ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
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Chapter 1, Problem 1.13P
Interpretation Introduction

(a)

Interpretation:

The resonance structure for the allyl anion that shows, along with the given structure, that the two CH2 carbons are equivalent and indistinguishable is to be drawn.

Concept introduction:

Most of the organic structures cannot be represented using single Lewis structure. Therefore, there exists more than one Lewis structure for representing a molecule or ion. These structures are known as resonance structures. These resonance structure combine together to give resonance hybrid that is lower in energy and is the most stable structure.

Interpretation Introduction

(b)

Interpretation:

The negative charge on each of the CH2 carbons is to be predicted.

Concept introduction:

Most of the organic structures cannot be represented using single Lewis structure. Therefore, there exists more than one Lewis structure for representing a molecule or ion. These structures are known as resonance structures. These resonance structure combine together to give resonance hybrid that is lower in energy and is the most stable structure.

Interpretation Introduction

(c)

Interpretation:

The single hybrid structure for the allyl anion that shows shared bonds as dashed lines and charges as partial charges is to be drawn.

Concept introduction:

Most of the organic structures cannot be represented using single Lewis structure. Therefore, there exists more than one Lewis structure for representing a molecule or ion. These structures are known as resonance structures. These resonance structure combine together to give resonance hybrid that is lower in energy and is the most stable structure.

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