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
Book Icon
Chapter 12, Problem 12.47P
Interpretation Introduction

(a)

Interpretation:

The mechanism and the product(s) for the given reaction are to be drawn.

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. Rearrangements and rotations about C=C bond are not permitted during the course of the reaction. The stereochemistry that describes the C=C bond remains the same in the product.

Interpretation Introduction

(b)

Interpretation:

The mechanism and the product(s) for the given reaction are to be drawn.

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. Rearrangements and rotations about C=C bond are not permitted during the course of the reaction. The stereochemistry that describes the C=C bond remains the same in the product.

Blurred answer
Students have asked these similar questions
Draw the complete mechanism for the reaction below, including stereochemistry.
Please draw out the whole mechanism for the following reaction.
For the following reactions draw the full mechanism of each one .

Chapter 12 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning