Given below are two statements :

Statement (I) : Benzyl chloride reacts faster in $S_N1$ mechanism than ethyl chloride.

Statement (II) : Ethyl carbocation intermediate is less stabilized by hyperconjugation than benzyl carbocation by resonance.

In the light of the above statements, choose the correct answer from the options given below :

Consider the above reaction

A. The reaction proceeds through a more stable radical intermediate.

B. The role of peroxide is to generate $${H^ \bullet }$$ (Hydrogen radical).

C. During this reaction, benzene is formed as a byproduct.

D. 1-Bromo-2-phenylethane is formed as the minor product.

E. The same reaction in absence of peroxide proceeds via carbocation intermediate.

Identify the correct statements. Choose the correct answer from the options given below :

Consider the following reactions giving major product. Identify the correct reaction.

Given below are two statements :

Statement I : ' $\mathrm{C}-\mathrm{Cl}$ ' bond is stronger in $\mathrm{CH}_2=\mathrm{CH}-\mathrm{Cl}$ than $\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{Cl}$

Statement II : The given optically active molecule, on

hydrolysis gives a solution that can rotate the plane polarized light.

In the light of the above statements, choose the correct answer from the options given below