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  2. Sulfamic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfamic_acid

    Sulfamic acid is preferable to hydrochloric acid in household use, due to its intrinsic safety. If inadvertently mixed with hypochlorite based products such as bleach , it does not form chlorine gas, whereas the most common acids would; the reaction ( neutralisation ) with ammonia , produces a salt, as depicted in the section above.

  3. 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 ...

  4. Edwards equation - Wikipedia

    en.wikipedia.org/wiki/Edwards_equation

    H is a measure of the basicity of the nucleophile relative to protons, as defined by the equation: = + where the pK a is that of the conjugate acid of the nucleophile and the constant 1.74 is the correction for the pK a of H 3 O +. E n is the term Edwards introduced to account for the polarizability of the nucleophile.

  5. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    Protic solvents react with strong nucleophiles with good basic character in an acid/base fashion, thus decreasing or removing the nucleophilic nature of the nucleophile. The following table shows the effect of solvent polarity on the relative reaction rates of the S N 2 reaction of 1-bromobutane with azide (N 3 – ).

  6. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    A typical mixture is 3 parts of concentrated sulfuric acid and 1 part of 30 wt. % hydrogen peroxide solution; [1] other protocols may use a 4:1 or even 7:1 mixture. A closely related mixture, sometimes called "base piranha", is a 5:1:1 mixture of water, ammonia solution (NH 4 OH, or NH 3 (aq)), and 30% hydrogen peroxide.

  7. Synthesis of nucleosides - Wikipedia

    en.wikipedia.org/wiki/Synthesis_of_nucleosides

    Synthesis of nucleosides involves the coupling of a nucleophilic, heterocyclic base with an electrophilic sugar. The silyl-Hilbert-Johnson (or Vorbrüggen) reaction, which employs silylated heterocyclic bases and electrophilic sugar derivatives in the presence of a Lewis acid, is the most common method for forming nucleosides in this manner.

  8. Superacid - Wikipedia

    en.wikipedia.org/wiki/Superacid

    This definition was refined by Ronald Gillespie in 1971, as any acid with an H 0 value lower than that of 100% sulfuric acid (−11.93). [3] George A. Olah prepared the so-called " magic acid ", so named for its ability to attack hydrocarbons , by mixing antimony pentafluoride (SbF 5 ) and fluorosulfonic acid (FSO 3 H). [ 4 ]

  9. Acid salt - Wikipedia

    en.wikipedia.org/wiki/Acid_salt

    Acid salts are a class of salts that produce an acidic solution after being dissolved in a solvent. Its formation as a substance has a greater electrical conductivity than that of the pure solvent. [1] An acidic solution formed by acid salt is made during partial neutralization of diprotic or polyprotic acids.