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  2. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Tetrafluoroethane (a haloalkane) is a colorless liquid that boils well below room temperature (as seen here) and can be extracted from common canned air canisters by simply inverting them during use. The haloalkanes (also known as halogenoalkanes or alkyl halides) are alkanes containing one or more halogen substituents. [1]

  3. Aryl halide - Wikipedia

    en.wikipedia.org/wiki/Aryl_halide

    In organic chemistry, an aryl halide (also known as haloarene) is an aromatic compound in which one or more hydrogen atoms, directly bonded to an aromatic ring are replaced by a halide. Haloarenes are different from haloalkanes because they exhibit many differences in methods of preparation and properties. The most important members are the ...

  4. Gilman reagent - Wikipedia

    en.wikipedia.org/wiki/Gilman_reagent

    A conjugated 1,4 addition using a Gilman reagent with an arbitrary R group. These reagents are useful because, unlike related Grignard reagents and organolithium reagents, they react with organic halides to replace the halide group with an R group (the Corey–House reaction).

  5. Wurtz reaction - Wikipedia

    en.wikipedia.org/wiki/Wurtz_reaction

    In organic chemistry, the Wurtz reaction, named after Charles Adolphe Wurtz, is a coupling reaction in which two alkyl halides are treated with sodium metal to form a higher alkane. 2 R−X + 2 Na → R−R + 2 NaX. The reaction is of little value except for intramolecular versions, such as 1,6-dibromohexane + 2 Na → cyclohexane + 2 NaBr.

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    On a day when Josh Allen became the first player to have three touchdown passes and three rushing TDs in the same game, it was a play during which Buffalo's quarterback didn't reach the end zone ...

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    Stein’s victory coattails will help. Cooper limited his time out of the state because he was worried that Robinson might use legislative tricks to seize power as acting governor.

  9. E1cB-elimination reaction - Wikipedia

    en.wikipedia.org/wiki/E1cB-elimination_reaction

    An example of the E1cB reaction mechanism in the degradation of a hemiketal under basic conditions. The E1cB elimination reaction is a type of elimination reaction which occurs under basic conditions, where the hydrogen to be removed is relatively acidic, while the leaving group (such as -OH or -OR) is a relatively poor one.

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