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