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  2. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    Example of a reduction–oxidation reaction between sodium and chlorine, with the OIL RIG mnemonic [1] Redox (/ ˈ r ɛ d ɒ k s / RED-oks, / ˈ r iː d ɒ k s / REE-doks, reduction–oxidation [2] or oxidation–reduction [3]: 150 ) is a type of chemical reaction in which the oxidation states of the reactants change. [4]

  3. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).

  4. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    An example is the oxidation state of phosphorus in H 3 PO 3 (structurally diprotic HPO(OH) 2) taken nominally as +3, while Allen electronegativities of phosphorus and hydrogen suggest +5 by a narrow margin that makes the two alternatives almost equivalent:

  5. Reducing agent - Wikipedia

    en.wikipedia.org/wiki/Reducing_agent

    An agent's oxidation state describes its degree of loss of electrons, where the higher the oxidation state then the fewer electrons it has. So initially, prior to the reaction, a reducing agent is typically in one of its lower possible oxidation states; its oxidation state increases during the reaction while that of the oxidizer decreases.

  6. Oxide - Wikipedia

    en.wikipedia.org/wiki/Oxide

    Iron silicate, Fe 2 SiO 4, the mineral fayalite, is one of many examples of a ternary oxide. For many metal oxides, the possibilities of polymorphism and nonstoichiometry exist as well. [3] The commercially important dioxides of titanium exists in three distinct structures, for example. Many metal oxides exist in various nonstoichiometric states.

  7. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    The oxidation of primary alcohols to carboxylic acids normally proceeds via the corresponding aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH) 2) by reaction with water. Thus, the oxidation of a primary alcohol at the aldehyde level without further oxidation to the carboxylic acid is possible by performing the reaction ...

  8. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    An example of organic reaction: oxidation of ketones to esters with a peroxycarboxylic acid Retrosynthetic analysis can be applied to design a complex synthesis reaction. Here the analysis starts from the products, for example by splitting selected chemical bonds, to arrive at plausible initial reagents.

  9. Oxygen compounds - Wikipedia

    en.wikipedia.org/wiki/Oxygen_compounds

    These compounds form by oxidation of alkali metals with larger ionic radii (K, Rb, Cs). For example, potassium superoxide (KO 2) is an orange-yellow solid formed when potassium reacts with oxygen. Hydrogen peroxide (H 2 O 2) can be produced by passing a volume of 96% to 98% hydrogen and 2 to 4% oxygen through an electric discharge. [7]