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  2. Formal charge - Wikipedia

    en.wikipedia.org/wiki/Formal_charge

    Formal charges in ozone and the nitrate anion. In chemistry, a formal charge (F.C. or q*), in the covalent view of chemical bonding, is the hypothetical charge assigned to an atom in a molecule, assuming that electrons in all chemical bonds are shared equally between atoms, regardless of relative electronegativity.

  3. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    As an example, summing bond orders in the ammonium cation yields −4 at the nitrogen of formal charge +1, with the two numbers adding to the oxidation state of −3: The sum of oxidation states in the ion equals its charge (as it equals zero for a neutral molecule). Also in anions, the formal (ionic) charges have to be considered when nonzero.

  4. 1,2-Bis (diphenylphosphino)ethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Bis(diphenylphosphino...

    (C 6 H 5) 2 PCH 2 CH 2 P(C 6 H 5) 2 (CH 2 C 6 H 5)]Br + NaOH → (C 6 H 5) 2 PCH 2 CH 2 P(O)(C 6 H 5) 2 + C 6 H 5 CH 3 + NaBr. Hydrogenation of dppe gives the ligand ...

  5. Chlorine - Wikipedia

    en.wikipedia.org/wiki/Chlorine

    Even though nitrogen in NCl 3 is bearing a negative charge, the compound is usually called nitrogen trichloride. Chlorination of metals with Cl 2 usually leads to a higher oxidation state than bromination with Br 2 when multiple oxidation states are available, such as in MoCl 5 and MoBr 3. Chlorides can be made by reaction of an element or its ...

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

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

    To define a formal reduction potential for a biochemical reaction, the pH value, the concentrations values and the hypotheses made on the activity coefficients must always be clearly indicated. When using, or comparing, several formal (or apparent) reduction potentials they must also be internally consistent.

  7. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    The formal charge of an atom is computed as the difference between the number of valence electrons that a neutral atom would have and the number of electrons that belong to it in the Lewis structure. Electrons in covalent bonds are split equally between the atoms involved in the bond.

  8. Dichlorocarbene - Wikipedia

    en.wikipedia.org/wiki/Dichlorocarbene

    In 1835, the French chemist Auguste Laurent recognised chloroform as CCl 2 • HCl (then written as C 8 Cl 8 • H 4 Cl 4) [a] in his paper on analysing some organohalides. Laurent also predicted a compound seemingly consisting of 2 parts dichlorocarbene which he named Chlorétherose (possibly Tetrachloroethylene, which was not known to exist at the time.) [8]

  9. Chloralkali process - Wikipedia

    en.wikipedia.org/wiki/Chloralkali_process

    The ion-permeable ion-exchange membrane at the center of the cell allows only the sodium ions (Na +) to pass to the second chamber where they react with the hydroxide ions to produce caustic soda (NaOH) (B in figure): [1] Na + + OH − → NaOH The overall reaction for the electrolysis of brine is thus: 2NaCl + 2 H 2 O → Cl 2 + H 2 + 2NaOH