Chapter 1 Notes

Structure and Bonding 11
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The general rule of bonding. Atoms strive to attain a complete outer shell of valence electrons
(Section 1.2). H wants 2 electrons. Second row elements want 8 electrons.
nonbonded electron pair
H C N O X X = F, Cl, Br, I
Usual number of bonds

in neutral atoms 1 4 3 2 1
Number of nonbonded 0 0 1 2 3
electron pairs
The sum (# of bonds + # of lone pairs) = 4 for all elements except H.
Formal charge (FC) is the difference between the number of valence electrons of an atom and the
number of electrons it owns (Section 1.3C). See Sample Problem 1.5 for a stepwise example.
number of number of electrons

Definition: formal charge = valence electrons an atom "owns"
Examples:
C C C
C shares 8 electrons. Each C shares 6 electrons. C shares 6 electrons.

C "owns" 4 electrons. Each C "owns" 3 electrons. C has 2 unshared electrons.
FC = 0 FC = +1 C "owns" 5 electrons.
FC = 1
Curved arrow notation shows the movement of an electron pair. The tail of the arrow always
begins at an electron pair, either in a bond or a lone pair. The head points to where the electron pair
moves (Section 1.5).
Move an electron pair to O.
O O
H C N H H C N H
A B
Use this electron pair to form a double bond.
Electrostatic potential plots are color-coded maps of electron density, indicating electron rich and
electron deficient regions (Section 1.11).
Chapter 12
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A properly drawn Lewis structure shows the number of bonds and lone pairs present around each atom
in a molecule. In a valid Lewis structure, each H has 2 electrons, and each second row element has no
more than 8. This is the first step needed to determine many properties of a molecule.
Geometry [linear, trigonal planar, or tetrahedral] (Section 1.6)
Lewis structure Hybridization [sp, sp2, or sp3] (Section 1.8)
Types of bonds [single, double, or triple] (Sections 1.3, 1.9)
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The basic principles:
Resonance occurs when a compound cannot be represented by a single Lewis structure.
Two resonance structures differ only in the position of nonbonded electrons and bonds.
The resonance hybrid is the only accurate representation for a resonance-stabilized compound. A
hybrid is more stable than any single resonance structure because electron density is delocalized.

O O O
CH3CH2 C CH3CH2 C CH3CH2 C delocalized charges

O O O
delocalized bonds
resonance structures hybrid
The difference between resonance structures and isomers:

Two isomers differ in the arrangement of both atoms and electrons.
Resonance structures differ only in the arrangement of electrons.
O O O
CH3 C CH3CH2 C CH3CH2 C
O CH3 O H O H
isomers resonance structures
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The number of groups around an atom determines both its geometry (Section 1.6) and hybridization
(Section 1.8).
Number of Geometry Bond angle (o) Hybridization Examples

groups
2 linear 180 sp BeH2, HCCH
3 trigonal planar 120 sp2 BF3, CH2=CH2
4 tetrahedral 109.5 sp3 CH4, NH3, H2O
Structure and Bonding 13
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Shorthand methods are used to abbreviate the structure of organic molecules.
CH3 H CH3
= CH3 C C C CH3 = (CH3)2CHCH2C(CH3)3
H H CH3
skeletal structure isooctane condensed structure
A carbon bonded to four atoms is tetrahedral in shape. The best way to represent a tetrahedron is to
draw two bonds in the plane, one in front, and one behind.
Four equivalent drawings for CH4
H H HH H H
C
C C C
H H H
H H H H H HH
Each drawing has two solid lines, one wedge, and one dashed line.
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Bond length decreases across a row and increases down a column of the periodic table (Section
1.6A).
C H > N H > O H H F < H Cl < H Br
increasing bond length

Bond length decreases as the number of electrons between two nuclei increases (Section 1.10A).
CH3 CH3 < CH2 CH2 < H C C H
Bond length increases as the percent s-character decreases (Section 1.10B).
Csp H Csp2 H Csp3 H
Bond length and bond strength are inversely related. Shorter bonds are stronger bonds (Section
1.10)
longest CC bond shortest CC bond
weakest bond C C C C C C
strongest bond
increasing bond strength

Chapter 14
Sigma () bonds are generally stronger than bonds (Section 1.9).
C C C C C C
1 strong bond 1 stronger bond 1 stronger bond

1 weaker bond 2 weaker bonds
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Electronegativity increases across a row and decreases down a column of the periodic table.
A polar bond results when two atoms of different electronegativity are bonded together. Whenever
C or H is bonded to N, O or any halogen, the bond is polar.
A polar molecule has either one polar bond, or two or more bond dipoles that reinforce.

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Structure and Bonding 11

nonbonded electron pair

Usual number of bonds

The sum (# of bonds + # of lone pairs) = 4 for all elements except H.

number of number of electrons

C shares 8 electrons. Each C shares 6 electrons. C shares 6 electrons.

Geometry [linear, trigonal planar, or tetrahedral] (Section 1.6)

Lewis structure Hybridization [sp, sp2, or sp3] (Section 1.8)

Types of bonds [single, double, or triple] (Sections 1.3, 1.9)

RReessoonnaannccee ((SSeeccttiioonn 11..55))

The difference between resonance structures and isomers:

isomers resonance structures

Number of Geometry Bond angle (o) Hybridization Examples

Four equivalent drawings for CH4

increasing bond length

CH3 CH3 < CH2 CH2 < H C C H

increasing bond length

Bond length increases as the percent s-character decreases (Section 1.10B).

Csp H Csp2 H Csp3 H

increasing bond length

increasing bond strength

Sigma () bonds are generally stronger than bonds (Section 1.9).

1 strong bond 1 stronger bond 1 stronger bond

EElleeccttrroonneeggaattiivviittyy aanndd ppoollaarriittyy ((SSeeccttiioonn 11..1111,, 11..1122))

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