Classify the following species into carbocation,free radical,and carbanion:
$CH_3^{\bullet}, CH_3^{+}, \bar{C}H_3, (CH_3)_3C^{\bullet}, (CH_3)_3C^{+}, (CH_3)_2CH^{+}, (CH_3)_3\bar{C}:, (CH_3)_3\ddot{C}H, C_6H_5CH_2^{\bullet}, CH_3\ddot{C}H_2, C_6H_5CH_2^{+}, CH_2=CHCH_2^{\bullet}, CH_2=CHCH_2^{+}$

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Carbocation: $CH_3^{+}, (CH_3)_3C^{+}, (CH_3)_2CH^{+}, C_6H_5CH_2^{+}, CH_2=CHCH_2^{+}$
Free radical: $CH_3^{\bullet}, (CH_3)_3C^{\bullet}, C_6H_5CH_2^{\bullet}, CH_2=CHCH_2^{\bullet}$
Carbanion: $\bar{C}H_3, (CH_3)_3\bar{C}:, CH_3\ddot{C}H_2$

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Similar Questions

For the given reaction,the total number of possible products formed by the tertiary carbocation of $A$ is $.........$.

Among the given species,which carbocations are resonance stabilized?

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

Carbocation as an intermediate is likely to be formed in the reaction:

The orbital picture of a triplet carbene can be drawn as

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