Describe the following mechanisms with an example.
a. Friedel Craft’s Alkylation.
b. Sulphonation.
c. Nitration.
d. Halogenation.
Answers
Answer:
1. Friedel-Crafts Alkylation refers to the replacement of an aromatic proton with an alkyl group. This is done through an electrophilic attack on the aromatic ring with the help of a carbocation. The Friedel-Crafts alkylation reaction is a method of generating alkylbenzenes by using alkyl halides as reactants.
2. Sulfonation is a reversible reaction that produces benzenesulfonic acid by adding sulfur trioxide and fuming sulfuric acid. The reaction is reversed by adding hot aqueous acid to benzenesulfonic acid to produce benzene.
3. Nitration is a general class of a chemical process for the introduction of a nitro group into an organic chemical compound. More loosely the term also is applied incorrectly to the different process of forming nitrate esters between alcohols and nitric acid, as occurs in the synthesis of nitroglycerin.
4. Halogenation is a chemical reaction that involves the addition of one or more halogens to a compound or material. The pathway and stoichiometry of halogenation depends on the structural features and functional groups of the organic substrate, as well as on the specific halogen.