Chemistry, asked by Sudhalatwal8804, 1 year ago

discuss various methods of reduction of esters giving the products formed

Answers

Answered by LuvKapoor003
0
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A new method for reduction of esters to aldehydes through silyl acetal intermediates involves a single‐step hydrosilylation catalyzed by a readily available iridium complex, [{Ir(coe)2Cl}2] (see scheme; coe=cyclooctene). 

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Answered by topanswers
0

1. Generally, Esters are reduced to alcohols by reacting it with lithium aluminum hydride.

Example:  Propyl ethanoate is reduced to propanol and ethanol.

2. Esters are reduced into aldehydes with help of di-isobutyl aluminum hydride (DIBAL).

3. Thioesters are reduced into aldehydes with a palladium catalyst and silyl hydride.

4. Esters are reduced to ethers with the help of Et3SiH. Here, the catalyst is InBr3.

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