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Ch.8 - Basic Concepts of Chemical Bonding

Chapter 8, Problem 96b

Mothballs are composed of naphthalene, C10H8, a molecule that consists of two six-membered rings of carbon fused along an edge, as shown in this incomplete Lewis structure:

(b) Do you expect the C—C bond lengths in the molecule to be similar to those of C—C single bonds, C ═ C double bonds, or intermediate between C—C single and C ═ C double bonds?

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Hi everyone, so I asked. The following statements is true For the bond length infinite three. If you look at a typical band lint for Cinnabon, This is 154 km for double bond, This is 133 km. If you look at the length of the single bonds, We see that they live between 133 and 154. This is going to be C. The carbon carbon bond length of three are similar to the intermediate between the carbon, carbon. Single bonds in the carbon carbon double bonds, and this is because it exhibits a resonance hybrid. So the bonds are average, they're gonna be somewhere in between. Thanks for watching my video and I hope it was up for
Related Practice
Textbook Question

The following three Lewis structures can be drawn for N2O:

(a) Using formal charges, which of these three resonance forms is likely to be the most important?

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Textbook Question

The following three Lewis structures can be drawn for N2O:

(b) The N—N bond length in N2O is 1.12 Å, slightly longer than a typical N ≡N bond; and the N— O bond length is 1.19 Å, slightly shorter than a typical N ═O bond (see Table 8.4). Based on these data, which resonance structure best represents N2O?

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Textbook Question

Mothballs are composed of naphthalene, C10H8, a molecule that consists of two six-membered rings of carbon fused along an edge, as shown in this incomplete Lewis structure:(a) Draw all of the resonance structures of naphthalene. How many are there?

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Textbook Question

Mothballs are composed of naphthalene, C10H8, a molecule that consists of two six-membered rings of carbon fused along an edge, as shown in this incomplete Lewis structure:

(c) Not all of the C—C bond lengths in naphthalene are equivalent. Based on your resonance structures, how many C—C bonds in the molecule do you expect to be shorter than the others?

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Textbook Question

a. Triazine, C3H3N3, is like benzene except that in triazine every other C—H group is replaced by a nitrogen atom. Draw the Lewis structure(s) for the triazine molecule.

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Textbook Question

Ortho-Dichlorobenzene, C6H4Cl2, is obtained when two of the adjacent hydrogen atoms in benzene are replaced with Cl atoms. A skeleton of the molecule is shown here. (a) Complete a Lewis structure for the molecule using bonds and electron pairs as needed.

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