The reactivity order towards an \(S_N1\) reaction is determined by the stability of the carbocation intermediate.
Allyl chloride forms an allyl carbocation, which is resonance-stabilized, making it more stable.
Ethyl chloride forms a primary carbocation, which is less stable than the allyl carbocation.
Chlorobenzene, however, does not undergo \(S_N1\) reactions readily because the carbocation would be destabilized due to the aromatic ring.
Thus, the reactivity order is III>I>II.
(i) What is a rate determining step?
Write two characteristic properties of transition metals.
Write short notes on the following: Denaturation of protein & Nucleic acid