Home
Class 12
CHEMISTRY
Explain why Grignard reagents should b...

Explain why
Grignard reagents should be prepared under anhydrous conditions.

Text Solution

Verified by Experts

Grignard reagents are very reactive. These are readily decomposed by compounds containing acidic lıydrogen (protic solvents), even water, as follows:
` underset("Grignard reagent")(RMgX) +H_2 O to underset("Alkane ")(RH) + Mg (OH) X `
Therefore, Grignard reagent is generally prepared in dry ether under anhydrous conditions.
Promotional Banner

Topper's Solved these Questions

  • GENERAL PRINCIPLES AND PROCESS OF ISOLATION OF ELEMENTS

    BETTER CHOICE PUBLICATION|Exercise Question Bank (6.6 OXIDATION-REDUCTION)|15 Videos
  • ORGANIC COMPOUND WITH FUNCTIONAL GROUP CONTANING OXYGEN-II

    BETTER CHOICE PUBLICATION|Exercise Question Bank (12.9 Uses of Carboxylic Acids)|4 Videos

Similar Questions

Explore conceptually related problems

Grignard reagent can be prepared in:

The gland which works under stress conditions.

Explain why: Al utensils should not be kept in water over night.

Explain the process of inspiration under normal conditions.

Why should weeds be removed?

Explain why is thionyl chloride method preferred for preparing alkyl chlorides from alcohol ?

BETTER CHOICE PUBLICATION-HALOALKANES AND HALOARENES-QUESTIONS
  1. Write a chemical reaction to illustrate Saytzeff's rule.

    Text Solution

    |

  2. Which metal is used in the preparation of Grignard's regent from haloa...

    Text Solution

    |

  3. Explain why Grignard reagents should be prepared under anhydrous con...

    Text Solution

    |

  4. The treatment of alkyl chlorides with aqueous KOH leads to the formati...

    Text Solution

    |

  5. The treatment of alkyl halides with alcoholic KOH leads to the formati...

    Text Solution

    |

  6. Complete the following reaction : CH3 CH2 Br + KOH(aq) to

    Text Solution

    |

  7. Write the structure of the major organic product in each of the follow...

    Text Solution

    |

  8. Explain why is thionyl chloride method preferred for preparing alkyl c...

    Text Solution

    |

  9. Out of HCl and SOCl2 which is preferred for converting ethanol into ch...

    Text Solution

    |

  10. Primary alkyl halide C4 H9 Br (A) is reacted with alcoholic KOH to giv...

    Text Solution

    |

  11. How do the products differ when ethyl bromide reacts separately with K...

    Text Solution

    |

  12. The treatment of alkyl halides with KNO2 leads of the formation of alk...

    Text Solution

    |

  13. Alkyl halides react with AgNO2 to give R-NO2not R-ONO.Why?

    Text Solution

    |

  14. The treatment of alkyl halides with alcoholic KOH leads to the formati...

    Text Solution

    |

  15. Alkyl halides react with AgNO2 to give R-NO2not R-ONO.Why?

    Text Solution

    |

  16. Rearrange the compounds of each of the following sets in order of reac...

    Text Solution

    |

  17. Allyl choride is more reactive than r-propyl chloride towards nucleoph...

    Text Solution

    |

  18. Haloalkanes react with potassium cyanide (KCN) to give alkyl cyanide, ...

    Text Solution

    |

  19. Although chlorine is an electron withdrawing group, yet it is ortho-, ...

    Text Solution

    |

  20. How will you convert the following : Isopropylbromide to Propene

    Text Solution

    |