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  2. -yne - Wikipedia

    en.wikipedia.org/wiki/-yne

    The position of unsaturation is indicated by a numerical locant immediately preceding the "-yne" suffix, or locants in the case of multiple triple bonds. Locants are chosen to be as low as possible. While generally used as a suffix, "-yne" is also used as an infix to name substituent groups that are triply bound to the parent compound.

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched. Eller, Gernot A. (2006). "Improving the Quality of Published Chemical Names with Nomenclature Software" (PDF). Molecules. 9 (11): 915– 928.

  4. Category:Chemistry suffixes - Wikipedia

    en.wikipedia.org/wiki/Category:Chemistry_suffixes

    Download as PDF; Printable version; ... Help. Pages in category "Chemistry suffixes" The following 12 pages are in this category, out of 12 total. ... -yne This page ...

  5. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/.../IUPAC_nomenclature_of_chemistry

    IUPAC states that, "As one of its major activities, IUPAC develops Recommendations to establish unambiguous, uniform, and consistent nomenclature and terminology for specific scientific fields, usually presented as: glossaries of terms for specific chemical disciplines; definitions of terms relating to a group of properties; nomenclature of chemical compounds and their classes; terminology ...

  6. -ene - Wikipedia

    en.wikipedia.org/wiki/-ene

    If the other suffix starts with a consonant or "y", the final "-e" remains, e.g. "-enediyne" (which has the "-ene" suffix and also the "-yne" suffix, for a compound with a double bond and two triple bonds.) A Greek number prefix before the "-ene" indicates how many double bonds there are in the compound, e.g. butadiene.

  7. Ethynyl group - Wikipedia

    en.wikipedia.org/wiki/Ethynyl_group

    In organic chemistry, an ethynyl group is a functional group with the formula −C≡CH, representing an acetylene molecule with one fewer hydrogen atom.. Ethynyl group (HC≡C–), also designated as an acetylenic group (from acetylene), is referred to in IUPAC chemical nomenclature with the -yne suffix.

  8. Alk- - Wikipedia

    en.wikipedia.org/wiki/Alk-

    Prefixes, suffixes, and infixes are known as organic chemistry affixes. These affixes provide details about the molecule's structure, such as the quantity of carbon atoms, the kind of carbon-to-carbon bonds, and the existence of functional groups. [2] The following are a few typical additions in organic chemistry: Prefixes

  9. IUPAC nomenclature of inorganic chemistry - Wikipedia

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

    The names "caffeine" and "3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione" both signify the same chemical compound.The systematic name encodes the structure and composition of the caffeine molecule in some detail, and provides an unambiguous reference to this compound, whereas the name "caffeine" simply names it.