Which of the following carbocations will unde | vedclass

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(C) Carbocations undergo rearrangement to form more stable carbocations (e.g.,from primary to secondary or tertiary,or to a more substituted position)

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(C) Carbocations undergo rearrangement to form more stable carbocations (e.g.,from primary to secondary or tertiary,or to a more substituted position).$(1)$ This is a primary carbocation adjacent to a quaternary carbon. It will undergo a methyl shift to form a more stable tertiary carbocation.$(2)$ This is a secondary carbocation. It can undergo a hydride shift to form a more stable tertiary carbocation.$(3)$ This is a secondary carbocation. It can undergo a hydride shift to form a more stable tertiary carbocation.$(4)$ This is a secondary carbocation. It can undergo a hydride shift to form a more stable tertiary carbocation.Since all the given carbocations can rearrange to form more stable structures,the correct option is $C$.

Which of the following carbocations will undergo rearrangement?

Similar Questions

In the following carbocation,the $H$ or $CH_3$ group that is most likely to migrate to the positively charged carbon is:

What is the correct order of stability for free radicals?

Find the correct stability order for the following carbocations:

Arrange the following free radicals in the correct order of their stability:
$(i)$ $CH_2=\dot{C}H$
$(ii)$ $\dot{C}H_3$
$(iii)$ $CH_3-\dot{C}H-CH_3$
$(iv)$ $(CH_3)_3\dot{C}$

For the given reaction,the total number of possible products formed by the tertiary carbocation of $A$ is $.........$.

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