enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Phenolphthalein - Wikipedia

    en.wikipedia.org/wiki/Phenolphthalein

    Phenolphthalein (/ f ... is a chemical compound with the formula C 20 H 14 O 4 and is often written as ... it will turn pink immediately upon addition of the peroxide ...

  3. Kastle–Meyer test - Wikipedia

    en.wikipedia.org/wiki/Kastle–Meyer_test

    The Kastle–Meyer test is a presumptive blood test, first described in 1903, in which the chemical indicator phenolphthalein is used to detect the possible presence of hemoglobin. It relies on the peroxidase -like activity of hemoglobin in blood to catalyze the oxidation of phenolphthalin (the colorless reduced form of phenolphthalein) into ...

  4. Diphenyl oxalate - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_oxalate

    This chemical is the double ester of phenol with oxalic acid. Upon reaction with hydrogen peroxide, 1,2-dioxetanedione is formed, along with release of the two phenols. [2] The dioxetanedione then reacts with a dye molecule, decomposing to form carbon dioxide and leaving the dye in an excited state.

  5. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Dialkyl peroxides, e.g., dicumyl peroxide, are synthesized by addition of hydrogen peroxide to alkenes or by O-alkylation of hydroperoxides. Diacyl peroxides are typically prepared by treating hydrogen peroxide with acid chlorides or acid anhydrides in the presence of base: [1] H 2 O 2 + 2 RCOCl → (RCO 2) 2 + 2 HCl H 2 O 2 + (RCO) 2 O → ...

  6. Peroxide - Wikipedia

    en.wikipedia.org/wiki/Peroxide

    The peroxide group is marked in blue. R, R 1 and R 2 mark hydrocarbon moieties. The most common peroxide is hydrogen peroxide (H 2 O 2), colloquially known simply as "peroxide". It is marketed as solutions in water at various concentrations. Many organic peroxides are known as well. In addition to hydrogen peroxide, some other major classes of ...

  7. Fenton's reagent - Wikipedia

    en.wikipedia.org/wiki/Fenton's_reagent

    Fenton's reagent is a solution of hydrogen peroxide (H 2 O 2) and an iron catalyst (typically iron(II) sulfate, FeSO 4). [1] It is used to oxidize contaminants or waste water as part of an advanced oxidation process.

  8. Cumene hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Cumene_hydroperoxide

    Cumene hydroperoxide is the organic compound with the formula C 6 H 5 C(CH 3) 2 OOH; this oily liquid is classified as an organic hydroperoxide. [2] Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and 2-phenylpropan-2-ol. [3] It is produced by treatment of cumene with oxygen, an autoxidation.

  9. Hydroquinone - Wikipedia

    en.wikipedia.org/wiki/Hydroquinone

    Hydroquinone, also known as benzene-1,4-diol or quinol, is an aromatic organic compound that is a type of phenol, a derivative of benzene, having the chemical formula C 6 H 4 (OH) 2. It has two hydroxyl groups bonded to a benzene ring in a para position. It is a white granular solid. Substituted derivatives of this parent compound are also ...