Without looking back, propose a mechanism for the

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L. G. Wade Jr

Problem 7P Chapter 22

Organic Chemistry | 8th Edition

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Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L. G. Wade Jr

Organic Chemistry | 8th Edition

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Problem 7P

Without looking back, propose a mechanism for the hydrolysis of this iminium salt to the alkylated ketone. The first step is attack by water, followed by loss of a proton to give a carbinolamine. Protonation on nitrogen allows pyrrolidine to leave, giving the protonated ketone.

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Chapter 22, Problem 7P is Solved
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Textbook: Organic Chemistry
Edition: 8
Author: L. G. Wade Jr
ISBN: 9780321768414

Organic Chemistry was written by and is associated to the ISBN: 9780321768414. The full step-by-step solution to problem: 7P from chapter: 22 was answered by , our top Chemistry solution expert on 05/06/17, 06:41PM. Since the solution to 7P from 22 chapter was answered, more than 256 students have viewed the full step-by-step answer. The answer to “Without looking back, propose a mechanism for the hydrolysis of this iminium salt to the alkylated ketone. The first step is attack by water, followed by loss of a proton to give a carbinolamine. Protonation on nitrogen allows pyrrolidine to leave, giving the protonated ketone.” is broken down into a number of easy to follow steps, and 45 words. This full solution covers the following key subjects: Ketone, leave, attack, back, carbinolamine. This expansive textbook survival guide covers 25 chapters, and 1336 solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8.

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