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H production

De Raedt, H. Product formula algorithms for solving the time-dependent Schrodinger equation. Comput. Phys. Rep. 7 (1987) 1-72. [Pg.30]

Fig. 12. Unipol PP process where A is the polymerization reactor B, recycle gas compressor C, recycle gas cooler D, product discharge tank E, impact copolymer reactor F, recycle gas compressor G, recycle gas cooler and H, product discharge tank (134). Fig. 12. Unipol PP process where A is the polymerization reactor B, recycle gas compressor C, recycle gas cooler D, product discharge tank E, impact copolymer reactor F, recycle gas compressor G, recycle gas cooler and H, product discharge tank (134).
Fig. 2. World sugar balance, where represents opening stocks H, production consumption and ending stocks (9,10). Fig. 2. World sugar balance, where represents opening stocks H, production consumption and ending stocks (9,10).
Mazur " obtained 2a-alkyl-5a-H (3) or 4 -alkyl-5 -H products (6) by direct alkylation of either 5a-H (1) or 5 -H-3-keto steroids (4) with alkyl halides under basic conditions. In general, formation and alkylation of the more stable enolate ion is observed in this procedure. [Pg.86]

Substrate RCf,H4CH0 R Time (h) Product Product of Hydrolysis ... [Pg.670]

Thompson, G. H. "Production of Transplutonium Elements," Navratil, J.D. Schulz, W. W. (Eds.), American Chemical... [Pg.375]

Chloro-7-nitroquinoxaline (103, Q = Cl, R = H) gave a separable mixture of 6-nitro-3-piperidinoquinoxaline [103, Q = N(CH2)2, R = H] (product of amino-lysis) and 6-nitro-2,3-dipiperidinoquinoxaline [103, Q = R = N(CH2)s] (product of an additional amination) [excess HN(CH2)5, Et20, 20°C, <4h the amination product was least in an inert atmosphere and most in an oxygen atmosphere, inferrring an addition-oxidation mechanism]. [Pg.153]

Hydrazinocarbonylmethyl-2(l//)-quinoxalinone (112) gave 3-azidoformyl-methyl-2(l//)-quinoxalinone (113) (crude material uncharacterized) and thence 3-oxo-3,4-dihydro-2-quinoxalinecarbonitrile (114) [NaN02, H2O, 5°C solid azide, which redissolved on prolonged stirring then 95°C, 2 h product (114) (27% after separation from a major tricyclic product) a mechanism for this one-pot reaction is suggested]... [Pg.338]

Silane (X) Reaclion Time (h) Products (C ) L nrcacled Silane... [Pg.174]

Our groups developed a catalytic C-CN bond cleavage of organonitriles catalyzed by the Fe complex (Scheme 49) [163, 164]. In this reaction, an organonitrile R-CN and EtsSiH are converted into EtsSiCN as a result of the C-CN bond cleavage and the Si-CN bond formation, and the R-H product. This is the first example of the catalytic C-CN bond cleavage of acetonitrile. [Pg.61]

R= OH, Products 2, 4, 6, 4-tetrahydro5 chalcone 5,7,4 -trihydro) avanone R= H, Products 2, 4, 4-trihydroxychalcone 7,4 -dihydroxyflavanone, which requires operation of reductase E1... [Pg.211]

Adams, J.P, Von Elbe, J.H., and Amundson, C.H., Production of a betacyanine concentrate by fermentation of red beet juice with Candida utilis, J. Food ScL, 41, 78, 1976. [Pg.296]

Cai, YZ. and Corke, H., Production and properties of spray-dried Amaranthus beta-cyanin pigments, J. Food ScL, 65, 1248, 2000. [Pg.325]

Films on Pt/CdS/Naflon have been constructed for use in Investigations of photoasslsted H production from H2O. [Pg.566]

Host-guest complex Irradiation time (h) Product ... [Pg.34]

Zr-H Activity (mol P/mol Zr/h) Product selectivity at 0% conversion Final product selectivity... [Pg.176]

Schein, C. H., Production of soluble recombinant proteins in bacteria, Bio/Technology, 7, 1141, 1989. [Pg.125]

Stream Feed (3) kmol/h Product (4) kmol/h C°, kJ/kmol K ... [Pg.162]


See other pages where H production is mentioned: [Pg.16]    [Pg.618]    [Pg.826]    [Pg.964]    [Pg.472]    [Pg.113]    [Pg.698]    [Pg.134]    [Pg.14]    [Pg.618]    [Pg.826]    [Pg.837]    [Pg.964]    [Pg.240]    [Pg.201]    [Pg.254]    [Pg.963]    [Pg.55]    [Pg.86]    [Pg.121]    [Pg.439]    [Pg.196]    [Pg.129]    [Pg.158]    [Pg.98]    [Pg.35]    [Pg.202]    [Pg.115]    [Pg.231]    [Pg.427]   
See also in sourсe #XX -- [ Pg.353 ]




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C-H activation products

C-H insertion product

C-S-H product

Ideal Gas Sensible Enthalpies, hT - hs (kjkmol), of Combustion Products

Synthesis of Natural Products and Pharmaceuticals via Catalytic C-H Functionalization

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