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
Question
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Chapter 12, Problem 12.48P
Interpretation Introduction

(a)

Interpretation:

How the given epoxide can be produced from an alkene is to shown.

Concept introduction:

An epoxide can be produced from an alkene using a peroxyacid (RCO3H), also called a peracid. Treatment of an alkene with a peroxyacid (or peracid) produces an epoxide. The reagent MCPBA, a peroxyacid, can form an epoxide in a one-step reaction with an alkene. The stereochemistry that describes the C=C bond remains the same in the product.

Interpretation Introduction

(b)

Interpretation:

How the given epoxide can be produced from an alkene is to shown.

Concept introduction:

An epoxide can be produced from an alkene using a peroxyacid (RCO3H), also called a peracid. Treatment of an alkene with a peroxyacid (or peracid) produces an epoxide. The reagent MCPBA, a peroxyacid, can form an epoxide in a one-step reaction with an alkene.

Interpretation Introduction

(c)

Interpretation:

How the given epoxide can be produced from an alkene is to be shown.

Concept introduction:

An epoxide can be produced from an alkene using a peroxyacid (RCO3H), also called a peracid. Treatment of an alkene with a peroxyacid (or peracid) produces an epoxide. The reagent MCPBA, a peroxyacid, can form an epoxide in a one-step reaction with an alkene.

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Students have asked these similar questions
Provide the mechanism for each step of the given reaction, showing the major product as well.
Synthesize the resulting product using the following compounds using the appropriate reaction steps.
Draw the product for the following alkene addition (hydrogenation) reaction.

Chapter 12 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

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