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Use bromine water (Br2) or acidified permanganate (H+/MnO4-) With permanganate: add the permanganate to the alkane and no reaction will occur, add the permanganate to the alkene and you will form a diol the solution will also turn from purple to colourless. With bromine water: add the bromine water to the alkane (plus you need sunlight) and you get a substitution reaction, this is a slow reaction. Add the bromine water to the alkene and you get an immediate addition reaction (this one does not need sunlight). When bromine water reacts with an alkene it is decolourised, the reddish brown bromine water turns from brown to colourless. This is because alkenes are unsaturated and contain a carbon to carbon double bond. If you did the bromine water test in a dark place say a cupboard then the alkene would decolourise but the alkane wouldn't because it needs UV/sunlight in order to react. in practice the cupboard is not necessary as the speed of decolourisation is so much faster with the alkene.
If alkene is straight chain and alkane has one tertiary carbon atom then alkylation of alkene takes place and a substituted alkane is produced.
Yes, if the alkane is cyclic and the alkene is not.
2-butene is an alkene
Its a cycloalkene
Use bromine water (Br2) or acidified permanganate (H+/MnO4-) With permanganate: add the permanganate to the alkane and no reaction will occur, add the permanganate to the alkene and you will form a diol the solution will also turn from purple to colourless. With bromine water: add the bromine water to the alkane (plus you need sunlight) and you get a substitution reaction, this is a slow reaction. Add the bromine water to the alkene and you get an immediate addition reaction (this one does not need sunlight). When bromine water reacts with an alkene it is decolourised, the reddish brown bromine water turns from brown to colourless. This is because alkenes are unsaturated and contain a carbon to carbon double bond. If you did the bromine water test in a dark place say a cupboard then the alkene would decolourise but the alkane wouldn't because it needs UV/sunlight in order to react. in practice the cupboard is not necessary as the speed of decolourisation is so much faster with the alkene.
If alkene is straight chain and alkane has one tertiary carbon atom then alkylation of alkene takes place and a substituted alkane is produced.
Yes, if the alkane is cyclic and the alkene is not.
It is an alkene
2-butene is an alkene
alkene
Alkene
Its a cycloalkene
alkane
Alkene + Cl2 or Br2 --> Adducts (addition products) dichloor alkane, dibroom alkane
unsaturation
no