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  2. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.

  3. Cyclopentane - Wikipedia

    en.wikipedia.org/wiki/Cyclopentane

    Cyclopentane (also called C pentane) [4] is a highly flammable alicyclic hydrocarbon with chemical formula C 5 H 10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane.

  4. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

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  5. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.

  6. Chemical table file - Wikipedia

    en.wikipedia.org/wiki/Chemical_table_file

    An MDL Molfile is a file format for holding information about the atoms, bonds, connectivity and coordinates of a molecule.. The molfile consists of some header information, the Connection Table (CT) containing atom info, then bond connections and types, followed by sections for more complex information.

  7. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes. A Newman projection visualizes the conformation of a chemical bond from front to back, with the front atom represented by the intersection of three lines (a dot) and the back atom as a circle.

  8. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The σ from the 2p is more non-bonding due to mixing, and same with the 2s σ. This also causes a large jump in energy in the 2p σ* orbital. The bond order of diatomic nitrogen is three, and it is a diamagnetic molecule. [12] The bond order for dinitrogen (1σ g 2 1σ u 2 2σ g 2 2σ u 2 1π u 4 3σ g 2) is three because two electrons are now ...

  9. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    This is because the bond angle for an alkene, C-C=C, is 122°, while the bond angle for an alkane, C-C-C, is 112°. When these carbons form a small ring, the alkene which has a larger bond angle will have to compress more than the alkane causing more bond angle strain. [4] Cycloalkenes have a lower melting point than cycloalkanes of the same size.