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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. 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.

  4. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    Unlike chlorates, which disproportionate very slowly to form chloride and perchlorate, iodates are stable to disproportionation in both acidic and alkaline solutions. From these, salts of most metals can be obtained. Iodic acid is most easily made by oxidation of an aqueous iodine suspension by electrolysis or fuming nitric acid. Iodate has the ...

  5. Iodine - Wikipedia

    en.wikipedia.org/wiki/Iodine

    This is an accepted version of this page This is the latest accepted revision, reviewed on 9 January 2025. This article is about the chemical element. For other uses, see Iodine (disambiguation). Chemical element with atomic number 53 (I) Iodine, 53 I Iodine Pronunciation / ˈ aɪ ə d aɪ n, - d ɪ n, - d iː n / (EYE -ə-dyne, -⁠din, -⁠deen) Appearance lustrous metallic gray solid, black ...

  6. Hypervalent organoiodine compounds - Wikipedia

    en.wikipedia.org/wiki/Hypervalent_organoiodine...

    The latter can occur with organometallized arenes such as an arylstannane or -silane (a nucleophilic aromatic substitution reaction) or unfunctionalized arenes in the presence of a Brønsted or Lewis acid (an electrophilic aromatic substitution reaction). Diaryliodonium salts react with nucleophiles at iodine, replacing one ligand to form the ...

  7. Hypophosphorous acid - Wikipedia

    en.wikipedia.org/wiki/Hypophosphorous_acid

    Because hypophosphorous acid can reduce elemental iodine to form hydroiodic acid, which is a reagent effective for reducing ephedrine or pseudoephedrine to methamphetamine, [11] the United States Drug Enforcement Administration designated hypophosphorous acid (and its salts) as a List I precursor chemical effective November 16, 2001. [12]

  8. Hydrogen iodide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_iodide

    Hydrogen iodide (HI) is a diatomic molecule and hydrogen halide. Aqueous solutions of HI are known as hydroiodic acid or hydriodic acid, a strong acid.Hydrogen iodide and hydroiodic acid are, however, different in that the former is a gas under standard conditions, whereas the other is an aqueous solution of the gas.

  9. 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 ...