Consider the following statements. Of these s | vedclass

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(C) $(I)$ $CH_3O-CH_2^+$ is stabilized by resonance due to the lone pair on oxygen,making it more stable than the primary carbocation $CH_3-CH_2^+$. S

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$I, II$ and $III$ are correct

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(C) $(I)$ $CH_3O-CH_2^+$ is stabilized by resonance due to the lone pair on oxygen,making it more stable than the primary carbocation $CH_3-CH_2^+$. Statement $(I)$ is correct.$(II)$ $Me_2CH^+$ is a secondary carbocation,which is more stable than the primary carbocation $CH_3-CH_2-CH_2^+$ due to hyperconjugation and inductive effects. Statement $(II)$ is correct.$(III)$ $CH_2=CH-CH_2^+$ is an allyl carbocation,which is stabilized by resonance,making it more stable than the primary carbocation $CH_3-CH_2-CH_2^+$. Statement $(III)$ is correct.$(IV)$ $CH_2=CH^+$ is a vinylic carbocation where the positive charge is on an $sp$-hybridized carbon. This is highly unstable compared to the $sp^3$-hybridized primary carbocation $CH_3-CH_2^+$. Statement $(IV)$ is incorrect.Therefore,statements $(I), (II),$ and $(III)$ are correct.

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

Consider the following statements. Of these statements:
$(I) \ CH_3O-CH_2^+$ is more stable than $CH_3-CH_2^+$
$(II) \ Me_2CH^+$ is more stable than $CH_3-CH_2-CH_2^+$
$(III) \ CH_2=CH-CH_2^+$ is more stable than $CH_3-CH_2-CH_2^+$
$(IV) \ CH_2=CH^+$ is more stable than $CH_3-CH_2^+$

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

The reaction of methyltrichloroacetate $(Cl_{3}CCO_{2}Me)$ with sodium methoxide $(NaOMe)$ generates

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Consider the following statements. Of these statements:$(I) \ CH_3O-CH_2^+$ is more stable than $CH_3-CH_2^+$$(II) \ Me_2CH^+$ is more stable than $CH_3-CH_2-CH_2^+$$(III) \ CH_2=CH-CH_2^+$ is more stable than $CH_3-CH_2-CH_2^+$$(IV) \ CH_2=CH^+$ is more stable than $CH_3-CH_2^+$