Which of the following will react faster through the $S_N 1$ mechanism?

  • A
    $H_2C=CH-CH_2Cl$
  • B
    Chlorobenzene
  • C
    $CH_2=CHCl$
  • D
    $CH_3CH_2Cl$

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Similar Questions

The major product obtained in the following reaction is $C_2H_5ONa + (CH_3)_3C-Cl \rightarrow$

What is the product formed when $Ethyl \ bromide$ reacts with alcoholic $Silver \ nitrite$ $(AgNO_2)$?

Chloroform on reduction with zinc dust and water gives:

Given below are two statements:
Statement-$I$: High concentration of strong nucleophilic reagent with secondary alkyl halides which do not have bulky substituents will follow $S_{N}2$ mechanism.
Statement-$II$: $A$ secondary alkyl halide when treated with a large excess of ethanol follows $S_{N}1$ mechanism.
In the light of the above statements,choose the most appropriate from the options given below:

$(i) \, (CH_3)_2CH-CH_2Br \xrightarrow{C_2H_5OH} (CH_3)_2CH-CH_2OC_2H_5 + HBr$
$(ii) \, (CH_3)_2CH-CH_2Br \xrightarrow{C_2H_5O^-} (CH_3)_2CH-CH_2OC_2H_5 + Br^-$
The reaction mechanisms for $(i)$ and $(ii)$ are respectively:

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