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

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

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.28P

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