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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. Metal peroxide - Wikipedia

    en.wikipedia.org/wiki/Metal_peroxide

    The first class mostly contains the peroxides of the alkali and alkaline earth metals whereas the covalent peroxides are represented by such compounds as hydrogen peroxide and peroxymonosulfuric acid (H 2 SO 5). In contrast to the purely ionic character of alkali metal peroxides, peroxides of transition metals have a more covalent character. [1]

  4. 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 ...

  5. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    Many industrial peroxides are produced using hydrogen peroxide. Reactions with aldehydes and ketones yield a series of compounds depending on conditions. Specific reactions include addition of hydrogen peroxide across the C=O double bond: R 2 C=O + H 2 O 2 → R 2 C(OH)OOH. In some cases, these hydroperoxides convert to give cyclic diperoxides:

  6. Ionic bonding - Wikipedia

    en.wikipedia.org/wiki/Ionic_bonding

    Ionic bonding is a type of chemical bonding that involves the electrostatic attraction between oppositely charged ions, or between two atoms with sharply different electronegativities, [1] and is the primary interaction occurring in ionic compounds.

  7. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    Hydroxyl radicals are also produced during UV-light dissociation of H 2 O 2 (suggested in 1879) and likely in Fenton chemistry, where trace amounts of reduced transition metals catalyze peroxide-mediated oxidations of organic compounds. In organic synthesis hydroxyl radicals are most commonly generated by photolysis of 1-Hydroxy-2(1H ...

  8. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    A bond of higher bond order also exerts greater repulsion since the pi bond electrons contribute. [10] For example in isobutylene, (H 3 C) 2 C=CH 2, the H 3 C−C=C angle (124°) is larger than the H 3 C−C−CH 3 angle (111.5°). However, in the carbonate ion, CO 2− 3, all three C−O bonds are equivalent with angles of 120° due to resonance.

  9. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    A hydrogen bond (H-bond), is a specific type of interaction that involves dipole–dipole attraction between a partially positive hydrogen atom and a highly electronegative, partially negative oxygen, nitrogen, sulfur, or fluorine atom (not covalently bound to said hydrogen atom). It is not a covalent bond, but instead is classified as a strong ...