Verified Solution • 2025–26 Session moderate

QJEEM24Ch4189: JEE Main 2024 Chemistry - Class 12 JEEM24Ch4189 Solution: Given below are two statements : one is labelled as Assertion…

Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R).

Assertion (A) : SN2 reaction of C6H5CH2Br occurs more readily than the SN2 reaction of CH3CH2Br.

Reason (R) : The partially bonded unhybridized p-orbital that develops in the trigonal bipyramidal transition state is stabilized by conjugation with the phenyl ring.

In the light of the above statements, choose the most appropriate answer from the options given below :

Multiple Choice Options

  • A Both (A) and (R) are correct but (R) is not the correct explanation of (A)
  • B Both (A) and (R) are correct and (R) is the correct explanation of (A)
  • C (A) is not correct but (R) is correct
  • D (A) is correct but (R) is not correct

Step-by-Step Verified Solution

To determine the correct answer, we need to analyze both the Assertion (A) and the Reason (R) independently, as well as see if the Reason (R) provides the correct explanation for the Assertion (A).

Assertion (A) Analysis:

Assertion (A) states that SN2 reaction of C6H5CH2Br occurs more readily than the SN2 reaction of CH3CH2Br. In an SN2 reaction, the rate depends on the nucleophile as well as the substrate. Specifically, SN2 reactions proceed through a backside attack mechanism, leading to the formation of a transition state where the nucleophile and the leaving group are simultaneously bonded to the carbon atom. The benzyl group C6H5CH2− is more stable for SN2 reactions compared to the ethyl group CH3CH2− because the benzyl carbon's partial positive charge in the transition state is stabilized by the resonance of the phenyl ring.

Reason (R) Analysis:

Reason (R) explains that the partially bonded unhybridized p-orbital that develops in the trigonal bipyramidal transition state is stabilized by conjugation with the phenyl ring. This means that the presence of the phenyl ring can delocalize and stabilize the charge in the transition state, facilitating the SN2 reaction.

Combining Assertion (A) and Reason (R):

Given that the phenyl ring in C6H5CH2Br can indeed stabilize the transition state through conjugation more effectively than an ethyl group, both the Assertion (A) and Reason (R) are correct. Furthermore, Reason (R) provides a valid explanation for Assertion (A), reinforcing why the SN2 reaction occurs more readily for C6H5CH2Br.

Thus, the most appropriate answer is:

Option B: Both (A) and (R) are correct and (R) is the correct explanation of (A)

Related Learning Resources & Exam Preparation