Organic Chemistry
Organic Chemistry
11th Edition
ISBN: 9781118133576
Author: T. W. Graham Solomons, Craig Fryhle
Publisher: Wiley, John & Sons, Incorporated
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Chapter 13, Problem 41P
Interpretation Introduction

Interpretation:

The structure of the product of reaction in which cyclopentadiene undergoing a Diels–Alder reaction with ethene at 160°180°C is to be written.

Concept introduction:

A Diels–Alder reaction is one between a conjugate diene and a reactant containing a double bond (dienophile)to forma product. The product is called adduct.

Diels–Alder reactions are highly stereospecific. The configuration of the dienophile is retained in the product and the reaction is a syn addition reaction.

The dienes react with dienophiles in cis forms rather than trans forms.

Endo is favored in the transition state of a Diels–Alder reaction because it has a lower energy.

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