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  2. List of isomers of nonane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_nonane

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  3. List of isomers of tridecane - Wikipedia

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  4. 3-Methylheptane - Wikipedia

    en.wikipedia.org/wiki/3-Methylheptane

    3-Methylheptane is a branched alkane isomeric to octane. Its structural formula is CH 3 CH 2 CH(CH 3)CH 2 CH 2 CH 2 CH 3. It has one stereocenter. Its refractive ...

  5. Octane - Wikipedia

    en.wikipedia.org/wiki/Octane

    N-octane has 23 constitutional isomers. 8 of these isomers have one stereocenter; 3 of them have two stereocenters. (3S,4S)-3,4-Dimethylhexane (top left) and (3R,4R)-3,4-Dimethylhexane (top right) are non-superimposable mirror images, so they are chiral enantiomers.

  6. Electron configurations of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electron_configurations_of...

    However there are numerous exceptions; for example the lightest exception is chromium, which would be predicted to have the configuration 1s 2 2s 2 2p 6 3s 2 3p 6 3d 4 4s 2, written as [Ar] 3d 4 4s 2, but whose actual configuration given in the table below is [Ar] 3d 5 4s 1.

  7. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    The boiling point of 89.7 °C is 0.3 °C higher than the value of 89.4 °C predicted by Wiener's formula, based on the structure of the molecule and the boiling point of n-heptane. [2] [3] The speed of sound at 3 MHz is 1149.5 m/s at 20 °C and 889.5 m/s at 80 °C. [7] [8] [9]

  8. Periodic table (electron configurations) - Wikipedia

    en.wikipedia.org/wiki/Periodic_table_(electron...

    Og, 118, oganesson : 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 10 4p 6 5s 2 4d 10 5p 6 6s 2 4f 14 5d 10 6p 6 7s 2 5f 14 6d 10 7p 6 Note that these electron configurations are given for neutral atoms in the gas phase, which are not the same as the electron configurations for the same atoms in chemical environments.

  9. Tetramethylethylene - Wikipedia

    en.wikipedia.org/wiki/Tetramethylethylene

    It can be prepared by base-catalyzed isomerization of 2,3-dimethyl-1-butene. [2] Another route involves direct dimerization of propylene. [3] It can also be produced by photolysis of tetramethylcyclobutane-1,3-dione. [4]