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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. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    Under ideal conditions the reaction produces 50% of both the alcohol and the carboxylic acid (it takes two aldehydes to produce one acid and one alcohol). [5] This can be economically viable if the products can be separated and both have a value; the commercial conversion of furfural into furfuryl alcohol and 2-furoic acid is an example of this ...

  4. Acid–base reaction - Wikipedia

    en.wikipedia.org/wiki/Acidbase_reaction

    In chemistry, an acidbase reaction is a chemical reaction that occurs between an acid and a base.It can be used to determine pH via titration.Several theoretical frameworks provide alternative conceptions of the reaction mechanisms and their application in solving related problems; these are called the acidbase theories, for example, Brønsted–Lowry acidbase theory.

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  6. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    [15] In Lewis theory an acid, A, and a base, B, form an adduct, AB, where the electron pair forms a dative covalent bond between A and B. This is shown when the adduct H 3 N−BF 3 forms from ammonia and boron trifluoride , a reaction that cannot occur in water because boron trifluoride hydrolizes in water.

  7. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    Iodine chloride vapour tends to chlorinate phenol and salicyclic acid, since when iodine chloride undergoes homolytic dissociation, chlorine and iodine are produced and the former is more reactive. However, iodine chloride in tetrachloromethane solution results in iodination being the main reaction, since now heterolytic fission of the I–Cl ...

  8. Iodic acid - Wikipedia

    en.wikipedia.org/wiki/Iodic_acid

    When iodic acid acts as oxidizer, then the product of the reaction is either iodine, or iodide ion. Under some special conditions (very low pH and high concentration of chloride ions, such as in concentrated hydrochloric acid), iodic acid is reduced to iodine trichloride , a golden yellow compound in solution and no further reduction occurs.

  9. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    The E and C parameters refer, respectively, to the electrostatic and covalent contributions to the strength of the bonds that the acid and base will form. The equation is −ΔH = E A E B + C A C B + W. The W term represents a constant energy contribution for acidbase reaction such as the cleavage of a dimeric acid or base.