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Q. The acid catalysed hydration of alkene involves the following three steps.
I. Nucleophilic attack of water on carbocation.
II. Protonation of alkene to form carbocation by the electrophilic attack of $H _{3} O ^{+}$.
III. Deprotonation to form an alcohol.
Identify the sequence for the mechanism of reaction in the acid catalysed hydration of alkenes.

Alcohols Phenols and Ethers

Solution:

The mechanism of the given reaction involves the following three steps.
Step I Protonation of alkene to form carbocation by electrophilic attack of $H _{3} O ^{+}$.
$H _{2} O + H ^{+} \longrightarrow H _{3} O ^{+}$
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Step II Nucleophilic attack of water on carbocation.
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Step III Deprotonation to form an alcohol.
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