Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
8th Edition
ISBN: 9780135213711
Author: Paula Bruice
Publisher: PEARSON+
Question
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Chapter 28, Problem 38P

(a)

Interpretation Introduction

Interpretation:

A mechanism should be proposed for the given reaction.

Concept introduction:

Pericyclic reactions are “ any concerted reaction in which bonds are formed or brocken in a cyclic transition state”.  There is a single transition state from start to finish, in contrast to a stepwise reaction.

In an electrocyclic reaction “one new sigma- bond is formed or brocken.”

Pearson eText Organic Chemistry -- Instant Access (Pearson+), Chapter 28, Problem 38P , additional homework tip  1

Diels-alder reaction is a cycloaddition reaction which is occurs between a conjugated diene and substituted alkene to form cyclohexene ring system.  This concerted reaction can be accelerated by heating or using some catalysts.

Mechanism gives the step wise processes occurs in a particular reaction.

(b)

Interpretation Introduction

Interpretation:

The product should be determined for the given reaction if trans-2-butene were used instead of ethene.

Concept introduction:

Pericyclic reactions are “ any concerted reaction in which bonds are formed or brocken in a cyclic transition state”.  There is a single transition state from start to finish, in contrast to a stepwise reaction.

In an electrocyclic reaction “one new sigma- bond is formed or brocken.”

Pearson eText Organic Chemistry -- Instant Access (Pearson+), Chapter 28, Problem 38P , additional homework tip  2

Diels-alder reaction is a cycloaddition reaction which is occurs between a conjugated diene and substituted alkene to form cyclohexene ring system.  This concerted reaction can be accelerated by heating or using some catalysts.

Mechanism gives the step wise processes occurs in a particular reaction.

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