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  2. Acetaldehyde (data page) - Wikipedia

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

    0.2521 mPa·s at 10 °C 0.2307 mPa·s at 20 °C Thermodynamic properties. Phase behavior Triple point? K (? °C), ? ... log 10 of Acetaldehyde vapor pressure.

  3. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    The equilibrium constant is 6 × 10 −7 at room temperature, thus that the relative amount of the enol form in a sample of acetaldehyde is very small. [27] At room temperature, acetaldehyde ( CH 3 CH=O ) is more stable than vinyl alcohol ( CH 2 =CHOH ) by 42.7 kJ/mol: [ 28 ] Overall the keto-enol tautomerization occurs slowly but is catalyzed ...

  4. Fluoral - Wikipedia

    en.wikipedia.org/wiki/Fluoral

    Trifluoroacetaldehyde, trifluoroethanal, or fluoral, [2] is a fluorinated derivative of acetaldehyde with the formula CF 3 CHO. It is a gas at room temperature. It is a gas at room temperature. Fluoral is used to introduce trifluoromethyl groups into organic compounds.

  5. 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]

  6. Chloral - Wikipedia

    en.wikipedia.org/wiki/Chloral

    Chloral is produced commercially by the chlorination of acetaldehyde in the presence of hydrochloric acid, producing chloral hydrate. Ethanol can also be used as a feedstock. This reaction is catalyzed by antimony trichloride: H 3 CCHO + 3 Cl 2 + H 2 O → Cl 3 CCH(OH) 2 + 3 HCl. The chloral hydrate is distilled from the reaction mixture.

  7. Dichloroacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Dichloroacetaldehyde

    Dichloroacetaldehyde is a highly volatile liquid that is easily soluble in water to form Hydrates. A geminal diol, also known as monohydrate, 2,2-dichloro-1,1-ethanediol, is formed in water.

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  9. Alcohol flush reaction - Wikipedia

    en.wikipedia.org/wiki/Alcohol_flush_reaction

    The idea that acetaldehyde is the cause of the flush is also shown by the clinical use of disulfiram (Antabuse), which blocks the removal of acetaldehyde from the body via ALDH inhibition. The high acetaldehyde concentrations described share similarity to symptoms of the flush (flushing of the skin, accelerated heart rate, shortness of breath ...