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  2. Eudysmic ratio - Wikipedia

    en.wikipedia.org/wiki/Eudysmic_ratio

    A racemic mixture is an equal mixture of both enantiomers, which may be easier to manufacture than a single enantiomeric form. Indacrinone Enantiomers. It is often the case that only a single one of the enantiomers contains all of the wanted bioactivity, the distomer is often less active, has no desired activity or may even be toxic. [6]

  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. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    A mixture of equal amounts of each enantiomer, a racemic mixture or a racemate, does not rotate light. [7] [8] [9] Stereoisomers include both enantiomers and diastereomers. Diastereomers, like enantiomers, share the same molecular formula and are also nonsuperposable onto each other; however, they are not mirror images of each other. [10]

  5. Kinetic resolution - Wikipedia

    en.wikipedia.org/wiki/Kinetic_resolution

    Kinetic resolution is a possible method for irreversibly differentiating a pair of enantiomers due to (potentially) different activation energies. While both enantiomers are at the same Gibbs free energy level by definition, and the products of the reaction with both enantiomers are also at equal levels, the Δ G ‡ {\displaystyle \Delta G ...

  6. Stereoselectivity - Wikipedia

    en.wikipedia.org/wiki/Stereoselectivity

    An example of modest stereoselectivity is the dehydrohalogenation of 2-iodobutane which yields 60% trans-2-butene and 20% cis-2-butene. [5] Since alkene geometric isomers are also classified as diastereomers, this reaction would also be called diastereoselective.

  7. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    Le Bel-van't Hoff rule states that for a structure with n asymmetric carbon atoms, there is a maximum of 2 n different stereoisomers possible. As an example, D-glucose is an aldohexose and has the formula C 6 H 12 O 6. Four of its six carbon atoms are stereogenic, which means D-glucose is one of 2 4 =16 possible stereoisomers. [20] [21]

  8. 6 Ways to Lose Weight Without Exercising This Year

    www.aol.com/lifestyle/6-ways-lose-weight-without...

    Practicing relaxation techniques like meditation or breathing patterns could help manage general stress, as well as stress around overeating or weight loss.. brizmaker/istockphoto Plenty of Rest

  9. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    A living system usually deals with two enantiomers of the same compound in drastically different ways. In biology, homochirality is a common property of amino acids and carbohydrates . The chiral protein-making amino acids , which are translated through the ribosome from genetic coding, occur in the L form.