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  2. Radical (chemistry) - Wikipedia

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

    Radical elimination can be viewed as the reverse of radical addition. In radical elimination, an unstable radical compound breaks down into a spin-paired molecule and a new radical compound. Shown below is an example of a radical elimination reaction, where a benzoyloxy radical breaks down into a phenyl radical and a carbon dioxide molecule. [7]

  3. nth root - Wikipedia

    en.wikipedia.org/wiki/Nth_root

    The principal root of a positive real number is thus also a positive real number. As a function, the principal root is continuous in the whole complex plane, except along the negative real axis. An unresolved root, especially one using the radical symbol, is sometimes referred to as a surd [2] or a radical. [3]

  4. 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]

  5. Nested radical - Wikipedia

    en.wikipedia.org/wiki/Nested_radical

    The nested radicals in this solution cannot in general be simplified unless the cubic equation has at least one rational solution. Indeed, if the cubic has three irrational but real solutions, we have the casus irreducibilis, in which all three real solutions are written in terms of cube roots of complex numbers. On the other hand, consider the ...

  6. Radical clock - Wikipedia

    en.wikipedia.org/wiki/Radical_clock

    In chemistry, a radical clock is a chemical compound that assists in the indirect methodology to determine the kinetics of a free-radical reaction. The radical-clock compound itself reacts at a known rate, which provides a calibration for determining the rate of another reaction.

  7. Elimination reaction of free radicals - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction_of...

    Radicals can undergo a disproportionation reaction through a radical elimination mechanism (See Fig. 1). Here a radical abstracts a hydrogen atom from another same radical to form two non-radical species: an alkane and an alkene. Radicals can also undergo an elimination reaction to generate a new radical as the leaving group.

  8. Trivalent group 14 radicals - Wikipedia

    en.wikipedia.org/wiki/Trivalent_group_14_radicals

    A trivalent group 14 radical (also known as a trivalent tetrel radical) is a molecule that contains a group 14 element (E = C, Si, Ge, Sn, Pb) with three bonds and a free radical, having the general formula of R 3 E•. Such compounds can be categorized into three different types, depending on the structure (or equivalently the orbital in which ...

  9. Hydroperoxyl - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxyl

    The hydroperoxyl radical, also known as the hydrogen superoxide, is the protonated form of superoxide with the chemical formula HO 2, also written HOO •. This species plays an important role in the atmosphere and as a reactive oxygen species in cell biology.

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