Key Idea Alkyl halides are more reactive towards nucleophilic substitution. Reactivity depends upon the stability of carbocation intermediate formed. Among the given halides, aryl halide (C6H5X) is least reactive towards nucleophile as in it the C−X bond acquire some double bond character due to resonance. Presence of electron withdrawing groups like −NO2 at ortho and para positions facilitate the nucleophilic displacenent of −X of aryl halide. Among alkyl halides, 3∘ halides are more reactive as compared to 2∘ halides due to the formation of more stable carbocation. Hence, the order of reactivity of C−X bond towards nucleophile is as 
The correct order of increasing reactivity of C X bond towards nucleophile in the following compounds is NEET 2010 Chemistry, Haloalkanes and…
NEET UG 2010 — Chemistry Organic Chemistry
The correct order of increasing reactivity of CX bond towards nucleophile in the following compounds is 
Held on 30 Apr 2010 · Verified 9 Jul 2026.
Options
- A
I < II < IV < III
- B
II < III < I < IV
- C
IV < III < I < II
- D
III < II < I < IV
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