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  2. Pyramidal inversion - Wikipedia

    en.wikipedia.org/wiki/Pyramidal_inversion

    Pyramidal inversion in nitrogen and amines is known as nitrogen inversion. [8] It is a rapid oscillation of the nitrogen atom and substituents, the nitrogen "moving" through the plane formed by the substituents (although the substituents also move - in the other direction); [ 9 ] the molecule passing through a planar transition state . [ 10 ]

  3. Umpolung - Wikipedia

    en.wikipedia.org/wiki/Umpolung

    In organic chemistry, umpolung (German: [ˈʔʊmˌpoːlʊŋ]) or polarity inversion is the chemical modification of a functional group with the aim of the reversal of polarity of that group. [ 1 ] [ 2 ] This modification allows secondary reactions of this functional group that would otherwise not be possible. [ 3 ]

  4. Molecular symmetry - Wikipedia

    en.wikipedia.org/wiki/Molecular_symmetry

    An inversion center is a special case of having a rotation-reflection axis about an angle of 180° through the center. Examples are xenon tetrafluoride (a square planar molecule), where the inversion center is at the Xe atom, and benzene (C 6 H 6) where the inversion center is at the center of the ring.

  5. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    In chemistry, absolute configuration refers to the spatial arrangement of atoms within a molecular entity (or group) that is chiral, and its resultant stereochemical description. [1] Absolute configuration is typically relevant in organic molecules where carbon is bonded to four different substituents .

  6. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...

  7. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    The energy difference between gauche and anti is 0.9 kcal/mol associated with the strain energy of the gauche conformer. The anti conformer is, therefore, the most stable (≈ 0 kcal/mol). The three eclipsed conformations with dihedral angles of 0°, 120°, and 240° are transition states between conformers. [6]

  8. Suspension (chemistry) - Wikipedia

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

    In chemistry, a suspension is a heterogeneous mixture of a fluid that contains solid particles sufficiently large for sedimentation. The particles may be visible to the naked eye , usually must be larger than one micrometer , and will eventually settle , although the mixture is only classified as a suspension when and while the particles have ...

  9. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    In organic chemistry, a ring flip (also known as a ring inversion or ring reversal) is the interconversion of cyclic conformers that have equivalent ring shapes (e.g., from a chair conformer to another chair conformer) that results in the exchange of nonequivalent substituent positions. [1]