NEET2024Chemistry
Q.
The compound that will undergo S1 reaction with the fastest rate is:

- A
1
- B
2
- C
3
- D
4
Solution
S1 rate is controlled by carbocation stability.
Option 2 generates a benzylic-secondary cation that is resonance-stabilised by the ring, the most stable among the choices. Bromobenzene cannot ionise (no stable aryl cation), and the cyclohexyl options give a primary or secondary alkyl cation without resonance stabilisation.
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