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  2. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    The hydroamination reaction is approximately thermochemically neutral. The reaction however suffers from a high activation barrier, perhaps owing to the repulsion of the electron-rich substrate and the amine nucleophile. The intermolecular reaction also is accompanied by highly negative changing entropy, making it unfavorable at higher ...

  3. Alkoxylation - Wikipedia

    en.wikipedia.org/wiki/Alkoxylation

    Alkoxylation is a chemical reaction that involves the addition of an epoxide to another compound. The usual manifestation of this reaction is ethoxylation of alcohols (ROH), in which case ethylene oxide is the alkoxylating agent: ROH + C 2 H 4 O → ROCH 2 CH 2 OH. Another industrially significant epoxide is propylene oxide (PO, OCH 2 CHCH 3 ...

  4. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    The structure of a typical methoxy group. In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen.This alkoxy group has the formula R−O−CH 3.

  5. Methanation - Wikipedia

    en.wikipedia.org/wiki/Methanation

    Methanation reaction over different carried metal catalysts including Ni, [4] Ru [5] and Rh [6] has been widely investigated for the production of CH 4 from syngas and other power to gas initiatives. [3] Nickel is the most widely used catalyst due to its high selectivity and low cost. [1]

  6. Oxidative coupling of methane - Wikipedia

    en.wikipedia.org/wiki/Oxidative_coupling_of_methane

    The oxidative coupling of methane (OCM) is a potential chemical reaction studied in the 1980s for the direct conversion of natural gas, primarily consisting of methane, into value-added chemicals. Although the reaction would have strong economics if practicable, no effective catalysts are known, and thermodynamic arguments suggest none can exist.

  7. Hydroxymethylation - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylation

    A common method for hydroxymethylation involves the reaction of formaldehyde with active C-H and N-H bonds: R 3 C-H + CH 2 O → R 3 C-CH 2 OH R 2 N-H + CH 2 O → R 2 N-CH 2 OH. A typical active C-H bond is provided by a terminal acetylene [1] or the alpha protons of an aldehyde. [2]

  8. Hydroacylation - Wikipedia

    en.wikipedia.org/wiki/Hydroacylation

    Hydroacylation is a type of organic reaction in which an electron-rich [1] unsaturated hydrocarbon inserts into a formyl C-H bond. With alkenes, the product is a ketone: RCHO + CH 2 =CHR' → RC(O)CH 2 CH 2 R' With an alkyne instead, the reaction produces an α,β-unsaturated ketone. [2] The reaction requires a metal catalyst or a radical ...

  9. Cracking (chemistry) - Wikipedia

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

    The actual reaction is known as homolytic fission and produces alkenes, which are the basis for the economically important production of polymers. [ 6 ] Thermal cracking is currently used to "upgrade" very heavy fractions or to produce light fractions or distillates, burner fuel and/or petroleum coke .