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  2. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The smaller number is always used, not the sum of the constituents numbers. The side chains are: an ethyl- at carbon 4, an ethyl- at carbon 8, and a butyl- at carbon 12. Note: the −O−CH 3 at carbon atom 15 is not a side chain, but it is a methoxy functional group. There are two ethyl- groups. They are combined to create, 4,8-diethyl.

  3. Skeletal formula - Wikipedia

    en.wikipedia.org/wiki/Skeletal_formula

    The skeletal formula of hexane, with carbons number one and three labelled The Lewis structure of hexane, for reference The 3d ball representation of hexane, with carbon (black) and hydrogen (white) shown explicitly. It does not matter which end of the chain one starts numbering from, as long as consistency is maintained when drawing diagrams.

  4. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    The carbons of the chain are conventionally numbered from 1 to n, starting from the end which is closest to the carbonyl. If the carbonyl is at the very beginning of the chain (carbon 1), the monosaccharide is said to be an aldose, otherwise it is a ketose. These names can be combined with the chain length prefix, as in aldohexose or ...

  5. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    From Figure 1, oxy subunits are take precedence over acyclic carbon chain subunits. The preferred CRU is chosen as that with the lowest possible locant (s) for substituents . In the example, there is a bromo-substituted -CH 2 -CH 2 - subunit. 1-Bromoethane-1,2-diyl is chosen in preference to 2- bromoethane-1,2-diyl as the former has a lower ...

  6. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    Find the longest carbon chain in the molecule. If that chain does not contain the double bond, name the compound according to the alkane naming rules. Otherwise: Number the carbons in that chain starting from the end that is closest to the double bond. Define the location k of the double bond as being the number of its first carbon.

  7. Bicyclic molecule - Wikipedia

    en.wikipedia.org/wiki/Bicyclic_molecule

    Numbering of the carbon chain always begins at one bridgehead atom (where the rings meet) and follows the carbon chain along the longest path, to the next bridgehead atom. Then numbering is continued along the second longest path and so on. Fused and bridged bicyclic compounds get the prefix bicyclo, whereas spirocyclic compounds get the prefix ...

  8. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The prefixes sec (from "secondary") and tert (from "tertiary") refer to the number of additional side chains (or carbons) connected to the first butyl carbon. The prefix "iso" or "iso" means "isolated" while the prefix 'n-' stands for "normal". Butan-2-yl (sec-butyl) group is chiral. The carbon atom at position 2 is a stereocenter.

  9. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Number of C atoms Number of isomers [3] [4] Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl ...