The reaction of propene with $H_{3} O^{+}$ will proceed with which of the following intermediates ?

C H_{3} - C H_{2} - ⨁ O H_{2} | C H_{2}

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C H_{3} - ⨁ C H - O H | C H_{2}

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C H_{3} - ⨁ O H_{2} | C H - C H_{3}

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C H_{3} - O H | C H - C H_{3}

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Solution

The correct option is A $C H_{3} - ⨁ C H - O H | C H_{2}$
Hydration of alkene proceeds by the formation of a carbocation intermidate most stable the caarbocation most stable the intermidate.Here $2^{o}$ protonated alcohol is the most stableamong all others.

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Similar questions

The reaction of propene with HOCl $(C l_{2} + H_{2} O)$ proceeds through the intermediate:

A g N O_{3}

C H_{3} - C H_{2} - C H_{2} - O H

C H_{3} - C H = C H - O H

C H_{3} - C H = C H - C H_{2} - O H

C H_{3} - C H = C H - O H

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