Which of the following carbocations lacks hyperconjugative stability?

  • A
    $A = CH_3CH_2^+$
  • B
    $B = (CH_3)_3C^+$
  • C
    $C = (CH_3)_2CH^+$
  • D
    $D = CH_3^+$

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In the above reaction,the left-hand side and right-hand side rings are named as '$A$' and '$B$' respectively. They undergo ring expansion. The correct statement for this process is:

Arrange the $(C-H)$ bonds $x, y$ and $z$ in decreasing order of their bond dissociation energies in homolysis.

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Choose the most reasonable reaction intermediate for the following reaction.

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