(a) Explain why compound A, when treated with one equivalent of NaOEt, followed by acidification, is completely...

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(a) Explain why compound A, when treated with one equivalent of NaOEt, followed by acidification, is completely converted into compound B.

(b) Write a curved-arrow mechanism for this conversion.

(c) Give the structure of the only product formed when diethyl a-methyladipate (compound C) reacts in the Dieckmann condensation. Explain your reasoning. A CH3 -COEt H3C. B COEt EtO2C .COzEt CH3

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Organic Chemistry

ISBN: 9781936221349

6th Edition

Authors: Marc Loudon, Jim Parise

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Question Posted: Dec 07, 2023 07:08 AM

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(a) Explain why compound A, when treated with one equivalent of NaOEt, followed by acidification, is completely...

Question:

A CH3 -CO₂Et H3C. B CO₂Et EtO2C с .COzEt CH3

Step by Step Answer:

a b An ordinary Claisen condensation is driven to completion by ionization of ...View the full answer

Organic Chemistry

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