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Compounds and Uses

The most common oxidation states and the corresponding electronic configuration of mthenium are +2 and +3 (t5 ). Compounds are usually octahedral. Compounds in oxidations states from —2 and 0 (t5 ) to +8 have various coordination geometries. Important appHcations of mthenium compounds include oxidation of organic compounds and use in dimensionally stable anodes (DSA). [Pg.177]

Many grades of PVB and PVF resias are made, and most are eventually compounded and used as multicomponent products. Individual product MSDSs need to be consulted prior to handling and each product should be handled appropriately and ia accordance with good iadustrial hygiene and safety practices, which iaclude appropriate skin, respiratory, and eye protection. [Pg.451]

U. von Sacken, Q. Zhong, Tao Zheng, and J.R. Dahn, Phenolic Resin Precursor Pregraphitic Carbonaceous Insertion Compounds and Use as Anodes in Rechargeable Batteries, Canadian Patent Application 2,146,426... [Pg.386]

Chemoautotroph An organism that obtains its energy from the oxidation of chemical compounds and uses only organic compounds as a source of carbon. Example nitrifiers. [Pg.609]

The Mukaiyama aldol reaction can provide access to a variety of (3-hydroxy carbonyl compounds and use of acetals as reactants can provide (3-alkoxy derivatives. The issues of stereoselectivity are the same as those in the aldol addition reaction, but the tendency toward acyclic rather than cyclic TSs reduces the influence of the E- or Z-configuration of the enolate equivalent on the stereoselectivity. [Pg.86]

The instability of 5-aminoimidazoles (96) has led to in situ acylation being used to obtain stable compounds and using this approach several derivatives have been prepared. For example, a solution of the appropriate 5-nitroimidazole (97) in ethyl acetate was reduced with Raney nickel, and the resulting solution of 5-aminoimidazole (96) then treated with an acid chloride to give the amides (118 R1 = Me, R2 = S02Me, COPh, R3 = alkyl, aryl, hetaryl) (25-45%) [82IJC(B)1087],... [Pg.30]

Used in the manufacture of pharmaceuticals, dye intermediates, explosives, various inorganic and organic nitrates, nitro compounds and used industrially for ore flotation, metallurgy, photoengraving, and reprocessing spent nuclear fuel. [Pg.330]

B We write the combustion reaction for each compound, and use that reaction to determine the compound s heat of combustion. [Pg.129]

Mortimer and co-workers extended these studies to many other CoL2X2 compounds and, using estimated or measured enthalpies of sublimation and heat capacities of the complexes and the ligands, were able to derive the corresponding Co-L mean bond dissociation enthalpies [238]. [Pg.185]

Atomic charges, effective charges at reacting centres, and HOMO and LUMO energies have been calculated for nitrobenzene, nitrosobenzene, A-phenylhydrazine, diphenyldiazine, A,A -diphenyldiazine-A-oxide, and A,A -diphenyUiydrazine, compared with kinetic data for the hydrogenation of these compounds, and used to propose a mechanism for the hydrogenation of nitrobenzene. [Pg.246]

Thus, to conduct successful analyses for many organic and inorganic compounds at trace concentrations, it is necessary to extract these compounds and use a concentration step prior to analysis. Many of the techniques developed for preconcentration are described in specialized books [10]. Proper choice of the extracting solvent can often be the critical step in the procedure. [Pg.565]

Because of the different experimental conditions, the solvent/amine pair plays a crucial role in the formation of the iiii stereoisomer. Systematic study of the influence of the nature of the base, the reagent/base ratio, and the nature of the solvent (donating power), was performed with the phosphonatocavitands 12a and 12b (Table 1). The procedure is highly solvent dependent the iiii stereoisomer is the major product obtained in toluene, associated with minor amount of iiio isomer. When the reaction is run in acetone other isomers are predominant (ioio, iioo, oooi) and the iiii stereoisomer is not observed. The use of catalytic amount of this amine (0.2 equiv) [64] did not lead to any extractable compounds, and using eight equivalents of amine to trap all the HCl formed, did not change dramatically the yield and the isomer ratio (entries 5 and 6, Table 1). In the presence of triethylamine the iiii and iiio isomers were formed in 28.5% and 7% yields respectively. [Pg.66]

Table 8.4 Mono- and bimetallic iron- ruthenium- and osmium-based catalysts prepared from carbonyl compounds and used in the CO hydrogenation reaction. Table 8.4 Mono- and bimetallic iron- ruthenium- and osmium-based catalysts prepared from carbonyl compounds and used in the CO hydrogenation reaction.
Reduction of a range of allyl and benzyl chlorides at a stainless steel cathode in dimethylformamide in the presence of carbonyl compounds and using a sacrificial anode of aluminium or zinc, leads to a Reformatsky-type reaction in 40-80 % yields. Allyl halide give products by reaction at both the a- and y-positions. Tetra-chioromethane and bromotrifluoromethane take part in similar reactions provided a... [Pg.134]

We here further demonstrate the merits of Fe -exchanged montmorillonite over the conventional homogeneous acid catalysts, applying it to other types of liquid-phase carbon-carbon bond-forming reactions between carbonyl compounds and useful nucleophilic carbanion reagents such as silyl ketene acetal (an ester... [Pg.371]

In one of the first studies of the vapor-phase mutagenicity of polluted urban air, Alfheim and co-workers (1985) collected both ambient particles and vapor-phase compounds and used the Salmonella typhlmurium reversion assay. The direct activities ( —S9) of the extracts generally exceeded the promutagenicities (+ S9), and furthermore, the vapor-phase mutagenicity ranged from 0 to 88% of the total activity. [Pg.502]

Preservatives. Sulfur compounds, such as sulfur dioxide and sodium bisulfite, are used commercially to preserve the color of various food products, such as orange juice, dehydiated fruits and vegetables, such as apricots, carrots, peaches, pears, potatoes, and many odiers. Concentrated sulfur dioxide is used in wine-making to destroy certain bacteria. The color preservation of canned green beans and peas is enhanced by dipping the produce in a sulfite solution prior to canning. In 1986, some of these compounds and uses were put under closer regulation in the United States. [Pg.1575]

The applicants then appealed to the CCPA where they had better luck. The CCPA began its written opinion by reminding the USPTO Appeal Board that it was impermissible to negate inventiveness based on the method used by the applicants for discovering their invention.135 Second, they noted that the obviousness determination must be based on a comparison of the claimed matter and the prior art. As such, the prior art at the time of the invention was the natural strawberry and its attendant taste. From this, there was no basis for selecting the claimed compound and using it... [Pg.277]

Urea derivatives are an important class of carbonyl compounds and useful chemical intermediates in the synthesis of pharmaceuticals, agricultural chemicals, and dyes and they are also used as antioxidants in gasoline and additives in plastics [51-54]. [Pg.66]

Hundreds of reports have been published on electrophilic mercuration of a variety of aromatic compounds and uses of the resulting organomercurials in synthesis [5, 7-11]. Although in this chapter, we will not discuss synthetic applica-... [Pg.120]

Table 6.1 also lists the resonance frequency for each nucleus at 7.0463 T, which corresponds to a resonance frequency of 300 MHz for 3H. Also listed in the table are useful reference compounds and useful ranges of detection in parts per million. Chemical shift data are only useful if properly referenced. In fact, excluding H and 13C data, we must exercise extreme caution when comparing chemical shifts from different sources because most other nuclei have seen more than one compound used as a reference. [Pg.316]

In this experiment, you will examine physical and chemical properties of representative alcohols and phenols. You will be able to compare the differences in chemical behavior between these compounds and use this information to identify an unknown. [Pg.312]

As a result, specific kinds of vibration modes always appear at similar frequencies for different molecules then, it is feasible to construct a table of characteristic absorption frequencies. Typical absorption band tables for significant bonds included in polyatomic molecules are reported in ref. [58], Subsequently, using the typical absorption frequencies, it is relatively simple to recognize the occurrence of functional groups in unidentified compounds, and use this information to get structural information about these substances in order to identify them. [Pg.166]

Just as there are many formulations, there are many ways to compound and process the requisite raw materials into an adhesive formulation. The methods chosen and how they are used also influence the final physical properties of the adhesive. The important processes to be considered in compounding and use of epoxy adhesives can be listed as follows ... [Pg.392]

Do not guess a starting material and try every possible reaction to convert it to the target compound. Rather, begin with the target compound and use a retrosynthetic analysis to simplify it. [Pg.377]


See other pages where Compounds and Uses is mentioned: [Pg.339]    [Pg.337]    [Pg.13]    [Pg.13]    [Pg.108]    [Pg.208]    [Pg.300]    [Pg.21]    [Pg.271]    [Pg.450]    [Pg.183]    [Pg.196]    [Pg.1]    [Pg.135]    [Pg.2494]    [Pg.232]    [Pg.155]    [Pg.136]    [Pg.240]    [Pg.1]   


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