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  2. Ylide - Wikipedia

    en.wikipedia.org/wiki/Ylide

    An ylide (/ ˈ ɪ l aɪ d /) [1] or ylid (/ ˈ ɪ l ɪ d /) is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached to a heteroatom with a formal positive charge (usually nitrogen, phosphorus or sulfur), and in which both atoms have full octets of electrons.

  3. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    Pyridinium refers to the cation [C 5 H 5 NH] +. It is the conjugate acid of pyridine. Many related cations are known involving substituted pyridines, e.g. picolines ...

  4. Radical disproportionation - Wikipedia

    en.wikipedia.org/wiki/Radical_disproportionation

    Radical disproportionation encompasses a group of reactions in organic chemistry in which two radicals react to form two different non-radical products. Radicals in chemistry are defined as reactive atoms or molecules that contain an unpaired electron or electrons in an open shell. The unpaired electrons can cause radicals to be unstable and ...

  5. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    Pyridinium p-toluenesulfonate (PPTS) is a colourless solid salt of pyridine and p-toluenesulfonic acid. Uses. In organic synthesis, PPTS is used as a weakly acidic ...

  6. Casus irreducibilis - Wikipedia

    en.wikipedia.org/wiki/Casus_irreducibilis

    Moreover, if the polynomial degree is a power of 2 and the roots are all real, then if there is a root that can be expressed in real radicals it can be expressed in terms of square roots and no higher-degree roots, as can the other roots, and so the roots are classically constructible. Casus irreducibilis for quintic polynomials is discussed by ...

  7. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Radical dimerization of pyridine with elemental sodium or Raney nickel selectively yields 4,4'-bipyridine, [98] or 2,2'-bipyridine, [99] which are important precursor reagents in the chemical industry. One of the name reactions involving free radicals is the Minisci reaction.

  8. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    The hydroxyl radical can damage virtually all types of macromolecules: carbohydrates, nucleic acids , lipids (lipid peroxidation) and amino acids (e.g. conversion of Phe to m-Tyrosine and o-Tyrosine). The hydroxyl radical has a very short in vivo half-life of approximately 10 −9 seconds and a high reactivity. [5]

  9. Nested radical - Wikipedia

    en.wikipedia.org/wiki/Nested_radical

    In the case of two nested square roots, the following theorem completely solves the problem of denesting. [2]If a and c are rational numbers and c is not the square of a rational number, there are two rational numbers x and y such that + = if and only if is the square of a rational number d.