HydrocarbonsHard
Question
A hydrocarbon, ′X′(C3H4) decolourise bromine in carbon tetrachloride forming ′Y′ . ′X′ gave a red precipitate of a compound ′Z′ with ammonical cuprous chloride and formed a carbonyl compound with dilute sulphuric acid in the presence of Hg+2 ions. X, Y, and Z are given by the set −
Options
A.CH2 = C = CH2, CH2Br - CBr2 - CH2Br, CH3 - C ≡ C - Cu
B.CH3 − C ≡ CH, CH3 − CBr2 − CHBr2, CH3 − C ≡ C − Cu
C.CH3 − C ≡ CH, CH3 − CBr = CHBr, CH2Cu − C ≡ CH
D.CH2 = C = CH2, CH2Br − CH = CHBr, CH3 − C ≡ C − Cu
More Hydrocarbons Questions
In the reaction -CH3CH2CH = CH2 the product obtained is...Which of the following compound undergoes dehydrochlorination most easily when treated with alcoholic KOH -...Which branched chain isomer of the hydrocarbon with molecular mass 72 u gives only one isomer of mono substituted alkylh...A sample of petrol has an octane number of 60. It means it has the same knocking as a mixture of -...The addition of HBr to alkene in the presence of a peroxide is -...