A hydrocarbon `X` has molecular formula `C_(8)H_(18).` Substitution of a hydrogen of `X

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

A hydrocarbon X has the molecular formula C_(5)H_(8) and it does not has any sp^(2) or sp- hybridized carbons. How many different IUPAC names are possible for X ?

Pentane has the molecular formula C_(5)H_(12) . It has

Assign structures for the following: (a) An alkyne (X) has molecular formula C_(5) H_(8) . It reacts neither with sodamide nor with ammoniacal cuprous chloride. (b) A hydrocarbon Y decolourises bromine water. On ozonolysis it gives 3-methyl butanal and formaldehyde. Give the name of the compound. (c) A hydrocarbon (Z) has molecular formula C_(8)H_(10) . It does not decolourise bromine water and is oxidised to benzoic acid on heating with K_(2)Cr_(2)O_(7) . It can also have three other isomers A, B and C. Write the structures of Z, A, B and C.

A hydrocarbon has molecular formula X(C_(6)H_(6)) . Also, X has triple bonds as the only type of unsaturation, i.e., it has neither double bonds nor any ring structure. How many different IUPAC name can be assigned to X ?

Ethane, with the molecular formula C_(2)H_(6) has