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  2. Meso compound - Wikipedia

    en.wikipedia.org/wiki/Meso_compound

    The meso compound must not be confused with a 50:50 racemic mixture of the two optically-active compounds, although neither will rotate light in a polarimeter. It is a requirement for two of the stereocenters in a meso compound to have at least two substituents in common (although having this characteristic does not necessarily mean that the ...

  3. Mesoionic compounds - Wikipedia

    en.wikipedia.org/wiki/Mesoionic_compounds

    Mesoionic compounds are a subclass of betaines. [1] Examples are sydnones and sydnone imines (e.g. the stimulant mesocarb ), münchnones , [ 1 ] [ 2 ] and mesoionic carbenes . The formal positive charge is associated with the ring atoms and the formal negative charge is associated either with ring atoms or an exocyclic nitrogen or other atom. [ 3 ]

  4. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    On the other hand, an organic compound with multiple stereogenic carbons is typically, but not always, chiral. In particular, if the stereocenters are configured in such a way that the molecule can take a conformation having a plane of symmetry or an inversion point, then the molecule is achiral and is known as a meso compound.

  5. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    These include meso compounds, cis–trans isomers, E-Z isomers, and non-enantiomeric optical isomers. Diastereomers seldom have the same physical properties. In the example shown below, the meso form of tartaric acid forms a diastereomeric pair with both levo- and dextro-tartaric acids, which form an enantiomeric pair.

  6. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    However, compounds that contain an even number of asymmetric atoms sometimes lack chirality because they are arranged in mirror-symmetric pairs, and are known as meso compounds. For instance, meso tartaric acid (shown on the right) has two asymmetric carbon atoms, but it does not exhibit enantiomerism because there is a mirror symmetry plane.

  7. Descriptor (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Descriptor_(Chemistry)

    Pseudoasymmetry occurs when four different substituents are attached to one carbon atom, two of which differ only by their absolute stereochemical configuration. Examples of such are meso compounds such the tropane alkaloids; the parent compound is tropine, whose systematic name is (1R, 3r, 5S)-8-methyl-8

  8. Tacticity - Wikipedia

    en.wikipedia.org/wiki/Tacticity

    An example of m diads in a polypropylene molecule. ... (formerly meso diad, as in a meso compound, ... Laboratory of Polymers and Biomaterials, Dept. of Chemistry ...

  9. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    The achiral meso compound (1R,2S)-1,2-diphenyloxirane arises from cis-stilbene, though peroxide epoxidations of the cis-isomer produce both cis- and trans-epoxide products. For example, using tert-butyl hydroperoxide, oxidation of cis-stilbene produces 0.8% cis-stilbene oxide, 13.5% trans-stilbene oxide, and 6.1% benzaldehyde.