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  2. Ethanol fermentation - Wikipedia

    en.wikipedia.org/wiki/Ethanol_fermentation

    The energy released by this exothermic reactions is used to phosphorylate two ADP molecules, yielding two ATP molecules, and to reduce two molecules of NAD+ to NADH. (2) The two pyruvate molecules are broken down, yielding two acetaldehyde molecule and giving off two molecules of carbon dioxide.

  3. Mixed acid fermentation - Wikipedia

    en.wikipedia.org/wiki/Mixed_acid_fermentation

    Ethanol is the most commonly used biofuel and can be produced on large scale via fermentation. The maximum theoretical yield for the production of ethanol was achieved around 20 years. [14] [15] A plasmid that carried the pyruvate decarboxylase and alcohol dehydrogenase genes from the bacteria Z. mobilis was used by scientists.

  4. Acetone–butanol–ethanol fermentation - Wikipedia

    en.wikipedia.org/wiki/Acetone–butanol–ethanol...

    The ABE fermentation pathway generally proceeds in two phases. In the initial acidogenesis phase, the cells grow exponentially and accumulate acetate and butyrate. The low pH along with other factors then trigger a metabolic shift to the solventogenesis phase, in which acetate and butyrate are used to produce the solvents. [4]

  5. Ethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate

    Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.

  6. Saponification - Wikipedia

    en.wikipedia.org/wiki/Saponification

    Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis. When the carboxylate is long chain, its salt is called a soap. The saponification of ethyl acetate gives sodium acetate and ethanol: C 2 H 5 O 2 CCH 3 + NaOH → C 2 H 5 OH + NaO 2 CCH 3

  7. Pharmacology of ethanol - Wikipedia

    en.wikipedia.org/wiki/Pharmacology_of_ethanol

    The model is most accurate when used to estimate BAC a few hours after drinking a single dose of alcohol in a fasted state, and can be within 20% CV of the true value. [ 121 ] [ 122 ] It is less accurate for BAC levels below 0.2 g/L (alcohol is not eliminated as quickly as predicted) and consumption with food (overestimating the peak BAC and ...

  8. Sugar alcohol - Wikipedia

    en.wikipedia.org/wiki/Sugar_alcohol

    Sugar alcohols can be, and often are, produced from renewable resources.Particular feedstocks are starch, cellulose and hemicellulose; the main conversion technologies use H 2 as the reagent: hydrogenolysis, i.e. the cleavage of C−O single bonds, converting polymers to smaller molecules, and hydrogenation of C=O double bonds, converting sugars to sugar alcohols.

  9. Transesterification - Wikipedia

    en.wikipedia.org/wiki/Transesterification

    Transesterification is used to synthesize enol derivatives, which are difficult to prepare by other means. Vinyl acetate, which is cheaply available, undergoes transesterification, giving access to vinyl ethers: [5] [6] ROH + AcOCH=CH 2 ROCH=CH 2 + AcOH. The reaction can be effected with high enantioselectivity when mediated with a lipase. [7]