Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Solvent carbon tetrachloride

Contrary to the results obtained with carbon tetrachloride solvent and entirely in accord with the postulate that the effect arises from the steric hindrance to solvation, the rates of cleavage of ArSnR3 compounds in methanol decrease on increasing the size of the group R. This is shown by the rate coefficients in Table 265, though it is difficult to draw any conclusion from the Arrhenius parameters... [Pg.384]

It is possible to calculate the mole fraction of carbon tetrachloride (solvent) in a similar manner. However, simply subtracting the mole fraction of chloroform from 1 will give the same value. [Pg.180]

Carbon Tetrachloride Solvents, refrigerant, aerosols, fire extinguishers, grease solvents. 96 2B... [Pg.369]

Williams and coworkers preliminarily reported that CO oxidation on Pt/Al203 is faster in the presence of water solvent than in the presence of ethanol [141]. We then studied CO oxidation on platinum surface in the presence of different solvents, and identified obvious solvent effects, namely, CO oxidation takes place the most easily with water solvent, the least easily with carbon tetrachloride solvent, and follows the overall trend of water > ethanol > methanol > cyclohexane > benzene carbon tetrachloride [67]. We subsequently took advantage of the solvent effect to design a diagnosing tool to pin down low-coverage CO at the liquid-solid interface, by flushing the liquid-solid interface with water and carbon tetrachloride individually [67]. [Pg.258]

The radiotracer method for estimating efficiency of initiation was applied by Bevington and Eaves (32) to polymerization in benzene and in carbon tetrachloride. Whereas they had calculated that about 47% of the radicals from AIBN initiate polymer chains in DMF solvent, efficiency in benzene was about 50% and in carbon tetrachloride about 30%. This low efficiency in carbon tetrachloride is attributed to attack of radicals from AIBN on the carbon tetrachloride solvent, especially at high concentrations of solvent. Chains initiated by secondary radicals derived in this way from the solvent would not be detected by the tracer method. [Pg.421]

Moyer, B.A., McDowell, W.J., Ontko, R.J., Bryan, S.A., Case, G.N. Complexation of strontium in the synergistic extraction system dicyclohexano-18-crown-6, versatic acid, carbon tetrachloride. Solvent Extr. Ion Exch. (1986), 4(1), 83-93. [Pg.378]

The n.m.r. spectrum (60 MHz., carbon tetrachloride solvent with t.ctramethylsilane as an internal reference) shows a complex multiplet centered at 431 Hz. attributable to the aromatic protons, and two doublets centered at 326 and 313 Hz., respectively, attributable to the olefinic protons. [Pg.63]

Finally, MIC was reacted with a slight excess of a-naphthol in the presence of a catalyst in carbon tetrachloride solvent to produce the desired pesticide carbaryl. [Pg.295]

Although the 2,3-dimethyl and 3,4-dimethyl ethers of L-rhamnose were known, the 2,4-dimethyl ether had not been synthesized prior to its preparation through a trifluoroacetyl intermediate. - The synthesis started from methyl 2,3-0-isopropylidene-a-L-rhamnopyranoside this was methylated and the acetal group removed, to give methyl 4-0-methyl-a-L-rhamnopyranoside (6). Conversion to the 2,3-bis(trifluoroacetate) (7) was readily achieved with trifluoroacetic anhydride in the presence of sodium trifluoroacetate. As expected, the trifluoroacetate (7) was completely de-acylated by treatment with alcohol, regenerating (6) this process was complete after 25 min. at room temperature. The procedure for selective de-esterification was based on the observation that, if excess carbon tetrachloride (6 vol.) is present, very little methanolysis occurs. By use of a mixed methanol-carbon tetrachloride solvent (65 35 vol./vol.), the meth-... [Pg.64]

Densities were measured using a density gradient column (toluene/carbon tetrachloride solvent). [Pg.117]

Properties Clear amber liquid. D 0.99. Soluble in acetone, alcohol, benzene, carbon tetrachloride, solvent naphtha, and ligroin insoluble in water, but can hydrolyze. [Pg.1012]

The decomposition of dinitrogen pentoxide has been studied in carbon tetrachloride solvent (CCI4) at a certain temperature ... [Pg.552]

Carbon tetrachloride solvent anomaly with silica, 142 Celite, 172 Charcoal, 168-169 See also Graphite eluotropic series on, 197-199 oxidized, 168 standardization of, 138 Charge transfer, 51-52 Chemical interaction, adsorbate-adsorbent, 225-226... [Pg.208]

Physical Parameters. Povidone-iodine is obtained as yellowish-brown, amorphous powder with slight typical characteristic odour. The aqueous solutions have a pH 2 it may be made more neutral (but less stable) by the addition of sodium bicarbonate. It is fomid to be soluble in ethanol and water almost insoluble in chloroform, carbon tetrachloride, solvent ether, hexane and acetone. Interestingly, its solutions do not respond to the familiar blue colouP starch-test, when prepared even fi-eshly. [Pg.289]

Fig. 5.6. Mossbauer spectrum of a rapidly frozen solution of SnBr4 in tetrahydrofuran-carbon tetrachloride solvent mixture [Ve 76]... Fig. 5.6. Mossbauer spectrum of a rapidly frozen solution of SnBr4 in tetrahydrofuran-carbon tetrachloride solvent mixture [Ve 76]...
A certain first-order reaction is 35.5 percent complete in 4.90 min at 25°C. What is its rate constant The decomposition of dinitrogen pentoxide has been studied in carbon tetrachloride solvent (CCI4) at a certain temperature ... [Pg.608]

In the preparation of 9-bromoanthracene, the reaction progress is easily followed, since NBS (a reactant) and sucdnimide (a product) are both nearly insoluble in carbon tetrachloride. The NBS is more dense than the carbon tetrachloride solvent, and as the reaction proceeds this solid disappears from the bottom of the reaction flask and the less dense sucdnimide forms and floats on the surface of the reaction solution. [Pg.391]

Electrophilic Bromination of Benzene in the Gas Phase and in Carbon Tetrachloride Solvent... [Pg.68]

The first overtone of a free hydroxyl group in dilute CCI4 solution or a low-density gas is at about 7090 cm (1410 nm). This peak is at different positions for primary, secondary, and tertiary alcohols, as seen in Figure 5.1. Primary and secondary butanols can be split into doublets by rotational isomerization. The splits are better seen in Figure 5.2, in the second derivation spectra of the same spectral region. Maeda et al. observed an additional peak in the first overtone region when they subtracted the spectrum at a lower temperature from that at a higher one. They felt that temperature effects further separated species that were weakly bonded to the carbon tetrachloride solvent and a terminal free OH of a self-associated species. [Pg.64]

Dinitrogen pentoxide, N2O5, decomposes when heated in carbon tetrachloride solvent. [Pg.609]

Solutions of the complexes were prepared in spectral grade benzene or carbon tetrachloride solvents, which were deaerated with prepurified nitrogen before use in order to minimize oxidation of the chromium complexes. The flow rate for the SCOT column was determined by injecting 40 to 50y 1 of methane and measuring the time of elution. The resultant linear gas velocity in ft/sec was then converted to volume flow rate in ml/min by the appropriate conversion factors. Flow rates for the packed column were determined by use of a soap-film flow meter. [Pg.498]

Chemicals Carbon tetrachloride Solvent Rare, all animals... [Pg.98]

Thus, in carbon tetrachloride solvent, the dimer consists of 45% of I and 55% of II. In benzene solvent, the alkylation product, III, was also formed. [Pg.281]


See other pages where Solvent carbon tetrachloride is mentioned: [Pg.466]    [Pg.496]    [Pg.376]    [Pg.143]    [Pg.376]    [Pg.466]    [Pg.26]    [Pg.506]    [Pg.376]    [Pg.172]    [Pg.248]    [Pg.391]    [Pg.966]    [Pg.95]    [Pg.143]    [Pg.371]    [Pg.265]    [Pg.110]    [Pg.5688]    [Pg.702]    [Pg.576]    [Pg.702]    [Pg.198]    [Pg.408]   


SEARCH



Carbon solvents

Carbon tetrachlorid

Carbon tetrachloride

Solvent carbonate

© 2024 chempedia.info