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  2. 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.

  3. Glycerol and potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Glycerol_and_potassium...

    Potassium permanganate (KMnO 4) is a dark violet colored powder. Its reaction with glycerol (commonly known as glycerin or glycerine) (C 3 H 5 (OH) 3) is highly exothermic, resulting rapidly in a flame, along with the formation of carbon dioxide and water vapour:

  4. Ethanol fermentation - Wikipedia

    en.wikipedia.org/wiki/Ethanol_fermentation

    Fermentation of sugar to ethanol and CO 2 can also be done by Zymomonas mobilis, however the path is slightly different since formation of pyruvate does not happen by glycolysis but instead by the Entner–Doudoroff pathway. Other microorganisms can produce ethanol from sugars by fermentation but often only as a side product. Examples are [4]

  5. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    By removing ethylene by oxidation, the permanganate delays the ripening, increasing the fruit's shelf life up to 4 weeks without the need for refrigeration. [ 52 ] [ 53 ] [ 54 ] The chemical reaction, in which ethylene (C 2 H 4 ) is oxidised by potassium permanganate (KMnO 4 ) to carbon dioxide (CO 2 ), manganese oxide (MnO 2 ) and potassium ...

  6. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    A permanganate (/ p ər ˈ m æ ŋ ɡ ə n eɪ t, p ɜːr-/) [1] is a chemical compound with the manganate(VII) ion, MnO − 4, the conjugate base of permanganic acid.Because the manganese atom has a +7 oxidation state, the permanganate(VII) ion is a strong oxidising agent.

  7. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Glycol cleavage is a specific type of organic chemistry oxidation. The carbon–carbon bond in a vicinal diol (glycol) is cleaved and instead the two oxygen atoms become double-bonded to their respective carbon atoms. Depending on the substitution pattern in the diol, these carbonyls will be ketones and/or aldehydes. [1]

  8. Acetic acid bacteria - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid_bacteria

    Specific oxidation reactions occur through oxidative fermentation, which creates vinegar as a byproduct. In the biotechnological industry, these bacteria's oxidation mechanism is exploited to produce a number of compounds such as l-ascorbic acid, dihydroxyacetone, gluconic acid, and cellulose. [ 4 ]

  9. Chemical chameleon - Wikipedia

    en.wikipedia.org/wiki/Chemical_chameleon

    The reaction proceeds in alkaline conditions under the influence of a reducing agent. Sodium hydroxide, potassium hydroxide, and ammonium hydroxide can be used to alkalize the permanganate solution, while a variety of reducing agents can be used, sugars being common.