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  2. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    An example of such an enantiomer is the sedative thalidomide, which was sold in a number of countries around the world from 1957 until 1961. It was withdrawn from the market when it was found to cause birth defects. One enantiomer caused the desirable sedative effects, while the other, unavoidably [23] present in equal quantities, caused birth ...

  3. Enantioselective synthesis - Wikipedia

    en.wikipedia.org/wiki/Enantioselective_synthesis

    Enantioselective synthesis, also called asymmetric synthesis, [1] is a form of chemical synthesis.It is defined by IUPAC as "a chemical reaction (or reaction sequence) in which one or more new elements of chirality are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereomeric) products in unequal amounts."

  4. Optical rotation - Wikipedia

    en.wikipedia.org/wiki/Optical_rotation

    Optical rotation, also known as polarization rotation or circular birefringence, is the rotation of the orientation of the plane of polarization about the optical axis of linearly polarized light as it travels through certain materials. Circular birefringence and circular dichroism are the manifestations of optical activity.

  5. Polarimeter - Wikipedia

    en.wikipedia.org/wiki/Polarimeter

    The optical rotation is proportional to the concentration of the optically active substances in solution. Polarimeters may therefore be applied for concentration measurements of enantiomer-pure samples. With a known concentration of a sample, polarimeters may also be applied to determine the specific rotation when characterizing a new substance.

  6. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Cis–trans isomerism, also known as geometric isomerism, describes certain arrangements of atoms within molecules. The prefixes " cis " and " trans " are from Latin: "this side of" and "the other side of", respectively. [ 1 ] In the context of chemistry, cis indicates that the functional groups (substituents) are on the same side of some plane ...

  7. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    In chemistry, absolute configuration refers to the spatial arrangement of atoms within a molecular entity (or group) that is chiral, and its resultant stereochemical description. [1] Absolute configuration is typically relevant in organic molecules where carbon is bonded to four different substituents. This type of construction creates two ...

  8. Specific rotation - Wikipedia

    en.wikipedia.org/wiki/Specific_rotation

    Definition. The CRC Handbook of Chemistry and Physics defines specific rotation as: For an optically active substance, defined by [α] θλ = α/γl, where α is the angle through which plane polarized light is rotated by a solution of mass concentration γ and path length l. Here θ is the Celsius temperature and λ the wavelength of the light ...

  9. Racemization - Wikipedia

    en.wikipedia.org/wiki/Racemization

    In chemistry, racemization is a conversion, by heat or by chemical reaction, of an optically active compound into a racemic (optically inactive) form. This creates a 1:1 molar ratio of enantiomers and is referred to as a racemic mixture (i.e. contain equal amount of (+) and (−) forms). Plus and minus forms are called Dextrorotation and ...