Arrange the carbanions,$(CH_3)_3\overline{C}$,$\overline{C}Cl_3$,$(CH_3)_2\overline{C}H$,$C_6H_5\overline{C}H_2$ in order of their decreasing stability:

  • A
    $(CH_3)_2\overline{C}H > \overline{C}Cl_3 > C_6H_5\overline{C}H_2 > (CH_3)_3\overline{C}$
  • B
    $\overline{C}Cl_3 > C_6H_5\overline{C}H_2 > (CH_3)_2\overline{C}H > (CH_3)_3\overline{C}$
  • C
    $(CH_3)_3\overline{C} > (CH_3)_2\overline{C}H > C_6H_5\overline{C}H_2 > \overline{C}Cl_3$
  • D
    $C_6H_5\overline{C}H_2 > \overline{C}Cl_3 > (CH_3)_3\overline{C} > (CH_3)_2\overline{C}H$

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Similar Questions

The decreasing order of hydride affinity for the following carbocations is:
$A: CH_2=CH-C^+(CH_3)_2$
$B: (C_6H_5)_3C^+$
$C: (CH_3)_3C^+$
$D: (Cyclopropyl)_3C^+$
Choose the correct answer from the options given below:

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:

Which is the most stable carbocation?

Classify the following species into carbocation,free radical,and carbanion:
$CH_3^{\bullet}, CH_3^{+}, \bar{C}H_3, (CH_3)_3C^{\bullet}, (CH_3)_3C^{+}, (CH_3)_2CH^{+}, (CH_3)_3\bar{C}:, (CH_3)_3\ddot{C}H, C_6H_5CH_2^{\bullet}, CH_3\ddot{C}H_2, C_6H_5CH_2^{+}, CH_2=CHCH_2^{\bullet}, CH_2=CHCH_2^{+}$

$p$ will be

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