Carbanion stabilityMediumQuestion 730008
Question
Carbanion stability order is:
- A3° < 2° < 1° < CH₃⁻Correct
- B3° > 2° > 1°
- CAll equal
- D1° > 2° > 3°
Correct answer
3° < 2° < 1° < CH₃⁻
Explanation
Carbanions (negatively charged carbon) are destabilised by electron-donating alkyl groups. More alkyl groups = less stable carbanion. So: tertiary < secondary < primary < methyl. Wait: the answer given is CH₃⁻ < 1° < 2° < 3° which means methyl is least stable — but that is wrong. Carbanion stability: 3° < 2° < 1° < CH₃⁻ (opposite of carbocations). The correct answer should reflect increasing stability for less substitution.