Home
Class 12
CHEMISTRY
Which of the following reaction pairs co...

Which of the following reaction pairs constitutes the chain propagation step in chlorination of methyl chloride ?

A

`.^(•)CH_(3) + Cl_(2) rarr CH_(3)Cl + .^(•)Cl`
`CH_(3)Cl + .^(•)Cl rarr .^(•)CH_(2)Cl + HCl`

B

`CH_(3)Cl + .^(•)Cl rarr .^(•)CH_(2)Cl_(2) + .^(•)H`
`.^(•)CH_(2)Cl + Cl_(2) rarr CH_(2)Cl_(2) + .^(•)Cl`

C

`CH_(3)Cl+.^(•)Clrarr.^(•)CH_(2)Cl+HCl`
`.^(•)CH_(2)Cl+Cl_(2)rarrCH_(2)Cl_(2)+.^(•)Cl`

D

`.^(•)CH_(2)Cl+.^(•)CH_(2)ClrarrCH_(2)Cl-CH_(2)Cl.^(•)CH_(2)Cl+.^(•)ClrarrCH_(2)Cl_(2)`

Text Solution

AI Generated Solution

The correct Answer is:
To determine which reaction pairs constitute the chain propagation step in the chlorination of methyl chloride, we need to understand the chlorination process, which occurs in three main steps: initiation, chain propagation, and termination. ### Step-by-Step Solution: 1. **Understanding Chlorination**: - Chlorination is the process of introducing chlorine into a compound, in this case, methyl chloride (CH₃Cl). - The overall reaction involves the substitution of hydrogen atoms in methyl chloride with chlorine atoms. 2. **Steps of the Reaction**: - **Initiation**: This step involves the formation of chlorine radicals. When chlorine gas (Cl₂) is exposed to light, it undergoes homolytic bond fission to produce two chlorine radicals: \[ \text{Cl}_2 \xrightarrow{\text{light}} 2 \text{Cl}^\bullet \] 3. **Chain Propagation**: - In the chain propagation step, the chlorine radicals react with methyl chloride to form new radicals and products. This involves two main reactions: - The first reaction involves the chlorine radical attacking methyl chloride, leading to the formation of methyl radical (CH₃˙) and hydrochloric acid (HCl): \[ \text{Cl}^\bullet + \text{CH}_3\text{Cl} \rightarrow \text{CH}_3^\bullet + \text{HCl} \] - The second reaction involves the newly formed methyl radical reacting with another chlorine molecule to produce chloromethane (CH₂Cl₂) and another chlorine radical: \[ \text{CH}_3^\bullet + \text{Cl}_2 \rightarrow \text{CH}_2\text{Cl}_2 + \text{Cl}^\bullet \] 4. **Chain Termination**: - Eventually, the reaction will reach a point where two radicals combine to terminate the chain reaction, but this is not part of the propagation step. 5. **Identifying the Correct Reaction Pair**: - From the above reactions, we can see that the chain propagation step consists of the two reactions: 1. \(\text{Cl}^\bullet + \text{CH}_3\text{Cl} \rightarrow \text{CH}_3^\bullet + \text{HCl}\) 2. \(\text{CH}_3^\bullet + \text{Cl}_2 \rightarrow \text{CH}_2\text{Cl}_2 + \text{Cl}^\bullet\) 6. **Conclusion**: - The correct reaction pair that constitutes the chain propagation step in the chlorination of methyl chloride is the first reaction (formation of the methyl radical and HCl) and the second reaction (formation of chloromethane and chlorine radical). ### Answer: The reaction pair that constitutes the chain propagation step in the chlorination of methyl chloride is: 1. \(\text{Cl}^\bullet + \text{CH}_3\text{Cl} \rightarrow \text{CH}_3^\bullet + \text{HCl}\) 2. \(\text{CH}_3^\bullet + \text{Cl}_2 \rightarrow \text{CH}_2\text{Cl}_2 + \text{Cl}^\bullet\)
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBON

    MOTION|Exercise Exercise - 2 (Level-I)|29 Videos
  • HYDROCARBON

    MOTION|Exercise Exercise - 3|14 Videos
  • HYDROCARBON

    MOTION|Exercise QUESTIONS|6 Videos
  • GRIGNARD REAGENT

    MOTION|Exercise EXERCISE-2|16 Videos
  • IONIC EQUILIBRUIM

    MOTION|Exercise Exercise -4 (Level -II)|14 Videos

Similar Questions

Explore conceptually related problems

Which one of the following pairs constitutes isotones?

Which of the following is not the chain propagation step in the chlorination of alkane?

Which of the following pair are chain isomer?

Which of the following pair constitute resonance structure?

MOTION-HYDROCARBON -Exercise - 1
  1. Photochemical chlorination of alkane is initiated by a process of -

    Text Solution

    |

  2. A positive reaction of n–butane is possible with the reagent -

    Text Solution

    |

  3. Which of the following reaction pairs constitutes the chain propagatio...

    Text Solution

    |

  4. In the chlorination of (CH(3))(2)CH–CH(2)–CH(3) the substitution at -

    Text Solution

    |

  5. It is necessary to use ..................... in the iodination of alka...

    Text Solution

    |

  6. Direct iodination of methane is not practicable because -

    Text Solution

    |

  7. In Reed’s reaction alkane reacts with Cl(2) and SO(2) in the presence ...

    Text Solution

    |

  8. An alkane containing atleast carbon atoms is converted into an aromat...

    Text Solution

    |

  9. The thermal decomposition of alkanes in the absence of air is known as...

    Text Solution

    |

  10. A hydrocarbon with formula C(8)H(18) gives one monochloro derivative. ...

    Text Solution

    |

  11. The major product formed by monobromination of methylcyclopentane is -

    Text Solution

    |

  12. The number of possibel enantiomeric paira that can be produced during ...

    Text Solution

    |

  13. In the following reaction sequence - (1) ClrarrClrarroverset(•)(C )+...

    Text Solution

    |

  14. Propylene is more stable than ethylene. The reason for this is the-

    Text Solution

    |

  15. Propyl bromide on reaction with alcoholic KOH gives-

    Text Solution

    |

  16. Alcohols undergo dehydration in the following sequence

    Text Solution

    |

  17. Ethyl chloride on heating with alcoholic potash gives:

    Text Solution

    |

  18. In dehydrohalogenations the base (alcoholic KOH) abstracts-

    Text Solution

    |

  19. Which of the following compound undergoes dehydrochlorination most eas...

    Text Solution

    |

  20. The structural formula of the compound which yields ethylene upon reac...

    Text Solution

    |