Octene
Several isomers of octene are known, depending on the position and the geometry of the double bond in the carbon chain.The simplest isomer is 1-octene, an alpha-olefin used primarily as a co-monomer in production of polyethylene via the solution polymerization process.Several useful structural isomers of the octenes are obtained by dimerization of isobutene and 1-butene.These branched alkenes are used to alkylate phenols to give precursors to detergents.[1] The dimerisation of isobutane generates diisobutenes This article about a hydrocarbon is a stub.
octaneoctynealkeneisomersdouble bond1-octenealpha-olefinmonomerpolyethylenepolymerizationstructural isomersisobutene1-butenephenolsdetergentsdiisobutenesAlkenesEthenePropeneButenePenteneHexeneHepteneNoneneDeceneDehydrohalogenationhaloalkaneDehydration reactionalcoholSemihydrogenationalkyneBamford–Stevens reactionBarton–Kellogg reactionBoord olefin synthesisChugaev eliminationCope reactionCorey–Winter olefin synthesisGrieco eliminationHofmann eliminationHorner–Wadsworth–Emmons reactionHydrazone iodinationJulia olefinationKauffmann olefinationMcMurry reactionPeterson olefinationRamberg–Bäcklund reactionShapiro reactionTakai olefinationWittig reactionOlefin metathesisEne reactionCope rearrangementHydrogenationHalogenationHydrationElectrophilic additionOxymercuration reactionHydroborationCyclopropanationEpoxidationDihydroxylationOzonolysisHydrohalogenationDiels–Alder reactionWacker processDehydrogenationFriedel-Crafts Alkylationhydrocarbon