In the Sommelet-Hauser rearrangement, a benzyl quaternary ammonium salt reacts with a strong base to give a

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In the Sommelet-Hauser rearrangement, a benzyl quaternary ammonium salt reacts with a strong base to give a benzyl tertiary amine, as exemplified below:

Suggest a mechanism for this rearrangement.

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Organic Chemistry

ISBN: 978-1118133576

11th edition

Authors: Graham Solomons, Craig Fryhle, Scott Snyder

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Question Posted: Apr 19, 2016 09:30 AM

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In the Sommelet-Hauser rearrangement, a benzyl quaternary ammonium salt reacts with a strong base to give a

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CH3 N-CH3 CH3 CH2 CH NH2 CH3 0%

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CH3 CH3 CH3 CH3 X ...View the full answer

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