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  2. Prochirality - Wikipedia

    en.wikipedia.org/wiki/Prochirality

    An sp 2-hybridized carbon atom, with re and si faces. In stereochemistry, prochiral molecules are those that can be converted from achiral to chiral in a single step. [1] [2] An achiral species which can be converted to a chiral in two steps is called proprochiral. [2]

  3. Chirality (mathematics) - Wikipedia

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

    An object that is not chiral is said to be achiral. A chiral object and its mirror image are said to be enantiomorphs. The word chirality is derived from the Greek χείρ (cheir), the hand, the most familiar chiral object; the word enantiomorph stems from the Greek ἐναντίος (enantios) 'opposite' + μορφή (morphe) 'form'.

  4. Point group - Wikipedia

    en.wikipedia.org/wiki/Point_group

    The four-dimensional point groups (chiral as well as achiral) are listed in Conway and Smith, [1] Section 4, Tables 4.14.3. Finite isomorphism and correspondences The following list gives the four-dimensional reflection groups (excluding those that leave a subspace fixed and that are therefore lower-dimensional reflection groups).

  5. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    Instead, both effects can also occur when the propagation direction of the electromagnetic wave together with the structure of an (achiral) material form a chiral experimental arrangement. [10] [11] This case, where the mutual arrangement of achiral components forms a chiral (experimental) arrangement, is known as extrinsic chirality. [12] [13]

  6. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    [4] [5] The configuration of other chiral compounds was then related to that of (+)-glyceraldehyde by sequences of chemical reactions. For example, oxidation of (+)-glyceraldehyde (1) with mercury oxide gives (−)-glyceric acid (2), a reaction that does not alter the stereocenter. Thus the absolute configuration of (−)-glyceric acid must be ...

  7. Enantioselective reduction of ketones - Wikipedia

    en.wikipedia.org/wiki/Enantioselective_reduction...

    Enantioselective ketone reductions convert prochiral ketones into chiral, non-racemic alcohols and are used heavily for the synthesis of stereodefined alcohols. [1]Carbonyl reduction, the net addition of H 2 across a carbon-oxygen double bond, is an important way to prepare alcohols.

  8. Mathematical formulation of the Standard Model - Wikipedia

    en.wikipedia.org/wiki/Mathematical_formulation...

    For the leptons, the gauge group can be written SU(2) l × U(1) L × U(1) R. The two U(1) factors can be combined into U(1) Y × U(1) l, where l is the lepton number. Gauging of the lepton number is ruled out by experiment, leaving only the possible gauge group SU(2) L × U(1) Y. A similar argument in the quark sector also gives the same result ...

  9. Specific rotation - Wikipedia

    en.wikipedia.org/wiki/Specific_rotation

    Values for specific rotation are reported in units of deg·mL·g −1 ·dm −1, which are typically shortened to just degrees, wherein the other components of the unit are tacitly assumed. [4] These values should always be accompanied by information about the temperature, solvent and wavelength of light used, as all of these variables can ...