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Similar Questions

Arrange the following carbanions in the decreasing order of their stability:
$(1) CH_3-CH_2^-, (2) CH_2=CH^-, (3) HC \equiv C^-$

Match the ions given in Column-$I$ with their nature given in Column-$II$.
Column-$I$ Column-$II$
$A$. $CH_3-O^{+}=CH-CH_3$ $1$. Stable due to resonance
$B$. $F_3C^{+}$ $2$. Destabilised due to inductive effect
$C$. $(CH_3)_3C^{-}$ $3$. Stabilised by hyperconjugation
$D$. $CH_3-CH^{+}-CH_3$ $4$. $A$ secondary carbocation

In the following species, the one which is likely to be the intermediate during benzoin condensation of benzaldehyde is

Which of the following cannot exist at room temperature?

Which of the following is the most stable carbanion?

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