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6.4 (i) is not correct; there are only eight valence electrons (should have ten); neither N nor C has an octet.
(ii) is not correct; C has too many valence electrons (has twelve); O has too few (each has six).
(iii) is not correct; S has too few valence electrons (needs two more).
6.5
(i) (ii) (iii)
(a) Group 7A 0 +1 +2
(b) Group 5A –2 –1 0
(c) Group 3A –4 –3 –2
6.7 (i) is not a resonance structure of the original because it is a different arrangement of atoms.
6.9 P can violate the octet rule and form more than the three bonds in PCl 3 by accepting additional electrons in
empty outer d orbitals; N does not have any d orbitals to violate the octet rule and so cannot form more than
the three bonds in NCl3.
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Chapter 6: Representing Molecules
6.10 In the order of decreasing formal charge, the list of structures is ii > iii > i.
Key Skills
6.1 a, c
6.2 b, e
6.3 c
6.4 a
6.1 Lewis first suggested that a chemical bond involves atoms that share electrons. He summarized much
of his theory of chemical bonding with the octet rule.
6.2 A Lewis symbol consists of an element’s symbol surrounded by dots representing the valence electrons.
A Lewis structure is a representation of the covalent bonds in a molecule.
The octet rule says that atoms will gain, lose, or share electrons to achieve noble gas configuration.
Example:
Bond length is defined as the distance between the nuclei of two covalently bonded atoms in a molecule.
Example:
6.4 The valence subshells of first-period elements can hold only two electrons, but in second-period
elements the subshells can hold a total of eight electrons. So, it is mainly second-period elements that
lose, gain, or share electrons attain the noble gas configuration. The octet rule can be violated by
higher-period elements expanding their valence shells into empty d orbitals.
6.5 According to the octet rule, atoms without d orbitals will lose, gain, or share electrons to achieve a noble gas
electron configuration. For hydrogen, the octet rule dictates that it has two electrons, giving it the
electronic configuration of the nearest noble gas, helium.
6.6 If the bond is formed between two atoms and consists of one shared pair of electrons, it is called a
single bond. A double bond is a multiple bond in which the atoms share two pairs of electrons; in a
triple bond, atoms share three pairs of electrons.
Single bond
e.g., C–C in ethane (C2H6)
Double bond
e.g., C=C in ethylene (C2H4)
Triple bond
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Chapter 6: Representing Molecules
Single bonds are longer than double bonds, and double bonds are longer than triple bonds.
6.7 Bond length is defined as the distance between the nuclei of two covalently bonded atoms in a molecule.
For a given pair of atoms (identical atoms), triple bonds are shorter than double bonds and double bonds are
shorter than single bonds. The shorter multiple bonds are also shorter than single bonds. The bond strength
can be quantified by measuring the quantity of energy required to break off. Because multiple bonds involve
the sharing of multiple pairs of electrons, the bond energies of double and triple bonds between two atoms
are higher than that of a single bond between the same atoms. In short, when bond length decreases, the
bond strength increases.
6.8 a. I and Cl should form a covalent compound; both the elements are nonmetals. The only possibility would
be ICl, iodine chloride.
b. Mg and F will form an ionic compound; Mg is a metal, whereas F is a nonmetal. The substance will be
MgF2, magnesium fluoride.
6.10 Electronegativity is the ability of an atom in a compound to draw electrons to itself that it shares in a
chemical bond with another atom, whereas electron affinity refers to an isolated atom’s ability to
attract an additional electron in the gas phase. Electron affinity is an experimentally measurable
quantity, whereas electronegativity is an estimated number that cannot be measured directly.
In general, electronegativity increases from left to right across a period in the periodic table. Within a
group, electronegativity decreases with increasing atomic number.
6.11 A polar covalent bond is a bond in which electrons are shared but are not shared equally by the two
atoms.
6.12 Strategy: Rearrange Equation 6.1 to solve for Q. Convert the resulting charge in coulombs to charge in
units of electronic charge.
Setup: The dipole moments must be converted from debye to C m and the distance between the ions
must be converted to meters.
3.336 1030 C m
µ = 1.24 D 4.137 1030 C m
1D
11010 m
r = 1.57 Å 1.57 1010 m
1Å
Solution: In coulombs:
µ 4.137 1030 C m
Q 10
2.635 1020 C
r 1.57 10 m
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Chapter 6: Representing Molecules
1 e
2.635 1020 C 0.164 e
1.6022 1019 C
Therefore, the partial charges on Cl and O in ClO are +0.164 and –0.164, respectively.
6.13 Strategy: Use Equation 6.1 to solve for the dipole moment, µ, of AlF.
Setup: The partial charges on Al and F are +0.019 and –0.019, respectively. In units of electronic
charge, this is 0.019 e–.
The charge units of electronic charge must be converted to coulombs and the distance between
the partial charges converted to meters. The calculated dipole moments should be expressed as
debyes (1 D = 3.336 × 10–30 C · m).
1.6022 1019 C
0.019 e 3.044 1021 C
1 e
1.0 1012 m
165 pm 1.65 1010 m
1 pm
Solution: µ=Q×r
µ = 5.023 × 10–31 C m
6.14 Strategy: Use Equation 6.1 to calculate the dipole moment of BrF assuming that the charges on Br and F
are +1 and –1, respectively; and use Equation 6.2 to calculate percent ionic character. The
magnitude of the charges must be expressed in coulombs (1 e– = 1.6022 × 10–19 C); the bond
length (r) must be expressed in meters (1 Å = 1 × 10–10 m); and the calculated dipole moment
should be expressed in debyes (1 D = 3.336 × 10–30 C m).
Setup: The bond length is 1.76 Å (1.76 × 10 –10 m) and the measured dipole moment of BrF is 1.42 D.
Solution: The expected dipole moment if the magnitude of charges were 1.6022 × 10–19 C is
µ=Q×r
µ = 2.820 × 10–29 C · m
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Chapter 6: Representing Molecules
1D
2.820 1029 C m 8.4532 D
3.336 1030 C m
1.42 D
100 % 16.8%
8.4532 D
6.15 Strategy: Use Equation 6.1 to calculate the dipole moment of BaO assuming that the charges on Ba and O
are +2 and –2, respectively. Then, rearrange Equation 6.2 to solve for the measured (observed)
dipole moment. The magnitude of the charges must be expressed in coulombs (1 e– = 1.6022 ×
10–19 C; therefore 2 e– = 2 × 1.6022 × 10–19 C, or 3.2044 × 10–19 C). The bond length (r) must be
expressed in meters (1 pm = 1 × 10–12 m); and the measured dipole moments should be
expressed in debyes (1 D = 3.336 × 10–30 C·m).
Setup: The bond length is 194 pm (1.94 × 10 –10 m) and the percent ionic character of the Ba–O bond is
85.3% or 85.3/100 = 0.853.
Solution: The expected dipole moment if the magnitude of charges were 3.2044 × 10–19 C is:
µ=Q×r
µ = 6.217 × 10–29 C · m
1D
6.217 1029 C m 18.636 D
3.336 1030 C m
µmeasured
0.853
18.636 D
µmeasured = 15.9 D
BY: 3.8 3.3 0.5; RY: 3.3 2.8 0.5; GY: 3.3 1.3 2.0; BG: 3.8 1.3 2.5
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