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Hydration of propene in presence of dilute sulphuric acid

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Answered by sweety9735
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Hydration of propene in the presence of dilute sulphuric acid will result in the formation of a carbocation as an intermediate. ... Thus, the hydroxide ion will attach to the secondary carbon of propene. Therefore, according to Markonikov's rule regioselectivity will be favoured over stereoselectivity.

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Hydration of propene in the presence of dilute sulphuric acid

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JinKazama1

JinKazama1 Ace

Hydration:

Hydration of Alkenes to form alcohols:

Acid Catalysed Hydration:

CH_3-CH=CH_2\xrightarrow{dil. H_2SO_4}\:\:CH_3-CH(OH)CH_3 \\ Prop-1-ene \:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:\:Propan-2-ol

\cdot Reaction is proceeded by stable carbocation intermediate due to protonation and Hence, Regioselectivity is decided by Markovinov's Rule.

\cdot Reaction is not stereoselective.

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