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  2. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ] [ 2 ] Number of C atoms

  3. Pentane - Wikipedia

    en.wikipedia.org/wiki/Pentane

    Pentane is an organic compound with the formula C 5 H 12 —that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane ...

  4. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    The simplest isomer of an alkane is the one in which the carbon atoms are arranged in a single chain with no branches. This isomer is sometimes called the n-isomer (n for "normal", although it is not necessarily the most common). However, the chain of carbon atoms may also be branched at one or more points.

  5. List of compounds with carbon number 5 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    C 5 F 6 O 3: hexafluoroglutaric acid anhydride: 376-68-1 C 5 F 8 O 2: hexafluoroglutaryl fluoride: 678-78-4 C 5 F 10: decafluorocyclopentane: 376-77-2 C 5 F 11 N: undecafluoropiperidine: 836-77-1 C 5 F 13 N: perfluoromethyldiethylamine: 758-48-5 C 5 FeO 4 S: tetracarbonyl carbonothioyl iron: 66517-47-3 C 5 FeO 5: iron pentacarbonyl: 13463-40-6 ...

  6. IUPAC nomenclature of organic chemistry - Wikipedia

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

    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. The side chains are grouped like this: 12-butyl-4,8-diethyl.

  7. Pyranose - Wikipedia

    en.wikipedia.org/wiki/Pyranose

    Common conformations are chair (C), boat (B), skew (S), half-chair (H) or envelope (E). The ring atoms are then numbered; the anomeric, or hemiacetal, carbon is always 1. Oxygen atoms in the structure are, in general, referred to by the carbon atom they are attached to in the acyclic form, and designated O. Then:

  8. Carbon compounds - Wikipedia

    en.wikipedia.org/wiki/Carbon_compounds

    In general bonds of carbon with other elements are covalent bonds. Carbon is tetravalent but carbon free radicals and carbenes occur as short-lived intermediates. Ions of carbon are carbocations and carbanions are also short-lived. An important carbon property is catenation as the ability to form long carbon chains and rings. [3]

  9. Open-chain compound - Wikipedia

    en.wikipedia.org/wiki/Open-chain_compound

    In chemistry, an open-chain compound (or open chain compound) or acyclic compound (Greek prefix α 'without' and κύκλος 'cycle') is a compound with a linear structure, rather than a cyclic one. [1] An open-chain compound having no side groups is called a straight-chain compound (also spelled as straight chain compound).