A dilute solution of bromine is added to samples of heptane and cyclohexene. The bromination reactions and mechanisms are compared.
Alkanes: Bromination (substitution reaction)
R-H + Br2 → R-Br + HBr
( colorless) (amber) (colorless)
UV light splits the bromine molecule into two reactive radicals, resulting in a very slow loss of amber bromine color. The radical bromine atoms can then go on to react with other species in solution (including each other) in a chain reaction.
Alkanes: Oxidation (no reaction)
Alkenes: Bromination (addition reaction)
RHC = CHR + Br2 → RHBrC-CBrHR
(colorless) (amber) (colorless)
This reaction proceeds at room temperature and does not require sunlight or UV radiation to initiate it. The rapid disappearance of the amber color of the bromine at room temperature is characteristic of reaction with alkenes.
Alkenes: Oxidation (reaction with KMnO4)
RHC = CHR + KMnO4 → RHOHC-CHROH + MnO2
(colorless) (purple) (colorless) (brown ppt.)
Reaction of an alkene with aqueous potassium permanganate results in addition of two hydroxyl groups to each side of the double bond to form a glycol.
To Conduct Demonstration:
Bromine in dichloromethane and potassium permanganate can cause burns; avoid contact with skin.
Margaret Asirvatham, Summer 1992.