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
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
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
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
formation of an enamine from a ketone,
Michael addition to an α,β-unsaturated carbonyl compound, and
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.
Transcribed Image Text:The following text is an excerpt focused on explaining a specific chemical reaction for educational purposes.
---
**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**.
1. **Draw the structure of the product of the enamine formed between acetophenone and dimethylamine.**
[There is an interactive drawing tool provided for drawing chemical structures, labeled as ChemDoodle®, with various controls for drawing molecular structures like bonds and atoms.]
---
This educational content prompts students to engage with the chemical process by drawing the intermediate enamine structure using interactive software. The diagram interface includes tools for editing molecular structures, indicative of steps in organic synthesis education.
Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
![The following text is an excerpt focused on explaining a specific chemical reaction for educational purposes.
---
**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**.
1. **Draw the structure of the product of the enamine formed between acetophenone and dimethylamine.**
[There is an interactive drawing tool provided for drawing chemical structures, labeled as ChemDoodle®, with various controls for drawing molecular structures like bonds and atoms.]
---
This educational content prompts students to engage with the chemical process by drawing the intermediate enamine structure using interactive software. The diagram interface includes tools for editing molecular structures, indicative of steps in organic synthesis education.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb1a68961-4ff0-4515-a729-3be4df9f661e%2Fb5b0d24f-d3af-4c3b-8e11-e70ed21145c4%2Ft322ro9_processed.png&w=3840&q=75)
