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  2. Pinnick oxidation - Wikipedia

    en.wikipedia.org/wiki/Pinnick_Oxidation

    Hydrogen peroxide (H 2 O 2) can be used as HOCl scavenger whose byproducts do not interfere in the Pinnick oxidation reaction: HOCl + H 2 O 2 → HCl + O 2 + H 2 O. In a weakly acidic condition, fairly concentrated (35%) H 2 O 2 solution undergoes a rapid oxidative reaction with no competitive reduction reaction of HClO 2 to form HOCl. HClO 2 ...

  3. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Potassium permanganate (KMnO 4) oxidizes primary alcohols to carboxylic acids very efficiently. This reaction, which was first described in detail by Fournier, [10] [11] is typically carried out by adding KMnO 4 to a solution or suspension of the alcohol in an alkaline aqueous solution. For the reaction to proceed efficiently, the alcohol must ...

  4. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  5. tert-Butyl hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_hydroperoxide

    In the Halcon process, molybdenum-based catalysts are used for this reaction: (CH 3) 3 COOH + CH 2 =CHCH 3 → (CH 3) 3 COH + CH 2 OCHCH 3. The byproduct t-butanol can be dehydrated to isobutene and converted to MTBE. On a much smaller scale, tert-butyl hydroperoxide is used to produce some fine chemicals by the Sharpless epoxidation. [4]

  6. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    The Dakin oxidation (or Dakin reaction) is an organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde (2-hydroxybenzaldehyde or 4-hydroxybenzaldehyde) or ketone reacts with hydrogen peroxide (H 2 O 2) in base to form a benzenediol and a carboxylate. Overall, the carbonyl group is oxidised, whereas the H 2 O 2 is reduced.

  7. Milas hydroxylation - Wikipedia

    en.wikipedia.org/wiki/Milas_hydroxylation

    The Milas hydroxylation is an organic reaction converting an alkene to a vicinal diol, and was developed by Nicholas A. Milas in the 1930s. [1] [2] The cis-diol is formed by reaction of alkenes with hydrogen peroxide and either ultraviolet light or a catalytic osmium tetroxide, [3] vanadium pentoxide, or chromium trioxide.

  8. In situ chemical oxidation - Wikipedia

    en.wikipedia.org/wiki/In_situ_chemical_oxidation

    The biggest difference between the two chemicals is that potassium permanganate is less soluble than sodium permanganate. [5] Potassium permanganate is a crystalline solid that is typically dissolved in water before application to the contaminated site. [3] Unfortunately, the solubility of potassium permanganate is dependent on temperature.

  9. Methyl hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Methyl_hydroperoxide

    Methyl hydroperoxide is the organic compound with the formula CH 3 OOH. It is a volaltile colorless liquid. It is a volaltile colorless liquid. In addition to being of theoretical interest as the simplest organic hydroperoxide , methyl hydroperoxide is an intermediate in the oxidation of methane . [ 1 ]