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  2. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    In organic chemistry, a coupling reaction is a type of reaction in which two reactant molecules are bonded together. Such reactions often require the aid of a metal catalyst.

  3. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    The Sandmeyer reaction is an example of a radical-nucleophilic aromatic substitution (S RN Ar). The radical mechanism of the Sandmeyer reaction is supported by the detection of biaryl byproducts. [8]

  4. Jahn–Teller effect - Wikipedia

    en.wikipedia.org/wiki/Jahn–Teller_effect

    The Jahn–Teller effect (JT effect or JTE) is an important mechanism of spontaneous symmetry breaking in molecular and solid-state systems which has far-reaching consequences in different fields, and is responsible for a variety of phenomena in spectroscopy, stereochemistry, crystal chemistry, molecular and solid-state physics, and materials science.

  5. Ion exchange - Wikipedia

    en.wikipedia.org/wiki/Ion_exchange

    Ion exchange resins are the physical medium that facilitates ion exchange reactions. The resin is composed of cross-linked organic polymers, typically polystyrene matrix and functional groups where the ion exchange process takes place.

  6. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    In organic chemistry, ethers are a class of compounds that contain an ether group—a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl). They have the general formula R−O−R′, where R and R′ represent the organyl groups.

  7. Debye–Hückel theory - Wikipedia

    en.wikipedia.org/wiki/Debye–Hückel_theory

    An English translation [21]: 217–63 of the article is included in a book of collected papers presented to Debye by "his pupils, friends, and the publishers on the occasion of his seventieth birthday on March 24, 1954". [21]: xv Another English translation was completed in 2019. [22]

  8. Wurtz–Fittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wurtz–Fittig_reaction

    The Wurtz–Fittig reaction is the chemical reaction of an aryl halide, alkyl halides, and sodium metal to give substituted aromatic compounds. [1] Following the work of Charles Adolphe Wurtz on the sodium-induced coupling of alkyl halides (the Wurtz reaction), Wilhelm Rudolph Fittig extended the approach to the coupling of an alkyl halide with an aryl halide.

  9. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    In commercial applications, the alkylating agents are generally alkenes, some of the largest scale reactions practiced in industry.Such alkylations are of major industrial importance, e.g. for the production of ethylbenzene, the precursor to polystyrene, from benzene and ethylene and for the production of cumene from benzene and propene in cumene process:

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