Question: (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

(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

A CH3 -COEt H3C. B COEt EtO2C .COzEt CH3

Step by Step Solution

3.25 Rating (154 Votes )

There are 3 Steps involved in it

1 Expert Approved Answer
Step: 1 Unlock

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

blur-text-image
Question Has Been Solved by an Expert!

Get step-by-step solutions from verified subject matter experts

Step: 2 Unlock
Step: 3 Unlock

Students Have Also Explored These Related Organic Chemistry 6th Questions!