Benzyl chloride undergoes S\(_{N}\)1 reactions easily because the benzylic carbocation formed is stable due to resonance stabilization. Chloro benzene, on the other hand, does not undergo S\(_{N}\)1 reaction readily because the lone pair of electrons on the oxygen atom of the aromatic ring is delocalized, making the C-Cl bond more stable and less likely to dissociate.
Hence, the assertion (A) and reason (R) are correct and R correctly explains A.
For the thermal decomposition of \( N_2O_5(g) \) at constant volume, the following table can be formed, for the reaction mentioned below: \[ 2 N_2O_5(g) \rightarrow 2 N_2O_4(g) + O_2(g) \] Given: Rate constant for the reaction is \( 4.606 \times 10^{-2} \text{ s}^{-1} \).
A hydrocarbon which does not belong to the same homologous series of carbon compounds is
The logic gate equivalent to the combination of logic gates shown in the figure is