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Most addition reactions to alkenes follow the mechanism of electrophilic addition.
- Halogenation: Addition of elementary bromine or chlorine to alkenes yield vicinal Dibromo- and dichloroalkenes, respectively. The decoloration of a solution of bromine in water is an analytical test for the presence of alkenes:
CH2=CH2 + Br2 → BrCH2-CH2Br
- Hydrohalogenation: Addition of hydrohalic acids like HCl or HBr to alkenes yield the corresponding haloalkanes.
CH3-CH=CH2 + HBr → CH3-CHBr-CH3 If the two carbon atoms at the double bond are linked to a different number of hydrogen atoms, the halogen is found preferentially at the carbon with less hydrogen substituents (Markovnikov's rule).
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