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  2. End group - Wikipedia

    en.wikipedia.org/wiki/End_group

    The thiocarbonate moiety can be functionalized at the R-group for end group analysis. The end group is a result of the propagation of chain-transfer agents during the free-radical polymerization process. The end groups can subsequently be modified by the reaction of the thiocarbonylthio compounds with nucleophiles and ionic reducing agents. [11]

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    Example: 2,2,3-trimethyl- . If there are both double bonds and triple bonds, "en" (double bond) is written before "yne" (triple bond). When the main functional group is a terminal functional group (a group which can exist only at the end of a chain, like formyl and carboxyl groups), there is no need to number it.

  4. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    IUPAC Polymer Nomenclature are standardized naming conventions for polymers set by the International Union of Pure ... End-groups are described with α- and ω-, e.g ...

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    This naming method generally follows established IUPAC organic nomenclature. Hydrides of the main group elements (groups 13–17) are given the base name ending with -ane, e.g. borane (B H 3), oxidane (H 2 O), phosphane (P H 3) (Although the name phosphine is also in common use, it is not recommended by

  6. IUPAC nomenclature of chemistry - Wikipedia

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

    In 1919, a group of chemists created the IUPAC with this idea, as well as the purpose of unionizing scientists and strengthening the international trade of science. IUPAC celebrated its 100th anniversary in 2019 and continues to regulate scientific terminology today.

  7. 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.

  8. Wikipedia:Naming conventions (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Wikipedia:Naming...

    The group numberings with Roman numbers and "A" and "B" suffixes (like VIIA, VIII) should not be used, as they are outdated and ambiguous. For example, in the CAS scheme "group VIIB" denotes manganese group (group 7), while in the old IUPAC scheme it denotes halogen group (group 17). If they are used at all, context should clarify (disambiguate ...

  9. Names for sets of chemical elements - Wikipedia

    en.wikipedia.org/wiki/Names_for_sets_of_chemical...

    Elements in groups 1–2 or 13–18, excluding hydrogen * Transition elements are sometimes referred to as transition metals † Although the heavier elements of groups 15 (Mc), 16 (Lv), 17 (Ts) and 18 (Og) have been notionally assigned to the indicated groups their chemical properties have not yet been experimentally confirmed.