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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. CH3 + excess CH₂CH₂OH • 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. NaOCH₂CH3

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. CH3 + excess CH₂CH₂OH • 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. NaOCH₂CH3

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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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. CH3 + excess CH₂CH₂OH • 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. NaOCH₂CH3
Transcribed Image Text: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. CH3 + excess CH₂CH₂OH • 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. NaOCH₂CH3
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