How many $1,2-$ shifts take place in the following carbocation to reach the most stable form?

  • A
    $2$
  • B
    $1$
  • C
    $3$
  • D
    $4$

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Similar Questions

Which of the following carbocations is the least stable?

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:

Which of the following carbocations will not undergo rearrangement?

Which is the most stable cation?

Using curved-arrow notation,show the formation of reactive intermediates when the following covalent bonds undergo heterolytic cleavage:
$(a)$ $CH_{3}-SCH_{3}$
$(b)$ $CH_{3}-CN$
$(c)$ $CH_{3}-Cu$

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