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  2. Standard electrode potential (data page) - Wikipedia

    en.wikipedia.org/wiki/Standard_electrode...

    The data below tabulates standard electrode potentials (E°), in volts relative to the standard hydrogen electrode (SHE), at: . Temperature 298.15 K (25.00 °C; 77.00 °F); ...

  3. Acetone (data page) - Wikipedia

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

    Vapor-liquid Equilibrium of Acetone/Ethanol [4] P = 760 mm Hg BP Temp. °C % by mole acetone liquid vapor 78.3: 0: 0 76.4: 3.3: 11.1 74.0: 7.8: 21.6 70.8: 14.9: 34.5 ...

  4. Table of standard reduction potentials for half-reactions ...

    en.wikipedia.org/wiki/Table_of_standard...

    The formal potential is thus the reversible potential of an electrode at equilibrium immersed in a solution where reactants and products are at unit concentration. [4] If any small incremental change of potential causes a change in the direction of the reaction, i.e. from reduction to oxidation or vice versa , the system is close to equilibrium ...

  5. 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:

  6. 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 ...

  7. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    Most of the worldwide production of phenol and acetone is now based on this method. In 2022, nearly 10.8 million tonnes of phenol was produced by the cumene process. [4] In order for this process to be economical, there must also be demand for the acetone by-product as well as the phenol. [5]

  8. 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.

  9. Spartan (chemistry software) - Wikipedia

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

    Electrostatic potential – The potential, ε p, is defined as the energy of interaction of a positive point charge located at p with the nuclei and electrons of a molecule. A surface for which the electrostatic potential is negative (a negative potential surface) delineates regions in a molecule which are subject to electrophilic attack.