Home
Class 12
CHEMISTRY
Explain as to why haloarenes are much le...

Explain as to why haloarenes are much less reactive than halo-alkanes towards nucleophilic substitution reactions.

Promotional Banner

Topper's Solved these Questions

  • HALOALKANES AND HALOARENES

    PRADEEP|Exercise ADDITIONAL QUESTIONS (LONG ANSWER QUESTIONS)|4 Videos

  • HALOALKANES AND HALOARENES

    PRADEEP|Exercise HIGHER ORDER THINKING SKILLS ((QUESTIONS AND PROBLEMS WITH ANSWERS/SOLUTION)|6 Videos

  • HALOALKANES AND HALOARENES

    PRADEEP|Exercise ADDITIONAL QUESTIONS (VERY SHORT ANSWER QUESTIONS)|64 Videos

  • GENERAL PRINCIPLES AND PROCESSES OF ISOLATION OF ELEMENTS

    PRADEEP|Exercise Curiosity Questions|2 Videos

  • ORGANIC COMPOUNDS CONTAINING NITROGEN

    PRADEEP|Exercise IMPORTANT QUESTIONS FOR BOARD EXAMINATION|27 Videos

Similar Questions

Explore conceptually related problems

Aryl halide is less reactive than halide towards nucleophilic substitution because

Haloarenes are less reactive than haloalkanes and haloalkenes. Explain.

(A) Greater the stability of carbanion, greater is its ease of formation and hence , more reactive is aryl halide. (R) Chlorobenzene is less reactive than p-chloroanisole towards nucleophilic substitution reactions.

Why a benzaldehyde less reactive than acetaldehyde towards nucleophilic addition reactions?

PRADEEP-HALOALKANES AND HALOARENES-ADDITIONAL QUESTIONS (SHORT ANSWER QUESTIONS)
  1. Give two reasons for low reactivity of aryl halides towards nucleophil...

    Text Solution

    |

  2. Chlorobenzene is extremely less reactive towards nucleophilic substitu...

    Text Solution

    |

  3. Account for the fact that halogen in chlorobenzene is less reactive th...

    Text Solution

    |

  4. Give reasons: (i). C-Cl bond length in chlorobenzene is shorter than...

    Text Solution

    |

  5. Account for the fact that C-X bond length in halobenzene is smaller th...

    Text Solution

    |

  6. Why do alkyl halides undergo alkaline hydrolysis more easily than aryl...

    Text Solution

    |

  7. Why are haloarenes more stable than haloalkanes and undergo electrophi...

    Text Solution

    |

  8. Explain as to why haloarenes are much less reactive than halo-alkanes ...

    Text Solution

    |

  9. Arrange the following compounds according to reactivity towards nucleo...

    Text Solution

    |

  10. the presence of electron withdrawing group at ortho and para positions...

    Text Solution

    |

  11. What is a nucleophilic substitution reaction? Write such a reaction, o...

    Text Solution

    |

  12. What do you undersetand by : (i) nucleophilic substitution ad (ii) e...

    Text Solution

    |

  13. How will you convert: (i) n-propyl bromide to iso-propyl bromide (...

    Text Solution

    |

  14. In the reaction : R-Br+Cl^(-) to R -Cl+Br^(-) The rates of react...

    Text Solution

    |

  15. Complete the following reaction equations: (i) CH(3)CH(2)Br+H(2)over...

    Text Solution

    |

  16. What happens when: (i). Methyl chloride is treated with alcoholic KC...

    Text Solution

    |

  17. What happens when: (i) Chlorobenzene is subjected to hydrolysis. (...

    Text Solution

    |

  18. The modified stem in grasses, strawberry Chrysanthemum is concerned wi...

    Text Solution

    |

  19. Identify the compounds X, Y and Z in each of the following sequence of...

    Text Solution

    |

  20. Write one use of each of the following: ((i) Chloroform (ii) Iodof...

    Text Solution

    |