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  2. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    A hydroxide ion acting as a nucleophile in an S N 2 reaction, converting a haloalkane into an alcohol. In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they ...

  3. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    The pH of a simple solution of an acid in water is determined by both and the acid concentration. For weak acid solutions, it depends on the degree of dissociation, which may be determined by an equilibrium calculation. For concentrated solutions of acids, especially strong acids for which pH < 0, the value is a better measure of acidity than ...

  4. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    For example, bases donating a lone pair from an oxygen atom are harder than bases donating through a nitrogen atom. Although the classification was never quantified it proved to be very useful in predicting the strength of adduct formation, using the key concepts that hard acid—hard base and soft acid—soft base interactions are stronger ...

  5. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    The rate equation for S N 2 reactions are bimolecular being first order in Nucleophile and first order in Reagent. The determining factor when both S N 2 and S N 1 reaction mechanisms are viable is the strength of the Nucleophile. Nuclephilicity and basicity are linked and the more nucleophilic a molecule becomes the greater said nucleophile's ...

  6. Superbase - Wikipedia

    en.wikipedia.org/wiki/Superbase

    Another type of organometallic superbase has a reactive metal exchanged for a hydrogen on a heteroatom, such as oxygen (unstabilized alkoxides) or nitrogen (metal amides such as lithium diisopropylamide). [23] The Schlosser base (or Lochmann-Schlosser base), the combination of n-butyllithium and potassium tert-butoxide, is commonly cited as a ...

  7. n-Butyllithium - Wikipedia

    en.wikipedia.org/wiki/N-Butyllithium

    n-BuLi reacts violently with water: C 4 H 9 Li + H 2 O → C 4 H 10 + LiOH. This is an exergonic and highly exothermic reaction. If oxygen is present the butane produced may ignite. BuLi also reacts with CO 2 to give lithium pentanoate: C 4 H 9 Li + CO 2 → C 4 H 9 CO 2 Li

  8. Hydrochloric acid - Wikipedia

    en.wikipedia.org/wiki/Hydrochloric_acid

    Cation exchange is widely used to remove ions such as Na + and Ca 2+ from aqueous solutions, producing demineralized water. The acid is used to rinse the cations from the resins. [25] Na + is replaced with H + and Ca 2+ with 2 H +. Ion exchangers and demineralized water are used in all chemical industries, drinking water production, and many ...

  9. Protic solvent - Wikipedia

    en.wikipedia.org/wiki/Protic_solvent

    In chemistry, a protic solvent is a solvent that has a hydrogen atom bound to an oxygen (as in a hydroxyl group −OH), a nitrogen (as in an amine group −NH 2 or −NH−), or fluoride (as in hydrogen fluoride). In general terms, any solvent that contains a labile H + is called a protic solvent.