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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. Ball-and-stick model - Wikipedia

    en.wikipedia.org/wiki/Ball-and-stick_model

    A plastic ball-and-stick model of proline. In chemistry, the ball-and-stick model is a molecular model of a chemical substance which displays both the three-dimensional position of the atoms and the bonds between them. [1]

  4. High-test peroxide - Wikipedia

    en.wikipedia.org/wiki/High-test_peroxide

    Hydrogen peroxide works best as a propellant in extremely high concentrations (roughly over 70%). Although any concentration of peroxide will generate some hot gas (oxygen plus some steam), at concentrations above approximately 67%, the heat of decomposing hydrogen peroxide becomes large enough to completely vaporize all the liquid at standard pressure.

  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. Chemical bonding of water - Wikipedia

    en.wikipedia.org/wiki/Chemical_bonding_of_water

    While valence bond theory is suitable for predicting the geometry and bond angle of H 2 O, its prediction of electronic states does not agree with the experimentally measured reality. In the valence bond model, the two sigma bonds are of identical energy and so are the two lone pairs since they both resides in the same bonding and nonbonding ...

  7. Hydrogen disulfide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_disulfide

    The structure of hydrogen disulfide is similar to that of hydrogen peroxide, with C 2 point group symmetry. Both molecules are distinctly nonplanar. The dihedral angle between the H a −S−S and S−S−H b planes is 90.6°, compared with 111.5° in H 2 O 2. The H−S−S bond angle is 92°, close to 90° for unhybridized divalent sulfur. [1]

  8. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    Dilithium is a gas-phase molecule with a much lower bond strength than dihydrogen because the 2s electrons are further removed from the nucleus. In a more detailed analysis [ 17 ] which considers the environment of each orbital due to all other electrons, both the 1σ orbitals have higher energies than the 1s AO and the occupied 2σ is also ...

  9. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    For example, the loss of blue color in leuco-methylene blue is selective for hydrogen peroxide. [21] Quantitative analysis of hydroperoxides can be performed using potentiometric titration with lithium aluminium hydride. [22] Another way to evaluate the content of peracids and peroxides is the volumetric titration with alkoxides such as sodium ...