(B) Alkenes undergo electrophilic addition reactions. $HOCl$ acts as a source of the electrophile $Cl^{+}$. In the first step,the electrophile $Cl^{+}

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(B) Alkenes undergo electrophilic addition reactions. $HOCl$ acts as a source of the electrophile $Cl^{+}$. In the first step,the electrophile $Cl^{+}$ attacks the double bond of propene to form a cyclic chloronium ion intermediate. Subsequently,the nucleophile $OH^{-}$ attacks the more substituted carbon atom to form the final product,chlorohydrin.

Class 11 Chemistry Hydrocarbons Alkene

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The reaction of propene with $HOCl$ proceeds via the addition of

IIT 2001 All IIT

A
$H^{+}$ in the first step
B
$Cl^{+}$ in the first step
C
$OH^{-}$ in the first step
D
$Cl^{+}$ and $OH^{-}$ in a single step

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Hydrocarbons

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Alkene

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IIT 2001 Paper All IIT years →

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The reaction of propene with $HOCl$ proceeds via the addition of

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$(R)-3-$bromocyclopentene (shown below) reacts with $Br_2/CCl_4$ to form two products,$Y$ and $Z$. $Y$ is not optically active (does not rotate plane-polarized light). What is the structure of $Y$?

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