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  2. 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.

  3. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Hydrogen fluoride: 1.86 A x OH Molecules with an OH at one end C 2 H 5 OH Ethanol: 1.69 O x A y: Molecules with an O at one end H 2 O Water: 1.85 N x A y: Molecules with an N at one end NH 3: Ammonia: 1.42 Nonpolar A 2: Diatomic molecules of the same element O 2: Dioxygen: 0.0 C x A y: Most hydrocarbon compounds C 3 H 8: Propane: 0.083 C x A y ...

  4. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    A typical mixture is 3 parts of concentrated sulfuric acid and 1 part of 30 wt. % hydrogen peroxide solution; [1] other protocols may use a 4:1 or even 7:1 mixture. A closely related mixture, sometimes called "base piranha", is a 5:1:1 mixture of water, ammonia solution ( NH 4 OH , or NH 3 (aq) ), and 30% hydrogen peroxide.

  5. Hydroperoxyl - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxyl

    Together with its conjugate base superoxide, hydroperoxyl is an important reactive oxygen species.Unlike • O − 2, which has reducing properties, HO • 2 can act as an oxidant in a number of biologically important reactions, such as the abstraction of hydrogen atoms from tocopherol and polyunstaturated fatty acids in the lipid bilayer.

  6. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    The O−O bond length in peroxides is about 1.45 Å, and the R−O−O angles (R = H, C) are about 110° (water-like). Characteristically, the C−O−O−H dihedral angles are about 120°. The O−O bond is relatively weak, with a bond dissociation energy of 45–50 kcal/mol (190–210 kJ/mol), less than half the strengths of C−C , C−H ...

  7. 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 → ...

  8. Hydrogen polyoxide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_polyoxide

    Hydrogen peroxide (H 2 O 2) is a common disinfectant and readily decomposes to form water and oxygen. Trioxidane (H 2 O 3) is rare and readily decomposes into water and singlet oxygen. Tetraoxidane (H 2 O 4) has been synthesized by reaction among peroxy radicals at low temperature. [1]

  9. High-test peroxide - Wikipedia

    en.wikipedia.org/wiki/High-test_peroxide

    High-test peroxide (HTP) is a highly concentrated (85 to 98%) solution of hydrogen peroxide, with the remainder consisting predominantly of water. In contact with a catalyst, it decomposes into a high-temperature mixture of steam and oxygen, with no remaining liquid water.

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