The products A and B in the following reaction sequence are : [figure]
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- [figure]
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Answer
(3) [figure]
Solution
Step 1 (Markovnikov addition; the more stable benzylic carbocation is formed):
C6H5-CH=CH2 HBr C6H5-CH(Br)-CH3
Step 2 (Grignard reagent):
C6H5-CH(Br)-CH3 Mg, dry ether C6H5-CH(MgBr)-CH3
Step 3 (carboxylation; as per NCERT, Grignard reagents react with CO2 to give, after hydrolysis, carboxylic acids):
C6H5-CH(MgBr)-CH3 [(ii) H3O+](i) CO2 C6H5-CH(CH3)-COOH = A
Step 4 (acid chloride, then amide):
A SOCl2 C6H5-CH(CH3)-COCl
CH3NH2 C6H5-CH(CH3)-CONHCH3 = B
∴ A = 2-phenylpropanoic acid and B = N-methyl-2-phenylpropanamide, as in option (3).
Answer: (3)