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Carbon compounds elemental analysis

The synthesis of hydroxy-3-aminoethane thiosulfuric acid (AETSAPPE) is shown in Scheme II. The same basic conditions used for the polymer synthesis were employed to synthesize the model compound (AETSAPPE) although the work-up conditions were less stringent. The structure was confirmed by carbon-13 NMR and elemental analysis. [Pg.283]

Traditionally, the molecular formula of a compound was derived from elemental analysis and its molecular weight which was determined independently. The concept of the degree of unsaturation of an organic compound derives simply from the tetravalency of carbon. For a non-cyclic hydrocarbon i.e. an alkane) the number of hydrogen atoms must be twice the number of carbon atoms plus two, any deficiency in the number of hydrogens must be due to the presence of unsaturation, i.e. double bonds, triple bonds or rings in the structure. [Pg.3]

Mesoionic 4-amino-l,2,3,5-thiatriazoles constitute the only class of mesoionic 1,2,3,5-thiatriazoles known. They are prepared by the reaction of l-amino-l-methyl-3-phenylguanidine with approximately 2 equivalents of thionyl chloride with pyridine as solvent (88ACS(B)63>. They are obtained as the yellow 1 1 pyridine complexes (17). The dark-violet mesoionic 1,2,3,5-thiatriazole (18) was liberated on treatment with aqueous potassium carbonate (Scheme 3). The structure is established on the basis of elemental analysis and spectroscopic data. In particular, the IR spectrum is devoid of NH absorptions. Compound (18) exhibits a long-wavelength absorption at 463 nm in methanol. When mixed with an equivalent amount of pyridinium chloride, complex (17) is formed and the absorption shifts to 350 mn. The mesoionic thiatriazoles are sensitive towards mineral acids and aqueous base and although reaction takes place with 1,3-dipolarophiles such as dimethyl acetylene-dicarboxylate, a mixture of products were obtained which were not identified. [Pg.737]

In this paper we present results which reconcile the widely different results just discussed ranging from a carbon aerosol dominated by secondary organic material on the one hand to a carbon aerosol composed largely of primary carbon compounds on the other. We have employed an approach which uses lead or elemental carbon as a tracer for primary emissions and combines several analysis techniques to reexamine the published ACHEX data. We also present a new data set from St. Louis which is analyzed in a similar manner to contrast the aerosol in a midwestern city with that on the California coast. [Pg.253]

In the chemical ionization mass spectrum of pentobarbital in Figure 22-4, the peak with the most significant intensity at the high end of the mass spectrum at mlz 227 is suspected to be MH+ If this is so. then the nominal mass of M is 226. The nitrogen rule tells us that a molecule with an even mass must have an even number of nitrogen atoms. If you know from elemental analysis that the compound contains only C, H. N. and O. how many atoms of carbon would you suspect are in the molecule ... [Pg.480]

A highly toxic gas that has been used in chemical warfare gives the following elemental analysis figures 12.1% carbon, 16.2% oxygen, and 71.7% chlorine by mass. Its molar mass is 98.9 g-moU1. Write the Lewis structure of this compound. [Pg.240]

In 1943, Hieber and Lagally reported that the reaction of anhydrous rhodium trichloride with carbon monoxide at 80°C, under pressure, and in the presence of silver and copper as halogen acceptors, gave a black crystalline product which, on the basis of elemental analysis, was formulated as Rh4(CO)n 75). The exact nature of this compound was established 20 years later by Dahl using three-dimensional X-ray analysis which led to its reformulation as Rh6(CO)i6 53). This discovery can be regarded as the birthday of the chemistry of high nuclearity clusters. [Pg.286]

Based on TGA and elemental analysis, up to one in 20 nanotube carbons (5 %) has been found to possess an aryl addend [174], For the preparation of PS-CNT nanocomposites, the same authors functionalized SWCNTs by in-situ generation of a diazonium compound from 4-(10-hydroxydecyl)aminobenzoate [175], From rheology data it was suggested that the reinforcement and dispersibility of the thus functionalized SWCNT-composites were improved over PS composites with pristine SWCNTs. [Pg.28]

Cyclotriveratrylenes are made by the condensation of veratrole with formaldehyde and were a curiosity when they were first prepared by Robinson in 1915 [47], At the time she believed the compound to be a dimer, 2,3,6,7-tetramethoxy-9,10-dihydroxyanthracene. The reason for this was that the composition of the original compound was determined by elemental analysis. This technique determines the percentage of hydrogen and carbon in the sample which would be identical for a dimer, trimer or any other cyclic product with the same proportion of carbon to... [Pg.23]

Elemental analysis of chlorinated samples of carbonic nanofibers and multiple wall nanotubes revealed that the abundance of chlorine in compounds obtained is 5,8 and 1,3 mass. %, respectively. [Pg.157]

Although the great majority of petroleum and coal-based pitch materials, as well as model compounds such as polyvinyl chloride, acenaphthylene, decacyclene and polynuclear aromatic hydrocarbons, form anisotropic graphitizable carbons, it is an almost impossible task to predict the type of optical texture of a coke from an elemental analysis of the pitch. The size, shape and reactivity of peri-condensed polynuclear aromatic molecules in the products of pyrolysis of a pitch play a more important role in determining optical texture. [Pg.19]

Calculation of the Empirical Formula Molecular formulas can be determined by a two-step process. The first step is the determination of an empirical formula, simply the relative ratios of the elements present. Suppose, for example, that an unknown compound was found by quantitative elemental analysis to contain 40.0% carbon and 6.67% hydrogen. The remainder of the weight (53.3%) is assumed to be oxygen. To convert these numbers to an empirical formula, we can follow a simple procedure. [Pg.1328]


See other pages where Carbon compounds elemental analysis is mentioned: [Pg.441]    [Pg.441]    [Pg.506]    [Pg.152]    [Pg.34]    [Pg.445]    [Pg.201]    [Pg.384]    [Pg.164]    [Pg.3]    [Pg.271]    [Pg.61]    [Pg.213]    [Pg.260]    [Pg.385]    [Pg.479]    [Pg.315]    [Pg.389]    [Pg.250]    [Pg.273]    [Pg.121]    [Pg.270]    [Pg.46]    [Pg.708]    [Pg.621]    [Pg.389]    [Pg.1054]    [Pg.39]    [Pg.281]    [Pg.376]    [Pg.165]    [Pg.71]    [Pg.4]    [Pg.1070]    [Pg.155]    [Pg.283]    [Pg.1529]    [Pg.713]    [Pg.1274]   
See also in sourсe #XX -- [ Pg.430 ]




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