattice enthalpies would
increase from Mn(II) to Zn(II).
In the spectrum of [Mo(CO)6], the ionization
energy around 8 eV was attributed to the t2g
electrons that are largely metal-based. The
differences in the 68 eV region can be
attributed to the lack of d electrons for Mg(II).
(b)
(c)
S20.4
(d)
19.4
19.5
The oxides FeO4 and Co2O9 contain iron and

cobalt in oxidation states +8 and +9
respectively, which are not stable for either
element.
Statement (c) is not true.
19.6
The most likely compounds of general

formula MM are rubidium and cesium
aurides, RbAu and CsAu, containing Au
19.7
The difference in density can be explained by

difference in atomic mass for Hf and Zr.
S20.5
F and 3F terms are possible.
S20.6
(a) 3P (called a triplet P term).

(b) 2D (called a doublet D term).
S20.7
F terms are 3T1g, 3T2g, and 3A2g. Similarly, D

terms are 1T2g and 1Eg.
S20.8
17500 cm1 and 22400 cm1.
S20.9
(i) The very low intensity of the band at 16,000
cm1 is a clue that it is a spin-forbidden
transition, probably 2Eg 4A2g.
(ii) Spin-allowed but Laporte-forbidden bands
typically have ~ 100 M1 cm1, so it is
likely that the bands at 17,700 cm1 and
23,800 cm1 are of this type.

(iii) The band at 32,400 cm1 is probably a charge
transfer band, since its intensity is too
high to be a ligand field (dd) band.
(a)
3050
(a) d6, low spin, no unpaired electrons, LFSE

= 2.40.
(b) d6, high spin, four unpaired electrons,
LFSE = 0.40.
-1
hyd H / kJ mol
2950
Exercises
20.1
20.7
2750
(f) d6, high spin, four unpaired electrons,

LFSE = 0.6 T.
(g) d10, 0 unpaired electrons, LFSE = 0.
20.2
Mn
2550
Ca2+
2450
2250
0
10
Number of d electrons
(b)
Ion
o (in cm1)
o (in kJ mol1
t2g
eg
configuration
LFSE (kJ mol1)
Ca2+
0
0
t2g0
eg0
0
No.
There are two ways for a complex to develop
a large value of 0, by possessing ligands that
are -acids or by possessing ligands that are
strong -bases (or both).
20.3
2+
2650
(d) d3, three unpaired electrons, low spin,

LFSE = 1.20.
(e) d , low spin, no unpaired electrons, LFSE
= 2.40.
Fe2+
V2+
Fe2+
10400
124.2
t2g4 eg2
49.7
Co2+
9300
111.1
t2g5 eg2
88.9
V2+
12600
150.5
t2g3 eg0
Cr2+
13900
166.1
t2g3 eg1
180.6
99.6
Ni2+
8300
99.2
t2g6 eg2
119
Cu2+
12600
150.5
t2g6 eg3
90.3
Mn2+
7800
93.2
t2g3
eg2
0
Zn2+
0
0
t2g6 eg4
0
Spin-only contributions are:

(c) The straight line now shows the expected
trend in hydH as a function of cationic radius
only without electronic effects.
3050
N
3+
[Co(NH3)6]
[Fe(OH2)6]2+
[Fe(CN)6]3
[Cr(NH3)6]3+
[W(CO)6]
[FeCl4]2
[Ni(CO)4]
20.4
20.5
0
4
1
3
0
4
0
B = [(N)(N +
2)]1/2
0
4.9
1.7
3.9
0
4.9
0
[CoCl4]2 is blue, [Co(NH3)6]2+ is yellow,

[Co(OH2)6]2+ is pink.
-1
hyd H / kJ mol
2950
Complex
2750
Mn2+
Cu2+
Fe2+
V2+
Co2+
2650
2550
Ca2+
2450
2350
2250
0
10
Number of d electrons
20.8
Shift from square planar to tetragonal

complex.
20.9
Elongated octahedron.
20.10
The electronic excited state of Ti(OH2)63+ has

the configuration t2g0eg1, and so the excited
state possesses eg degeneracy. Therefore, the
single electronic transition is really the
superposition of two transitions, one from an
Oh ground-state ion to an Oh excited-state ion,
and a lower energy transition from an Oh
ground-state ion to a lower energy distorted
excited-state ion.
20.11
(a) 6S
(a) The chromium complex.

(b) The Fe3+ complex.
(d) The ruthenium complex.

(e) The Co2+ complex.
There are two factors that lead to the values:
(i) decreasing ionic radius from left to right
across the d block, and (ii) LFSE.
Zn2+
Ni2+
Cr2+
2850
(c) [Fe(CN)6]3
20.6
Zn2+
Cu2+
Co2+
2350
(c) d5, low spin, one unpaired electron. LFSE

is 2.00.
Ni2+
Cr2+
2850
36

(b) 4F
the intense yellow color is due to LMCT

transitions.
(c) D
(d) 3P
20.12
20.23
The Cl atom lone pairs of electrons can form

molecular orbitals with dxz and dyz. These
metal atomic orbitals are -antibonding MOs,
and so they will be raised in energy.
20.24
The oxidation state of manganese in

permanganate anion is Mn(VII), which is d0.
Therefore, no ligand field transitions are
possible.
(a) 3F.
(b) 5D
(c) 6S
20.13
(a) 2S.
(b) 1D, 3P, 1S. The ground term is 3P.
20.14
B = (12920 cm1)/(15) = 861.33 cm1 and C =

3167.7 cm1.
20.15
(a) 1A1g.
(b) 2T2g.
(c) 6A1g.
20.16
The difference in energy between the two

transitions, E(t2) E(e) = 13700 cm1, is just
equal to T.
(a) 0 = 8500 cm1 and B 770 cm1.

(b) 0 = 10,750 cm1 and B 720 cm1.
20.17
20.18
The presence of two moderate-intensity bands

in the visible/near-UV spectrum of
[Co(NH3)6]3+ suggests that it is low spin. The
very weak band in the red corresponds to a
spin-forbidden transition such as 3T2g 1A1g.
No spin-allowed transitions are possible for
the Fe3+; the complex is expected to be
colorless. The d6 Co3+ ion in [CoF6]3 is also
high spin, but in this case a single spinallowed transition makes the complex colored
and gives it a one-band spectrum.
20.19
Ammonia and cyanide ion are both -bases,

but cyanide is also a -acid.
20.20
First, the intense band at relatively high

energy is undoubtedly a spin-allowed chargetransfer transition. The two bands with max =
60 and 80 M1 cm1 are probably spin-allowed
ligand field transitions. The very weak peak
is most likely a spin-forbidden ligand field
transition.
20.21
The faint green color, which is only observed

when looking through a long pathlength of
bottle glass, is caused by spin-forbidden
ligand field transitions.
20.22
The blue-green color of the Cr3+ ions in

[Cr(H2O)6]3+ is caused by spin-allowed but
Laporte-forbidden ligand field transitions.
The relatively low molar absorption
coefficient is the reason that the intensity of
the color is weak. The oxidation state of
chromium in dichromate dianion is Cr(VI);
CHAPTER 21
Self-tests
S21.1
k2(NO2) = 100.71 = 5.1 M1s1
S21.2
S21.3 KE = 1 M1, k = 1.2 102 s1.
Exercises
21.1
Dissociative.
21.2
The rate of an associative process depends on

the identity of the entering ligand so it is not
an inherent property of [M(OH2)6]n+.
21.3
d.
21.4 rate =
21.14
(kKE[Mn(OH2)62+][X])/(1
(a) cis-[PtCl2(PR3)2].
(b) trans-[PtCl2(PR3)2].
+ KE[X ])
(c) trans-[PtCl2(NH3)(py)].
You can distinguish d from a by varying the
nature of X. If k varies as X varies, then the
reaction is a. If k is relatively constant as X
varies, then the reaction is d.
21.5
21.15
The order of increasing rate is [Ir(NH3)6]3+ <

[Rh(NH3)6]3+ < [Co(NH3)6]3+ < [Ni(OH2)6]2+
< [Mn(OH2)6]2+.
21.16
(a) Decreased rate.
Metal centers with high oxidation numbers

have stronger bonds to ligands than metal
centers with low oxidation numbers.
Furthermore, period 5 and 6 d-block metals
have stronger metal ligand bonds.
(b) Decreased rate.

(c) This change will have little or no effect on
the rate.
(d) Decreased rate.
21.6
The greater steric hindrance.
21.7
This is a case of dissociative activation.
21.8
Mechanism must be dissociative.
21.9
Yes - for a detectable amount of [Ni(CN)5]3

to build up in solution, the forward rate
constant kf must be numerically close to or
greater than the reverse rate constant kr.
{[Co(N3)(NH3)5]2+, [V(OH2)6]2+}
{[Co(N3)(NH3)5]2+, [V(OH2)5]2+, H2O}
A possible mechanism is loss of one

dimethyl sulfide ligand, followed by the
coordination of 1,10-phenanthroline.
[(NH3)5CoN=N=NV(OH2)5]4+ [(NH3)5Co
N=N=NV(OH2)5]4+
21.10
21.11
21.17
The inner-sphere pathway:
[Co(N3)(NH3)5]2+ + [V(OH2)6]2+
[[Co(N3)(NH3)5]2+, [V(OH2)6]2+}
{[Co(N3)(NH3)5]2+, [V(OH2)5]2+, H2O}

[(NH3)5CoN=N=NV(OH2)5]4+
[(NH3)5CoN=N=NV(OH2)5]4+ [Co(OH2)6]2+ +
[V(N3)(OH2)5]2+
The outer sphere pathway:
[Co(N3)(NH3)5]2+ + [V(OH2)6]2+
{[Co(N3)(NH3)5]2+ [V(OH2)6]2+}
{[Co(N3)(NH3)5]2+,[V(OH2)6]2+} {[Co(N3)(NH3)5]+ ,
[V(OH2)6]3+}
{[Co(N3)(NH3)5] +,[V(OH2)6]3+} + H2O
[Co(NH3)5(OH2)]2+ + [V(OH2)6]3+ + N3
21.12
(a) Rate decreases.
21.18
Appears to be an inner-sphere electron

transfer reaction.
21.19
The reduction of [Co(NH3)5(OH)]2+ proceeds

via
inner-sphere
mechanism.
The
[Co(NH3)5(H2O)]3+ has no bridging ligands
and the only mechanistic pathway for the
electron-transfer is outer sphere. Both
reactions with [Ru(NH3)6]2+ as a reducing
agent likely proceed via the same mechanism,
the outer-sphere mechanism
21.20
(a) k = 4.53 103 dm3mol1s1
(b) The rate decreases.

(c) The rate decreases.
(d) Rate increase.
21.13
(i) The general trend: octahedral Co(III)

complexes undergo dissociatively activated
ligand substitution.
(b) k = 1.41 102 dm3mol1s1
(ii) The anomalously high rate of substitution

by OH signals an alternate path, that of base
hydrolysis.
(iii) The implication is that a complex without
protic ligands will not undergo anomalously
fast OH ion substitution.
The reduction of the Ru complex is more

thermodynamically favoured and faster.
21.21
(a) k11 (Cr3+/Cr2+) = 1 105 dm3mol1s1; k22

(Ru3+/Ru2+ for the hexamine complex) = 6.6
o
103 dm3mol1s1; f12 = 1; K12 = e [nF /RT]
38

where o = 0.07 V (0.41V) = 0.48 V; n = 1;
F = 96485 C; R = 8.31 Jmol1K1 and T = 298
K. Using these values gives K12 = 1.32 108.
Substitution of these values in the MarcusCross relationship gives k12 = 2.95 103
dm3mol1s1.
(b) k11 (Cr3+/Cr2+) = 1 105 dm3mol1s1; k22
(Fe3+/Fe2+ for the aqua complex) = 1.1
o
dm3mol1s1; f12 = 1; K12 = e[nF /RT] where o
= 0.77 V (0.41V) = 1.18 V; n = 1; F =
96485 C; R = 8.31 Jmol1K1 and T = 298 K.
Using these values we get K12 = 9.26 1019.
dm3mol1s1.
(c) k11 (Cr3+/Cr2+) = 1 105 dm3mol1s1;
k22 (Ru3+/Ru2+ for the bipy complex) = 4 108
o
dm3mol1s1; f12 = 1; K12 = e[nF /RT] where o
= 1.26 V (0.41V) = 1.67 V; n = 1; F =
96485 C; R = 8.31 Jmol1K1 and T = 298 K.
Using these values gives K12 = 1.81 1028.
dm3mol1s1.
21.22
The product will be [W(CO)5(NEt3)], and the

quantum yield will be 0.4.
21.23
~250 nm.
S22.9
S22.10 PMe3 would be preferred, because of its

smaller size.
S22.11 Fluorenyl compounds are more reactive than
indenyl.
S22.12 The decrease in both coordination number and
oxidation number by 2.
S22.13 The ethyl group in [Pt(PEt3)2(Et)(Cl)] is prone
to -hydride elimination.
Exercises
22.1
(c) Hexcarbonylvanadium(0), 17e; can be

easily reduced to [V(CO6)]
(d) Tetracarbonylferrate(2), 18e;
(e)
Tris(pentamethylcyclopentadienyl)lanthanum(
III), 18e;
(f) 3-allyltricarbonylchloridoiron(II), 18e
(g) Tetracarbonyltriethylphosphineiron(0)
18e
(h)
Dicarbonylmethyltriphenylphosphinerhodium
(I),16e; a square planar complex, undergoes
oxidative addition easily.
Self-tests
S22.1
No.
S22.2
Electron count, 16; oxidation number, +2.
S22.3
Dibromocarbonylmethylbis(triphenylphosphine)iridium(III).
S22.4
Fe(CO)5
S22.5
(a) 6-C7H8 = 6 electrons, Mo atom = 6.

carbonyl = 2 electrons, total = 18.
(i)
Chloridomethylbis(triphenylphosphine)pallad
ium(II), 16e; a square planar complex,
undergoes oxidative addition easily
(j) 5-cyclopentadienyl-4tetraphenylcyclobutadienecobalt(I), 18e
(k) 5-cyclopentadienyldicarbonylferrate(0),
18e
(b) 7-C7H7+ = 6 electrons, Mo atom = 6, 3

COs = 6, total = 18.
(l) 6-benzene-6cycloheptatrienechromium(0), 18e
S22.6
Mn2(CO)10 + 2 Na 2Na[Mn(CO)5]
(m) Trichloridobis(5cyclopentadineyl)tanatalum(V), 18e
Na[Mn(CO)5] + CH3I [Mn(CH3)(CO)5] + NaI

[Mn(CH3)(CO)5] + PPh3 [Mn(COCH3)
(CO)4(PPh3)]
S22.8
(a) Pentacarbonyliron(0), 18e;

(b) Decacarbonyldimanganese(0), 18e;
CHAPTER 22
S22.7 Bridging
TA tetrahedron with 4 terminal Cp rings and

four capping COs.
(n) 5-cyclopentadineylnitrosylnickel(II),16e
; a rather reactive complex
22.2
It will not.
22.3
(a) 2
(b) No. Deviations from the rule are common

for cyclopentadienyl complexes to the right of
the d block.
(b) Can be 5, 3, or 1.
(c) 6, 4, and 2.
(d) 2 and .
22.9
The Ir complex. It has an A mechanism.
22.10
(a) [Fe(CO)4]2 The trend involved is the

greater affinity for a cation that a species with
a higher negative charge has.
(e) 8, 6, 4, 2.
22.4
(b) The rhenium complex. The trend involved

is the greater MH bond enthalpy for a period
6 metal ion relative to a period 4 metal ion in
the same group.
(a) 16, very common for group 9 and group

10 elements.
(b) 18.
(c) 18.
22.5
(1) Mo(s) + 6 CO(g) Mo(CO)6(s)
(high
temperature and pressure required)
(2) 2 CoCO3(s) + 2 H2(g) + 8 CO(g)
Co2(CO)8(s) + 2 CO2 + 2 H2O
22.11
(a) 3 (b) 2 (c) 12
22.12
(i) Reduce Mn2(CO)10 with Na to give

Mn(CO)5; react with MeI to give
MnMe(CO)5. (ii), Oxidize with Br2. to give
MnBr(CO)5; displace the bromide with MeLi
to give MnMe(CO)5.
22.13
Mo(CO)5(C(OCH3)Ph)
22.14
The reason that the second method is

preferred is kinetic.
22.6
A complex that has Cs symmetry will have the

greatest number of bands. A fragment with
D3h symmetry will give rise to one band, a
fragment with C3v symmetry will give rise to
two bands, and a fragment with Cs symmetry
will give rise to three bands.
22.7
(a) CO bands of the trimethylphosphine

complex are 100 cm1 or more lower in
frequency. PMe3 is primarily a -donor
ligand. PF3 is primarily a -acid ligand.
(b) CO bands of the Cp* complex are lower
in frequency than the corresponding bands of
the Cp complex. Cp* is a stronger donor
ligand than Cp.
22.8
(a)
40
22.18
22.19
22.15
(a) Reflux Mo(CO)6 with cycloheptatriene to

give [Mo(6-C7H8)(CO)3]; treat with the trityl
tetrafluoroborate to give [Mo(7C7H7)(CO)3]BF4.
(b) React [IrCl(CO)(PPh3)2] with MeCl, then
expose to CO atmosphere to give
[IrCl2(COMe)(CO)(PPh3)2].
Considering that Cp can both slip and

rotate, at room temperature we see only one
resonance as an effect of averaging the proton
environments. At 40C we observe two
different signals of equal intensity. This tells
us that there are two different environments,
both of which contain two Cp rings.
(a) [Fe(5-C5H5)2] + CH3COCl
3
5
5
[Fe( -C5H5)( -C5H4COCH3)] + HCl
AlCl
(b)
22.20
22.16
See resource section 5. dz2 and s orbitals have

an a1 symmetry and thus have correct
symmetry to form the MOs with the a1
symmetry-adapted orbital on Cp rings.
Therefore, three a1 MOs will be formed.
22.21
The reason that the Ni complex is protonated

at a carbon atom is that a more stable (i.e., 18electron) product is formed.
22.22
(a)
(b)
The compound B shows two 1H NMR

resonances due to Fe-H proton and the
aromatic Cp ring. C shows a single 1H NMR
resonance because of aromatic Cp ring.
22.17
In either case compounds formed are

tetraalkyl titanium(IV) complexes, TiR4.
Neither the methyl or trimethylsilyl groups
have hydrogens. Thus, unlike [TiEt4],
[TiMe4] and [Ti(CH2SiMe3)4] cannot undergo
a low energy -hydride elimination
decomposition reaction.
22.23
One of the possible routes involves initial slip

of Cp ring from 5 to 3 bonding mode
creating a 16-electron complex that can
coordinate a phosphine ligand producing new
18-electron [Mo(3-C5H5)(CO)3Me(PR3)]
complex. This complex loses one CO ligand
giving a new 16-electron intermediate
[Mo(3-C5H5)(CO)2Me(PR3)] that converts to
the stable 18-electron complex

[Mo(5-C5H5)(CO)2Me(PR3)].
Exercises
23.1
2 Ln3+(aq) + 3 H2(g) + 6 H2O(l)
The second route starts with CO insertion (or

methyl group migration) to produce a 16electron acyl complex. This complex can
coordinate one PR3 ligand to give an 18electron species, which if heated can lose one
CO ligand and undergo reverse alkyl group
migration.
22.24
(a) 86; 90
(b) Yes for trigonal prismatic; no for
octahedral arrangement.
(c) The iron complex probably contains an
octahedral Fe6 array, whereas the cobalt
complex probably contains a trigonalprismatic Co6 array.
22.25
(a) SiCH3 group

(b) Iodine atom
22.26
The cobalt complex will exhibit faster

exchange. This is because metalmetal bond
strengths increase down a group in the dblock.
(a) 2 Ln(s) + 6 H3O+(aq)

(b) The potentials for the Ln0/Ln3+ oxidations
in acid solution range from a low of 1.99 V
for europium to 2.38 V.
(c) Ce4+, Eu2+.
23.2
23.3
The lanthanide contraction.

Unusual oxidation states were used in
separation procedures.
23.4
UF6 is a molecular solidits solid state

structure contains isolated, octahedral UF6
molecules held together via relatively weak
intermolecular forces. UF3 and UF4 form
network solids in which each U atom is
surrounded by nine and eight fluorines
respectively.
23.5
Could contain Pu(III), Pu(IV), Pu(V), and

even Pu(VI) species. Addition of F to the
solution is likely going to precipitate PuF3.
23.6
See Figure 23.16. Bond order is 3. All these

fragments are linear because this geometry
maximizes the strong -overlap between 2p
orbitals on the oxygen atoms and 6dz2 and 5fz3
orbitals on the An atom.
23.7
Tb3+: 7F6
Nd3+: 4I9/2
Ho3+: 5I8
CHAPTER 23
Self-tests
S23.1
H6.
Er3+: 4I15/2
S23.2
Likely to result in a product containing two

(Cp)2Ln units bridged by a ligand system. In
fact the product consists of two (Cp)2Ln units
bridged by a hydrido ligand.
Lu3+: 1S0
S23.2
S23.4
23.8
(a) Correct
(b) Incorrect - Ln3+ cations exchange water
molecules very rapidly
UO22+ if sufficient oxygen is present.
(c) Correct
23.9
It would shake the theoretical foundation of

the claim that the lanthanide 4f subshell is
rather inert. A good candidate could be Pr.
23.10
Both have 2+ as a stable oxidation state.
23.11
With the lanthanoids, the 5d orbitals are

empty, and the 4f orbitals are deeply buried in
the inert [Xe] core and cannot participate in
bonding.
23.12
NpCl4 + 4NaCp NpCp4 + 4NaCl
THF, Low temp.
23.13
The 5f orbitals of the actinide ions interact

strongly with ligand orbitals, and the splitting
of the 5f subshell, as well as the color of the
complex, varies as a function of ligand.
42
24.7
23.14
Rock-salt structure.
CHAPTER 24
Self-tests
S24.1
(a) From SrCO3 and TiO2 in 1 : 1 ratio. The

two are grinded together and heated.
(b) 3 : 2 stoichiometry (SrCO3 : TiO2);
alternatively, it can be prepared from SrTiO3
and SrO in 2 : 1 stoichiometry.
For the 1 : 1 Na:Re ratio the structure type

can be described as that of perovskite
(CaTiO3).
24.8
Below 122 K.
24.9
ZnCr2S4; NiLi2F4
24.10
All except Gd2Ba2Ti2Cu2O11 (compound c),

are superconductors.
24.11
White Ta2O5 reacts with ammonia at high

temperature to produce red Ta3N5.
24.12
(a) By heating a 1 : 1 mixture of MgCO3 (or
Mg(NO3)2) and (NH4)2Cr2O7 at high
temperature.
Formation of a glass is favoured for the

substances that have polyhedral, cornersharing oxygen atoms and that can retain the
coordination sphere around a glass-forming
element while having variable bond angles
around O atom.
(b) By coprecipitating La3+ and Fe3+

hydroxides and then, after filtration, heating
the precipitate and eliminating water
CaF2 is an ionic compound - on cooling, Ca2+

and F ions simply pack into the fluorite
structure.
(c) By heating Ta2O5 under a flow of NH3 at

high temperature.
SiO2 has a framework structure composed of

SiO4 tetrahedra connected through O atoms
shared at corners. The SiO bond has
significant covalent character and is very
strong. This network is not easily broken (and
reformed) with temperature.
S24.2
Because K+ is a larger ion than Na+.
S24.3
The A2+ ions (Fe2+ in this example) occupy

tetrahedral sites and the B3+ ions (Cr3+)
occupy octahedral sites.
S24.4
MCM-41.
Exercises
24.1
(d) By heating a molar mixture of LiH and

MgH2 (under hydrogen or an inert gas) in a
direct reaction, or by heating a mixture of the
elements under hydrogen.
24.2
(e) Can be prepared from solution of CuBr2

and KF as a precipitate.
24.13
(f) Can be prepared starting from sodium

gallate, NaGaO2 and sodium silicate. The
reaction would be undertaken hydrothermally
in a sealed reaction vessel.
BeO, B2O3, and to some extent GeO2 are glass

forming. Transition metal and rare earth
oxides are typically nonglass-forming
oxides.
24.14
Any metal sulfide glasses would involve

metalloid and non-metal sulfides.
24.15
1. Direct combination of lithium and TiS2 at

elevated temperatures. 2. Electrointercalation.
24.16
Both [Co(5-C5H5)2] and [Co(5-C5Me5)2] are

19-electron species and can be easily oxidized
to 18-electron species. Ferrocene [Fe(5C5H5)2] is an 18- electron compound and
cannot be easily oxidized.
24.17
The Mo6S8 units are bonded via Mo S

bridges. The S atoms in one cube donate an
electron pair from a filled p orbital to the
empty 4dz2 orbital on Mo located on a
neighbouring cube.
(a) LiCoO2
(b) Sr2WMnO6
24.3
The electronic conductivity of the solid

increases owing to formation of (Ni1xLix)O.
24.4
FexO contains vacancies.
24.5
Using electron
diffaction.
24.6
(a) Na+
(b) Ca2+ or Na+
microscopy
and
X-ray
24.18
Be, Ga, Zn, and P all form stable tetrahedral

units with oxygen. Mg would prefer an
octahedral environment (i.e., the structure of
brucite, Mg(OH)2), whereas Cl would likely
be an anion.
24.19
The following zeotypes are possible: (AlP)O4,

(BP)O4, (ZnP2)O6.
24.20
Ambidentate ligands.
24.21
10.6%; however elevated temperatures for

decomposition are required to liberate the
hydrogen gas.
24.22
LixMg1x/22y/3AlyH2z; heating an alloy with

desired Li : Mg : Al ratio (which can be
prepared by mulling) under H2 atmosphere.
(b) Top-down: precise control over the spatial

relationships between nanoscale entities, but
limited to the design of rather large nanoscale
items.
Bottom-up: precise spatial control over atoms
and molecules relative to each other, but the
long-range spatial arrangement is often
difficult to realize.
24.31
(a) reacting species and additives must be

solvated; stable nuclei of nanometer
dimensions must be formed from solution;
growth of particles to the final desired size.
(b) So that nucleation fixes the total number
of particles and growth leads to a controlled
size and a narrow size distribution.
(c) Stabilizers prevent unwanted Ostwald
ripening.
24.23
Because it is thermodynamically unstable.
24.24
The Cu site in Egyptian blue is square planar

and thus has a centre of symmetry; in copper
aluminate spinel blue, the site is tetrahedral
with no centre of symmetry.
24.32
Smaller particles present in the solution

dissolve and this redisolved material
precipitates again but on the surface of
existing particles.
24.25
In the solution an anionic radical S3 is

present. In solution polysulfide, radical anions
are very sensitive to O2 from the atmosphere;
upon oxidation the colour is lost.
(a) High efficiency of light absorption (b)
efficient electron-hole separation process and
(c) high surface area of bulk material.
24.33
(a)
24.26
24.27
BN > C(diamond) > AlP > InSb.
24.28
In Na2C60, all of the tetrahedral holes are

filled with sodium cations within the closepacked array of fulleride anions. In Na3C60,
all of the tetrahedral holes and all of the
octahedral holes are filled with sodium
cations within the fcc lattice of fulleride
anions.
24.29
(a) 1.256 103 nm2 versus 1.256 107 nm2 (a

factor of 104).
(b) The 10 nm particle can be considered a
nanoparticle, whereas the 1000 nm particle
cannot.
(c) A true nanoparticle should have a
localized
surface
plasmon
without
characteristic momentum and of high
intensity.
24.30
(a) Top-down: requires one to carve out

nanoscale features from a larger object e.g.
lithography.
Bottom up: requires one to build up
nanoscale features from smaller entities e.g.
thin film deposition of quantum wells.
(b) i) Solution based: grow the core in

solution and add the additive and material for
the growth of shell. ii) Vapor-deposition:
deposit the material for the core and then the
material for the shell.
(c) Biosensing.
24.34
Hexagonal boron nitride, Sheet silicates,

Molybdenum sulphide.
CHAPTER 25
Self-tests
S25.1
Cyclohexanecarboxaldehyde.
S25.2
the rate of hydroformylation will be decreased

by added phosphine.
S25.3
Bands near 1465 cm1
S25.4
Not an active catalyst; contains SiOH

groups, which are only moderate Brnsted
acids.
44
S25.5
The polymerization of mono-substituted

alkenes introduces sterogenic centres along
the carbon chain at every other position.
Without R groups attached to the Zr centre
there is no preference for specific binding of
new alkenes during polymerization and thus
the repeat is random or atactic.
catalyst, [RhCl(PPh3)3], is shown in Figure

25.5.
25.6
Hydrogenation is faster for hexene than for

cis-4-methyl-2-pentene (a factor of 2910/990
3). It is also faster for cyclohexene than for
1-methylcyclohexene (a factor of 3160/60
53). In both cases, the alkene that is
hydrogenated slowly has a greater degree of
substitution and so is sterically more
demanding. The reaction (C) (D) is the
rate-determining step for hydrogenation by
RhCl(PPh3)3.
25.7
The selectivity step is the hydride migration

onto
the
coordinated
prop-1-en
in
[HCo(CO)4(H2C=CHCH3)] complex.
25.8
The resulting polymer is going to be isotactic:

it is going to have a high melting point and
will be semicrystalline.
25.9
The transformation of (E) into [CoH(CO)4]

and product must be the rate-determining step
in the absence of added PBu3. In the presence
of added PBu3, the formation of either (A) or
(E),
or
their
phosphine-substituted
equivalents, is the rate-determining step.
25.10
HI would hydrolyse MeCOOMe and produce

MeI and MeCOOH (instead of water). The
reaction of the ethanolic acid with the acetyl
iodide (produced at the end of the catalytic
cycle) leads to ethanoic anhydride.
25.11
(a) ROMP can result in reduced steric strain,

thereby providing a thermodynamic driving
force for the reaction.
(b) RCM results in the loss of ethane, and by
removing this gas, the position of equilibrium
can easily be driven to favour the ring
product.
25.12
(a)
Exercises
25.1
25.2
25.3
25.4
25.5
(a) Genuine example of catalysis; the

platinum can be recovered unchanged after
many turnovers
(b) Not an example of catalysis as the
activation energy of the reaction is not
lowered.
(c) Not an example of catalysis as both
substances are consumed.
(a) The amount of product formed per unit
time per unit amount of catalyst.
(b) A measure of how much of the desired
product is formed relative to undesired byproducts
(c) A substance that increases the rate of a
reaction but is not itself consumed.
(d) A sequence of chemical reactions, each
involving the catalyst, that transform the
reactants into products.
(e) In cases where a heterogeneous catalyst
does not remain a finely divided pure
substance with a large surface area under the
reaction conditions, it must be dispersed on a
support material.
(a) Since the substances are all present in the
same phase, this is an example of
homogeneous catalysis.
(b) Heterogeneous catalysis the reactants
and products are in the liquid phase but the
catalyst is a solid.
(c) The substrate and catalyst are in the same
phase so this is homogeneous catalysis.
(a) Since water is a thermodynamically stable
compound, it would not be a worthwhile
endeavour to try to develop a catalyst to split
water into hydrogen and oxygen.
(b) As with (a) you would be trying to
catalyze the decomposition of a very stable
compound so it would not be worthwhile.
(c) This would be a candidate for catalyst
development, however the process can be
readily set up with existing technology.
(b)
The catalytic cycle for homogeneous

hydrogenation of alkenes by Wilkinsons
S26.2
The proteins tertiary structure can place any

particular atom or group in a suitable position
for axial coordination.
S26.3
If a patient was given an intravenous fluid

containing KCl instead of NaCl, the potential
across the cell membrane would collapse,
with severe consequences.
S26.4
Calmodulin does not bind to the pump unless

Ca2+ is coordinated to it. As the Ca2+
concentration increases in the cell, the Cacalmodulin complex is formed. The binding
of this Ca-calmodulin complex to the pump is
thus a signal informing the pump that the
cytoplasmic Ca2+ level has risen above a
certain level and to start pumping Ca2+ out.
S26.5
Starting from a Fe(II) porphyrin complex (L

is a neutral axial ligand throughout the
sequence) we first obtain a peroxo bridged
Fe(III) porphyrin dimer. Peroxo bridge can
oxidatively cleave producing two equivalents
of oxido Fe(IV) porphyrin monomers. This
rather reactive species can react with another
equivalent of the starting Fe(II) porphyrin
complex producing an oxido-bridged Fe(III)
porphyrin dimer.
S26.6
Hydrogen bonding and replacement of one

cysteine with a histidine should lead to an
increase in the reduction potential of an Fe-S
cluster.
S26.7
There is greater covalence in blue Cu centres

than in simple Cu(II) compounds.
S26.8
Likely to be highly oxidizing, and probably

diamagnetic with a preference for squareplanar geometry.
S26.9
Species such as CH3Hg+ and (CH3)2Hg are

hydrophobic and can penetrate cell
membranes. Cobalamins are very active
methyl-transfer reagents that can methylate
anything in the cell, which is bad news for the
human body
(c) Yes.
25.13
(a) When Al3+ replaces Si4+ on lattice site, the

charge is balanced by H3O+, increasing the
acidity of the solid catalyst.
(b) Other 3+ ionsfor example Ga3+, Co3+, or
Fe3+, would have similar effect as Al3+.
25.14
Because it increases the surface area.
25.15
The steps necessary for deuterium substitution

into an alkane include the dissociative
chemisorption of an RH bond, the
dissociative chemisorption of D2, and the
dissociation of RD. The second observation
(a given ethyl group is completely deuterated
before another one incorporates any
deuterium) can be explained by invoking a
mechanism for rapid deuterium exchange of
the methyl group in the chemisorbed
CHR(CH3) group (R = C(CH3)2(C2H5)).
25.16
Platinum not only has a strong tendency to

chemisorb H2, but it also has a strong
tendency to chemisorb CO.
25.17
Electrocatalysts are compounds that are

capable of reducing the kinetic barrier for
electrochemical reactions.
25.18
(a) While it is true that a catalyst introduces a

new reaction pathway it does so by lowering
the Gibbs energy of activation, not enthalpy
of activation.
(b) First, the catalyst does not make the Gibbs
energy of a reaction more favourable but
rather the Gibbs energy of activation. Second,
even if the Gibbs energy of activation was
implied, a catalyst is not only reducing the
Gibbs energy, but it can also dictate the
formation of a specific product.
(c) The ZieglerNatta catalyst is a
heterogeneous catalyst.
(d) Highly favourable Gibbs energies for the
attachment of reactants and products to a
catalyst are not good for catalysis at all.
CHAPTER 26
Self-tests
S26.1
S26.10 Spectroscopic measurements that are metal

specific, such as EPR, could be used on both
enzyme and isolated cofactor. Attempts could
be made to grow single crystals from the
solution and perform single-crystal X-ray
diffraction and EXAFS to reveal molecular
geometry, bond distances, and angles between
Fe or Mo and the sulphur ligands.
S26.11 Cu(I) has an ability to undergo linear
coordination by sulphur-containing ligands.
Uncomplexed Fe2+ is present at very low

concentrations.
Exercises
46

For a channel or ionophore to be Na+ specific
it must have smaller cavity than K-channel.
Ca2+ is going to bind more tightly than either
Na+ or K+ to the residues that have negative
charge. It is also a cation of a s-block element
and has no LFSE that could dictate a preferred
geometry. Cl is obviously different from the
other three by being an anion. Thus, to move
Cl we would need to have a large cavity and
rely on hydrogen bonds formed with NH and
OH functional groups.
Exercises
27.1
Both have a preference for square planar

geometry that seems to be necessary for the
activity of Pt(II) anticancer drugs. Au(III) is
also a soft Lewis acid, meaning that it has low
preference for Cl and O-donor ligands. The
major difference is that Au(III) is easily
reduced under hypoxic conditions to Au(I),
which prefers linear geometry as in [AuCl2].
26.2
The larger size of lanthanides is compensated

for by their higher charge, although they are
likely to have higher coordination numbers.
27.2
26.3
Co(II) commonly adopts distorted tetrahedral

and five-coordinate geometries typical of
Zn(II) in enzymes. When substituted for
Zn(II), the enzyme generally retains catalytic
activity. Zn(II) is d10 and therefore colourless;
however, Co(II) is d7, and its peaks in the
UV-Vis spectrum are quite intense.
Copper slowly oxidises in air producing

copper oxides. The epidermis is slightly
acidic, meaning a small amount of the oxide
can dissolve to produce Cu2+, which is water
soluble and can pass through the skin.
27.3
B(OH)3, H2, CO, and OH. In neutral or

mildly acidic medium it would be protonated
to
produce
hydrogenboranocarbonate.
Hydrogenboranocarbonate can eliminate OH
to produce [H3BCO] adduct. [H3BCO] is
unstable when not under CO atmosphere and
CO can be easily displaced by water
molecules. The intermediate aquo adduct
[H3B(OH2)] rapidly decomposes to give
H2BOH and H2. H2BOH reacts rapidly with
another two water molecules to produce the
final products B(OH)3 and two more
equivalents of H2.
27.4
Choose a trace element (not CHNOPS); list

what its important chemical properties are,
including
aqueous
chemistry,
redox
chemistry; identify proteins in which such an
element appears; discuss how the elements
chemical properties suit it for its task.
27.5
Gallium(III) can bind to transferrin and

lactoferrin, and can even be incorporated into
ferritin. These enzymes use nitrogen and
oxygen donors to bind iron. Since Ga(III) also
has a good affinity for the same donors, it can
compete with Fe(III) for the binding sites
27.6
In the strongly acidic environment (pH ~ 3)

that abounds in organic acids, Bi(III)
compounds form polymeric species and
clusters that can form a protective layer (or
coating) on the stomach.
26.1
26.4
Acidity of coordinated water molecules is in

the order Fe(III) > Zn(II) > Mg(II). Ligandbinding rates are Mg(II) > Zn(II) > Fe(III).
26.5
Either EPR or Mssbauer spectroscopy.
26.6
The two central lines correspond to Fe3+. The

two new ones show a larger quadrupole
coupling and a higher isomer shift,
characteristics consistent with high-spin Fe2+.
Since the signals from Fe2+ and Fe3+ in the
reduced form are well separated, there is no
delocalization.
26.7
The change in structure suggests that the

coupling of proton and electron transfer can
also occur at the P-cluster by controlling
protonation of the exchangeable ligands.
26.8
Co(I) and Co(III); Fe(II) or Zn(II)
26.9
Would
indicate
the
presence
of
photosynthesis and consequently some lifeform that is capable of photosynthesis.
26.10
EPR spectroscopy; use of isotopically labelled

water molecules, for example H217O, can be
combined with Raman and IR spectroscopies.
CHAPTER 27
Self-tests
S27.1
By modifying R substituents (R1R5) on the

ligand backbone.

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What are the main topics covered in the document?

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What is the structure of the self-tests and exercises provided?

What is the structure of the self-tests and exercises provided?

Answers to self-tests and exercises

Please note that just the final numerical

779967m , 1.28 10 m or 1280 nm.

3d set of orbitals, 5 orbitals

The s electron already present in Li repels the

Period 4, Group 2, s block

Generally, going down a group the atomic

For a given value of n, the angular momentum

n2 (e.g., n2 = 1 for n = 1, n2 = 4 for n = 2, etc.)

When n = 5, l = 3 (for the f orbitals) and ml =

Comparing the plots for 1s (Figure 1.10) and

E(He+)/E(Be3+) = Z2(He+)/Z2(Be3+) = 22/42 =

E(H, n = 1) E(H, n = 6) = 13.6 eV 0.378

0.544eV , The discrepancy is due to the

ANSWERS TO SELF-TESTS AND EXERCISES

Each 4p orbital has one nodal plane; the total

The first ionization energies of strontium,

Both the first and the second ionization

dxy Function: xyR (r ) Label: xy

The 1s electrons shield the positive charge

1.70, 2.05, 2.40, 2.75, 3.10, 3.45, 3.80

The higher value of I2 for Cr relative to Mn is

Both of these atoms have an electron

See Figure 1.22 and the inside front cover of

In general, I1, Ae, and all increase from left

ANSWERS TO SELF-TESTS AND EXERCISES

general increase across the period is the

One 2s and three 2p

(c) Trigonal bipyramidal

Bond length (shortest to longest): CN, C=N,

Tetrahedral and octahedral

The single bond covalent radii decrease if we

ANSWERS TO SELF-TESTS AND EXERCISES

As a consequence of these two trends, the

2(Si-O) (Si=O) = 2(466 kJ) (640 kJ) =

Therefore two single bonds will always be

If N2 were to exist as N4 molecules with the

The atoms that obey the octet rule are O in

AD < BD < AC < AB

The configuration of C22 would be 1g21u2

ANSWERS TO SELF-TESTS AND EXERCISES

1g21u2 1u4. The bond order would be [22+4] = 2.

See figure 2.18. The bond order would be

See figure 2.22.

(a) The 5p and 5s of I, and the 4p and 4s of Br

Probably not stable in isolation; unstable in solution.

(a) (1/2)((2 + 4 + 2) (2 + 2)) = 2

(b) (1/2)((2 + 4 + 2) (2 + 4)) = 1

(a) Bond order increases from 2 to 2.5; bond

The line at about 15.2 eV corresponds to

Four atomic orbitals can yield

Your molecular orbital diagram for the N2

(a) Hypothetical example of (4c,2e) bonding;

(b) It is electron precise. It could very well

P- type lattice of chloride anions with caesium