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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 ...
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 ...
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 ...
The benzilic acid rearrangement is formally the 1,2-rearrangement of 1,2- diketones to form α- hydroxy – carboxylic acids using a base. This reaction receives its name from the reaction of benzil with potassium hydroxide to form benzilic acid. First performed by Justus von Liebig in 1838, [ 1 ] it is the first reported example of a ...
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.
English chemist John Daniell (left) and physicist Michael Faraday (right), both credited as founders of electrochemistry. Electrochemistry is the branch of physical chemistry concerned with the relationship between electrical potential difference and identifiable chemical change. These reactions involve electrons moving via an electronically ...
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 ...
Redox indicator. A redox indicator (also called an oxidation-reduction indicator) is an indicator which undergoes a definite color change at a specific electrode potential. The requirement for fast and reversible color change means that the oxidation-reduction equilibrium for an indicator redox system needs to be established very quickly.