A compound 'X' on ozonolysis followed by reduction gives an aldehyde, `C_(2)H_(4)O` and 2-butanoic. Compound 'X' is:

A compound 'X' on ozonolysis followed by reduction gives an aldehyde, C_(2)H_(4)O and 2-butanone. Compound 'X' is:

An organic compound [A] C_(6)H_(10) , on reduction first gives [B] C_(6)H_(12) , and finally [C] C_(6)H_(14) . [A] on ozonolysis followed by hydrolysis gives two aldehydes [D] C_(2)H_(4)O , and [E] C_(2)H_(2)O . Oxidation of [B] with acidified KMnO_(4) gives acid [F] C_(4)H_(8)O_(2) . Determine the structures of the compounds [A] to [F] with proper reasoning.

An alkene with molecular formula C_(7)H_(14) on reductive ozonolysis followed by hydrolysis gives , an aldehyde with molecular formula C_(3)H_(6)O and a ketone . The ketone is :

An organic compound (A) C_(6)H_(10) on reduction, first give (B) C_(6)H_(12) and finally (C) C_(6)H_(14) (A) on reaction with ozone followed by hydrolysis is presence of Zn gives two aldehydes C_(2)H_(4)O (D) and C_(2)H_(2)O_(2) (E) Oxdation of (B) with acidified KMnO_(4) gives acid (F) C_(3)H_(6)O_(2) Determine structures of (A) to (F) with proper reasoning.

An organic compound C_(6)H_(12)(X) on reduction gives C_(6)H_(14)(Y) . X on ozonolysis gives two aldehydes C_(2)H_(4)O(I) and C_(4)H_(8)O(II) . Identify the compounds X, Y and aldehydes (I) and (II).