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  2. Stereoselectivity - Wikipedia

    en.wikipedia.org/wiki/Stereoselectivity

    In chemistry, stereoselectivity [1] is the property of a chemical reaction in which a single reactant forms an unequal mixture of stereoisomers during a non-stereospecific creation of a new stereocenter or during a non-stereospecific transformation of a pre-existing one. [2]

  3. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  4. Diastereomer - Wikipedia

    en.wikipedia.org/wiki/Diastereomer

    In the case of saccharides, when drawn in the Fischer projection the erythro isomer has two identical substituents on the same side and the threo isomer has them on opposite sides. [7] When drawn as a zig-zag chain, the erythro isomer has two identical substituents on different sides of the plane (anti).

  5. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    If they are on opposite sides, it is E (Ger. entgegen, opposite). [8] Since chlorine has a larger atomic number than hydrogen, it is the highest-priority group. [ 9 ] Using this notation to name the above pictured molecules, molecule I is ( Z )-1,2-dichloroethene and molecule II is ( E )-1,2-dichloroethene.

  6. Antarafacial and suprafacial - Wikipedia

    en.wikipedia.org/wiki/Antarafacial_and_suprafacial

    The suprafacial shift is symmetry-forbidden because orbitals with opposite algebraic signs overlap. The symmetry allowed antarafacial shift would require a strained transition state and is also unlikely. In contrast a symmetry allowed and suprafacial [1,5]-hydride shift is a common event. [2]

  7. Stereochemistry - Wikipedia

    en.wikipedia.org/wiki/Stereochemistry

    Stereochemistry, a subdiscipline of chemistry, studies the spatial arrangement of atoms that form the structure of molecules and their manipulation. [1] The study of stereochemistry focuses on the relationships between stereoisomers, which are defined as having the same molecular formula and sequence of bonded atoms (constitution) but differing in the geometric positioning of the atoms in space.

  8. Zeta potential - Wikipedia

    en.wikipedia.org/wiki/Zeta_potential

    In the colloidal chemistry literature, it is usually denoted using the Greek letter zeta (ζ), hence ζ-potential. The usual units are volts (V) or, more commonly, millivolts (mV). From a theoretical viewpoint, the zeta potential is the electric potential in the interfacial double layer (DL) at the location of the slipping plane relative to a ...

  9. Partial charge - Wikipedia

    en.wikipedia.org/wiki/Partial_charge

    Yet one can point to zones within the assemblage where less than a full charge resides, such as the area around an atom's nucleus. This is possible in part because particles are not like mathematical points—which must be either inside a zone or outside it—but are smeared out by the uncertainty principle of quantum mechanics. Because of this ...