Chemistry, asked by shivi7975, 1 year ago

which one of the following compound will undergo faster hydrolysis reaction by snl mechanism

Answers

Answered by patelpurv71

Explanation:

C6H5CH2Cl will undergo faster hydrolysis reaction by SN1 mechanism. This is because the carbocation formed from C6H5CH2Cl is resonance stabilized. SN1 mechanism is favored by a stable carbocation. Therfore C6H5CH2Cl will undergo faster hydrolysis reaction by SN1 mechanism.

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