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COMEDK20269 May 2026Evening ShiftChemistryHaloalkanes and HaloarenesActual

With reference to the two statements Assertion and Reason, choose the correct option. Assertion: The order of reactivity towards S_N 1 reaction is: C₆ H₅- CH₂ Br > (CH₃ )₃- C - Br > (CH₃ )₂- CH - Br. Reason: Among the given 3 compounds the Benzyl carbocation formed is the most stable while Isopropyl carbocation is the least stable one.

Options

  1. ABoth Assertion and Reason are correct and Reason is the correct explanation of Assertion
  2. BBoth Assertion and Reason are correct but Reason is not the correct explanation of Assertion
  3. CReason is correct but Assertion is wrong
  4. DAssertion is correct but Reason is wrong

Correct answer

A. Both Assertion and Reason are correct and Reason is the correct explanation of Assertion

Step-by-step solution

The reactivity of alkyl halides towards S _ N 1 reactions depends on the stability of the intermediate carbocation formed during the rate-determining step. The carbocations formed from the given alkyl halides are: 1. Benzyl carbocation ( C ₆ H ₅ CH ₂^+ ) from C ₆ H ₅ CH ₂ Br 2. tert-Butyl carbocation ( ( CH ₃)₃ C ^+ ) from ( CH ₃)₃ CBr 3. Isopropyl carbocation ( ( CH ₃)₂ CH ^+ ) from ( CH ₃)₂ CHBr The benzyl carbocation is highly stabilized by the delocalization of the positive charge over the benzene ring through

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