[" An organic compound "A(C_(4)H_(10)" o) has "],[" two enantiomeric forms and on "],[" dehydration it gives B(major "],[" product) and "C" (minor product).B "],[" and C are treated with HBr/ Peroxide "],[" and the compounds so produced "],[" were subjected to alkaline hydrolysis "],[" then- "]

Compound A and B, both were treated with NaOH , producing a single compound C. Compound C is:

Wthanol is dehydrated as, Major products (A),(B) and (C ) are respectively :

An organic compound (A) , C_(4)H_(8)Cl_(2) on hydrolysis forms another compound (B) , C_(4)H_(8)O . If all possible structures of (B) visualised above in (a) and (b) are treated with Zn - Hg/HCl , what are the products ?

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 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. Compounds B and D are :