Chemistry by OpenStax (2015-05-04)
Chemistry by OpenStax (2015-05-04)
1st Edition
ISBN: 9781938168390
Author: Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher: OpenStax
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Chapter 8, Problem 33E

How are the following similar, and how do they differ?

(a) σ molecular orbitals and π molecular orbitals

(b) ψ for an atomic orbital and ψ for a molecular orbital

(c) bonding orbitals and antibonding orbitals

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(a) Write a single Lewis structure for SO3 , and determine the hybridization at the S atom. (b) Are there other equivalent Lewis structures for the molecule? (c) Would you expect SO3 to exhibit delocalized π bonding?
Azo dyes are organic dyes that are used for many applications,such as the coloring of fabrics. Many azo dyes arederivatives of the organic substance azobenzene, C12H10N2.A closely related substance is hydrazobenzene, C12H12N2.The Lewis structures of these two substances are given (Recall the shorthand notation used for benzene.)(a) What is the hybridization at the N atom in each of thesubstances? (b) How many unhybridized atomic orbitalsare there on the N and the C atoms in each of the substances?(c) Predict the N—N—C angles in each of thesubstances. (d) Azobenzene is said to have greater delocalizationof its π electrons than hydrazobenzene. Discussthis statement in light of your answers to (a) and (b). (e) Allthe atoms of azobenzene lie in one plane, whereas thoseof hydrazobenzene do not. Is this observation consistentwith the statement in part (d)? (f) Azobenzene is an intensered-orange color, whereas hydrazobenzene is nearly colorless.Which molecule would be a better one to use in…
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Chapter 8 Solutions

Chemistry by OpenStax (2015-05-04)

Ch. 8 - Explain why a carbon atom cannot form five bonds...Ch. 8 - What is the hybridization of the central atom in...Ch. 8 - A molecule with the formula AB3 could have one of...Ch. 8 - Methionine, CH3SCH2CH2CH(NH2)CO2H, is an amino...Ch. 8 - Sulfuric acid is manufactured by a series of...Ch. 8 - Two important industrial chemicals, ethene, C2H4,...Ch. 8 - For many years after they were discovered, it was...Ch. 8 - Consider nitrous acid, HNO2 (HONO). (a) Write a...Ch. 8 - Strike-anywhere matches contain a layer of KClO3...Ch. 8 - Identify the hybridization of each carbon atom in...Ch. 8 - Write Lewis structures for NF3 and PP5. On the...Ch. 8 - In addition to NF3, two other fluoro derivatives...Ch. 8 - The bond energy of a C—C single bond averages 347...Ch. 8 - For the carbonate ion, CO32, draw all of the...Ch. 8 - A useful solvent that will dissolve salts as well...Ch. 8 - For the molecule allene, H2C=C=CH2, give the...Ch. 8 - Identify the hybridization of the central atom in...Ch. 8 - Describe the molecular geometry and hybridization...Ch. 8 - For each of the following molecules, indicate the...Ch. 8 - For each of the following structures, determine...Ch. 8 - Draw the orbital diagram for carbon in CO2 showing...Ch. 8 - Sketch the distribution of electron density in the...Ch. 8 - How are the following similar, and how do they...Ch. 8 - If molecular orbitals are created by combining...Ch. 8 - Can a molecule with an odd number of electrons...Ch. 8 - Can a molecule with an even number of electrons...Ch. 8 - Why are bonding molecular orbitals lower in energy...Ch. 8 - Calculate the bond order for an ion with this...Ch. 8 - Explain why an electron in the bonding molecular...Ch. 8 - Predict the valence electron molecular orbital...Ch. 8 - Determine the bond order of each member of the...Ch. 8 - For the first ionization energy for an N2...Ch. 8 - Compare the atomic and molecular orbital diagrams...Ch. 8 - Which of the period 2 homonuclear diatomic...Ch. 8 - A friend tells you that the 2s orbital for...Ch. 8 - True or false: Boron contains 2s22p1 valence...Ch. 8 - What charge would be needed on F2 to generate an...Ch. 8 - Predict whether the MO diagram S2 would show s-p...Ch. 8 - Explain why N22+ is diamagnetic, while O24+, which...Ch. 8 - Using the MO diagrams, predict the bond order for...
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