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. H3C CH3 H20 NaOH • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • 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
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Chapter13: Substitution
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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.
H3C
CH3
H2O
NaOH
• You do not have to consider stereochemistry.
• Include all valence lone pairs in your answer.
• Do not include counter-ions, e.g., Nat, I', in your answer.
• In cases where there is more than one answer, just draw one.
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Transcribed Image Text:[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 in the following reaction. H3C CH3 H2O NaOH • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Nat, I', in your answer. • In cases where there is more than one answer, just draw one. C opy aste C. Previous Next Email Instructor Save and Ex Cengage Learning | Cengage Technical Support 5:48 PI 82°F 3/28/20
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