Home
Class 12
CHEMISTRY
Explain the fact that in aryl ethers, (i...

Explain the fact that in aryl ethers, (i) the alkoxy group activates the benzene ring towards electrophilic substitution and (ii) it directs the incoming substituents to ortho and para positions in benzene ring.

Text Solution

Verified by Experts

NA
Promotional Banner

Topper's Solved these Questions

  • ALCOHOL,PHENOL AND ETHERS

    CENGAGE CHEMISTRY|Exercise Exercises Linked Comprehension|60 Videos
  • ALCOHOL,PHENOL AND ETHERS

    CENGAGE CHEMISTRY|Exercise Exercises Multiple Correct|35 Videos
  • ALCOHOL,PHENOL AND ETHERS

    CENGAGE CHEMISTRY|Exercise Exercises Subjective|25 Videos
  • ALIPHATIC AND AROMATIC ALDEHYDES AND KETONES

    CENGAGE CHEMISTRY|Exercise Archives Subjective|29 Videos

Similar Questions

Explore conceptually related problems

Explain the fact that in alkyl aryl ethers, alkoxy group : (i) activates the benzene ring towards electrons subsitution. (ii) directs the incoming substitudents word ortho and para positions in the ring.

A group which deactivates the benzene ring towards electrophilic substitution but directs the incoming group towards o- and p- position is

Which of the following group(s) activate the benzene ring towards electrophilic substitution reaction.

Which of the following froups groups deactivates the benzene ring towards electrophilic substitution ?

Which of the following substituents deactivates the benzene ring towards electrophilic substitution?

CENGAGE CHEMISTRY-ALCOHOL,PHENOL AND ETHERS-Exercises Concept Application
  1. Give two reactions that show the acidic nature of phennol. Compare the...

    Text Solution

    |

  2. Explain why is ortho-nitrophenol more acidic than ortho-methoxyphenol ...

    Text Solution

    |

  3. Explain how does the (---OH) group attached to a carbon of benzene rin...

    Text Solution

    |

  4. Give the equations of the following reactions: i. Oxidation of prop...

    Text Solution

    |

  5. Explain the following with an example: i. Kolbe's reaction ii. R...

    Text Solution

    |

  6. Write the mechanism of hydration of ethene to yield ethanol.

    Text Solution

    |

  7. How are the following conversions carried out ? i. Propene rarr Pro...

    Text Solution

    |

  8. Name the reagents used in the following reactions: i. Oxidation of ...

    Text Solution

    |

  9. Given reason for the higher boiling point of ethanol in comparison to ...

    Text Solution

    |

  10. Give the IUPAC names of the following ethers: C(2)H(5)OCH(2)--overse...

    Text Solution

    |

  11. Write the names of reagents and equations for the preparation of follo...

    Text Solution

    |

  12. Illustrate with examples the limitations of Williamson's synthesis for...

    Text Solution

    |

  13. How is 1-propoxyproapane synthesised from propan-1-ol ? Write mechanis...

    Text Solution

    |

  14. Preparation of ethers by acid dehydration of secondary or tetiary alco...

    Text Solution

    |

  15. Write the equation of the reaction of hydrogen iodide with : (i) 1-p...

    Text Solution

    |

  16. Explain the fact that in aryl ethers, (i) the alkoxy group activates t...

    Text Solution

    |

  17. Write the mechanism of the reaction of Hiwith methoxymethane.

    Text Solution

    |

  18. Write the equations of the following reactions: i. Friedel-Crafts r...

    Text Solution

    |

  19. Show how would you synthesisse the following alcohols form approprite ...

    Text Solution

    |

  20. when 3-methylbutan-2-ol is treated with HBr, the following reaction ta...

    Text Solution

    |