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 propenenitrile and nitroethane. Sn ? ChemDoodle 9

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 propenenitrile and nitroethane. Sn ? ChemDoodle 9

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 28VC

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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.

Question

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 propenenitrile and nitroethane.
IF
ChemDoodle
9

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