Consider the following compound $(X)$:
$H-C \equiv C-CH_2-CH(CH_3)-CH_3$
The most stable and least stable carbon radicals,respectively,produced by homolytic cleavage of the corresponding $C-H$ bond are:

  • A
    $II, IV$
  • B
    $III, II$
  • C
    $I, IV$
  • D
    $II, I$

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Arrange the following carbocations in increasing order of stability:
$1. \, (CH_3)_2 - \overset{+}{C} - CH_2 - CH_3$
$2. \, (CH_3)_3 - \overset{+}{C}$
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The stability order of the following carbocations is:

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