During the carbocation rearrangement of , which group will predominantly migrate to the positively c β Reaction Mechanism Chemistry Question
Question
During the carbocation rearrangement of $CH_3-C(CH_3)(Ph)-C^+H_2$, which group will predominantly migrate to the positively charged carbon?
Answer: C
π‘ Solution & Explanation
The migratory aptitude (migrating tendency) generally follows the order: $Hydride > Aryl > Alkyl$. Among the groups attached to the adjacent carbon (methyl and phenyl), the phenyl group is more electron-rich and has a higher migrating tendency to form the more stable tertiary carbocation.
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