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  2. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    Valence shell electron pair repulsion (VSEPR) theory (/ ˈ v ɛ s p ər, v ə ˈ s ɛ p ər / VESP-ər, [1]: 410 və-SEP-ər [2]) is a model used in chemistry to predict the geometry of individual molecules from the number of electron pairs surrounding their central atoms. [3]

  3. 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.

  4. Hydroperoxyl - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxyl

    The hydroperoxyl radical, also known as the hydrogen superoxide, is the protonated form of superoxide with the chemical formula HO 2, also written HOO •. This species plays an important role in the atmosphere and as a reactive oxygen species in cell biology.

  5. Trigonal pyramidal molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_pyramidal...

    However, the three hydrogen atoms are repelled by the electron lone pair in a way that the geometry is distorted to a trigonal pyramid (regular 3-sided pyramid) with bond angles of 107°. In contrast, boron trifluoride is flat, adopting a trigonal planar geometry because the boron does not have a lone pair of electrons.

  6. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Benzoyl peroxide and hydrogen peroxide are used as bleaching and "maturing" agents for treating flour to make its grain release gluten more easily; the alternative is letting the flour slowly oxidize by air, which is too slow for the industrialized era. Benzoyl peroxide is an effective topical medication for treating most forms of acne.

  7. Lipid peroxidation - Wikipedia

    en.wikipedia.org/wiki/Lipid_peroxidation

    Phototherapy may cause lipid peroxidation, leading to the rupture of red blood cell cell membranes. [9] End-products of lipid peroxidation may be mutagenic and carcinogenic. [10] For instance, the end-product MDA reacts with deoxyadenosine and deoxyguanosine in DNA, forming DNA adducts to them, primarily M 1 G. [10]

  8. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    This hydrogen peroxide then releases hydrogen peroxide: [(HO) 3 B(OOH)] − + H 2 O ⇌ B(OH) − 4 + H 2 O 2 Several metal hydroperoxide complexes have been characterized by X-ray crystallography, for example: triphenylsilicon and triphenylgermanium hydroperoxides can be obtained by reaction of initial chlorides with excess of hydrogen ...

  9. Dioxygen difluoride - Wikipedia

    en.wikipedia.org/wiki/Dioxygen_difluoride

    The structure of dioxygen difluoride resembles that of hydrogen peroxide, H 2 O 2, in its large dihedral angle, which approaches 90° and C 2 symmetry. This geometry conforms with the predictions of VSEPR theory. Dioxygen difluoride's structure