Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction он H2SO4 (trace) +CH3OH reflux You do not have to consider stereochemistry. Include all valence lone pairs in your answer. . Do not include counter-ions, eg, Na+, 1, in your answer. In cases where there is more than one answer, just draw one.
Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction он H2SO4 (trace) +CH3OH reflux You do not have to consider stereochemistry. Include all valence lone pairs in your answer. . Do not include counter-ions, eg, Na+, 1, in your answer. In cases where there is more than one answer, just draw one.
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
Chapter7: Alkynes
Section: Chapter Questions
Problem 7.30P
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Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction.
- You do not have to consider stereochemistry.
- Include all valence lone pairs in your answer.
- Do not include counter-ions, e.g., Na+, I-, in your answer.
- In cases where there is more than one answer, just draw one.
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