Carbocation as an intermediate is likely to be formed in the reaction:
- A$Acetone + HCN \xrightarrow{-OH} \text{acetone cyanohydrin}$
- B$Hexane \xrightarrow{\text{anhy. } AlCl_3 / HCl} \text{isomerization}$
- C$Propene + Cl_2 \xrightarrow{hv} 2-\text{chloropropane}$
- D$Ethyl bromide + \text{aq. } KOH \xrightarrow{\Delta} \text{ethyl alcohol}$
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Similar Questions
Provide four formulas of carbocations.
Easy
View SolutionFind the correct stability order for the following carbocations:
Difficult
View SolutionWhich of the following carbocations is the least stable?
The bond dissociation energy of the $C-H$ bond for the compounds: $(I)\ CH_3-H, (II)\ CH_3-CH_2-H, (III)\ CH_2=CH-CH_2-H, (IV)\ C_6H_5-H$ follows the order:
Medium
View SolutionArrange the following carbanions in the decreasing order of stability:
$I. \ p-Br-C_6H_4-CH_2^-$
$II. \ C_6H_5-CH_2^-$
$III. \ p-CH_3O-C_6H_4-CH_2^-$
$IV. \ p-CHO-C_6H_4-CH_2^-$
$V. \ p-CH_3-C_6H_4-CH_2^-$
Choose the correct answer from the options given below:
$I. \ p-Br-C_6H_4-CH_2^-$
$II. \ C_6H_5-CH_2^-$
$III. \ p-CH_3O-C_6H_4-CH_2^-$
$IV. \ p-CHO-C_6H_4-CH_2^-$
$V. \ p-CH_3-C_6H_4-CH_2^-$
Choose the correct answer from the options given below:
DifficultJEE MAIN 2026
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