enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Sulfuryl chloride - Wikipedia

    en.wikipedia.org/wiki/Sulfuryl_chloride

    Sulfuryl chloride is used as a source of Cl 2.Because it is a pourable liquid, it is considered more convenient than Cl 2 to dispense.. Sulfuryl chloride is used in the conversion of C−H to C−Cl adjacent to activating substituents such as carbonyls and sulfoxides: [5] [6]

  3. Reed reaction - Wikipedia

    en.wikipedia.org/wiki/Reed_reaction

    The reaction occurs via a free radical mechanism. UV-light initiates homolysis of chlorine, producing a pair of chlorine atoms: . Chain initiation: Thereafter a chlorine atom attacks the hydrocarbon chain, freeing hydrogen to form hydrogen chloride and an alkyl free radical.

  4. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    The cheletropic reactions of 1,3-dienes with sulfur dioxide have been extensively investigated in terms of kinetics (see above for general reaction). In the first quantitative measurement of kinetic parameters for this reaction, a 1976 study by Isaacs and Laila measured the rates of addition of sulfur dioxide to butadiene derivatives.

  5. Johnson–Corey–Chaykovsky reaction - Wikipedia

    en.wikipedia.org/wiki/Johnson–Corey...

    The reaction mechanism for the Johnson–Corey–Chaykovsky reaction consists of nucleophilic addition of the ylide to the carbonyl or imine group. A negative charge is transferred to the heteroatom and because the sulfonium cation is a good leaving group it gets expelled forming the ring.

  6. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    In the presence of certain reducing agents, one of the sulfur-carbon bonds of the sulfonyl group is cleaved, leading to sulfur-free organic products. Depending on the nature of the substrate and reaction conditions, alkyl sulfones afford either the corresponding alkanes or olefins (the Julia olefination ).

  7. Catalytic oxidation - Wikipedia

    en.wikipedia.org/wiki/Catalytic_oxidation

    Consequently, it is flared (converted to carbon dioxide). One challenge is that methanol is more easily oxidized than is methane. [3] Catalytic oxidation with oxygen or air is a major application of green chemistry. There are however many oxidations that cannot be achieved so straightforwardly.

  8. Partial oxidation - Wikipedia

    en.wikipedia.org/wiki/Partial_oxidation

    Partial oxidation (POX) is a type of chemical reaction. It occurs when a substoichiometric fuel-air mixture is partially combusted in a reformer, creating a hydrogen-rich syngas which can then be put to further use, for example in a fuel cell. A distinction is made between thermal partial oxidation (TPOX) and catalytic partial oxidation (CPOX).

  9. Peters four-step chemistry - Wikipedia

    en.wikipedia.org/wiki/Peters_four-step_chemistry

    The third reaction, known as radical consumption layer, where most of the heat is released, and the first reaction, also known as fuel consumption layer, occur in a narrow region at the flame. The fourth reaction is the hydrogen oxidation layer, whose thickness is much larger than the former two layers.