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A hydrohalogenation reaction is the electrophilic addition of hydrogen halides like hydrogen chloride or hydrogen bromide to alkenes to yield the corresponding haloalkanes. [ 1 ] [ 2 ] [ 3 ] 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 fewer ...
Example Classification notes (type of addition, molecule location, regiochemistry, stereochemistry, etc.) Hydrohalogenation: Can occur either in syn or anti addition fashion, depending on the solution it is in; 50% of each orientation. This reaction is considered Markovnikov because the halogen substituent attaches to the more substituted carbon.
In organic chemistry, the hydrohalogenation reaction is used to prepare halocarbons. For example, chloroethane is produced by hydrochlorination of ethylene : [ 5 ] C 2 H 4 + HCl → CH 3 CH 2 Cl
With the holidays approaching, polls show that 82% of Americans plan to gather for the holidays to share celebrations, gifts, memories — and sometimes, unintentionally, germs. "Such gatherings ...
When you buy a bottle of vitamins from a nutrition store, you’ll probably notice a best-by date on the bottom of the jar. But that inscribed number isn’t a hard-and-fast rule—there is some ...
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Example of hydrohalogenation: addition of HBr to an alkene. Hydrohalogenation involves addition of H−X to unsaturated hydrocarbons. This reaction results in new C−H and C−X σ bonds. The formation of the intermediate carbocation is selective and follows Markovnikov's rule. The hydrohalogenation of alkene will result in haloalkane. The ...