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  2. Chirality (chemistry) - Wikipedia

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

    Chiral molecules will usually have a stereogenic element from which chirality arises. The most common type of stereogenic element is a stereogenic center, or stereocenter. In the case of organic compounds, stereocenters most frequently take the form of a carbon atom with four distinct (different) groups attached to it in a tetrahedral geometry.

  3. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    The term "chiral" in general is used to describe the object that is non-superposable on its mirror image. [18] In chemistry, chirality usually refers to molecules. Two mirror images of a chiral molecule are called enantiomers or optical isomers. Pairs of enantiomers are often designated as "right-", "left-handed" or, if they have no bias ...

  4. Chiral media - Wikipedia

    en.wikipedia.org/wiki/Chiral_media

    For example, an isotropic chiral material can comprise a random dispersion of handed molecules or inclusions, such as a liquid consisting of chiral molecules. Handedness can also be present at the macroscopic level in structurally chiral materials .

  5. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Chiral purity is a measure of the purity of a chiral drug. Other synonyms employed include enantiomeric excess , enantiomer purity, enantiomeric purity, and optical purity. Optical purity is an obsolete term since today most of the chiral purity measurements are done using chromatographic techniques (not based on optical principles).

  6. Axial chirality - Wikipedia

    en.wikipedia.org/wiki/Axial_chirality

    Two types of molecules having axial chirality: allenes (left) and binaryl atropisomers (right) In chemistry, axial chirality is a special case of chirality in which a molecule contains two pairs of chemical groups in a non-planar arrangement about an axis of chirality so that the molecule is not superposable on its mirror image.

  7. Chirality timeline - Wikipedia

    en.wikipedia.org/wiki/Chirality_timeline

    Chiral molecules in the receptors in our noses can tell the difference between these things. Chirality affects biochemical reactions, and the way a drug works depends on what kind of enantiomer it is. Many drugs are chiral and it is important that the shape of the drug matches the shape of the cell receptor it is meant to affect.

  8. Scientists warn of ‘unprecedented’ risks of research into ...

    www.aol.com/mirror-bacteria-may-constitute...

    The report said that if a cell with natural chirality can be created from lifeless molecules, then, in theory, a mirror-image cell could be created from mirror-image molecules using the same ...

  9. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Chiral molecules can differ in their chemical properties, but are identical in their physical properties, which can make distinguishing enantiomers challenging. Absolute configurations for a chiral molecule (in pure form) are most often obtained by X-ray crystallography , although with some important limitations.