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  2. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene is a fundamental ligand in transition metal alkene complexes. One of the first organometallic compounds, Zeise's salt is a complex of ethylene. Useful reagents containing ethylene include Pt(PPh 3) 2 (C 2 H 4) and Rh 2 Cl 2 (C 2 H 4) 4. The Rh-catalysed hydroformylation of ethylene is conducted on an industrial scale to provide ...

  3. Shell higher olefin process - Wikipedia

    en.wikipedia.org/wiki/Shell_higher_olefin_process

    The Shell higher olefin process (SHOP) is a chemical process for the production of linear alpha olefins via ethylene oligomerization and olefin metathesis invented and exploited by Shell plc. [1] The olefin products are converted to fatty aldehydes and then to fatty alcohols , which are precursors to plasticizers and detergents .

  4. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2). [ 1 ] [ 2 ] This chemical reaction entails the net addition of a formyl group ( −CHO ) and a hydrogen atom to a carbon-carbon double bond .

  5. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde is mainly produced industrially by hydroformylation of ethylene: ... but is a lung and eye irritant and is a combustible liquid. References

  6. Ethenolysis - Wikipedia

    en.wikipedia.org/wiki/Ethenolysis

    In organic chemistry, ethenolysis is a chemical process in which internal olefins are degraded using ethylene (H 2 C=CH 2) as the reagent. The reaction is an example of cross metathesis. The utility of the reaction is driven by the low cost of ethylene as a reagent and its selectivity.

  7. β-Hydride elimination - Wikipedia

    en.wikipedia.org/wiki/Β-Hydride_elimination

    In Hydroformylation, β-hydride elimination can act as a side reaction that influences product regioselectivity. [4] For example, in the hydroformylation of open chain unsaturated ethers, it reverses the formation of branched metal-alkyl intermediates at high temperatures, leading to a greater yield of linear products.