The given question involves understanding the mechanism and stability of SN2 reactions in organic chemistry, specifically comparing the reactivities between benzyl bromide (C6H5CH2Br) and ethyl bromide (CH3CH2Br).
SN2 Reaction Overview:
Explanation:
Therefore, the correct answer is: Both (A) and (R) are correct and (R) is the correct explanation of (A).
Explanation:
1. Assertion (A): Correct. - In \( C_6H_5CH_2Br \), the \( CH_2-Br \) bond is connected to a benzyl group. The phenyl ring allows for stabilization of the transition state via resonance, facilitating the \( S_N2 \) reaction. This makes the reaction proceed more readily compared to \( CH_3CH_2Br \), where no such stabilization exists.
2. Reason (R): Correct. - The unhybridized \( p \)-orbital formed during the trigonal bipyramidal transition state interacts with the conjugated system of the phenyl ring, providing extra stabilization.
3. Conclusion: Both (A) and (R) are correct, and (R) is the correct explanation for (A).
Final Answer is option (3).
The reaction represented by \( A \rightarrow B \) follows first-order kinetics. At a given temperature, 20% of the reaction is completed in 223 s. The time taken to complete 50% of the reaction at the same temperature is _________ s (rounded off to the nearest integer).