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).
Which one of the following graphs accurately represents the plot of partial pressure of CS₂ vs its mole fraction in a mixture of acetone and CS₂ at constant temperature?
