The major products ' A ' and ' B ', respectively, are

In organic reactions, the type of reagent and reaction conditions (such as temperature and concentration of acid) play a key role in determining the products. Pay attention to electrophilic substitution mechanisms for aromatic compounds.




To determine the major products ' A ' and ' B ', let's analyze the reactions shown in the image.
The initial compound is isobutylene, and the reactions involve sulfuric acid (H2SO4) at different conditions:
For the formation of product 'A':
Cold, concentrated H2SO4 is used. This typically leads to an addition reaction where the alkene undergoes electrophilic addition with H2SO4, resulting in the formation of an alkyl hydrogen sulfate.
The reaction mechanism involves the protonation of the double bond, forming a carbocation, followed by the nucleophilic attack of HSO4-.
For the formation of product 'B':
Heating with H2SO4 at 80°C is performed. Under these conditions, the previously formed alkyl hydrogen sulfate can undergo elimination to form the corresponding alcohol.
This results in a dehydration reaction, leading to the formation of isopropanol (secondary alcohol).
The correct answer option is as shown in the image:
In the given reaction, electrophilic substitution of the phenyl group with a sulfate group is induced. The major products are:
The correct IUPAC name of (CH₃)₃C-CH₂Br is:
Statement I: High concentration of strong nucleophilic reagent with secondary alkyl halides which do not have bulky substituents will follow \(S_N2\) mechanism.
Statement II: A secondary alkyl halide when treated with a large excess of ethanol follows \(S_N1\) mechanism.
In the light of the above statements, choose the most appropriate from the questions given below: