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Relative yield

The first mfonnation on the HE vibrational distribution was obtained in two landmark studies by Pimentel [39] and Polanyi [24] in 1969 both studies showed extensive vibrational excitation of the HE product. Pimental found that tire F + H2 reaction could pump an infrared chemical laser, i.e. the vibrational distribution was inverted, with the HF(u = 2) population higher than that for the HF(u = 1) level. A more complete picture was obtained by Polanyi by measuring and spectrally analysing tlie spontaneous emission from vibrationally excited HE produced by the reaction. This infrared chemiluminescence experiment yielded relative populations of 0.29, 1 and 0.47 for the HF(u =1,2 and 3)... [Pg.876]

The maximum yield of 2-alkylseIenazole is 25%. In this way. 4-methylselenazole (7) was obtained starting from hydrogen cyanide, hydrogen selenide and chloroacetone. It is the only known selenazole not substituted in the 2-position. The yield relative to chloroacetone is very low (2.5%) (Scheme 2). [Pg.220]

The notion that carbocation formation is rate determining follows from our previous experience and by observing how the reaction rate is affected by the shucture of the aUcene Table 6 2 gives some data showing that alkenes that yield relatively stable carbocations react faster than those that yield less stable carbocations Protonation of ethylene the least reactive aUcene m the table yields a primary carbocation protonation of 2 methylpropene the most reactive m the table yields a tertiary carbocation As we have seen on other occa sions the more stable the carbocation the faster is its rate of formation... [Pg.248]

Modifications of Processes Based on Air Oxidation ofp-Xylene. Since the mid-1970s, starting in Japan, several companies have developed oxidation processes to yield relatively pure forms of terephthaUc acid without a separate purification. These products, normally called medium purity terephthahc acids, contain 200—300 ppm 4-formylbenzoic acid and trace amounts of acetic acid and thus do not meet normal specifications for the highest purity grades available (80,81). [Pg.490]

The sodium salt of CS [9005-22-5] is prepared by reaction of cellulose with sulfuric acid in alcohol followed by sodium hydroxide neutrali2ation (20). This water-soluble product yields relatively stable, clear, and highly viscous solutions. Introduced as a thickener for aqueous systems and an emulsion stabilizer, it is now of no economic significance. [Pg.265]

Figure 14.1 The McCabe-Thiele diagram for the calculation of the number of theoretical stages required to separate two liquids to yield relatively pure products... Figure 14.1 The McCabe-Thiele diagram for the calculation of the number of theoretical stages required to separate two liquids to yield relatively pure products...
Some of these difficulties can be circumvented. In particular a cavity-type Stark effect spectrograph has been built which seems capable of yielding relative intensities of near-by lines to within two or three per cent.32 Barrier values for acetaldehyde and fluoro-ethane have been obtained which are in excellent agreement with those from the frequency method described below. From Eq. (1) it can be seen that the error in v is... [Pg.378]

Another application of this method is the stereoselective addition of (7 )-2-hydroxy-l,2,2-triphenylethyl acetate, via the lithium enolate, to propenal (acrolein) which affords mainly the ester 13 (d.r. 92 8). When the acid, obtained in the subsequent alkaline hydrolysis, is converted into the ammonium salt derived from (.S)-l -phenylethylaminc, and the salt recrystallized once, then the amine liberated (/f)-3-hydroxy-4-pentenoic acid is obtained in 41 % yield [relative to the (/ )-acetate] and >99.8% ee82. [Pg.492]

Expts. 18-20 carried out with the TMPCl/EtAlCl2 system showed more promising results. For example, Exp. 20 yielded relatively high molecular weight poly(P-PIN), M = 8200, and Ieff = 105%, which is close to the theoretical value. [Pg.4]

B. In contrast, when a weak acid dissolves in water, it remains mostly undissociated, yielding relatively... [Pg.171]

Another metal that has attracted interest for use as electrode material is rhodium, inspired by its high activity in the catalytic oxidation of CO in automotive catalysis. It is found that Rh is a far less active catalyst for the ethanol electro-oxidation reaction than Pt [de Souza et al., 2002 Leung et al., 1989]. Similar to ethanol oxidation on Pt, the main reactions products were CO2, acetaldehyde, and acetic acid. Rh, however, presents a significant better CO2 yield relative to the C2 compounds than Pt, indicating a... [Pg.195]

Once potent ligands for a viral protein are identified, further advancement depends on demonstrating activity in cells. Unfortunately, reproducible in vitro viral replication assays for HCV have not been reported. There are scattered reports that a very low level of genome replication, or even virus production, can be observed under certain circumstances [56]. However, recently specific sequences yielding relatively reproducible replication, at consistently detectable levels have been reported [57]. In the coming years these may allow routine assays suitable for compound evaluation to be developed, but to date drug discovery must rely on other cell culture models. [Pg.74]

Apart from a few reports" on solid acid catalyzed esterification of model compounds, to our knowledge utilization of solid catalysts for biodiesel production from low quality real feedstocks have been explored only recently. 12-Tungstophosphoric acid (TPA) impregnated on hydrous zirconia was evaluated as a solid acid catalyst for biodiesel production from canola oil containing up to 20 wt % free fatty acids and was found to give ester yield of 90% at 200°C. Propylsulfonic acid-functionalized mesoporous silica catalyst for esterification of FFA in flotation beef tallow showed a superior initial catalytic activity (90% yield) relative to a... [Pg.280]

The reductive coupling of of dienes containing amine groups in the backbones allows for the production of alkaloid skeletons in relatively few steps [36,46,47]. Epilupinine 80 was formed in 51% yield after oxidation by treatment of the tertiary amine 81 with PhMeSiEh in the presence of catalytic 70 [46]. Notably, none of the trans isomer was observed in the product mixture (Eq. 11). The Cp fuMcTIIF was found to catalyze cyclization of unsubstituted allyl amine 82 to provide 83. This reaction proceeded in shorter time and with increased yield relative to the same reaction with 70 (Eq. 12) [47]. Substitution of either alkene prevented cyclization, possibly due to competitive intramolecular stabilization of the metal by nitrogen preventing coordination of the substituted olefin, and resulted in hydrosilylation of the less substituted olefin. [Pg.234]

M) and at low current levels yields relatively smooth surfaces, even in the absence of leveling agents. [Pg.252]

R3N—N=0, but this then readily undergoes C—N fission to yield relatively complex products. With aromatic tertiary amines, ArNR2, nitrosation can take place not on N but at the activated p-position of the nucleus (cf. p. 137) to yield a C-nitroso compound ... [Pg.121]

Attempts to understand hardness from first principles have resulted in empirical equations that represent good curve fitting, but yield relatively little understanding (Gao, 2006). [Pg.6]

In Eq. (6) the hydrogen attached to the oxygen has protonic character and the hydrogen attached to the zinc has hydridic character. Such bonds, with considerable ionic character, would be expected to yield intense bands in the IR, whereas a largely covalent bond would yield relatively weak IR... [Pg.15]


See other pages where Relative yield is mentioned: [Pg.287]    [Pg.49]    [Pg.177]    [Pg.107]    [Pg.121]    [Pg.286]    [Pg.535]    [Pg.32]    [Pg.208]    [Pg.20]    [Pg.433]    [Pg.339]    [Pg.228]    [Pg.265]    [Pg.335]    [Pg.194]    [Pg.198]    [Pg.156]    [Pg.234]    [Pg.401]    [Pg.328]    [Pg.252]    [Pg.551]    [Pg.150]    [Pg.195]    [Pg.159]    [Pg.140]    [Pg.199]    [Pg.199]    [Pg.116]    [Pg.93]   
See also in sourсe #XX -- [ Pg.138 , Pg.146 ]




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