Home
Class 11
CHEMISTRY
Suggest a route for the preparation of n...

Suggest a route for the preparation of nitrobenzene starting from acetylene?

Text Solution

AI Generated Solution

To prepare nitrobenzene starting from acetylene, we can follow these steps: ### Step 1: Convert Acetylene to Benzene 1. **Starting Material**: Begin with acetylene (C₂H₂), which has the structure CH≡CH. 2. **Reaction**: Treat acetylene with a red hot iron (Fe) tube. This process involves heating the acetylene, which leads to the formation of benzene (C₆H₆) as a major product. 3. **Mechanism**: When three moles of acetylene (3 C₂H₂) are heated, they undergo a cyclization reaction, where the carbon atoms interact and rearrange to form the six-membered aromatic ring of benzene. ### Step 2: Nitration of Benzene ...
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBONS

    MODERN PUBLICATION|Exercise NCERT FILE (NCERT EXEMPLAR PROBLEMS) (MATCH TYPE QUESTIONS)|4 Videos
  • HYDROCARBONS

    MODERN PUBLICATION|Exercise NCERT FILE (NCERT EXEMPLAR PROBLEMS) (Assertion and Reason Type Questions)|3 Videos
  • HYDROCARBONS

    MODERN PUBLICATION|Exercise NCERT FILE (NCERT EXEMPLAR PROBLEMS) (Multiple Choice Questions (Type-II))|9 Videos
  • HALOALKANES AND HALOARENES

    MODERN PUBLICATION|Exercise UNIT PRACTICE TEST|12 Videos
  • HYDROGEN

    MODERN PUBLICATION|Exercise UNIT PRACTICE TEST (for Board Examination)|9 Videos

Similar Questions

Explore conceptually related problems

Lithium hydride can be used to prepare other useful hydrides. Beryllium hydride is one of them. Suggest a route for the preparation of beryllium hydride starting from lithium hydride. Write chemical equations involved in the process.

The rate determining step for the preparation of nitrobenzene from benzen is

Which of the following is an appropriate set of reactants for the preparation of 1-methoxy-4-nitrobenzene and why?

MODERN PUBLICATION-HYDROCARBONS-NCERT FILE (NCERT EXEMPLAR PROBLEMS) (SHORT ANSWER QUESTIONS)
  1. Why do alkenes prefer to undergo electrophilec addition reaction while...

    Text Solution

    |

  2. Alkynes on reduction with sodium in liquid ammonia form trans alkenes....

    Text Solution

    |

  3. Rotation around carbon-carbon single bond of ethane is not completely ...

    Text Solution

    |

  4. Draw Newman and Sawhorse projections for the eclipsed and staggered co...

    Text Solution

    |

  5. The intermediate carbocation formed in the reactions of HI, HBr, and H...

    Text Solution

    |

  6. What will be product obtained as a result of following reaction and wh...

    Text Solution

    |

  7. How will you convert benzene into: (i) p-nitrobromobenzene (ii) ...

    Text Solution

    |

  8. Arrange the following set of compounds in the order of decreasing reac...

    Text Solution

    |

  9. Despite their -I effect, halogens are o- and p- directing in haloarene...

    Text Solution

    |

  10. Why does presence of a nifro group make the benzene ring less reactive...

    Text Solution

    |

  11. Suggest a route for the preparation of nitrobenzene starting from acet...

    Text Solution

    |

  12. Predict the major product(s) of the following reactions and explain th...

    Text Solution

    |

  13. Nucleophiles and electrophiles are reaction intermediates having elect...

    Text Solution

    |

  14. The relative reactivity of 1^(@), 2^(@) and 3^(@) hydrogen's towards c...

    Text Solution

    |

  15. Write the structures and names of products obtained in the reactions o...

    Text Solution

    |

  16. Write hydrocarbon radicals that can be formed as intermediates during ...

    Text Solution

    |

  17. An alkane C(8)H(18) is obtained as the only product on subjecting a pr...

    Text Solution

    |

  18. The ring systems having following characteristics are aromatic. (i) ...

    Text Solution

    |

  19. Which of the following compounds are aromatic according to Huckel's ru...

    Text Solution

    |

  20. Suggest a route to prepare ethyl hydrogensulphate (CH(3)-CH(2)-OSO(2)-...

    Text Solution

    |