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  2. Molecular symmetry - Wikipedia

    en.wikipedia.org/wiki/Molecular_symmetry

    Elements. The point group symmetry of a molecule is defined by the presence or absence of 5 types of symmetry element. Symmetry axis: an axis around which a rotation by. 360 ∘ n {\displaystyle {\tfrac {360^ {\circ }} {n}}} results in a molecule indistinguishable from the original. This is also called an n -fold rotational axis and abbreviated Cn.

  3. Axial chirality - Wikipedia

    en.wikipedia.org/wiki/Axial_chirality

    Axial chirality. In chemistry, axial chirality is a special case of chirality in which a molecule contains two pairs of chemical groups in a non-planar arrangement about an axis of chirality so that the molecule is not superposable on its mirror image. [1][2] The axis of chirality (or chiral axis) is usually determined by a chemical bond that ...

  4. Chirality (chemistry) - Wikipedia

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

    Chirality (chemistry) Two enantiomers of a generic amino acid that are chiral. (S)-Alanine (left) and (R)-alanine (right) in zwitterionic form at neutral pH. In chemistry, a molecule or ion is called chiral (/ ˈkaɪrəl /) if it cannot be superposed on its mirror image by any combination of rotations, translations, and some conformational changes.

  5. Fischer projection - Wikipedia

    en.wikipedia.org/wiki/Fischer_projection

    Fischer projections were originally proposed for the depiction of carbohydrates and used by chemists, particularly in organic chemistry and biochemistry. The use of Fischer projections in non-carbohydrates is discouraged, as such drawings are ambiguous and easily confused with other types of drawing. The main purpose of Fischer projections is ...

  6. Woodward–Hoffmann rules - Wikipedia

    en.wikipedia.org/wiki/Woodward–Hoffmann_rules

    Thermolysis converts 1 to (E,E) geometric isomer 2, but 3 to (E,Z) isomer 4.. The Woodward–Hoffmann rules (or the pericyclic selection rules) [1] are a set of rules devised by Robert Burns Woodward and Roald Hoffmann to rationalize or predict certain aspects of the stereochemistry and activation energy of pericyclic reactions, an important class of reactions in organic chemistry.

  7. C2-Symmetric ligands - Wikipedia

    en.wikipedia.org/wiki/C2-Symmetric_ligands

    In homogeneous catalysis C2-symmetric ligands refer to ligands that lack mirror symmetry but have C2 symmetry (two-fold rotational symmetry). Such ligands are usually bidentate and are valuable in catalysis. [1] The C2 symmetry of ligands limits the number of possible reaction pathways and thereby increases enantioselectivity, relative to ...

  8. Cahn–Ingold–Prelog priority rules - Wikipedia

    en.wikipedia.org/wiki/Cahn–Ingold–Prelog...

    In organic chemistry, the Cahn–Ingold–Prelog (CIP) sequence rules (also the CIP priority convention; named after Robert Sidney Cahn, Christopher Kelk Ingold, and Vladimir Prelog) are a standard process to completely and unequivocally name a stereoisomer of a molecule. [1][2]: 26 The purpose of the CIP system is to assign an R or S ...

  9. Symmetry element - Wikipedia

    en.wikipedia.org/wiki/Symmetry_element

    Symmetry element. In chemistry and crystallography, a symmetry element is a point, line, or plane about which symmetry operations can take place. In particular, a symmetry element can be a mirror plane, an axis of rotation (either proper and improper), or a center of inversion. [ 1 ][ 2 ][ 3 ] For an object such as a molecule or a crystal, a ...