Home
Class 12
CHEMISTRY
Arrange the following free radicals in t...

Arrange the following free radicals in the order of decreasing stability: methyl `(I)`, vinyl `(II)`, allyl `(III)`, benzyl `(IV)`

A

`IgtIIgtIIIgtIV`

B

`IIIgtIIgtIgtIV`

C

`IIgtIgtIVgtIII`

D

`IVgtIIIgtIgtII.`

Text Solution

Verified by Experts

The correct Answer is:
D

Among the alkyl free radicals, tertiary alkyl radicals are the most stable and methyl radical is least stable. Benzyl and allyl free radicals are resonance stabilized and are more stable than alkyl free radicals. Vinyl radical is least stable since the odd electron is present on `sp^(2)` C atom

Resonance in benzyl radical
`CH_(2)=CH-overset(cdot)CH_(2)harroverset(cdot)CH_(2)-CH=CH_(2)`
Resonance in allyl radical `therefore` order is Benzyl (I)`gt` Allyl (II)`gt` Methyl (Ill)`gt` Vinyl (II).
Promotional Banner

Topper's Solved these Questions

  • BASIC PRINCIPLES OF ORGANIC CHEMISTRY

    DINESH PUBLICATION|Exercise SELECTED STRAIGHT OBJECTIVE TYPE MCQS|64 Videos
  • BASIC PRINCIPLES OF ORGANIC CHEMISTRY

    DINESH PUBLICATION|Exercise LINKED COMPREHENSION TYPE MCQS|10 Videos
  • BASIC PRINCIPLES OF ORGANIC CHEMISTRY

    DINESH PUBLICATION|Exercise Matrix Type Questions|2 Videos
  • ALKALI EARTH METALS

    DINESH PUBLICATION|Exercise Unit test-12|5 Videos
  • BIOMOLECULES

    DINESH PUBLICATION|Exercise MATRIX - MATCH TYPE|8 Videos

Similar Questions

Explore conceptually related problems

Arrange the following free radiacals in order of decreasing stability. Methyl (I), Vinyl(II), Allyl(III), Benzyl(IV)

Arrange the following free radicals in order of decreasing stability: Methyl(I), Vinly(II), Allyl(III), Benzyl(IV)

Rank thefollowing radicals in order of decreasing stability

Arrange the following free radicals in decreasing order of stability:

Arrange the following free radicals in decreasing order of stability :

Arrange the following free radicals in increasing order of stability:

Arrange the following radicals in decreasing order of their stability.

A arrange the following resonating structures in the order of decreasing stability .

DINESH PUBLICATION-BASIC PRINCIPLES OF ORGANIC CHEMISTRY-REVISION QUESTIONS FROM COMPETITIVE EXAMS.
  1. In the compound HC-=C-CH=CH2, the hybridizations of C-2 and C-3 carbon...

    Text Solution

    |

  2. Which of the following carbocations will be the most stable?

    Text Solution

    |

  3. Arrange the following free radicals in the order of decreasing stabili...

    Text Solution

    |

  4. Which isomer of hexane has only two different sets of structurally equ...

    Text Solution

    |

  5. The number of primary, secondary and tertiary carbons in 3,4-dimethylh...

    Text Solution

    |

  6. Which of the following is a 3 methyl butyl group.

    Text Solution

    |

  7. An example of electrophile is

    Text Solution

    |

  8. Which among the following free radicals is most stable

    Text Solution

    |

  9. The molecule which is free from angular strain is

    Text Solution

    |

  10. The reaction CH(2)=CH-CH(3)+HBrrarrCH(3)underset(Br)underset(|)CHCH(...

    Text Solution

    |

  11. IUPAC name is

    Text Solution

    |

  12. In which of the following species, all the three types of hybrid carbo...

    Text Solution

    |

  13. The correct IUPAC name of the acid is

    Text Solution

    |

  14. How many sigma(sigma) bonds are there in CH2=CH-CH = CH2 ?

    Text Solution

    |

  15. The common names of the lower fatty acids are obtained from

    Text Solution

    |

  16. How many sigma and pi bonds are present in the given compound Ph-CH=un...

    Text Solution

    |

  17. The IUPAC name of

    Text Solution

    |

  18. Which one of the following forms propanenitrile as the major product ?

    Text Solution

    |

  19. All carbon atoms sp^(2) hybridised in

    Text Solution

    |

  20. Hyperconjugation is most useful for stabilizing which of the following...

    Text Solution

    |