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  2. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/wiki/Phosphoric_acids_and...

    A general formula for such cyclic compounds is [HPO 3] x where x = number of phosphoric units in the molecule. When metaphosphoric acids lose their hydrogens as H +, cyclic anions called metaphosphates are formed. An example of a compound with such an anion is sodium hexametaphosphate (Na 6 P 6 O 18), used as a sequestrant and a food additive.

  3. Phosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Phosphoric_acid

    Phosphoric acid (orthophosphoric acid, monophosphoric acid or phosphoric(V) acid) is a colorless, odorless phosphorus-containing solid, and inorganic compound with the chemical formula H 3 P O 4. It is commonly encountered as an 85% aqueous solution , which is a colourless, odourless, and non- volatile syrupy liquid.

  4. Phosphorus oxoacid - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_oxoacid

    In chemistry, phosphorus oxoacid (or phosphorus acid) is a generic name for any acid whose molecule consists of atoms of phosphorus, oxygen, and hydrogen. [1] There is a potentially infinite number of such compounds. Some of them are unstable and have not been isolated, but the derived anions and organic groups are present in stable salts and ...

  5. Oxygen compounds - Wikipedia

    en.wikipedia.org/wiki/Oxygen_compounds

    The oxidation state of oxygen is −2 in almost all known compounds of oxygen. The oxidation state −1 is found in a few compounds such as peroxides . Compounds containing oxygen in other oxidation states are very uncommon: − 1 ⁄ 2 ( superoxides ), − 1 ⁄ 3 ( ozonides ), 0 (elemental, hypofluorous acid ), + 1 ⁄ 2 ( dioxygenyl ), +1 ...

  6. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Ethers (R−O−R) consist of an oxygen atom between the two attached carbon chains. The shorter of the two chains becomes the first part of the name with the -ane suffix changed to -oxy, and the longer alkane chain becomes the suffix of the name of the ether. Thus, CH 3 OCH 3 is methoxymethane, and CH 3 OCH 2 CH 3 is methoxyethane (not ...

  7. Phosphoryl group - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_group

    Contrary to biology, biochemistry and biomedicine branches, in organic and inorganic chemistry branches, and in the branch of chemical nomenclature (see IUPAC), the correct name for the −P(=O)(−O −) 2 group is not "phosphoryl", but phosphonato, and the correct name for the −P(=O)(−OH) 2 group is phosphono, and the term phosphoryl ...

  8. 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.

  9. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    The main purpose of chemical nomenclature is to disambiguate the spoken or written names of chemical compounds: each name should refer to one compound. Secondarily, each compound should have only one name, although in some cases some alternative names are accepted. Preferably, the name should also represent the structure or chemistry of a compound.