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  2. Meso compound - Wikipedia

    en.wikipedia.org/wiki/Meso_compound

    One of the two meso isomers of 1,2,3,4-tetrafluorospiropentane, with S 4 symmetry. Since a meso isomer has a superposable mirror image, a compound with a total of n chiral centers cannot attain the theoretical maximum of 2 n stereoisomers if one of the stereoisomers is meso. [4] A meso isomer need not have a mirror plane.

  3. Dimethylhexane - Wikipedia

    en.wikipedia.org/wiki/Dimethylhexane

    2,5-Dimethylhexane; 3,3-Dimethylhexane; 3,4-Dimethylhexane [Wikidata This page was last edited on 27 April 2022, at 16:52 (UTC). Text is available under the ...

  4. 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.

  5. 1,2,3,4-Butanetetracarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/1,2,3,4-Butanetetra...

    1,2,3,4-Butanetetracarboxylic acid is an organic compound with the formula HO 2 CCH 2 CH(CO 2 H)CH(CO 2 H)CH 2 CO 2 H. It is one of the simplest stable tetracarboxylic acids. The compound exists as two diastereomers, meso and the (R,R)/(S,S) pair. All are white solids. The compound is produced by oxidation of tetrahydrophthalic anhydride. [1]

  6. File:Octane stereo isomers 10 3 4 dimethylhexane.svg

    en.wikipedia.org/wiki/File:Octane_stereo_isomers...

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  8. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    This page was last edited on 18 November 2024, at 00:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

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