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  2. Thorpe–Ingold effect - Wikipedia

    en.wikipedia.org/wiki/Thorpe–Ingold_effect

    The Thorpe–Ingold effect, gem-dimethyl effect, or angle compression is an effect observed in chemistry where increasing steric hindrance favours ring closure and intramolecular reactions. The effect was first reported by Beesley, Thorpe , and Ingold in 1915 as part of a study of cyclization reactions . [ 1 ]

  3. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  4. List of unsolved problems in chemistry - Wikipedia

    en.wikipedia.org/wiki/List_of_unsolved_problems...

    Protein folding problem: Is it possible to predict the secondary, tertiary and quaternary structure of a polypeptide sequence based solely on the sequence and environmental information? Inverse protein-folding problem: Is it possible to design a polypeptide sequence which will adopt a given structure under certain environmental conditions?

  5. Flippin–Lodge angle - Wikipedia

    en.wikipedia.org/wiki/Flippin–Lodge_angle

    Because chemical reactions take place in three dimensions, their quantitative description is, in part, a geometry problem. Two angles, first the Bürgi–Dunitz angle, , and later the Flippin–Lodge angle, , were developed to describe the approach of the reactive atom of a nucleophile (a point off of a plane) to the reactive atom of an ...

  6. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    3) are considered examples of a two π electron system, which are stabilized relative to the open system, despite the angle strain imposed by the 60° bond angles. [11] [12] Planar ring molecules with 4n π electrons do not obey Hückel's rule, and theory predicts that they are less stable and have triplet ground states with two unpaired ...

  7. Prelog strain - Wikipedia

    en.wikipedia.org/wiki/Prelog_strain

    In organic chemistry, transannular strain (also called Prelog strain after chemist Vladimir Prelog) is the unfavorable interactions of ring substituents on non-adjacent carbons. These interactions, called transannular interactions, arise from a lack of space in the interior of the ring , which forces substituents into conflict with one another.

  8. Ligand cone angle - Wikipedia

    en.wikipedia.org/wiki/Ligand_cone_angle

    In coordination chemistry, the ligand cone angle (θ) is a measure of the steric bulk of a ligand in a transition metal coordination complex. It is defined as the solid angle formed with the metal at the vertex of a cone and the outermost edge of the van der Waals spheres of the ligand atoms at the perimeter of the base of the cone.

  9. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    A bond angle is the geometric angle between two adjacent bonds. Some common shapes of simple molecules include: Linear: In a linear model, atoms are connected in a straight line. The bond angles are set at 180°. For example, carbon dioxide and nitric oxide have a linear molecular shape.