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  2. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    Chirality (/ k aɪ ˈ r æ l ɪ t i /) is a property of asymmetry important in several branches of science. The word chirality is derived from the Greek χείρ (kheir), "hand", a familiar chiral object. An object or a system is chiral if it is distinguishable from its mirror image; that is, it cannot be superposed (not to be confused with ...

  3. Chirality (chemistry) - Wikipedia

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

    In the achiral molecules, X and Y (with no subscript) represent achiral groups, whereas X R and X S or Y R and Y S represent enantiomers. Note that there is no meaning to the orientation of an S 2 axis, which is just an inversion. Any orientation will do, so long as it passes through the center of inversion.

  4. Stereocenter - Wikipedia

    en.wikipedia.org/wiki/Stereocenter

    A chirality center (chiral center) is a type of stereocenter. A chirality center is defined as an atom holding a set of four different ligands (atoms or groups of atoms) in a spatial arrangement which is non-superposable on its mirror image. Chirality centers must be sp 3 hybridized, meaning that a chirality center can only have single bonds. [5]

  5. Chirality (mathematics) - Wikipedia

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

    A general definition of chirality based on group theory exists. [2] It does not refer to any orientation concept: an isometry is direct if and only if it is a product of squares of isometries, and if not, it is an indirect isometry. The resulting chirality definition works in spacetime. [3] [4]

  6. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    A chirality center is also called a chiral center [16] [17] [18] or an asymmetric center. [19] Some sources use the terms stereocenter , stereogenic center , stereogenic atom or stereogen to refer exclusively to a chirality center, [ 16 ] [ 18 ] [ 20 ] while others use the terms more broadly to refer also to centers that result in diastereomers ...

  7. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Absolute configuration is typically relevant in organic molecules where carbon is bonded to four different substituents. This type of construction creates two possible enantiomers . Absolute configuration uses a set of rules to describe the relative positions of each bond around the chiral center atom.

  8. Chiral knot - Wikipedia

    en.wikipedia.org/wiki/Chiral_knot

    The simplest chiral knot is the trefoil knot, which was shown to be chiral by Max Dehn. All nontrivial torus knots are chiral. The Alexander polynomial cannot distinguish a knot from its mirror image, but the Jones polynomial can in some cases; if V k (q) ≠ V k (q −1), then the knot is chiral, however the converse is not true.

  9. Chiral inversion - Wikipedia

    en.wikipedia.org/wiki/Chiral_inversion

    Chiral inversion is the process of conversion of one enantiomer of a chiral molecule to its mirror-image version with no other change in the molecule. [1] [2] [3] [4]Chiral inversion happens depending on various factors (viz. biological-, solvent-, light-, temperature- induced, etc.) and the energy barrier energy barrier associated with the stereogenic element present in the chiral molecule. 2 ...