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L hydrogenation

Typical brines received at an Arkansas bromine plant have 3—5 g/L bromide, 200—250 g/L chloride, 0.15—0.20 g/L ammonia, 0.1—0.3 g/L hydrogen sulfide, 0.01—0.02 g/L iodide, and additionally may contain some dissolved organics, including natural gas and cmde oil. The bromide-containing brine is first treated to remove natural gas, cmde oil, and hydrogen sulfide prior to introduction into the contact tower (48). [Pg.285]

D. 2(S)-(fl-tert-Butoxycarbonyl-a-(R)-hydroxyethyl)-4-(R)-hydroxy-pyrrolidine- 1-carboxylic acid, tert-butyl ester. The identical procedure was followed, in this case using the (,S)-BINAP catalyst (5)-l. Hydrogenation is conducted for 64 hr, and the reaction mixture is then transferred to a 250-mL, round-bottomed flask and concentrated to dryness. The residue is dissolved in 17 mL of methanol and cooled to 15°C. After the slow addition of 7 mL of DI water, the solution is aged for 15 min gradually forming a thin slurry. More DI water (75 mL) is added over 1 hr and the mixture is allowed to stand for an additional 1 hr at 15°C. The resulting crystals (Note 19) are filtered at 15°C, washed with 10 mL of 1 4-MeOH water, and then dried overnight in a vacuum oven (35°C, 686 mm) to yield 7.0 g (70%) of (R)-hydroxy ester 4b (Note 20). [Pg.94]

Another type of steric effect results from interactions between diene substituents. Adoption of the s-cis conformation of the diene in the TS brings the d.v-oricnlcd 1- and 4-substituents on a diene close together. /(-1,3-Pcnladicnc is 103 times more reactive than 4-methyl-l,3-pentadiene toward the very reactive dienophile tetracyanoethylene. This is because the unfavorable interaction between the additional methyl substituent and the C(l) hydrogen in the s-cis conformation raises the energy of the TS.20... [Pg.480]

Dhainaut, F. (2006) Reduction des oxides d azote par l hydrogene sur des catalyseurs a base de metaux nobles supportes, PhD thesis, University of Fille, France. [Pg.321]

Pirez, M. (2004) Reduction catalytique selective des oxides d azote (NO. ) provenant d effluents gazeux industriels par l hydrogene ou le methane, Ph D Thesis, University of Lille, France. [Pg.324]

Figure 10.21 Relative stain removal after 60 min bleaching at 60 °C [233] 6.5 x 10 3 mol/l hydrogen peroxide in buffer solution. Relative share (%) of the protolytic forms of hydrogen peroxide in the total amount at 60 °C ( 0-0 negligible in this range)... Figure 10.21 Relative stain removal after 60 min bleaching at 60 °C [233] 6.5 x 10 3 mol/l hydrogen peroxide in buffer solution. Relative share (%) of the protolytic forms of hydrogen peroxide in the total amount at 60 °C ( 0-0 negligible in this range)...
Figure 10.28 Effect of temperature on the whiteness index of linen bleached using urea-activated hydrogen peroxide [243], Treated with 7 g/l hydrogen peroxide and 8 g/l urea for 150 min at pH 6 and 50 1 liquor ratio... Figure 10.28 Effect of temperature on the whiteness index of linen bleached using urea-activated hydrogen peroxide [243], Treated with 7 g/l hydrogen peroxide and 8 g/l urea for 150 min at pH 6 and 50 1 liquor ratio...
Becker, L., Hydrogen Storage, available at http //www.csa.com/discoveryguides/hydrogen/ overview.php, March 2007. [Pg.407]

Flow injection analysis has been used for the automated determination of hydrogen sulfide in seawater [20]. A low-sensitivity flow injection analysis manifold for concentrations up to 200 imol/l hydrogen sulfide had a detection limit of 0.12 xmol/l. Sulfide standards were calibrated by colorimetric measurement of the excess tri-iodide ion remaining after reaction of sulfide with iodine. The coefficient of variation was less than 1% at concentrations greater than 10 imol/l. The method was fast, accurate, sensitive enough for most natural waters, and could be used both for discrete and continuous analysis. [Pg.126]

Mora, V., J.C.Pairon, R.Gamier, J.Laureillard, F.Lionnet, L.Hoguet, A.Schaeffer, M.L.Efthymiou, and P.Brochard. 1992. Intoxication aigue par l hydrogene arsenie dans une fonderie de... [Pg.117]

Wood, W. SHydrogen Peroxide, Royal Institute of Chemistry Lectures, London, 1954,11. Schumb, W. C., Satterfield, C. N., and Wentworth, R. L., Hydrogen Peroxide, Reinhold Publishing, New York, 1955, 52. [Pg.158]

Mechanistic study revealed that the reaction proceeds through intramolecular 1,3-hydrogen migration, and the chiral rhodium catalyst differentiates the enantiotopic C-l hydrogens of allylic alcohols (Scheme 29).53... [Pg.84]

G.J. Kramer, J. Huijsmans, D. Austgen, Clean and green hydrogen, World Hydrogen Energy Conference, 13-16 June 2006, Lyon. Association Franpuse de l Hydrogene, Paris, France (2006). [Pg.334]

Engen, J.R. Gmeiner, W.H. Smithgall, T.E. Smith, D.L. Hydrogen exchange shows peptide binding stabilizes motions in Hck SH2. Biochemistry 1999, 38, 8926-8935. [Pg.373]

Wang, L. Pan, H. Smith, D.L. Hydrogen exchange-mass spectrometry. Optimization of digestion conditions. Mol. Cell. Proteomics 2002, 1, 132-138. [Pg.374]

With cyclic substrates, the formation of the new double bond depends on the availability of a cw-/l-hydrogen, which is required for the -elimination... [Pg.107]


See other pages where L hydrogenation is mentioned: [Pg.20]    [Pg.302]    [Pg.145]    [Pg.39]    [Pg.300]    [Pg.454]    [Pg.352]    [Pg.210]    [Pg.204]    [Pg.436]    [Pg.319]    [Pg.21]    [Pg.32]    [Pg.291]    [Pg.232]    [Pg.338]    [Pg.1552]    [Pg.1608]    [Pg.1612]    [Pg.397]    [Pg.169]    [Pg.25]    [Pg.204]    [Pg.166]    [Pg.116]    [Pg.234]    [Pg.107]   
See also in sourсe #XX -- [ Pg.45 ]




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1.4- Dithienylbuta-l,3-diyne, reaction with hydrogen sulfide

2-Trimethylsilyloxy-l,3-butadiene, reaction hydrogenation

4- Phenyl-9- perhydropyrido oxazin-l-one catalytic hydrogenation

Asymmetric Hydrogenations - The Monsanto L-Dopa Process

But-2-yne-l,4-diol hydrogenation

Calf, G. E., Garnett, J. L., isotopic Hydrogen

Calf, G. E., Garnett, J. L., isotopic Hydrogen Labeling of Heterocyclic Compounds

Calf, G. E., Garnett, J. L., isotopic Hydrogen One-Step Methods

Hex-l-ene, hydrogenation

Homodienyl-l,5-hydrogen shift

Hydrogenation of 2-butyne-l ,4-diol

Hydrogenation of buta-l,3-diene

Hydrogenation of buta-l,3-diene over

L/-»3/Hydrogen-migration

Reaction L.—(a) Addition of Hydrogen Cyanide to Aldehydes or Ketones

The Application of DuPHOS Rhodium(l) Catalysts for Commercial Scale Asymmetric Hydrogenation

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