Identify the correct stability order.

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(C) Let us analyze each option:$A$: The isopropyl carbanion $(CH_3-CH^--CH_3)$ is less stable than the ethyl carbanion $(CH_3-CH_2^-)$ due to the grea

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(C) Let us analyze each option:$A$: The isopropyl carbanion $(CH_3-CH^--CH_3)$ is less stable than the ethyl carbanion $(CH_3-CH_2^-)$ due to the greater $+I$ effect of the two methyl groups.$B$: Cyclobutadiene is anti-aromatic ($4\pi$ electrons),while $1,3-$butadiene is non-aromatic. Thus,$1$,$3$-butadiene is more stable.$C$: The carbocation $(MeO)_2C^+$ is highly stabilized by the resonance effect $(+M)$ of the two methoxy groups,making it significantly more stable than the tert-butyl carbocation $(t-Bu^+)$,which is only stabilized by hyperconjugation and the $+I$ effect.$D$: The tris(trifluoromethyl)methyl carbanion is extremely stable due to the strong $-I$ effect of the three $CF_3$ groups,making it much more stable than the isopropyl carbanion.

Similar Questions

Which of the following can show hyperconjugation?

The decreasing order of stability of the following anions is:
$(P)$ $p-OCH_3-C_6H_4-CH_2^-$
$(Q)$ $p-CHO-C_6H_4-CH_2^-$
$(R)$ $p-Cl-C_6H_4-CH_2^-$
$(S)$ $p-CH_3-C_6H_4-CH_2^-$

Given below are two statements:
Statement $I$: On the basis of inductive effect,the order of stability of alkyl carbanions is $CH_3^- > CH_3CH_2^- > (CH_3)_2CH^- > (CH_3)_3C^-$.
Statement $II$: Allyl and benzyl carbanions are more stabilised by inductive effect and not by resonance effect.

Explain the inductive effect with a suitable example.

Among the following,the most acidic compound is

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