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A compound X with molecular formula C7H8...

A compound X with molecular formula `C_7H_8` is treated with `Cl_2` in presence of `FeCl_3`. Which of the following compounds are formed during the reaction?

A

B

C

D

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem step by step, we need to analyze the given compound \( C_7H_8 \) and its reaction with \( Cl_2 \) in the presence of \( FeCl_3 \). ### Step 1: Identify the Structure of Compound X The molecular formula \( C_7H_8 \) suggests that the compound could be a derivative of toluene, which has the structure: - A benzene ring (C6H6) with a methyl group (CH3) attached. - The structure can be represented as: \[ \text{C}_6\text{H}_5\text{CH}_3 \] ### Step 2: Understand the Reaction Conditions The reaction involves \( Cl_2 \) and \( FeCl_3 \): - \( FeCl_3 \) acts as a catalyst and helps in generating the electrophile \( Cl^+ \) from \( Cl_2 \). - This reaction is a type of electrophilic aromatic substitution (EAS), where the electrophile (chlorine) will replace one of the hydrogen atoms on the aromatic ring. ### Step 3: Determine the Electrophilic Substitution Mechanism In electrophilic aromatic substitution: - The electrophile \( Cl^+ \) will attack the benzene ring. - The position of substitution will depend on the nature of the substituents on the ring. Since the methyl group (–CH3) is an electron-donating group, it will direct the incoming electrophile to the ortho and para positions. ### Step 4: Identify the Possible Products The substitution can occur at: - **Ortho position**: where the chlorine atom replaces a hydrogen atom adjacent to the methyl group. - **Para position**: where the chlorine atom replaces a hydrogen atom opposite the methyl group. Thus, the products formed will be: 1. **Ortho-chlorotoluene** (Cl at ortho position) 2. **Para-chlorotoluene** (Cl at para position) ### Step 5: Determine the Major Product - The para product is generally favored due to less steric hindrance compared to the ortho product. - Therefore, while both ortho and para products are formed, the para product is the major product. ### Conclusion The compounds formed during the reaction of \( C_7H_8 \) with \( Cl_2 \) in the presence of \( FeCl_3 \) are ortho-chlorotoluene and para-chlorotoluene, with para-chlorotoluene being the major product. ### Final Answer The compounds formed are ortho-chlorotoluene and para-chlorotoluene. ---

To solve the problem step by step, we need to analyze the given compound \( C_7H_8 \) and its reaction with \( Cl_2 \) in the presence of \( FeCl_3 \). ### Step 1: Identify the Structure of Compound X The molecular formula \( C_7H_8 \) suggests that the compound could be a derivative of toluene, which has the structure: - A benzene ring (C6H6) with a methyl group (CH3) attached. - The structure can be represented as: \[ \text{C}_6\text{H}_5\text{CH}_3 ...
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