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  2. Ultraviolet–visible spectroscopy of stereoisomers - Wikipedia

    en.wikipedia.org/wiki/Ultraviolet–visible...

    Ultraviolet–visible spectroscopy (UV–vis) can distinguish between enantiomers by showing a distinct Cotton effect for each isomer. UV–vis spectroscopy sees only chromophores, so other molecules must be prepared for analysis by chemical addition of a chromophore such as anthracene.

  3. Chiral analysis - Wikipedia

    en.wikipedia.org/wiki/Chiral_analysis

    Able to differentiate between enantiomers and from the racemate; (+) from (-) and (±) Spectroscopic: Polarimetry: Polarimetry uses the innate property of chiral molecules to rotate the plane-polarized light in equal and opposite direction. This method can be used to distinguish between enantiomers and from the racemate; (+) from (-) and (±)

  4. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    There are three common naming conventions for specifying one of the two enantiomers (the absolute configuration) of a given chiral molecule: the R/S system is based on the geometry of the molecule; the (+)- and (−)- system (also written using the obsolete equivalents d- and l-) is based on its optical rotation properties; and the D/L system is based on the molecule's relationship to ...

  5. Chirality (chemistry) - Wikipedia

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

    Enzymes, which are chiral, often distinguish between the two enantiomers of a chiral substrate. One could imagine an enzyme as having a glove-like cavity that binds a substrate. If this glove is right-handed, then one enantiomer will fit inside and be bound, whereas the other enantiomer will have a poor fit and is unlikely to bind.

  6. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    Each enantiomer of a chiral compound typically rotates the plane of polarized light that passes through it. The rotation has the same magnitude but opposite senses for the two isomers, and can be a useful way of distinguishing and measuring their concentration in a solution. For this reason, enantiomers were formerly called "optical isomers".

  7. Fischer projection - Wikipedia

    en.wikipedia.org/wiki/Fischer_projection

    The use of Fischer projections in non-carbohydrates is discouraged, as such drawings are ambiguous and easily confused with other types of drawing. The main purpose of Fischer projections is to show the chirality of a molecule and to distinguish between a pair of enantiomers. Some notable uses include drawing sugars and depicting isomers. [1]

  8. Ohio State warns students not to incite violence at campus ...

    www.aol.com/ohio-state-warns-students-not...

    The university's statement went on to say that "when protected speech becomes incitement or threats of violence," Ohio State President Ted Carter and university leaders have made it clear they ...

  9. Stereospecificity - Wikipedia

    en.wikipedia.org/wiki/Stereospecificity

    The quality of stereospecificity is focused on the reactants and their stereochemistry; it is concerned with the products too, but only as they provide evidence of a difference in behavior between reactants. Of stereoisomeric reactants, each behaves in its own specific way. Stereospecificity towards enantiomers is called enantiospecificity.