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  2. Seyferth–Gilbert homologation - Wikipedia

    en.wikipedia.org/wiki/Seyferth–Gilbert...

    The Seyferth–Gilbert homologation is a chemical reaction of an aryl ketone 1 (or aldehyde) with dimethyl (diazomethyl)phosphonate 2 and potassium tert-butoxide to give substituted alkynes 3. [ 1 ] [ 2 ] Dimethyl (diazomethyl)phosphonate 2 is often called the Seyferth–Gilbert reagent .

  3. Wikipedia:Discord - Wikipedia

    en.wikipedia.org/wiki/Wikipedia:DISCORD

    Authentication provides the "Authenticated Users" role, which allows members to know who you are on wiki, and is sometimes used for anti-raid/spam measures. This is not required, but benefits include the ability to send messages in more channels, embed multimedia, use reactions, and other minor permissions.

  4. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    This reaction is canonically known as the GGCG (Grignard-Grisius-Cormas-Gilman) reaction scheme. In this aspect, they are similar to organolithium reagents. Grignard reagents are rarely isolated as solids. Instead, they are normally handled as solutions in solvents such as diethyl ether or tetrahydrofuran using air-free techniques.

  5. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    An example of a simple chain reaction is the thermal decomposition of acetaldehyde (CH 3 CHO) to methane (CH 4) and carbon monoxide (CO). The experimental reaction order is 3/2, [4] which can be explained by a Rice-Herzfeld mechanism. [5] This reaction mechanism for acetaldehyde has 4 steps with rate equations for each step :

  6. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  7. Parikh–Doering oxidation - Wikipedia

    en.wikipedia.org/wiki/Parikh–Doering_oxidation

    The Parikh–Doering oxidation is an oxidation reaction that transforms primary and secondary alcohols into aldehydes and ketones, respectively. [1] The procedure uses dimethyl sulfoxide (DMSO) as the oxidant and the solvent, activated by the sulfur trioxide pyridine complex (SO 3 •C 5 H 5 N) in the presence of triethylamine or diisopropylethylamine as base.

  8. Flow chemistry - Wikipedia

    en.wikipedia.org/wiki/Flow_chemistry

    In batch the chemist works first followed by the chemical engineer. In flow chemistry this changes to a parallel approach, where chemist and chemical engineer work interactively. Typically there is a plant setup in the lab, which is a tool for both. This setup can be either commercial or noncommercial.

  9. Chemical reaction engineering - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction_engineering

    Chemical reaction engineering aims at studying and optimizing chemical reactions in order to define the best reactor design. Hence, the interactions of flow phenomena, mass transfer , heat transfer , and reaction kinetics are of prime importance in order to relate reactor performance to feed composition and operating conditions.