Question

The product S in the reaction given below is:

A.
B.
C.
D.

Answer 1

Friedel reaction is the introduction of alkyl or acyl groups into an aromatic structure in the presence of acid catalyst. They are of two types-Friedel Craft acylation and Friedel Craft alkylation.
While dehydration is the process of removal of water molecules from a compound. Aromatic sulfonation is a reaction in which ${\text{ - S}}{{\text{O}}_3}{\text{H}}$ group is attached to an aryl group.

Complete step by step solution:
The complete reaction mechanism of production of compounds Q, R, S from compound P is given below:

In the initial step, the given compound P is reacted with Grignard reagent, ${\text{C}}{{\text{H}}_3}{\text{MgBr}}$ in the presence of a solvent, ether, ${{\text{C}}_2}{{\text{H}}_5}{\text{O}}{{\text{C}}_2}{{\text{H}}_5}$. It produces an adduct with the Grignard reagent. It is then undergone hydrolysis which produces alcohol. This is the compound Q. This compound undergoes dehydration reaction in the presence of concentrated sulfuric acid. This compound having a carbocation, undergoes further Friedel Craft alkylation in which the compound is reacted with alkyl halide to produce a cyclopentane ring attached to the benzene group. This further undergoes Friedel Craft acylation in which the compound is reacted with the acyl chloride in the presence of aluminium chloride. It produces an aryl ketone.
Both Friedel Craft alkylation and acylation proceed by electrophilic aromatic substitution.
Thus the product S is .

Hence the correct option is C.

Note: Friedel Craft alkylation reaction is a type of electrophilic substitution. It involves an intermediate which is a carbocation. Commonly used alkylating agents are alkyl halides, alkenes, alcohols, etc. Also the most commonly used catalysts should be Lewis acids. They are ${\text{AlC}}{{\text{l}}_3}$ and ${\text{B}}{{\text{F}}_3}$.
Generally, acylation reaction is better than alkylation reaction. Friedel Craft acylation reaction has more advantages than the alkylation reaction.