A compound (A), `C_(4)H_(8)Cl_(2)` , on hydrolysis gives a product(B) which forms a 2,4-DNP derivation,but does not reduce Tollen's reagent. The compoun (A) has the structure:

An compound (A ) C_(4)H_(8)Cl_(2) on alkaline hydrolysis to give compound (B ) C_(4)H_(8)O which gives an oxime and positive Tollen's reagent test . What is the structure of (A) ?

Compound C_(4)H_(8)CI_(2) (A) on hydrolysis gives a compound C_(4)H_(8)O(B) which reacts with hydroxylamine and does not give any test with Tollens reagent . What are (A) and (B) ?

A dihalo alkane P, having formula C_(3)H_(6)Cl_(2), on hydrolysis gives a compound, that can reduce Tollen's reagent. The compound P is

An organic compound (A) , C_(4)H_(8)Cl_(2) on hydrolysis forms another compound (B) , C_(4)H_(8)O . If (B) does not responds to iodo form test , then identify possible structures of (A) and (B).

Compound (X) C_(4)H_(8)O gives positive haloform test but does not give 2,4 DNP derivation is :