-
At a low temp: 1,3-butadiene + 1 mol HBr->
- H3C-CH(Br)-CH=CH2
- kinetic product
- less stable
-
At a high temp: 1,3-butadiene + 1 mol HBr->
- H3C-CH=CH-CH2
- thermodynamic product
- more stable
-
alkene + NBS, heat/light->
substitution at the allylic carbon (C next to the double bond)
-
halogenated alkene + Li, pentane, alkyl halide->
alkene-R
-
Diels Alder Reaction
1,3-butadiene + ethene -> cyclohexene
-
1,3-butadiene --> cyclohexene (diels alder reaction)
ethene
-
1,3-butadiene --> 1,4-cyclohexadiene (diels alder reaction)
ethyne
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