ORGANIC CHEMISTRY - LOOSELEAF W/CONNECT
ORGANIC CHEMISTRY - LOOSELEAF W/CONNECT
6th Edition
ISBN: 9781266060144
Author: SMITH
Publisher: MCG
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Chapter 16.5, Problem 6P
Interpretation Introduction

(a)

Interpretation: The acid chloride which is needed to prepare the given ketones from benzene using a Friedel-Craft acylation is to be predicted.

Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. AlCl3 is used as Lewis acid which ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which is resonance stabilized. Then the electrophile reacts with benzene.

Interpretation Introduction

(b)

Interpretation: The acid chloride which is needed to prepare the given ketones from benzene using a Friedel-Craft acylation is to be predicted.

Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. AlCl3 is used as Lewis acid which ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which is resonance stabilized. Then the electrophile reacts with benzene.

Interpretation Introduction

(c)

Interpretation: The acid chloride which is needed to prepare the given ketones from benzene using a Friedel-Craft acylation is to be predicted.

Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. AlCl3 is used as Lewis acid which ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which is resonance stabilized. Then the electrophile reacts with benzene.

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Chapter 16 Solutions

ORGANIC CHEMISTRY - LOOSELEAF W/CONNECT

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