The Stork reaction is a condensation reaction between an enamine donor and an α,β-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence offormation of an enamine from a ketone,Michael addition to an α,β-unsaturated carbonyl compound, andhydrolysis of the enamine in dilute acid to regenerate the ketone.Consider the Stork reaction between cyclohexanone and propenal Draw the structure of the product of the enamine formed between cyclohexanone and dimethylamine.- Michael addition to an α,β-unsaturated carbonyl compound, and- hydrolysis of the enamine in dilute acid to regenerate the ketone. This question has multiple parts. Work all the parts to get the most points.The Stork reaction is a condensation reaction between an enamine donor and an a,ß-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of1. formation of an enamine from a ketone.2. Michael addition to an a,ß-unsaturated carbonyl compound, and3. hydrolysis of the enamine in dilute acid to regenerate the ketone.Consider the Stork reaction between cyclohexanone and propenal.Draw the structure of the product of the enamine formed between cyclohexanone and dimethylamine.opyasteChemDoodleSubmit

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This question has multiple parts. Work all the parts to get the most points. The Stork reaction is a condensation reaction between an enamine donor and an a,ß-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of 1. formation of an enamine from a ketone. 2. Michael addition to an a,ß-unsaturated carbonyl compound, and 3. hydrolysis of the enamine in dilute acid to regenerate the ketone. Consider the Stork reaction between cyclohexanone and propenal. Draw the structure of the product of the enamine formed between cyclohexanone and dimethylamine. opy aste

This question has multiple parts. Work all the parts to get the most points. The Stork reaction is a condensation reaction between an enamine donor and an a,ß-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of 1. formation of an enamine from a ketone. 2. Michael addition to an a,ß-unsaturated carbonyl compound, and 3. hydrolysis of the enamine in dilute acid to regenerate the ketone. Consider the Stork reaction between cyclohexanone and propenal. Draw the structure of the product of the enamine formed between cyclohexanone and dimethylamine. opy aste

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter23: Addition To A Carbonyl

Section: Chapter Questions

Problem 16E

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