Answered

Discover the best answers at Westonci.ca, where experts share their insights and knowledge with you. Experience the ease of finding accurate answers to your questions from a knowledgeable community of professionals. Get immediate and reliable solutions to your questions from a community of experienced professionals on our platform.

Draw the mechanism for the reaction of acetyl chloride (ethanoyl chloride) with the ethoxide anion to yield ethyl acetate (ethyl ethanoate)

Sagot :

Ethanoyl chloride is a common acyl chloride. Any other acyl chloride will function similarly.  Similarly, ethanol is regarded as a typical alcoholic beverage. simply substitute the CH3CH2 group with an alkyl group.

The first stage of the reaction (the addition stage) includes a nucleophilic attack on the relatively positive carbon atom by one of the lone pairs on an ethanol molecule's oxygen.

The second stage (elimination) occurs in two stages. The carbon-oxygen double bond reforms in the first step, releasing a chloride ion.

The ethanoyl chloride then removes a hydrogen ion, yielding ethyl ethanoate and hydrogen chloride.

To learn more about ethanoyl chloride please visit -
https://brainly.com/question/13043444
#SPJ4

Thanks for using our platform. We aim to provide accurate and up-to-date answers to all your queries. Come back soon. Thanks for stopping by. We strive to provide the best answers for all your questions. See you again soon. Westonci.ca is here to provide the answers you seek. Return often for more expert solutions.