[Review Topics] [References] Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed the following reaction. + H₂N • You do not have to consider stereochemistry. . Include all valence lone pairs in your answer. OH Do not include counter-ions, e.g., Nat, I, in your answer. - In cases where there is more than one answer, just draw one.

[Review Topics] [References] Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed the following reaction. + H₂N • You do not have to consider stereochemistry. . Include all valence lone pairs in your answer. OH Do not include counter-ions, e.g., Nat, I, in your answer. - In cases where there is more than one answer, just draw one.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 8E

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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. CI H₂N OH • 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. Sn [F
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