Chemistry: The Molecular Nature of Matter and Change - Standalone book
Chemistry: The Molecular Nature of Matter and Change - Standalone book
7th Edition
ISBN: 9780073511177
Author: Martin Silberberg Dr., Patricia Amateis Professor
Publisher: McGraw-Hill Education
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Chapter 11, Problem 11.52P
Interpretation Introduction

Interpretation:

The reason for the restricted rotation about the CN bond is to be explained. Also, the types of bonding involved are to be shown.

Concept introduction:

When bonds in a molecule can be expressed by different Lewis structures then resonance structures are used to depict the bonding in that molecule. This resonance structure has the same placement of atoms but different locations of bonding and lone pairs of electrons also one resonance form can be converted into another by moving lone pairs to bonding positions, and vice versa.

More important resonance structure selected as follows:

1. Always prefer smaller formal charge over the larger formal charge.

2. Always prefer the different non zero formal charge on adjacent atoms instead of the same non zero formal charge.

3. A more negative formal charge must be located on the most electronegative atom.

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Chapter 11 Solutions

Chemistry: The Molecular Nature of Matter and Change - Standalone book

Ch. 11 - Prob. 11.3PCh. 11 - Prob. 11.4PCh. 11 - Prob. 11.5PCh. 11 - Give the number and type of hybrid orbital that...Ch. 11 - What is the hybridization of nitrogen in each of...Ch. 11 - What is the hybridization of carbon in each of the...Ch. 11 - Prob. 11.9PCh. 11 - Prob. 11.10PCh. 11 - Prob. 11.11PCh. 11 - Prob. 11.12PCh. 11 - Phosphine (PH3) reacts with borane (BH3) as...Ch. 11 - The illustrations below depict differences in...Ch. 11 - Use partial orbital diagrams to show how the...Ch. 11 - Use partial orbital diagrams to show how the...Ch. 11 - Prob. 11.17PCh. 11 - Prob. 11.18PCh. 11 - Methyl isocyanate, , is an intermediate in the...Ch. 11 - Are these statements true or false? Correct any...Ch. 11 - Prob. 11.21PCh. 11 - Identify the hybrid orbitals used by the central...Ch. 11 - Prob. 11.23PCh. 11 - Identify the hybrid orbitals used by the central...Ch. 11 - Prob. 11.25PCh. 11 - Prob. 11.26PCh. 11 - Certain atomic orbitals on two atoms were combined...Ch. 11 - Prob. 11.28PCh. 11 - Antibonding MOs always have at least one node. Can...Ch. 11 - Prob. 11.30PCh. 11 - Prob. 11.31PCh. 11 - The molecular orbitals depicted are derived from...Ch. 11 - The molecular orbitals depicted below are derived...Ch. 11 - Prob. 11.34PCh. 11 - Use an MO diagram and the bond order you obtain...Ch. 11 - Prob. 11.36PCh. 11 - Prob. 11.37PCh. 11 - Prob. 11.38PCh. 11 - Prob. 11.39PCh. 11 - Epinephrine (or adrenaline; below) is a naturally...Ch. 11 - Prob. 11.41PCh. 11 - Isoniazid (below) is an antibacterial agent that...Ch. 11 - Prob. 11.43PCh. 11 - Prob. 11.44PCh. 11 - Prob. 11.45PCh. 11 - Prob. 11.46PCh. 11 - Tryptophan is one of the amino acids found in...Ch. 11 - Prob. 11.48PCh. 11 - Prob. 11.49PCh. 11 - Prob. 11.50PCh. 11 - Prob. 11.51PCh. 11 - Prob. 11.52PCh. 11 - Sulfur forms oxides, oxoanions, and halides. What...Ch. 11 - Prob. 11.54PCh. 11 - Use an MO diagram to find the bond order and...Ch. 11 - Acetylsalicylic acid (aspirin), the most widely...Ch. 11 - Prob. 11.57P
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