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  2. Metal peroxide - Wikipedia

    en.wikipedia.org/wiki/Metal_peroxide

    Few reactions are generally formulated for peroxide salt. In excess of dilute acids or water, they release hydrogen peroxide. [1] Na 2 O 2 + 2 HCl → 2 NaCl + H 2 O 2. Upon heating, the reaction with water leads to the release of oxygen. [1] Upon exposure to air, alkali metal peroxides absorb CO 2 to give peroxycarbonates.

  3. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    Molecular models of the different molecules active in Piranha solution: peroxysulfuric acid (H 2 SO 5) and hydrogen peroxide (H 2 O 2). Piranha solution, also known as piranha etch, is a mixture of sulfuric acid (H 2 SO 4) and hydrogen peroxide (H 2 O 2).

  4. Hydrogen peroxide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_peroxide

    Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.

  5. Asymmetric nucleophilic epoxidation - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_nucleophilic_ep...

    The mechanism of nucleophilic epoxidation begins with conjugate addition of the peroxide (or other O-nucleophilic species) to the enone. Metal ions or conjugate acids present in solution coordinate both the peroxide oxygen and the enolate oxygen. Attack of the enolate on the peroxide oxygen generates the epoxide product and releases a leaving ...

  6. Fenton's reagent - Wikipedia

    en.wikipedia.org/wiki/Fenton's_reagent

    The first stage of Fenton's reaction (oxidation of Fe 3+ with hydrogen peroxide) is used in Haber–Weiss reaction; Fenton's reagent can be used in organic synthesis reactions: e.g. hydroxylation of arenes via a free radical substitution; Conversion of benzene into phenol by using Fenton's reagent; Oxidation of barbituric acid into alloxan.

  7. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    The 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.

  8. Bleach activator - Wikipedia

    en.wikipedia.org/wiki/Bleach_activator

    Bleach activators react with hydrogen peroxide in aqueous solution to form peroxy acids. Peroxy acids are more active bleaches than hydrogen peroxide at lower temperatures (<60 °C) but are too unstable to be stored in their active form and hence must be generated in situ.

  9. 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 ...