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  2. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    Wacker process. The Wacker process or the Hoechst-Wacker process (named after the chemical companies of the same name) refers to the oxidation of ethylene to acetaldehyde in the presence of palladium (II) chloride and copper (II) chloride as the catalyst. [1] This chemical reaction was one of the first homogeneous catalysis with organopalladium ...

  3. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    The Wolff–Kishner reduction is a reaction used in organic chemistry to convert carbonyl functionalities into methylene groups. [1] [2] In the context of complex molecule synthesis, it is most frequently employed to remove a carbonyl group after it has served its synthetic purpose of activating an intermediate in a preceding step.

  4. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    Redox (/ ˈrɛdɒks / RED-oks, / ˈriːdɒks / 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] Oxidation is the loss of electrons or an increase in the oxidation state, while reduction is the gain of electrons or a decrease in the ...

  5. Carbonyl reduction - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_reduction

    Carbonyl reduction. Oxidation ladders such as this one are used to illustrate sequences of carbonyls which can be interconverted through oxidations or reductions. In organic chemistry, carbonyl reduction is the conversion of any carbonyl group, usually to an alcohol. It is a common transformation that is practiced in many ways. [1]

  6. Leclanché cell - Wikipedia

    en.wikipedia.org/wiki/Leclanché_cell

    A 1919 illustration of a Leclanché cell. The Leclanché cell is a battery invented and patented by the French scientist Georges Leclanché in 1866. [1] [2] [3] The battery contained a conducting solution (electrolyte) of ammonium chloride, a cathode (positive terminal) of carbon, a depolarizer of manganese dioxide (oxidizer), and an anode (negative terminal) of zinc (reductant).

  7. Mozingo reduction - Wikipedia

    en.wikipedia.org/wiki/Mozingo_reduction

    Organic redox reaction. The Mozingo reduction, also known as Mozingo reaction or thioketal reduction, is a chemical reaction capable of fully reducing a ketone or aldehyde to the corresponding alkane via a dithioacetal. [1][2] The reaction scheme is as follows: [3] The ketone or aldehyde is activated by conversion to cyclic dithioacetal by ...

  8. Bouveault–Blanc reduction - Wikipedia

    en.wikipedia.org/wiki/Bouveault–Blanc_reduction

    bouveault-blanc-reduction. RSC ontology ID. RXNO:0000119. The Bouveault–Blanc reduction is a chemical reaction in which an ester is reduced to primary alcohols using absolute ethanol and sodium metal. [1] It was first reported by Louis Bouveault and Gustave Louis Blanc in 1903. [2][3][4] Bouveault and Blanc demonstrated the reduction of ethyl ...

  9. Ruthenium tetroxide - Wikipedia

    en.wikipedia.org/wiki/Ruthenium_tetroxide

    Ruthenium tetroxide is the inorganic compound with the formula RuO 4. It is a yellow volatile solid that melts near room temperature. [2] It has the odor of ozone. [3] Samples are typically black due to impurities. The analogous OsO 4 is more widely used and better known.