An alkene (.A.) C16H16 on ozonolysis gives only one product (.B.) (.C8H8O.) . Compound (.B.) on reaction with NH2OH followed by reaction with H2SO4,Δ gives N- methyl benzamide the compound ‘A’ is -

Question

An alkene (.A.) C16H16 on ozonolysis gives only one product (.B.) (.C8H8O.) . Compound (.B.) on reaction with NH2OH followed by reaction with H2SO4,Δ gives N- methyl benzamide the compound ‘A’ is - (A) Option 1

(B)

(C)

(D)

Tardigrade Admin · Accepted Answer

Q. An alkene (A) C16​H16​ on ozonolysis gives only one product (B) (C8​H8​O) . Compound (B) on reaction with NH2​OH followed by reaction with H2​SO4​,Δ gives N− methyl benzamide the compound ‘A’ is -

Q. An alkene $(A)$ $C_{16} H_{16}$ on ozonolysis gives only one product $(B)$ $(C_{8} H_{8} O)$ . Compound $(B)$ on reaction with $N H_{2} O H$ followed by reaction with $H_{2} S O_{4}, Δ$ gives $N -$ methyl benzamide the compound $‘ A ’$ is -