Which of the following is the electrophile involved in the given reaction?

  • A
    Dichlorocarbene $(:CCl_2)$
  • B
    Trichloromethyl anion $(\overset{\ominus}{C}Cl_3)$
  • C
    Formyl cation $(\overset{\oplus}{C}HO)$
  • D
    Dichloromethyl cation $(\overset{\oplus}{C}HCl_2)$

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Similar Questions

Compare the stability of the following free radicals:
$(1)$ $CH_3 - \dot{CH} - CH_3$
$(2)$ $C_6H_5 - \dot{CH_2}$
$(3)$ $\dot{CH_2} - CH(CH_3)_2$
$(4)$ $\dot{CH_2} - CH_3$

For the following radicals,the correct order of their stability is

Arrange 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:

Which one of the carbanions is the least stable?

The stability of carbanions follows the order:
$I: CH_3CH_2CH_2\bar{C}H_2$
$II: CH_3\bar{C}HCH_2CH_3$
$III: (CH_3)_3\bar{C}$
$IV: CH_3\bar{C}(Ph)CH_2CH_3$

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