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  2. 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.

  3. Diastereomer - Wikipedia

    en.wikipedia.org/wiki/Diastereomer

    When the single bond between the two centres is free to rotate, cis/trans descriptors become invalid. Two widely accepted prefixes used to distinguish diastereomers on sp³-hybridised bonds in an open-chain molecule are syn and anti. Masamune proposed the descriptors which work even if the groups are not attached to adjacent carbon atoms.

  4. Pentane interference - Wikipedia

    en.wikipedia.org/wiki/Pentane_interference

    Pentane interference or syn-pentane interaction is the steric hindrance that the two terminal methyl groups experience in one of the chemical conformations of n-pentane.The possible conformations are combinations of anti conformations and gauche conformations and are anti-anti, anti-gauche +, gauche + - gauche + and gauche + - gauche − of which the last one is especially energetically ...

  5. Organostannane addition - Wikipedia

    en.wikipedia.org/wiki/Organostannane_addition

    When all reagents are achiral, only simple diastereoselectivity (syn versus anti, see above) must be considered. Addition takes place via an S E ' mechanism involving concerted dissociation of tin and C-C bond formation at the γ position.

  6. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    The disposition of the formed stereocenters is deemed syn or anti, depending if they are on the same or opposite sides of the main chain: Syn and anti products from an aldol (addition) reaction. The principal factor determining an aldol reaction's stereoselectivity is the enolizing metal counterion.

  7. endo–exo isomerism - Wikipedia

    en.wikipedia.org/wiki/Endo–exo_isomerism

    The prefix endo is reserved for the isomer with the substituent located closest, or "syn", to the longest bridge. The prefix exo is reserved for the isomer with the substituent located farthest, or "anti", to the longest bridge. Here "longest" and "shortest" refer to the number of atoms that comprise the bridge.

  8. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    a torsion angle between ±90° and 180° is called anti (a) a torsion angle between 30° and 150° or between −30° and −150° is called clinal (c) a torsion angle between 0° and ±30° or ±150° and 180° is called periplanar (p) a torsion angle between 0° and ±30° is called synperiplanar (sp), also called syn-or cis-conformation

  9. Klyne–Prelog system - Wikipedia

    en.wikipedia.org/wiki/Klyne–Prelog_system

    Anti or syn indicates the substituents are on opposite sides or the same side, respectively. Clinal substituents are found within 30° of either side of a dihedral angle of 60° (from 30° to 90°), 120° (90°–150°), 240° (210°–270°), or 300° (270°–330°).