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.
Consider the following two reactions A and B: 
The numerical value of [molar mass of $x$ + molar mass of $y$] is ___.
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?

Consider the following reaction sequence: 
Given: Compound (x) has percentage composition \(76.6%\ \text{C}\), \(6.38%\ \text{H}\) and vapour density \(=47\). Compound (y) develops a characteristic colour with neutral \(\mathrm{FeCl_3}\) solution. Identify the {INCORRECT statement.}