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Newman Projections definitions

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  • Newman Projection

    A visualization method showing the spatial arrangement of groups around a sigma bond by looking straight down the bond axis.
  • Sigma Bond

    A single covalent bond allowing free rotation, central to analyzing conformational changes in molecules.
  • Conformer

    A spatial arrangement of atoms resulting from rotation around a single bond, each with distinct energy and stability.
  • Dihedral Angle

    The angle between two largest groups on adjacent carbons, determining the relative orientation and stability of conformers.
  • Eclipsed Conformation

    A structure where groups on adjacent carbons overlap perfectly, resulting in highest energy and lowest stability.
  • Gauche Conformation

    A staggered arrangement with a 60° dihedral angle, where large groups are adjacent but not overlapping, yielding intermediate energy.
  • Anti Conformation

    A staggered arrangement with a 180° dihedral angle, placing large groups as far apart as possible for maximum stability.
  • Energy Diagram

    A plot showing how the energy of a molecule changes as the dihedral angle varies from 0° to 360°.
  • Stability

    A measure of how favorable a conformation is, with lower energy conformers being more favored.
  • Steric Repulsion

    The destabilizing effect caused by bulky groups being close together, increasing energy due to electron cloud overlap.
  • Staggered Conformation

    A general arrangement where groups on adjacent carbons are positioned to minimize overlap, enhancing stability.
  • Ethyl Group

    A two-carbon substituent often used in Newman projections to illustrate the effects of group size on energy.
  • Bond Rotation

    The movement around a sigma bond that leads to different spatial arrangements and energy levels.
  • Overlapping Groups

    A situation in Newman projections where substituents on adjacent carbons occupy the same spatial region, increasing energy.
  • Y-Axis

    The vertical axis on an energy diagram representing the relative energy or stability of conformers.