Home
Class 11
CHEMISTRY
When a benzene ring is attached to an al...

When a benzene ring is attached to an alkane with a functional group, it is considered as substituent instead of a parent

Promotional Banner

Topper's Solved these Questions

  • GENERAL ORGANIC CHEMISTRY

    AAKASH SERIES|Exercise Objective Exercise -1|204 Videos
  • GENERAL ORGANIC CHEMISTRY

    AAKASH SERIES|Exercise Objective Exercise -2|82 Videos
  • GENERAL ORGANIC CHEMISTRY

    AAKASH SERIES|Exercise Subjective Exercise -7|8 Videos
  • ENVIRONMENTAL CHEMISTRY

    AAKASH SERIES|Exercise EXERCISE ON PASSAGE (PASSAGE-III)|5 Videos
  • HYDROCARBONS

    AAKASH SERIES|Exercise ADDITIONAL PRACTICE SHEET ( LEVEL-II (PRACTICE SHEET (ADVANCED) (MATRIX MATCHING TYPE QUESTIONS)))|5 Videos

Similar Questions

Explore conceptually related problems

Position isomerism is due to the difference in the position of a functional group, multiple bond or substituent in the same carbon chain

In benzene diazonium chloride, the functional group is

Explain the fact that in aryl alkyl 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.

When an electron withdrawing or electron releasing group is attached to carbon chain, polarity is induced on the carbon atom and on the substituent attach to it. This permanent polarity is due electron displacement due to difference in electronegativities this is called inductive effect or I effect. The inducitve effect depends in the electronegativity of the substituent. The inductive effect is broadly classified as (i) negative inductive effect or -I effect. (ii) positive inductive effect or +I effect. The group which exhibits the maximum -I effect

When an electron withdrawing or electron releasing group is attached to carbon chain, polarity is induced on the carbon atom and on the substituent attach to it. This permanent polarity is due electron displacement due to difference in electronegativities this is called inductive effect or I effect. The inducitve effect depends in the electronegativity of the substituent. The inductive effect is broadly classified as (i) negative inductive effect or -I effect. (ii) positive inductive effect or +I effect. Which of the following statements is correct about inductive effect ?

When an electron withdrawing or electron releasing group is attached to carbon chain, polarity is induced on the carbon atom and on the substituent attach to it. This permanent polarity is due electron displacement due to difference in electronegativities this is called inductive effect or I effect. The inducitve effect depends in the electronegativity of the substituent. The inductive effect is broadly classified as (i) negative inductive effect or -I effect. (ii) positive inductive effect or +I effect. Stability of given anions in the decreasing order is (i) bar(C)H_(3) " (ii) "bar(C)H_(2)-NO_(2)" (iii) "bar(C)H_(2)Cl" (iv) "CH_(3)-bar(C)H_(2)

Explain OH group attached to benzene ring activates it towards electrophilic substitution.

AAKASH SERIES-GENERAL ORGANIC CHEMISTRY-Subjective Exercise -8
  1. The order of decreasing priority for functional groups is carboxylic a...

    Text Solution

    |

  2. The chain terminating groups like -COOH - CHO, -CN, etc. should always...

    Text Solution

    |

  3. When a benzene ring is attached to an alkane with a functional group, ...

    Text Solution

    |

  4. Compounds having the same molecular formula, same structure with diffe...

    Text Solution

    |

  5. Compounds having the same molecular formula, same structure with diffe...

    Text Solution

    |

  6. Structural isomerism is due to the difference in the linkage of atoms ...

    Text Solution

    |

  7. Structural isomerism is divided into chain, position, function group m...

    Text Solution

    |

  8. Stereoisomerism is due to the difference in arrangement of atoms or gr...

    Text Solution

    |

  9. Stereo isomers have same molecular formula but differ in the spatial a...

    Text Solution

    |

  10. Chain isomerism arises due to difference in the arrangement of carbon ...

    Text Solution

    |

  11. Chain isomers differ in the nature of the carbon chain (skeleton)

    Text Solution

    |

  12. Butane has 2 chain isomers: pentane has 3, hexane has 5 and heptane ha...

    Text Solution

    |

  13. Position isomerism is due to the difference in the position of a funct...

    Text Solution

    |

  14. Compounds having same molecule formula but difference functional group...

    Text Solution

    |

  15. Alchohol's ethers, aldehydes-ketones, carboxylic acids-esters, etc, ar...

    Text Solution

    |

  16. Metamerism is due to the presence of different alkyl groups attached t...

    Text Solution

    |

  17. Ketone secondary amines, ethers etc show metamerism

    Text Solution

    |

  18. Tautomerism is a special type of functional isomerism where the isomer...

    Text Solution

    |

  19. Configurational isomerism is further divided into geometrical isomeris...

    Text Solution

    |

  20. Geometrical isomerism arises due to restricted rotation about carbon-c...

    Text Solution

    |