The stability of the following carbanions is in the order of:

  • A
    $(a) > (b) > (c) > (d)$
  • B
    $(a) > (c) > (b) > (d)$
  • C
    $(b) > (a) > (c) > (d)$
  • D
    $(d) > (c) > (b) > (a)$

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Similar Questions

Which of the following carbocations will be most stable?

The order of decreasing stability of the carbanions is:
$1.$ $(CH_3)_3C^-$
$2.$ $(CH_3)_2CH^-$
$3.$ $CH_3CH_2^-$
$4.$ $C_6H_5CH_2^-$

Which of the following is the most stable form for the given structure after rearrangement?

Which free radical is most stable among the following?

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:

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