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  2. Ziegler process - Wikipedia

    en.wikipedia.org/wiki/Ziegler_process

    The Ziegler alcohol synthesis involves oligomerization of ethylene using triethylaluminium followed by oxidation. [2] The triethylaluminium is produced by action of aluminium, ethylene, and hydrogen gas. In the production process, two-thirds of the triethylaluminium produced is recycled back into the reactor, and only one-third is used to ...

  3. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH. It is an alcohol , with its formula also written as C 2 H 5 OH , C 2 H 6 O or EtOH, where Et stands for ethyl .

  4. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    In the IUPAC system, the name ethylene is reserved for the divalent group -CH 2 CH 2-. Hence, names like ethylene oxide and ethylene dibromide are permitted, but the use of the name ethylene for the two-carbon alkene is not. Nevertheless, use of the name ethylene for H 2 C=CH 2 (and propylene for H 2 C=CHCH 3) is still prevalent among chemists ...

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  6. Guerbet reaction - Wikipedia

    en.wikipedia.org/wiki/Guerbet_reaction

    These intermediates then react in an aldol condensation to the allyl aldehyde which the hydrogenation catalyst then reduces to the alcohol. [5] Guerbet Reaction Mechanism. The Cannizzaro reaction is a competing reaction when two aldehyde molecules react by disproportionation to form the corresponding alcohol and carboxylic acid.

  7. Transesterification - Wikipedia

    en.wikipedia.org/wiki/Transesterification

    The largest scale application of transesterification is in the synthesis of polyesters. [3] In this application, diesters undergo transesterification with diols to form macromolecules. For example, dimethyl terephthalate and ethylene glycol react to form polyethylene terephthalate and methanol, which is evaporated to drive the reaction forward.

  8. Distillation - Wikipedia

    en.wikipedia.org/wiki/Distillation

    Carbohydrate-containing plant materials are allowed to ferment, producing a dilute solution of ethanol in the process. Spirits such as whiskey and rum are prepared by distilling these dilute solutions of ethanol. Components other than ethanol, including water, esters, and other alcohols, are collected in the condensate, which account for the ...

  9. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    The reverse reaction of CM of two alpha-olefins, ethenolysis, can be favored but requires high pressures of ethylene to increase ethylene concentration in solution. The reverse reaction of RCM, ring-opening metathesis, can likewise be favored by a large excess of an alpha-olefin, often styrene .