Arrange the following carbocations in the inc | vedclass

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(A) The stability of carbocations increases with the number of electron-donating alkyl groups due to the $+I$ effect and hyperconjugation. The order o

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$2 < 4 < 1 < 3$

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(A) The stability of carbocations increases with the number of electron-donating alkyl groups due to the $+I$ effect and hyperconjugation. The order of stability is $3^\circ > 2^\circ > 1^\circ > ext{methyl}$.$3$: $(CH_3)_3C^+$ ($3^\circ$ carbocation)$1$: $CH_3-CH^+-CH_3$ ($2^\circ$ carbocation)$4$: $CH_3-CH_2^+$ ($1^\circ$ carbocation)$2$: $CH_3^+$ (Methyl carbocation)Thus,the increasing order of stability is $2 < 4 < 1 < 3$.

Arrange the following carbocations in the increasing order of stability with respect to their labels:
Label Carbocation
$1$ $CH_3-CH^+-CH_3$
$2$ $CH_3^+$
$3$ $(CH_3)_3C^+$
$4$ $CH_3-CH_2^+$

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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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$4. \, CH_3 - \overset{+}{C} H_2$
$5. \, \overset{+}{C} H_3$

The compound $(X)$ will be:

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Label	Carbocation
$1$	$CH_3-CH^+-CH_3$
$2$	$CH_3^+$
$3$	$(CH_3)_3C^+$
$4$	$CH_3-CH_2^+$

Arrange the following carbocations in the increasing order of stability with respect to their labels: LabelCarbocation$1$$CH_3-CH^+-CH_3$$2$$CH_3^+$$3$$(CH_3)_3C^+$$4$$CH_3-CH_2^+$