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  2. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    One approach to improving chemical reactions is the understanding of the underlying reaction mechanism. time-resolved spectroscopic techniques can be used to follow the dynamics of the chemical reaction. This technique requires a trigger for initiating the process, which is in most cases illumination of the compound.

  3. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    In one important reaction type, a main group organometallic compound of the type R-M (where R = organic group, M = main group centre metal atom) reacts with an organic halide of the type R'-X with formation of a new carbon-carbon bond in the product R-R'. The most common type of coupling reaction is the cross coupling reaction. [1] [2] [3]

  4. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    For example, protonation of methanol gives an electrophilic methylating reagent that reacts by the S N 2 pathway: CH 3 OH + H + → [CH 3 OH 2] + Similarly, methyl iodide and methyl triflate are viewed as the equivalent of the methyl cation because they readily undergo S N 2 reactions by weak nucleophiles. The methyl cation has been detected in ...

  5. Hydrogen auto-transfer - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_auto-transfer

    [1] [2] Mechanism of one type of carbonyl addition hydrogen auto-transfer reaction involving hydrometalation (step 2). [3] Hydrogen auto-transfer, also known as borrowing hydrogen, is the activation of a chemical reaction by temporary transfer of two hydrogen atoms from the reactant to a catalyst and return of those hydrogen atoms back to a ...

  6. Radical disproportionation - Wikipedia

    en.wikipedia.org/wiki/Radical_disproportionation

    In radical disproportionation reactions one molecule acts as an acceptor while the other molecule acts as a donor. [2] In the most common disproportionation reactions, a hydrogen atom is taken, or abstracted by the acceptor as the donor molecule undergoes an elimination reaction to form a double bond. [3]

  7. Riley oxidation - Wikipedia

    en.wikipedia.org/wiki/Riley_oxidation

    Allylic oxidation can be predicted by the substitution pattern on the olefin. In the case of 1,2-disubstituted olefins, reaction rates follow CH > CH 2 > CH 3: Geminally-substituted olefins react in the same order of reaction rates as above: [2] Trisubstituted alkenes experience reactivity at the more substituted end of the double bond.

  8. Cross dehydrogenative coupling - Wikipedia

    en.wikipedia.org/wiki/Cross_dehydrogenative_coupling

    Therefore, the CDC reaction has the advantages of high efficiency, Atom economy and environmental friendliness. Such reactions can be achieved or activated by transition-metal catalysis or oxidation reaction (e.g. benzoquinone, peroxides, O 2, hypervalent iodine), or by either photocatalysis or electrocatalysis. The mechanism and reactivity of ...

  9. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    In organic chemistry, methenium (also called methylium, carbenium, [2] methyl cation, or protonated methylene) is a cation with the formula CH + 3.It can be viewed as a methylene radical (: CH