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  2. Initiation (chemistry) - Wikipedia

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

    In chemistry, initiation is a chemical reaction that triggers one or more secondary reactions. Initiation creates a reactive centre on a molecule which produces a chain reaction . [ 1 ] The reactive centre generated by initiation is usually a radical , but can also be cations or anions . [ 2 ]

  3. Polymerisation inhibitor - Wikipedia

    en.wikipedia.org/wiki/Polymerisation_inhibitor

    In the simplest example oxygen can be used as it exists naturally in its triplet state (i.e. it is a diradical). This is referred to as air inhibition and is a diffusion-controlled reaction with rates typically in the order of 10 7 –10 9 mol −1 s −1 , [ 3 ] the resulting peroxy radicals (ROO•) are less reactive towards polymerisation.

  4. Thiol-ene reaction - Wikipedia

    en.wikipedia.org/wiki/Thiol-ene_reaction

    In organosulfur chemistry, the thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol (R−SH) and an alkene (R 2 C=CR 2) to form a thioether (R−S−R'). This reaction was first reported in 1905, [ 1 ] but it gained prominence in the late 1990s and early 2000s for its feasibility and wide range of applications.

  5. Radical initiator - Wikipedia

    en.wikipedia.org/wiki/Radical_initiator

    For example, di-tert-butyl peroxide (t-Bu OOt-Bu) gives two t-butoxy radicals (t-BuO•) and the radicals become methyl radicals (CH 3 •) with the loss of acetone. Benzoyl peroxide (( Ph C)OO) 2 ) generates benzoyloxyl radicals (PhCOO•), each of which loses carbon dioxide to be converted into a phenyl radical (Ph•).

  6. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    In organic chemistry, the E i mechanism (Elimination Internal/Intramolecular), also known as a thermal syn elimination or a pericyclic syn elimination, is a special type of elimination reaction in which two vicinal (adjacent) substituents on an alkane framework leave simultaneously via a cyclic transition state to form an alkene in a syn elimination. [1]

  7. Thermal runaway - Wikipedia

    en.wikipedia.org/wiki/Thermal_runaway

    Chemical reactions involving thermal runaway are also called thermal explosions in chemical engineering, or runaway reactions in organic chemistry.It is a process by which an exothermic reaction goes out of control: the reaction rate increases due to an increase in temperature, causing a further increase in temperature and hence a further rapid increase in the reaction rate.

  8. Chain-growth polymerization - Wikipedia

    en.wikipedia.org/wiki/Chain-growth_polymerization

    High energy initiation refers to the generation of chain carriers by radiation. Chemical initiation is due to a chemical initiator. For the case of radical polymerization as an example, chain initiation involves the dissociation of a radical initiator molecule (I) which is easily dissociated by heat or light into two free radicals (2 R°).

  9. Autoxidation - Wikipedia

    en.wikipedia.org/wiki/Autoxidation

    It is also an important concept in both industrial chemistry and biology. [4] Autoxidation is therefore a fairly broad term and can encompass examples of photooxygenation and catalytic oxidation . The common mechanism is a free radical chain reaction , where the addition of oxygen gives rise to hydroperoxides and their associated peroxy ...