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  2. Wacker process - Wikipedia

    en.wikipedia.org/wiki/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 chemistry ...

  3. Stephen aldehyde synthesis - Wikipedia

    en.wikipedia.org/wiki/Stephen_aldehyde_synthesis

    Organic redox reaction. Stephen aldehyde synthesis, a named reaction in chemistry, was invented by Henry Stephen (OBE / MBE). This reaction involves the preparation of aldehydes (R-CHO) from nitriles (R-CN) using tin (II) chloride (SnCl 2), hydrochloric acid (HCl) and quenching the resulting iminium salt ( [R-CH=NH 2] + Cl −) with water (H 2 ...

  4. 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 ...

  5. Blue bottle experiment - Wikipedia

    en.wikipedia.org/wiki/Blue_bottle_experiment

    The aqueous solution in the classical reaction contains glucose, sodium hydroxide and methylene blue. [14] In the first step an acyloin of glucose is formed. The next step is a redox reaction of the acyloin with methylene blue in which the glucose is oxidized to diketone in alkaline solution [6] and methylene blue is reduced to colorless leucomethylene blue.

  6. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    RXNO:0000226. 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.

  7. Rosenmund reduction - Wikipedia

    en.wikipedia.org/wiki/Rosenmund_reduction

    Rosenmund reduction. The Rosenmund reduction is a hydrogenation process in which an acyl chloride is selectively reduced to an aldehyde. The reaction was named after Karl Wilhelm Rosenmund, who first reported it in 1918. [1] The reaction, a hydrogenolysis, is catalysed by palladium on barium sulfate, which is sometimes called the Rosenmund ...

  8. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    Electron transfer reactions are central to myriad processes and properties in soils, and redox potential, quantified as Eh (platinum electrode potential relative to the standard hydrogen electrode) or pe (analogous to pH as -log electron activity), is a master variable, along with pH, that controls and is governed by chemical reactions and ...

  9. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    A chemical reaction is a process that leads to the chemical transformation of one set of chemical substances to another. [1] When chemical reactions occur, the atoms are rearranged and the reaction is accompanied by an energy change as new products are generated. Classically, chemical reactions encompass changes that only involve the positions ...