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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. 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]

  4. Chirality (chemistry) - Wikipedia

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

    Many chiral molecules have point chirality, namely a single chiral stereogenic center that coincides with an atom. This stereogenic center usually has four or more bonds to different groups, and may be carbon (as in many biological molecules), phosphorus (as in many organophosphates), silicon, or a metal (as in many chiral coordination compounds).

  5. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    are arranged around the chiral center carbon atom. With the hydrogen atom away from the viewer, if the arrangement of the CO→R→N groups around the carbon atom as center is counter-clockwise, then it is the L form. [14] If the arrangement is clockwise, it is the D form. As usual, if the molecule itself is oriented differently, for example ...

  6. Molecular configuration - Wikipedia

    en.wikipedia.org/wiki/Molecular_configuration

    R-S isomerism of thalidomide. Chiral center marked with a star(*). Hydrogen (not drawn) is projecting behind the chiral centre. Enantiomers are molecules having one or more chiral centres that are mirror images of each other. [2] Chiral centres are designated R or S. If the 3 groups projecting towards you are arranged clockwise from highest ...

  7. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Drugs that exhibit handedness are referred to as chiral drugs. Chiral drugs that are equimolar (1:1) mixture of enantiomers are called racemic drugs and these are obviously devoid of optical rotation. The most commonly encountered stereogenic unit, [2] that confers chirality to drug molecules are stereogenic center. Stereogenic center can be ...

  8. 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 ...

  9. Diastereomer - Wikipedia

    en.wikipedia.org/wiki/Diastereomer

    Erythritol is achiral (has at least one conformation with a plane or center of symmetry), whereas threitol is chiral. A useful English-language mnemonic device is that "threitol" and "chiral" both begin with consonants, whereas "erythritol" and "achiral" both begin with vowels. Another threo compound is threonine, one of the amino acids coded ...