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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. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    Generally, the choice of method is governed by the raw material and energy situations as well as by the availability of oxygen at a reasonable price. In general, 100 parts of ethene gives: 95 parts acetaldehyde; 1.9 parts chlorinated aldehydes; 1.1 parts unconverted ethene; 0.8 parts carbon dioxide; 0.7 parts acetic acid; 0.1 parts chloromethane

  4. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    A 3D model of ethyne (), the simplest alkyneIn organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. [1] The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula C n H 2n−2.

  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. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For example, CH 3-CH 3 is the alkane ethANe. The name of CH 2 =CH 2 is therefore ethENe. For straight-chain alkenes with 4 or more carbon atoms, that name does not completely identify the compound. For those cases, and for branched acyclic alkenes, the following rules apply: Find the longest carbon chain in the molecule.

  7. Hydroboration–oxidation reaction - Wikipedia

    en.wikipedia.org/wiki/Hydroboration–oxidation...

    The reaction was originally described by H.C. Brown in 1957 for the conversion of 1-hexene into 1-hexanol. [3] Hexanol synthesis. Knowing that the group containing the boron will be replaced by a hydroxyl group, it can be seen that the initial hydroboration step determines the regioselectivity. Hydroboration proceeds in an anti-Markovnikov manner.

  8. Acetylene - Wikipedia

    en.wikipedia.org/wiki/Acetylene

    Acetylene (systematic name: ethyne) is the chemical compound with the formula C 2 H 2 and structure H−C≡C−H. It is a hydrocarbon and the simplest alkyne . [ 8 ] This colorless gas is widely used as a fuel and a chemical building block.

  9. Steam cracking - Wikipedia

    en.wikipedia.org/wiki/Steam_cracking

    The propane dehydrogenation process may be accomplished through different commercial technologies. The main differences between each of them concerns the catalyst employed, design of the reactor and strategies to achieve higher conversion rates. [1] Olefins are useful precursors to myriad products. Steam cracking is the core technology that ...

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