Home
Class 12
CHEMISTRY
(A) Styrene on reaction with HBr gives 1...

(A) Styrene on reaction with HBr gives 1-bromo-1-phenyl ethane.
(R) Benzyl radical is more stable than alkyl radical

A

Both (A) and (R) are correct and (R) is the correct explanation of (A)

B

Both (A) and (R) are correct but (R) is not the correct explanation of (A)

C

(A) is True but (R) is False

D

Both (A) and (R) are false

Text Solution

Verified by Experts

The correct Answer is:
A
Promotional Banner

Topper's Solved these Questions

  • ALKYL AND ARYL HALIDES

    AAKASH SERIES|Exercise OBJECTIVE EXERCISE - 3 (PREVIOUS NEET/AIPMT QUESTIONS)|13 Videos
  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise Exercise 3.2|41 Videos
  • AMINES AND AZO COMPOUNDS

    AAKASH SERIES|Exercise PRACTICE SHEET - 6 (Integer answer type Questions)|9 Videos

Similar Questions

Explore conceptually related problems

(A) 2-Bromobutane on reaction with sodium ethoxide in ethanol gives 1-butene as a major product (R) 1-Butene is more stable than 2-butene

(A) Benzoyl peroxide can initiate free radical polymerisation. (R) Phenyl free radical is very stable.

(A) : Reaction of 1-butene with HBr gives 1-bromobutane as major product (R ) : Addition of hydrogen halides to alkenes proceeds according to Markovnikov's rule

Assertion (A) Propene on addition with hydrogen bromide in the presence of peroxide gives 1-bromopropane as the major product. Reason (R ) 1-bromopropane is the major product because it is formed through the stable carbocation. The correct answer is

Assertion (A) Reaction of 1 - butene with HBr gives 1 - bromobutane as major product. Reason ( R) Addtion of hydrogen halides to alkenes proceeds according to Markownikoff's rule. The correct answer is

(A): Styrene is more reactive than propylene towards cationic polymerization. (R): The carbocation resulting from styrene is more stable than that resulting from propylene.

The products of bond breaking, shown below, are not stable, and cannot be isolated for prolonged study. Such species are referred to as reactive intermediate, and are belived to be transient intermediates in many reactions. The general structures and names of four such intermediates are, Charged Intermediates Uncharged Intermediates Carbocations (called carbonium ions in the older literature) are electrophiles and carbananions are nucleophiles. Carbenes have only a valence shell sextet of electrons and are therefore electron deficient. In this sense they are elecrophiles, but the non-bonding electron pair also gives carbenes nucleophilic character. As a rule, the electrophilic character dominates carbene reactivity. Carbon radicals have only seven valence electrons, and may be considered electron deficient, however, they do not in general bond to nucleophilic electron pair, so their chemistry exhibits differences from that of conventional electrophiles. Radical intermediates are often called free radicals. Intermediates are in general stabilised with conjugation, electron donating and electron with drawing groups. Which of the following carbo cations is more stable?

How many of the following statements are correct? 1) The most stable conformer of cis-1, 3-cyclohexanediol is chair form. 2) Cis- 1, 3- cyclohexanediol is more stable than trans -1, 3-cyclohexanediol. 3) In Cis 1, 3-cyclohexanediol both the OH groups occupy equitorial positions. 4) The most stable conformer of trans -1, 4-cyclohexanediol is chair form. 5) The most stable conformer of cis-1, 4-cyclohexanediol is boat conformer.

AAKASH SERIES-ALKYL AND ARYL HALIDES-OBJECTIVE EXERCISE - 4 (ASSERTION (A) & REASON (R) TYPE QUESTIONS)
  1. (A) Towards SN2 reaction, order of reactivity is CH3Br > CH3CH2Br > (C...

    Text Solution

    |

  2. (A) Pure chloroform does not give precipitate with AgNO3 solution. (...

    Text Solution

    |

  3. (A) Addition of bromine to 2-butene yields 2,3-dibromobutane. (R) Br...

    Text Solution

    |

  4. (A) Thionyl chloride reacts with primary alcohols to form pure alkyl h...

    Text Solution

    |

  5. (A) The boiling points of alkyl halides decrease in the order RI > RBr...

    Text Solution

    |

  6. (A) KCN reacts with methyl chloride to give methyl cyanide and methyl ...

    Text Solution

    |

  7. (A) In monohaloarenes, further electrophilic substitution occurs at or...

    Text Solution

    |

  8. (A) Benzonitrile is prepared by the action of chlorobenzene with KCN ...

    Text Solution

    |

  9. (A) Styrene on reaction with HBr gives 1-bromo-1-phenyl ethane. (R) ...

    Text Solution

    |

  10. (A) NBS is a specific reagent for allylic bromination (R) Allylic br...

    Text Solution

    |

  11. (A) Benzyl bromide when kept in acetone - water, produces benzyl alcoh...

    Text Solution

    |

  12. (A) 2-Bromobutane on reaction with sodium ethoxide in ethanol gives 1-...

    Text Solution

    |

  13. (A) Chloral reacts with phenyl chloride to form DDT (R) It is an ele...

    Text Solution

    |

  14. (A) CH3overset(Cl)overset(|)(C)HCH2CH3overset(Alc.KOH)(rarr)CH3CH=CHCH...

    Text Solution

    |

  15. (A) Addition of HBr on but-2-ene gives two structural isomeric product...

    Text Solution

    |

  16. (A) The nature of the solvent can influence the rotation of plane pola...

    Text Solution

    |

  17. (A) SN2 reactions are exothermic (R) SN2 reactions are thermochemica...

    Text Solution

    |

  18. (A) Chloroform can be used as general anaesthetic. (R) In presence o...

    Text Solution

    |

  19. (A) Ethyl chloride gives C2H5CN as major product with alc. KCN but C2H...

    Text Solution

    |