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A organic compound A has molecular formula `C_(11)H_(14)O.A` on treatment with `H_(2)N-OH` yields two stereoisomer B and C having moleuclar formula `C_(11)H_(15)NO`. B and C on treatment with concentrated `H_(2)SO_(4)` yield D and E. D and E are respective isomer of B and C. D on alkaline hydrolysis produces optically active amine `F(C_(4)H_(11)N)` . E on alkaline hydrolysis produces aniline as one product. Find out structure of organic compound A :A. B. C. `Ph-CH_(2)-overset(O)overset(||)C-CH_(2)-CH_(2)-CH_(3)`D. `Ph-overset(O)overset(||)C-underset(CH_(3))underset(|)CH-CH_(2)CH_(3)` |
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Answer» Correct Answer - D |
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