In which of the following compounds,the $C-Cl$ bond ionization shall give the most stable carbocation?

  • A
    $tert$-Butyl chloride: $(CH_3)_3C-Cl$
  • B
    $1$-Phenylethyl chloride: $C_6H_5-CH(CH_3)-Cl$
  • C
    $2$-Nitroethyl chloride: $O_2N-CH_2-CH_2-Cl$
  • D
    Isopropyl chloride: $(CH_3)_2CH-Cl$

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