9701 w09 Ms 21

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS
GCE Advanced Subsidiary Level and GCE Advanced Level
MARK SCHEME for the October/November 2009 question paper

for the guidance of teachers
9701 CHEMISTRY
9701/21 Paper 21 (AS Structured Questions), maximum raw mark 60
This mark scheme is published as an aid to teachers and candidates, to indicate the requirements of
the examination. It shows the basis on which Examiners were instructed to award marks. It does not
indicate the details of the discussions that took place at an Examiners’ meeting before marking began,
which would have considered the acceptability of alternative answers.
Mark schemes must be read in conjunction with the question papers and the report on the
examination.
• CIE will not enter into discussions or correspondence in connection with these mark schemes.
CIE is publishing the mark schemes for the October/November 2009 question papers for most IGCSE,
GCE Advanced Level and Advanced Subsidiary Level syllabuses and some Ordinary Level
syllabuses.
www.xtremepapers.net
Page 2 Mark Scheme: Teachers’ version Syllabus Paper
GCE A/AS LEVEL – October/November 2009 9701 21
1 (a) same proton number/atomic number (1)

different mass number/nucleon number (1) [2]
(b) Ar =
(24 × 78.60 ) + (25 × 10.11) + (26 × 11.29 ) (1)
100
1886.4 + 252.75 + 293.54 2432.69

= =
100 100
which gives Ar = 24.33 (1)

penalise (–1) for misuse of significant figures [2]
(c)
isotopes number of
protons neutrons electrons

226
Ra 88 138 88
238
U 92 146 92
allow one mark for each correct column (3 × 1)

if there are no correct columns,
allow maximum one mark for a correct row [3]
(d) (i) Ra2+ (1)
(ii) less than (502 + 966)

allow answers in the range 1000–1400 kJ mol–1 (1)
ionisation energies decrease down the Group

or must be less than IE for Ba → Ba2+
or size of atom increases down Group/
electrons are further away from nucleus
or there is increased shielding down Group (1)
allow ecf on answer to (i) [3]
[Total: 10]
© UCLES 2009
2 (a) (i) configuration ends in s2

or there are two electrons in outermost/valence shell (1)
(ii) RaCO3/radium carbonate (1) [2]
(b) anode Br – → ½Br2 + e– (1)

cathode Ra2+ + 2e– → Ra (1) [2]
(c) (i) water slow reaction

gas bubbles
gas is colourless any 2 (2)
steam Mg glows
vigorous reaction
white solid formed any 2 (2)
(ii) Mg + H2O → MgO + H2 (1) [5]
(d) (i) Ra(s) + 2H2O(l) → Ra(OH)2(aq) + H2(g) eqn. (1)

s.s. (1)
(ii) radium dissolves/disappears

gas evolved
gas is colourless
heat evolved any 2 (2)
(iii) 10–14 (1)
(iv) more – no mark for this alone

because reactivity of metals increases down the Group
or electrons are further from nucleus
or IE is lower
or Ra is a stronger reducing agent (1) [6]
[Total: 15]
© UCLES 2009
3 (a) (i) CH4 + Cl2 → CH3Cl + HCl

–75 0 –82 –92 (1)
reaction = –82 + (–92) – (–75)

= –99 kJ mol–1 (1)
(ii) CH4 + I2 → CH3I + HI

broken C–H I–I made C–I H–I
410 151 240 299 (1)
reaction = –240 + (–299) + 410 + 151

= +22 kJ mol–1 (1)
(iii) activation energy is too great (1) [5]
(b) (i) initiation (1)

Cl2 + uvl → 2Cl (1)
propagation (1)
CH4 + Cl → CH3 + HCl

CH3 + Cl2 → CH3Cl + Cl both needed (1)
termination (1)
CH3 + CH3 → C2H6 or

CH3 + Cl → CH3Cl or
Cl + Cl → Cl2 (1)
(ii) CH3/methyl radical (1) [7]
© UCLES 2009
(c)
energy
I
Ea
CH4 + Cl2
∆H
CH3Cl + HCl
progress of reaction
correct placement of 16 kJ (1)
correct placement of –99 kJ (allow ecf on wrong calculation in (a) (i)) (1)
intermediate clearly shown at I (1)
correct ‘double peak’ shape (1)
second peak lower than first (1) [5]
[Total: max 16]
© UCLES 2009
4 (a) (i) C2H5O (1)
(ii) OH
(1)
(iii)
compound type of isomerism
A cis-trans or geometrical
D optical
allow one mark if both A and D are correctly identified

but in both cases, the type of isomerism is incorrect
(1 + 1) [4]
(b) (i) dehydration/elimination (1)
(ii) conc. H2SO4/P4O10/Al2O3/pumice etc. (1)
(iii) CH2=CHCH=CH2/butadiene/buta-1,3-diene (1) [3]
(c) (i) CH3CH2CH(OH)CH3 (1)
(ii) steam with H3PO4 catalyst or

conc. H2SO4 then water (1 + 1)
(iii) Cr2O72– /H+ (1) [4]
(d) functional group isomerism

or structural isomerism
not positional isomerism (1) [1]
[Total: 12]
© UCLES 2009
5 (a) G is HCHO/methanal (1) [1]
(b) (i) carboxylic acid/carboxyl/–CO2H

not acid (1)
(ii) H is CH3CO2H/ethanoic acid (1)
(iii) J is CH3CH(OH)CO2H/2-hydroxypropanoic acid

allow HOCH2CH2CO2H/3-hydroxypropanoic acid (1) [3]
(c) K is CH3COCO2H (1) [1]
(d) (i) L is
H CH3
C
O C O
O C O
C
H CH3
allow as ecf on HOCH2CH2CO2H/3-hydroxypropanoic acid
CH2 CH2
O C O
O C O
CH2 CH2
(1)
(ii) esterification
allow elimination/dehydration/condensation (1) [2]
[Total: 7]
© UCLES 2009

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UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS

GCE Advanced Subsidiary Level and GCE Advanced Level

MARK SCHEME for the October/November 2009 question paper

1 (a) same proton number/atomic number (1)

1886.4 + 252.75 + 293.54 2432.69

which gives Ar = 24.33 (1)

protons neutrons electrons

allow one mark for each correct column (3 × 1)

(d) (i) Ra2+ (1)

(ii) less than (502 + 966)

ionisation energies decrease down the Group

allow ecf on answer to (i) [3]

2 (a) (i) configuration ends in s2

(ii) RaCO3/radium carbonate (1) [2]

(b) anode Br – → ½Br2 + e– (1)

(c) (i) water slow reaction

(ii) Mg + H2O → MgO + H2 (1) [5]

(d) (i) Ra(s) + 2H2O(l) → Ra(OH)2(aq) + H2(g) eqn. (1)

(ii) radium dissolves/disappears

(iii) 10–14 (1)

(iv) more – no mark for this alone

3 (a) (i) CH4 + Cl2 → CH3Cl + HCl

reaction = –82 + (–92) – (–75)

(ii) CH4 + I2 → CH3I + HI

reaction = –240 + (–299) + 410 + 151

(iii) activation energy is too great (1) [5]

(b) (i) initiation (1)

CH4 + Cl → CH3 + HCl

CH3 + CH3 → C2H6 or

(ii) CH3/methyl radical (1) [7]

[Total: max 16]

4 (a) (i) C2H5O (1)

allow one mark if both A and D are correctly identified

(b) (i) dehydration/elimination (1)

(ii) conc. H2SO4/P4O10/Al2O3/pumice etc. (1)

(iii) CH2=CHCH=CH2/butadiene/buta-1,3-diene (1) [3]

(c) (i) CH3CH2CH(OH)CH3 (1)

(ii) steam with H3PO4 catalyst or

(iii) Cr2O72– /H+ (1) [4]

(d) functional group isomerism

5 (a) G is HCHO/methanal (1) [1]

(b) (i) carboxylic acid/carboxyl/–CO2H

(ii) H is CH3CO2H/ethanoic acid (1)

(iii) J is CH3CH(OH)CO2H/2-hydroxypropanoic acid

(c) K is CH3COCO2H (1) [1]

allow as ecf on HOCH2CH2CO2H/3-hydroxypropanoic acid

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