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  2. Ball-and-stick model - Wikipedia

    en.wikipedia.org/wiki/Ball-and-stick_model

    In chemistry, the ball-and-stick model is a molecular model of a chemical substance which displays both the three-dimensional position of the atoms and the bonds between them. [1] The atoms are typically represented by spheres , connected by rods which represent the bonds.

  3. Structural chemistry - Wikipedia

    en.wikipedia.org/wiki/Structural_chemistry

    Structural chemistry is a part of chemistry and deals with spatial structures of molecules (in the gaseous, liquid or solid state) and solids (with extended structures that cannot be subdivided into molecules). For structure elucidation [1] a range of different methods is used.

  4. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Wavy single bonds represent unknown or unspecified stereochemistry or a mixture of isomers. For example, the adjacent diagram shows the fructose molecule with a wavy bond to the HOCH 2 - group at the left. In this case the two possible ring structures are in chemical equilibrium with each other and also with the open-chain structure.

  5. Chemical structure - Wikipedia

    en.wikipedia.org/wiki/Chemical_structure

    A chemical structure of a molecule is a spatial arrangement of its atoms and their chemical bonds. Its determination includes a chemist 's specifying the molecular geometry and, when feasible and necessary, the electronic structure of the target molecule or other solid.

  6. Chemical bond - Wikipedia

    en.wikipedia.org/wiki/Chemical_bond

    A chemical bond is the association of atoms or ions to form molecules, crystals, and other structures. The bond may result from the electrostatic force between oppositely charged ions as in ionic bonds or through the sharing of electrons as in covalent bonds, or some combination of these effects.

  7. Lability - Wikipedia

    en.wikipedia.org/wiki/Lability

    The term is used to describe a transient chemical species.As a general example, if a molecule exists in a particular conformation for a short lifetime, before adopting a lower energy conformation (structural arrangement), the former molecular structure is said to have 'high lability' (such as C 25, a 25-carbon fullerene spheroid).

  8. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes. A Newman projection visualizes the conformation of a chemical bond from front to back, with the front atom represented by the intersection of three lines (a dot) and the back atom as a circle.

  9. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    Two main forms of isomerism are structural (or constitutional) isomerism, in which bonds between the atoms differ; and stereoisomerism (or spatial isomerism), in which the bonds are the same but the relative positions of the atoms differ. Isomeric relationships form a hierarchy. Two chemicals might be the same constitutional isomer, but upon ...