The final product (C) in the given reaction sequence is
To solve the problem, we need to identify the final product (C) in the given sequence of reactions. The reaction involves a carboxylic acid undergoing a series of steps to produce a specific organic compound.
- Reaction 1 (Formation of A): The carboxylic acid (C₆H₅COOH) reacts with thionyl chloride (SOCl₂) to form an acyl chloride (C₆H₅COCl). This reaction converts the -COOH group into an acyl chloride group (-COCl), which is a common intermediate for further reactions.
- Reaction 2 (Formation of B): The acyl chloride (C₆H₅COCl) reacts with aluminum chloride (AlCl₃), a Lewis acid, which facilitates the formation of a ketone structure by promoting the reaction with benzene to form benzophenone (C₆H₅COC₆H₅).
- Reaction 3 (Formation of C): The ketone (benzophenone) reacts with hydrazine (NH₂-NH₂) and potassium hydroxide (KOH) in the presence of heat, leading to the formation of diphenylmethane. This is a typical reaction where the ketone is reduced to the corresponding alkyl compound by hydrazine.
The given reactions involve:
1. Benzophenone: Benzophenone is an intermediate product (formed in Step 2), but it is not the final product.
2. Diphenyl methane: Diphenyl methane is the final product formed after the reduction of benzophenone in Step 3, making this the correct answer.
3. Diphenylmethanol: This is not the expected product from the given reaction sequence.
4. Benzoic acid: Benzoic acid is the starting material and is not the product in the given reaction sequence.
The final product (C) in the given reaction sequence is Diphenyl methane (Option 2).