The Michael reaction is a conjugate addition reaction between a stable nucleophilic enolate ion (the donor) and an a,ß-unsaturated carbonyl compound (the acceptor). Draw the structure of the product of the Michael reaction between propenal and diethyl malonate. Sn 11 ChemDoodle 96

The Michael reaction is a conjugate addition reaction between a stable nucleophilic enolate ion (the donor) and an a,ß-unsaturated carbonyl compound (the acceptor). Draw the structure of the product of the Michael reaction between propenal and diethyl malonate. Sn 11 ChemDoodle 96

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter23: Amines

Section: Chapter Questions

Problem 23.36P

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Concept explainers

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.

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The Michael reaction is a conjugate addition reaction between a stable nucleophilic enolate ion (the donor) and an a,ẞ-unsaturated carbonyl compound (the acceptor).
Draw the structure of the product of the Michael reaction between propenal and diethyl malonate.
IF
ChemDoodle
96

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