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  2. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    In chemistry, isovalent or second order hybridization is an extension of orbital hybridization, the mixing of atomic orbitals into hybrid orbitals which can form chemical bonds, to include fractional numbers of atomic orbitals of each type (s, p, d). It allows for a quantitative depiction of bond formation when the molecular geometry deviates ...

  3. Cyclopentane - Wikipedia

    en.wikipedia.org/wiki/Cyclopentane

    Cyclopentane can be fluorinated to give compounds ranging from C 5 H 9 F to perfluorocyclopentane C 5 F 10. Such species are conceivable refrigerants and specialty solvents. [15] [16] The cyclopentane ring is pervasive in natural products including many useful drugs. Examples include most steroids, prostaglandins, and some lipids.

  4. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    The bond angles in the table below are ideal angles from the simple VSEPR theory (pronounced "Vesper Theory") [citation needed], followed by the actual angle for the example given in the following column where this differs. For many cases, such as trigonal pyramidal and bent, the actual angle for the example differs from the ideal angle, and ...

  5. Pentagonal bipyramidal molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Pentagonal_bipyramidal...

    Structure of iodine heptafluoride, an example of a molecule with the pentagonal-bipyramidal coordination geometry. In chemistry, a pentagonal bipyramid is a molecular geometry with one atom at the centre with seven ligands at the corners of a pentagonal bipyramid. A perfect pentagonal bipyramid belongs to the molecular point group D 5h.

  6. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    This type of representation clearly illustrates the specific dihedral angle between the proximal and distal atoms. [ 2 ] This projection is named after American chemist Melvin Spencer Newman , who introduced it in 1952 as a partial replacement for Fischer projections , which are unable to represent conformations and thus conformers properly.

  7. Ring strain - Wikipedia

    en.wikipedia.org/wiki/Ring_strain

    In organic chemistry, ring strain is a type of instability that exists when bonds in a molecule form angles that are abnormal. Strain is most commonly discussed for small rings such as cyclopropanes and cyclobutanes, whose internal angles are substantially smaller than the idealized value of approximately 109°.

  8. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    An example of a common name is terpineol, the name of which can tell us only that it is an alcohol (because the suffix "-ol" is in the name) and it should then have a hydroxyl group (–OH) attached to it. The IUPAC naming system for organic compounds can be demonstrated using the example provided in the adjacent image.

  9. Trigonal pyramidal molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_pyramidal...

    This would result in the geometry of a regular tetrahedron with each bond angle equal to arccos(− ⁠ 1 / 3 ⁠) ≈ 109.5°. However, the three hydrogen atoms are repelled by the electron lone pair in a way that the geometry is distorted to a trigonal pyramid (regular 3-sided pyramid) with bond angles of 107°.

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