Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
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Chapter 12, Problem 12.19P
Interpretation Introduction

Interpretation:

The missing compounds (products) for the given reaction sequence from A to C are to be identified.

Concept introduction:

Alcohols, when heated with a strong acid, undergo an E1 elimination reaction to yield alkene. Heat favors elimination over substitution. The alkene that has been formed, as a result of the above reaction, is converted to an epoxide using the reagent MCPBA (peroxyacid). It is an electrophilic addition reaction of the peroxy group to an alkene. MCPBA contains the ‘peroxy’ (-COOOH) group, which acts as an electrophile and alkene acts as a nucleophile.

Epoxides undergo SN2, a type of reaction with strong nucleophiles, such as HO-. As the reaction is SN2, inversion of the configuration is observed in the substituted product. If chiral products are produced, then a mixture of stereoisomers is produced as a final product.

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Organic Chemistry: Principles and Mechanisms (Second Edition)

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