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  2. Olefin conversion technology - Wikipedia

    en.wikipedia.org/wiki/Olefin_conversion_technology

    Olefin Conversion Technology, also called the Phillips Triolefin Process, is the industrial process that interconverts propylene with ethylene and 2-butenes. [1] The process is also called the ethylene to propylene (ETP) process. In ETP, ethylene is dimerized to 1-butene, which is isomerized to 2-butenes.

  3. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Double-addition of chlorine gas to ethyne. Unsaturated compounds, especially alkenes and alkynes, add halogens: R−CH=CH−R' + X 2 → R−CHX−CHX−R' In oxychlorination, the combination of hydrogen chloride and oxygen serves as the equivalent of chlorine, as illustrated by this route to 1,2-dichloroethane:

  4. Transition metal alkene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkene...

    Structure of (acac)Rh(C 2 H 4)(C 2 F 4), distances (red) in picometers. [3]The bonding between alkenes and transition metals is described by the Dewar–Chatt–Duncanson model, which involves donation of electrons in the pi-orbital on the alkene to empty orbitals on the metal.

  5. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2. It is a colourless, flammable gas with a faint "sweet and musky " odour when pure. [ 7 ] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds ).

  6. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    The chief use of ethane is the production of ethylene (ethene) by steam cracking. Steam cracking of ethane is fairly selective for ethylene, while the steam cracking of heavier hydrocarbons yields a product mixture poorer in ethylene and richer in heavier alkenes (olefins), such as propene (propylene) and butadiene, and in aromatic hydrocarbons.

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The simplest alkene, ethylene (C 2 H 4) (or "ethene" in the IUPAC nomenclature) is the organic compound produced on the largest scale industrially. [ 5 ] Aromatic compounds are often drawn as cyclic alkenes, however their structure and properties are sufficiently distinct that they are not classified as alkenes or olefins. [ 3 ]

  8. Hydrovinylation - Wikipedia

    en.wikipedia.org/wiki/Hydrovinylation

    In organic chemistry, hydrovinylation is the formal insertion of an alkene into the C-H bond of ethylene (H 2 C=CH 2): . CH 2 =CHR + CH 2 =CH 2 → CH 3 −CHR−CH=CH 2. The more general reaction, hydroalkenylation, is the formal insertion of an alkene into the C-H bond of any terminal alkene.

  9. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    More research into this ethylene to acetaldehyde conversion resulted in a 1957 patent describing a gas-phase reaction using a heterogeneous catalyst. [7] In the meanwhile Hoechst AG joined the race and after a patent filing forced Wacker into a partnership called Aldehyd GmbH. The heterogeneous process ultimately failed due to catalyst ...