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  2. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Acetaldehyde occurs naturally in coffee, bread, and ripe fruit, [11] and is produced by plants. It is also produced by the partial oxidation of ethanol by the liver enzyme alcohol dehydrogenase and is a contributing cause of hangover after alcohol consumption. [ 12 ]

  3. Acetaldehyde (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde_(data_page)

    Print/export Download as PDF; Printable version; In other projects Wikidata item; ... log 10 of Acetaldehyde vapor pressure. Uses formula: ...

  4. Pyruvate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_decarboxylase

    The enzyme splits pyruvate into carbon dioxide and acetaldehyde. The reaction proceeds by attack of the nucleophilic thiazole carbon on the keto group. The intermediate loses carbon dioxide, giving an enol, in an irreversible step. Subsequently, free acetaldehyde is released and the TPP is regenerated. [7]

  5. 1,1-Diethoxyethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Diethoxyethane

    1,1-Diethoxyethane (acetaldehyde diethyl acetal) is a major flavoring component of distilled beverages, especially malt whisky [3] and sherry. [4] Although it is just one of many compounds containing an acetal functional group, this specific chemical is sometimes called simply acetal .

  6. 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 ...

  7. Aldehyde ferredoxin oxidoreductase - Wikipedia

    en.wikipedia.org/wiki/Aldehyde_ferredoxin...

    The main substrates for aldehyde ferredoxin oxidoreductase are acetaldehyde, phenylacetaldehyde, and isovalerdehyde, which is a metabolic product from common amino acids and glucose. [8] For example, acetaldehyde reaches its kcat/KM value up to 22.0 μM-1s-1. [8]

  8. 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.

  9. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    A two-stage distillation of the crude acetaldehyde follows. In the first stage, low-boiling substances, such as chloromethane, chloroethane and carbon dioxide, are separated. In the second stage, water and higher-boiling by-products, such as chlorinated acetaldehydes and acetic acid, are removed and acetaldehyde is obtained in pure form ...