A good Williamson synthesis of ethyl methyl ether would be What is wrong with the following proposed

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A good Williamson synthesis of ethyl methyl ether would be

What is wrong with the following proposed synthesis of ethyl methyl ether? First, ethanol is treated with acid to protonate the hydroxyl group (making it a good leaving group), and then sodium methoxide is added to displace water.

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Organic Chemistry

ISBN: 978-0321768414

8th edition

Authors: L. G. Wade Jr.

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Question Posted: Apr 29, 2016 01:00 PM

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A good Williamson synthesis of ethyl methyl ether would be What is wrong with the following proposed

Question:

CH3CH2O CH3 Nal sodium ethoxide methyl iodide ethyl methyl ether +Nat OCH CH3CH2-OH + H+ CH3CH-_-OH- CH CH 0CH → (incorrect synthesis of ethyl methyl ether)

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Proton transfer acidbase reactions are much faster th...View the full answer

Organic Chemistry

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