Home
Class 12
CHEMISTRY
Assertion (A) Hydrolysis of (-)-2-bromoo...

Assertion (A) Hydrolysis of (-)-2-bromooctane proceeds with inversion of configuration
Reason (R) This reaction proceeds through the formation of a carbocation.

A

Assertion and reason both are correct and reason is correct explanation of assertion

B

Assertion and reason both are wrong statements

C

Assertion is correct but reason is wrong statement

D

Assertion is wrong but reason is correct statement.

Text Solution

Verified by Experts

The correct Answer is:
C

Assertion is correct but reason is wrong statement
Correct Reason This reaction proceeds through `S_(N)2` mechanism, in which `""^(-)OH` ion attacks at `180^(@)` to the halogen atom of 2-bromooctane which leads to the inversion of configuration.
Promotional Banner

Topper's Solved these Questions

  • GENERAL PRINCIPLE AND PROCESSES OF ISOLATION OF ELEMENTS

    NCERT EXEMPLAR|Exercise General Principle And Processes Of Isolation Of Elements|55 Videos
  • P-BLOCK ELEMENTS

    NCERT EXEMPLAR|Exercise P-Block Elements|72 Videos

Similar Questions

Explore conceptually related problems

Assertion: Hydrolysis of (-)-2- bromooctane proceeds with inversion of configuration. Reason: This reaction prioceeds through the formation of a carbocation.

S_(N)1 // S_(N)2 proceeds through the formation of a carbocation.

S_(N)1 // S_(N)2 proceeds through the formation of a carbocation.

The above reaction proceeds through

S_(N)2 mechanism proceeds through formation of :

NCERT EXEMPLAR-HALOALKANES AND HALOARENES-Haloalkanes And Haloarenes
  1. Cyanide ion acts as an ambident nucleophille. From which end it acts a...

    Text Solution

    |

  2. Match the compounds given in column I with the effects given in Column...

    Text Solution

    |

  3. Match the items of Column I and Column II

    Text Solution

    |

  4. Match the structures of compounds given in Column I with the classes o...

    Text Solution

    |

  5. Match the reactions given in Column I with the types of reactions give...

    Text Solution

    |

  6. Match the structures given in Column I with the names in Column II

    Text Solution

    |

  7. Match the reactions given in Column I with the names givn in Column II...

    Text Solution

    |

  8. Assertion ( A) Phosphorus chlorides ( tri and penta) are preferred ove...

    Text Solution

    |

  9. Assertion( A) The boiling points of alkyl halides decrease in the orde...

    Text Solution

    |

  10. Assertion( A) KCN reacts with methyl chloride to give methyl isocyanid...

    Text Solution

    |

  11. Assertion (A) tert-butyl bromide undergoes Wurtz reaction to give 2,2,...

    Text Solution

    |

  12. Assertion (A) Presence of a nitro group at ortho or para position incr...

    Text Solution

    |

  13. Assertion: In monohaloarenes, further electrophilic substitution occur...

    Text Solution

    |

  14. Assertion: Aryl iodides can be prepared by reaction of arenes with iod...

    Text Solution

    |

  15. Assertion: It is difficult to replace chlorine by -OH in chlorobenzene...

    Text Solution

    |

  16. Assertion (A) Hydrolysis of (-)-2-bromooctane proceeds with inversion ...

    Text Solution

    |

  17. Assertion (A) Nitration of chlorobenzene leads to the formation of m-n...

    Text Solution

    |

  18. Some alkyl halides undergo substitutionn whereas some undergo eliminat...

    Text Solution

    |

  19. Some halogen containing compounds are useful in daily life. Some compo...

    Text Solution

    |

  20. Aryl halides are less reactive towards nucleophilic substitution react...

    Text Solution

    |