Tertiary butyl chloride undergoes $S_{N} 1$ reactions immediately .

True

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False

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Solution

The correct option is A True
True,
Tertiary butyl chloride forms a very stable carbocation as an intermediate hence it undergoes $S_{N} 1$ reaction mechanism.

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Similar questions

Why a tertiary substrate undergoes sn1 reaction.?

N a F

N a F

The systematic (IUPAC) name of tertiary butyl chloride is:

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