CH₂=CH₂ → P: The alkene ethene (CH₂=CH₂) reacts with Br₂ in the first step, which typically leads to the formation of 1,2-dibromoethane (P) through an electrophilic addition mechanism.
P → Q: 1,2-dibromoethane (P) then undergoes dehydrohalogenation with alcoholic KOH, leading to the formation of vinyl bromide (Q). The elimination of HBr forms the alkene CH₂=CH-Br.
Q → R: In the third step, NaNH₂ (Sodium amide) is used to dehydrohalogenate the vinyl bromide, resulting in the formation of acetylene (R), which is ethyne (CH≡CH).
R → S: Finally, the acetylene (R) undergoes partial hydrogenation using a red-hot iron tube to form benzene (C₆H₆).
Thus, the reactions are:
P: 1,2-dibromoethane.
Q: Vinyl bromide.
R: Acetylene (ethyne).
S: Benzene.
This sequence of reactions corresponds to option (D).