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alkene reactions
electrophilic addition reactions
Hydrogen-Halide addition reaction
H goes to other Hs, Markovnikov’s rule
Hammond postulate
the transition state is more similar in structure to the species to which it is more similar in energy.
Acid catalyzed hydration of alkenes without rearrangement
this involves a bridging mercurinium ion Hg2+, so there is not rearrangement
Hyrdoboration oxidation
1st step BH3 or THF, 2nd step HO, H2O2, antimarkovnikov concerted reaction, oxidation involves hydrogen peroxide, no carbocation rearrangement.
Di halide addition
concerted no rearrangement
addin water after Di halide addition
can add ether, OH or even another halide, follows markovnikovs
epoxidation
requires peroxyacids with two Os, concerted butterfly mechanism, forms O double bonded to both Carbons that were in the alkene, stereo specific
oxonlysis
uses ozone to split an alkene, ozone has 3 oxygens
addition of H2
syn, concerted addition