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

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

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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