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  2. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of decaphenylferrocene, [(η 5-C 5 Ph 5) 2 Fe]. [8] [9] Formation of decaphenylferrocene from its linkage isomer

  3. 1-Hexyne - Wikipedia

    en.wikipedia.org/wiki/1-Hexyne

    1-Hexyne is a hydrocarbon consisting of a straight six-carbon chain having a terminal alkyne. Its molecular formula is HC 2 C 4 H 9. A colorless liquid, it is one of three isomers of hexyne. [1] It is used as a reagent in organic synthesis.

  4. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon. [ 1 ] : 620 Hydrocarbons are examples of group 14 hydrides . Hydrocarbons are generally colourless and hydrophobic ; their odor is usually faint, and may be similar to that of gasoline or lighter fluid .

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The International Union of Pure and Applied Chemistry (IUPAC) recommends using the name "alkene" only for acyclic hydrocarbons with just one double bond; alkadiene, alkatriene, etc., or polyene for acyclic hydrocarbons with two or more double bonds; cycloalkene, cycloalkadiene, etc. for cyclic ones; and "olefin" for the general class – cyclic ...

  6. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    In organic chemistry, a cycloalkene or cycloolefin is a type of alkene hydrocarbon which contains a closed ring of carbon atoms and either one or more double bonds, but has no aromatic character. Some cycloalkenes, such as cyclobutene and cyclopentene , can be used as monomers to produce polymer chains. [ 1 ]

  7. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    In organic chemistry, a rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule. [1] Often a substituent moves from one atom to another atom in the same molecule, hence these reactions are usually intramolecular. In the example below ...

  8. Category:Hydrocarbons - Wikipedia

    en.wikipedia.org/wiki/Category:Hydrocarbons

    In chemistry, a hydrocarbon is an organic compound consisting only of carbon and hydrogen. They all consist of carbon backbone and atoms of hydrogen attached to that backbone, also see aliphatic hydrocarbons.

  9. Open-chain compound - Wikipedia

    en.wikipedia.org/wiki/Open-chain_compound

    For example, in living organisms, the open-chain isomer of glucose usually exists only transiently, in small amounts; D-glucose is the usual isomer; and L-glucose is rare. Straight-chain molecules are often not literally straight, in the sense that their bond angles are often not 180°, but the name reflects that they are schematically straight.