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In the following sequence of reactions, ...

In the following sequence of reactions, B is
`C_(6)H_(6) underset(FeCl_(3))overset(Cl_(2))to A overset(Na)to B`

A

chlorobenzene

B

benzyl chloride

C

diphenyl

D

chlorophenylmethane

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The correct Answer is:
To solve the problem, we need to analyze the given sequence of reactions step by step. ### Step 1: Identify Compound A 1. **Starting Material**: The starting compound is benzene (C₆H₆). 2. **Reagents**: The reagents used are chlorine gas (Cl₂) and iron(III) chloride (FeCl₃). 3. **Electrophilic Aromatic Substitution**: In the presence of FeCl₃, Cl₂ generates a chloronium ion (Cl⁺), which acts as an electrophile. 4. **Reaction Mechanism**: The π electrons of the benzene ring attack the electrophilic Cl⁺, resulting in the formation of chlorobenzene (C₆H₅Cl) as compound A. The reaction can be summarized as: \[ C_6H_6 + Cl_2 \xrightarrow{FeCl_3} C_6H_5Cl + HCl \] ### Step 2: Identify Compound B 1. **Starting Material**: The next step involves the compound A, which is chlorobenzene (C₆H₅Cl). 2. **Reagents**: The reagent used is sodium (Na). 3. **Reaction Type**: This reaction is a Wurtz reaction, where two molecules of chlorobenzene react with sodium to form biphenyl (C₁₂H₁₄). 4. **Reaction Mechanism**: The sodium reduces the chlorobenzene, leading to the coupling of two phenyl groups: \[ 2 C_6H_5Cl + 2 Na \rightarrow C_{12}H_{10} + 2 NaCl \] Here, biphenyl (C₁₂H₁₄) is formed as compound B. ### Final Compounds - **Compound A**: Chlorobenzene (C₆H₅Cl) - **Compound B**: Biphenyl (C₁₂H₁₄) ### Summary of Reactions 1. **C₆H₆ + Cl₂ (FeCl₃) → C₆H₅Cl (A)** 2. **2 C₆H₅Cl + 2 Na → C₁₂H₁₄ (B)**

To solve the problem, we need to analyze the given sequence of reactions step by step. ### Step 1: Identify Compound A 1. **Starting Material**: The starting compound is benzene (C₆H₆). 2. **Reagents**: The reagents used are chlorine gas (Cl₂) and iron(III) chloride (FeCl₃). 3. **Electrophilic Aromatic Substitution**: In the presence of FeCl₃, Cl₂ generates a chloronium ion (Cl⁺), which acts as an electrophile. 4. **Reaction Mechanism**: The π electrons of the benzene ring attack the electrophilic Cl⁺, resulting in the formation of chlorobenzene (C₆H₅Cl) as compound A. The reaction can be summarized as: \[ ...
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MODERN PUBLICATION-HALOALKANES AND HALOARENES-A. MULTIPLE CHOICE QUESTIONS (with only one correct answer)
  1. The most reactive nucleophile among the following is

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  2. In the reaction, the major product 'X' is

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  3. Chlorobenzene can be obtained from benzene diazonium chloride by

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  4. Which of the following is most reactive toward nucleophilic substituti...

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  5. The reaction fo toluenec with Cl(2) in presence of FeCl(3) gives predi...

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  6. During the conversion : C(6)H(5)CH(2)CH(3) overset((a))to X overset(...

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  7. The increasing order of hydrolysis of the following compounds is

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  8. Arrange the following compounds in order of increasing dipole moment, ...

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  9. In the following sequence of reactions, B is C(6)H(6) underset(FeCl(...

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  10. 2-Phenyl-2-chloropropane on treatment with alc. KOH gives mainly

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  11. The major product (Z) in the following reaction is :

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  12. Fluorobenzene is prepared by treating benzene diazonium chloride with ...

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  13. Chlorobenzene is commercially prepared by :

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  14. Chlorobenzene when heated with aqueous ammonia in the presence of Cu(2...

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  15. The structure of the major product formed in the reaction is

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  16. Which of the following will give yellow precipitateon shaking with an ...

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  17. Freon-12 is commonly used as

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  18. Which of the following is the correct structure of D.D.T.?

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  19. Benzene hexachloride (BHC) is used as :

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  20. When chloroform is exposed to light and damp air, it gives among other...

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