`C(C_(6)H_(12))`, and optically active dydrocarbon which on catalytic hydrogenation gives an optically inactive compound, `C_(6)H_(14)`.

Give the structures of (A),(B) and (C)( explanation is not required ). i. (A)(C_(4)H_(8)) that adds on HBr in the presence and in the absence of peroxide to give the same product, C_(4)H_(9)Br . ii. (B)(C_(4)H_(8)), which when treated with H_(2)O //H_(2)SO_(4) gives C_(4)H_(10)O that cannot be resolves into optical isomers. iii. (C)(C_(6)H_(12), an optically active hydrocarbon which on catalytic hydrogenation gives an optically inactive compound, C_(6)H_(14))

An optically active hydrocarbon X has molecular formula C_(6)H_(12) . X on catalytic hydrogenation gives optically inactive C_(6)H_(14).X could be

Give the structure of an optically active alkene (A) having the lowest molecular mass, which on catalytic hydrogenation gives an optically inactive compound (B) .

Which optically active compound on reduction with LiAlH_(4) will give optically inactive compound?

An optically active compound A with molecular formula C_(6)H_(14) undergoes catalytic hydrogenation to give an optically inactive product. Which of the following structures for A is/are consistent with all the data?

An optically active compound [A] C_(5)H_(13)N reacts with alkaline CHCl_(3) to give an optically active, compound [B]. [A] also reacts with nitrous acid to give an optically inactive alcohol [C] C_(5)H_(11)OH as the major product. What would be the structure of [A]?

An alkene (C_(6)H_(12)) is optically active.This on reductive oxonolysis gives