Home
Class 12
CHEMISTRY
A : Friedel-crafts alkylation of benzene...

A : Friedel-crafts alkylation of benzene occurs in the presence of Lewis acid.
R : The function of Lewis acid to generate electrophile.

A

If both Assertion & Reason are true and the reason is the correct explanation of the assertion, then mark (1).

B

If both Assertion & Reason are true but the reason is not the correct explanation of the assertion, then mark (2)

C

if Assertion is true statement but Reason is false, then mark (3)

D

If both Assertion and Reason are false statements, then mark (4)

Text Solution

AI Generated Solution

The correct Answer is:
To analyze the assertion and reason provided in the question, we will break down the concepts step by step. ### Step 1: Understanding the Assertion **Assertion (A):** Friedel-Crafts alkylation of benzene occurs in the presence of Lewis acid. - **Explanation:** Friedel-Crafts alkylation is a reaction where an alkyl group is introduced to a benzene ring. This reaction requires a catalyst, which is typically a Lewis acid (like AlCl3). The Lewis acid helps in the formation of a more reactive electrophile from the alkyl halide. ### Step 2: Understanding the Reason **Reason (R):** The function of Lewis acid is to generate electrophile. - **Explanation:** Lewis acids are electron pair acceptors. In the context of Friedel-Crafts alkylation, the Lewis acid interacts with the alkyl halide to create a carbocation (the electrophile) that can then react with the benzene ring. The generation of this electrophile is crucial for the reaction to proceed. ### Step 3: Evaluating the Truth of Assertion and Reason - Both the assertion and reason are true statements. Friedel-Crafts alkylation indeed requires a Lewis acid, and the primary role of the Lewis acid in this reaction is to generate the electrophile. ### Step 4: Checking if the Reason Explains the Assertion - The reason provided accurately explains the assertion. The presence of the Lewis acid is necessary to generate the electrophile that will react with benzene, thus validating the assertion. ### Conclusion - Both the assertion (A) and reason (R) are true, and the reason is the correct explanation of the assertion. ### Final Answer - **Assertion (A): True** - **Reason (R): True** - **Explanation:** The function of the Lewis acid in Friedel-Crafts alkylation is to generate the electrophile necessary for the reaction to occur. ---
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBONS

    AAKASH INSTITUTE|Exercise Assignment(Section - C) (Previous Years Questions)|69 Videos
  • HALOALKANES AND HALOARENES

    AAKASH INSTITUTE|Exercise ASSIGNMENT SECTION -D|15 Videos
  • HYDROGEN

    AAKASH INSTITUTE|Exercise ASSIGNMENT (SECTION - D) (Assertion-Reason Type question)|15 Videos

Similar Questions

Explore conceptually related problems

Lewis acids are called electrophiles. Why?

Alkylation of benzene with isobutene in the presence of sulphuric acid gives

The following is a Lewis acid

How benzene reacts with chlorine in the presence of light and in the presence of a Lewis acid?

The best Lewis acid is -

Which is the strongest Lewis acid?

AAKASH INSTITUTE-HYDROCARBONS-Assignment(Section - D) (Assertion -Reason Type Question)
  1. A : Generally, n-hexane and onwards can be sulphonated but isobutane a...

    Text Solution

    |

  2. A : When 2-fluoro butane is reacted with alcoholic KOH then butene-1 i...

    Text Solution

    |

  3. A: When butyne-2 is reacted with Na/liq. NH(3) then trans-butene-2 is ...

    Text Solution

    |

  4. A : has 12 pieelectrons i.e. 4n, pie electrons. R : It is an antiaro...

    Text Solution

    |

  5. A : Propene reacts with HBr in presence of H(2)O(2) gives 2-bromopropa...

    Text Solution

    |

  6. A : Boiling point of n-pentane is more than neopentane but the melting...

    Text Solution

    |

  7. A : Alkynes is more reactive than alkene towards electrophilic additio...

    Text Solution

    |

  8. A : But-1-yne has acidic hydrogen but but-2-yne does not R : In but-...

    Text Solution

    |

  9. A : CH(3)-CH(2)-underset(F)underset(|)CH-CH(3) on reaction with KNH(2)...

    Text Solution

    |

  10. A : Methane cannot be prepared by kolbe electrolytic reaction. R : In...

    Text Solution

    |

  11. A : Benzene on reaction with V(2)O(5) gives maleic anhydride at high t...

    Text Solution

    |

  12. A : The rate of sulphonation of benzene and deutrobenzene is different...

    Text Solution

    |

  13. A : Friedel-crafts alkylation of benzene occurs in the presence of Lew...

    Text Solution

    |

  14. A : The reaction between benzene and (CH(3))(3)C.COCl in the presence ...

    Text Solution

    |

  15. A : Addition of Br(2) in trans-but-2-ene in the presence of CCI(4) giv...

    Text Solution

    |

  16. A : Cyclohexane is more stable than cyclopentane. R : According to B...

    Text Solution

    |

  17. A : Addition of HBr in buta-1, 3-diene gives 3 bromo-but-1-ene as majo...

    Text Solution

    |

  18. A : Gauch conformer of ethylene glycol is most stable R : It is due ...

    Text Solution

    |

  19. A : But-2-ene is more stable than propene. R : Heat of hydrogenation ...

    Text Solution

    |

  20. A : Grignard reagent on reaction with alcohol form alkane. R : Alcoh...

    Text Solution

    |