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  2. 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 ...

  3. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Conversion of acetaldehyde to 1,1-diethoxyethane, R 1 = CH 3 R 2 = CH 3 CH 2. Acetaldehyde forms a stable acetal upon reaction with ethanol under conditions that favor dehydration. The product, CH 3 CH(OCH 2 CH 3) 2, is formally named 1,1-diethoxyethane but is commonly referred to as "acetal". [39]

  4. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  5. Ethanol fermentation - Wikipedia

    en.wikipedia.org/wiki/Ethanol_fermentation

    (3) The two molecules of NADH reduce the two acetaldehyde molecules to two molecules of ethanol; this converts NADH back into NAD+. Ethanol fermentation , also called alcoholic fermentation , is a biological process which converts sugars such as glucose , fructose , and sucrose into cellular energy , producing ethanol and carbon dioxide as by ...

  6. Vinyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Vinyl_alcohol

    At room temperature, acetaldehyde (H 3 CC(O)H) is more stable than vinyl alcohol (H 2 C=CHOH) by 42.7 kJ/mol. [3] Vinyl alcohol gas isomerizes to the aldehyde with a half-life of 30 min at room temperature. [1] H 2 C=CHOH → H 3 CC(O)H The industrial synthesis of acetaldehyde (Wacker process) proceeds via the intermediacy of a vinyl alcohol ...

  7. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    Acetylene hydrates to give acetaldehyde: [3] The process typically relies on mercury catalysts and has been discontinued in the West but is still practiced in China. The Hg 2+ center binds to a C≡C bond, which is then attacked by water.

  8. Alcohol dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Alcohol_dehydrogenase

    ADH2 is used by the yeast to convert ethanol back into acetaldehyde, and it is expressed only when sugar concentration is low. Having these two enzymes allows yeast to produce alcohol when sugar is plentiful (and this alcohol then kills off competing microbes), and then continue with the oxidation of the alcohol once the sugar, and competition ...

  9. Acetylene - Wikipedia

    en.wikipedia.org/wiki/Acetylene

    A number of bacteria living on acetylene have been identified. The enzyme acetylene hydratase catalyzes the hydration of acetylene to give acetaldehyde: [49] C 2 H 2 + H 2 O → CH 3 CHO. Acetylene is a moderately common chemical in the universe, often associated with the atmospheres of gas giants. [50]