Home
Class 11
CHEMISTRY
Is it possible to isolate pure staggered...

Is it possible to isolate pure staggered ethane or pure eclipsed ethane at room temperature?

Text Solution

Verified by Experts

The energy differences between staggered and eclipsed froms of ethane is just `12.55 "kJ mol"^(-1)` which is easily met by collisions of the molecules at room temperature. Therefore, it is not possible to isolate either pure staggered or pure eclipsed ethane at room temperature.
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBONS

    PRADEEP|Exercise NCERT QUESTION AND EXERCISES WITH ANSWERS|14 Videos
  • HYDROCARBONS

    PRADEEP|Exercise NCERT QUESTION AND EXERCISES WITH ANSWERS (NCERT EXCERCISES)|25 Videos
  • HYDROCARBONS

    PRADEEP|Exercise TEST YOUR GRIP (FILL IN THE BLANKS )|20 Videos
  • EQUILIBRIUM IN PHYSICAL AND CHEMICAL PROCESSES

    PRADEEP|Exercise Competition Focus (Jee(Main and advanced)/Medical Entrance) VIII. ASSERTION - REASON TYPE QUESTIONS (TYPE - II)|10 Videos
  • HYDROGEN

    PRADEEP|Exercise COMPETITION FOCUS (Assertion-Reason Type Questions) Type 2|15 Videos

Similar Questions

Explore conceptually related problems

Staggered and eclipsed form of ethane are

Staggered and eclipsed conformers of ethane are :

The ionisation energy of isolated pentavalent phosphorous atom is very large. How is it possible that when it goes into silicon lattice position to ralease its fifth electron at room temperature so that n-type semiconductor is obtained?

The most stable conformation of ethane chlorohydrin at room temperature is

Energy barrier between staggered and exlipsed form in ethane is

Which of the following molecules, in pure form, is /are ustable at room temperature?

PRADEEP-HYDROCARBONS-CONCEPTUAL Questions
  1. What are the main constituents of LPG ?

    Text Solution

    |

  2. a. Why are alkanes inert ? b. Why the (C----C) bond rather than (C...

    Text Solution

    |

  3. Is it possible to isolate pure staggered ethane or pure eclipsed ethan...

    Text Solution

    |

  4. Dehydration of alcohol to form an alkene is always carried out with co...

    Text Solution

    |

  5. Dehydration of 1-butanol or 2-butanol with conc. H2SO4 always gives th...

    Text Solution

    |

  6. Predict the major product of the following reaction: C(6)H(6)+(CH(3))(...

    Text Solution

    |

  7. Identify the organic products obtained in the following reaction :

    Text Solution

    |

  8. Predict the products of the following reaction

    Text Solution

    |

  9. Complete the following reactions with appropriate structures of produc...

    Text Solution

    |

  10. How will you prepare 3-methylbut-1-yne by starting with ethyne ?

    Text Solution

    |

  11. Predict the major product in the following reaction : R-C-=C-R under...

    Text Solution

    |

  12. Identify the product in the reaction PhC-=CMe overset(H3O^(+),Hg^(2+)?...

    Text Solution

    |

  13. How will you prepare (i) cis-pent-2-ene and trans-pent-2-ene by starti...

    Text Solution

    |

  14. Starting with ethyne, how will you prepare pentan-2-one ?

    Text Solution

    |

  15. How will you separate a mixture of ethane, ethylene and acetylene ?

    Text Solution

    |

  16. Give reasons for the following: CH2=CH^(Θ) is more basic than HC-=C^...

    Text Solution

    |

  17. Predict which of the following systems would be aromatic and why ?

    Text Solution

    |

  18. Ozonolysis of mesitylene gives

    Text Solution

    |

  19. Write the major product in each case

    Text Solution

    |

  20. Tert-Butylbenzene does not benzoic acid on oxidation with acidic KMnO(...

    Text Solution

    |