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  2. IUPAC nomenclature of chemistry - Wikipedia

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

    The Geneva Nomenclature of 1892 was created as a result of many other meetings in the past, the first of which was established in 1860 by August Kekulé. Another entity called the International Association of Chemical Societies (IACS) existed, and on 1911, gave vital propositions the new one should address: [ 2 ]

  3. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Chemical nomenclature however (with IUPAC nomenclature as the best example) is necessarily more restrictive: Its purpose is to standardize communication and practice so that, when a chemical term is used it has a fixed meaning relating to chemical structure, thereby giving insights into chemical properties and derived molecular functions. These ...

  4. IUPAC nomenclature of organic chemistry - Wikipedia

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

    To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...

  5. Naming of chemical elements - Wikipedia

    en.wikipedia.org/wiki/Naming_of_chemical_elements

    The Americans also wished to name element 106 seaborgium. This naming dispute ran from the 1970s (when the elements were discovered) to the 1990s, when the International Union of Pure and Applied Chemistry (IUPAC) created a tentative list of the element names for elements 104 to 109. The Americans, however, refused to agree with these names ...

  6. IUPAC nomenclature of inorganic chemistry 2005 - Wikipedia

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

    This naming method generally follows established IUPAC organic nomenclature. Hydrides of the main group elements (groups 13–17) are given -ane base names, e.g. borane, BH 3. Acceptable alternative names for some of the parent hydrides are water rather than oxidane and ammonia rather than azane.

  7. Alkylidene group - Wikipedia

    en.wikipedia.org/wiki/Alkylidene_group

    In standard IUPAC nomenclature, alkylidene groups are named by replacing the -yl in the corresponding alkyl group with -ylidene. [4] This practice is also often extended to common names. For example, the isopropyl group (IUPAC: prop-2-yl) −CH(CH 3) 2 corresponds to the isopropylidene group =C(CH 3) 2 (IUPAC: prop-2-ylidene).

  8. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    Polymer nomenclature usually applies to idealized representations meaning minor structural irregularities are ignored. A polymer can be named in one of two ways. Source-based nomenclature can be used when the monomer can be identified. Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven.

  9. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    The IUPAC numerical multiplier is a system of prefixes used in chemistry to indicate the number of atoms or groups in a molecule.