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.
Predict the major product $ P $ in the following sequence of reactions:
(i) HBr, benzoyl peroxide
(ii) KCN
(iii) Na(Hg), $C_{2}H_{5}OH$
Evaluate the integral: \[ \int \frac{3x^9 + 7x^8}{(x^2 + 2x + 5x^9)^2} \,dx= \]
If \( A(1,0,2) \), \( B(2,1,0) \), \( C(2,-5,3) \), and \( D(0,3,2) \) are four points and the point of intersection of the lines \( AB \) and \( CD \) is \( P(a,b,c) \), then \( a + b + c = ? \)