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 acetophenone and ethyl propenoate. (1 Draw the structure of the product of the enamine formed between acetophenone and dimethylamine. + 2 C P орy aste ChemDoodle

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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 α,β-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 α,β-unsaturated carbonyl compound, and
  3. hydrolysis of the enamine in dilute acid to regenerate the ketone.

Consider the Stork reaction between acetophenone and ethyl propenoate.

 

Draw the structure of the product of the enamine formed between acetophenone and dimethylamine.

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 acetophenone and ethyl propenoate.
(1 Draw the structure of the product of the enamine formed between acetophenone and dimethylamine.
+ 2 C P
орy aste
ChemDoodle
Transcribed Image Text: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 acetophenone and ethyl propenoate. (1 Draw the structure of the product of the enamine formed between acetophenone and dimethylamine. + 2 C P орy aste ChemDoodle
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