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  2. Tris(4-bromophenyl)ammoniumyl hexachloroantimonate - Wikipedia

    en.wikipedia.org/wiki/Tris(4-bromophenyl...

    Commonly known as magic blue, it is the hexachloroantimonate salt of an amine radical cation. It is a blue solid that reacts with many solvents but is soluble in acetonitrile . The compound is a popular oxidizing agent in organic and organometallic chemistry , with a reduction potential of 0.67 V versus ferrocene /ferrocenium ( acetonitrile ...

  3. Triethyloxonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Triethyloxonium_tetrafluo...

    The trimethyloxonium salt is available from dimethyl ether via an analogous route. [6] These salts do not have long shelf-lives at room temperature. They degrade by hydrolysis: [Et 3 O] + [BF 4] − + H 2 O → Et 2 O + EtOH + H + [BF 4] −. The propensity of trialkyloxonium salts for alkyl-exchange can be advantageous.

  4. Trimethyloxonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Trimethyloxonium_tetrafluo...

    The salt hydrolyzes readily: [Me 3 O] + [BF 4] − + H 2 O → Me 2 O + MeOH + H + [BF 4] −. Trimethyloxonium tetrafluoroborate is generally ranked as the strongest commercially available reagent for electrophilic methylation, [1] being stronger than methyl sulfonate esters, including methyl triflate and methyl fluorosulfonate ("magic methyl ...

  5. Salt (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Salt_(chemistry)

    In chemistry, a salt or ionic compound is a chemical compound consisting of an assembly of positively charged ions and negatively charged ions , [1] which results in a compound with no net electric charge (electrically neutral). The constituent ions are held together by electrostatic forces termed ionic bonds.

  6. Wikibooks - Wikipedia

    en.wikipedia.org/wiki/Wikibooks

    Growth of the eight largest Wikibooks sites (by language), July 2003–January 2010. Wikibooks (previously called Wikimedia Free Textbook Project and Wikimedia-Textbooks) is a wiki-based Wikimedia project hosted by the Wikimedia Foundation for the creation of free content digital textbooks and annotated texts that anyone can edit.

  7. Stevens rearrangement - Wikipedia

    en.wikipedia.org/wiki/Stevens_rearrangement

    The Stevens rearrangement in organic chemistry is an organic reaction converting quaternary ammonium salts and sulfonium salts to the corresponding amines or sulfides in presence of a strong base in a 1,2-rearrangement. [1] Stevens rearrangement overview. The reactants can be obtained by alkylation of the corresponding amines and sulfides.

  8. Experts Reveal the Biggest Nutrition Trends for 2025 - AOL

    www.aol.com/experts-reveal-biggest-nutrition...

    Staying hydrated is one of the most important, if not the most important, things you can do for your overall health. A well-hydrated body can reap improvements in sleep, mood, cognition, digestion ...

  9. Sodium methylsulfinylmethylide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methylsulfinylmethylide

    Sodium methylsulfinylmethylide (also called NaDMSO or dimsyl sodium) is the sodium salt of the conjugate base of dimethyl sulfoxide. This unusual salt has some uses in organic chemistry as a base and nucleophile. Since the first publication in 1965 by Corey et al., [2] a number of additional uses for this reagent have been identified. [3]