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 $C$.

Column $-I$	Column $-II$
$A$. Free radical	$1$. Trigonal planar
$B$. Carbocation	$2$. Pyramidal
$C$. Carbanion	$3$. Linear

Which of the following carbocations will undergo rearrangement?

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Which among the following carbocations has the maximum stability?

Due to the presence of an unpaired electron,free radicals are .........

The correct stability order for the following carbocations is:

Match the intermediates given in Column $-I$ with their probable structure in Column $-II$.

Column $-I$ Column $-II$

$A$. Free radical $1$. Trigonal planar

$B$. Carbocation $2$. Pyramidal

$C$. Carbanion $3$. Linear

Correct order of stability is

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