Home
Class 12
CHEMISTRY
Friedel - Crafts alkylation...

Friedel - Crafts alkylation

Text Solution

AI Generated Solution

### Step-by-Step Text Solution for Friedel-Crafts Alkylation **Step 1: Understand the Reaction Conditions** Friedel-Crafts alkylation is a reaction that occurs between a benzene ring and an alkyl halide in the presence of a Lewis acid catalyst, typically aluminum chloride (AlCl3). The alkyl halide can be any alkyl group, such as methyl chloride (CH3Cl) or ethyl chloride (C2H5Cl). **Hint:** Remember that a Lewis acid is a substance that can accept an electron pair, which is crucial for generating the electrophile in this reaction. --- ...
Promotional Banner

Topper's Solved these Questions

  • SOLUTIONS

    ICSE|Exercise MULTIPLE CHOICE QUESTIONS (Assertion and Reason based questions)|10 Videos
  • SPECIMEN QUESTION PAPER

    ICSE|Exercise QUESTION|140 Videos

Similar Questions

Explore conceptually related problems

Name the reagent used in the Friedel Craft's alkylation of anisole.

Give the equations for the following reactions in case of anisole: (i) Br_(2) in ethanoic acid medium. (ii) Mixture of conc. HNO_(3) and conc. H_(2)SO_(4) (iii) Friedel Craft's alkylation (iv) Friedel Craft's acylation (v) Conc. HI.

Friedel - Crafts acylation

Assertion : Alkyl benzene is not prepared by Friedel Craft alkylation of benzene. Reason : Grignard reagents react with hydroxyl group

Give reasons for the following in one or two sentences "Nitrobenzene does not undergo Friedel-Craft's alkylation."

Why following organic chlorides will not give a Friedel-Craft alkylation product when heated with benzene and AlCl_3 ? CH_2=CHCl ,

Statement-1: Phenol is more acidic than benzoic acid Statement-2: Fluorbenzene is les reactive than chlorobenzene towards electrophilic substitiution Statement-3: Friedel Craft alkylation is not possible in tertiary butyl benzene