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  2. Isopotential map - Wikipedia

    en.wikipedia.org/wiki/Isopotential_map

    In electromagnetism, Isopotential maps are a measure of electrostatic potential in space. The spatial derivatives of an electrostatic field indicate the contours of the electrostatic field, so isopotential maps show where another charged molecule might interact, using equipotential lines (isopotentials).

  3. Cation–π interaction - Wikipedia

    en.wikipedia.org/wiki/Cation–π_interaction

    Practically, this allows trends to be predicted qualitatively based on visual representations of electrostatic potential maps for a series of arenes. Electrostatic attraction is not the only component of cation–π bonding. For example, 1,3,5-trifluorobenzene interacts with cations despite having a negligible quadrupole moment.

  4. Spartan (chemistry software) - Wikipedia

    en.wikipedia.org/wiki/Spartan_(chemistry_software)

    Composite surfaces (maps): Electrostatic potential map (electrophilic indicator) – The most commonly employed property map is the electrostatic potential map. This gives the potential at locations on a particular surface, most commonly a surface of electron density corresponding to overall molecular size. [71]

  5. Electrochemical potential - Wikipedia

    en.wikipedia.org/wiki/Electrochemical_potential

    In generic terms, electrochemical potential is the mechanical work done in bringing 1 mole of an ion from a standard state to a specified concentration and electrical potential. According to the IUPAC definition, [4] it is the partial molar Gibbs energy of the substance at the specified electric potential, where the substance is in a specified ...

  6. Acetone (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetone_(data_page)

    Download as PDF; Printable version; In other projects Wikidata item; ... Vapor-liquid Equilibrium of Acetone/Ethanol [4] P = 760 mm Hg BP Temp. °C % by mole acetone ...

  7. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone is produced directly or indirectly from propene. Approximately 83% of acetone is produced via the cumene process; [24] as a result, acetone production is tied to phenol production. In the cumene process, benzene is alkylated with propylene to produce cumene, which is oxidized by air to produce phenol and acetone:

  8. Acetoacetate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Acetoacetate_decarboxylase

    The production of acetone by acetoacetate decarboxylase-containing or clostridial bacteria was utilized in large-scale industrial syntheses in the first half of the twentieth century. In the 1960s, the industry replaced this process with less expensive, more efficient chemical syntheses of acetone from petroleum and petroleum derivatives. [ 6 ]

  9. Poisson–Boltzmann equation - Wikipedia

    en.wikipedia.org/wiki/Poisson–Boltzmann_equation

    The Poisson–Boltzmann equation can be applied to biomolecular systems. One example is the binding of electrolytes to biomolecules in a solution. This process is dependent upon the electrostatic field generated by the molecule, the electrostatic potential on the surface of the molecule, as well as the electrostatic free energy. [13]