Stoichiometric names table

The stoichiometric name of the compound is then formed by combining the name of the electropositive constituent, cited first, with that of the electronegative constituent, both suitably qualified by any necessary multiplicative prefixes ( mono , di , tri , tetra , penta , etc., given in Table IV). The multiplicative prefixes precede the names they multiply, and are joined directly to them without spaces or hyphens. The final vowels of multiplicative prefixes should not be elided (although monoxide , rather than monooxide , is an allowed exception because of general usage). The two parts of the name are separated by a space in English. 

More structural information is obtained by augmenting the stoichiometric name by a structural descriptor. The descriptor is based on electron-counting relationships2 and is presented in Table IR-6.2. 

Thus, aU hyphens in the table are true parts of the names. The symbols > and < placed next to an element symbol both denote two single bonds connecting the atom in question to two other atoms. For a given compound, the various systematic names, if applicable, are given in the order stoichiometric names, substitutive names, additive names and hydrogen names. Acceptable names that are not entirely systematic (or not formed according to any of the systems mentioned above) are given at the end after a semicolon. No order of preference is implied by the order in which formulae and names are listed. Reprinted by permission of lUPAC. 

We now proceed as we did for the stoichiometric case, namely to develop defect- concentration equations for the non-stoichiometric case. Consider the effect of Anti-Frenkel defect production. From Table 2-1, we get Kaf with its associated equation, kAF In Table 2-2, we use Kxi for X-interstitial sites. Combining these, we get ... 

The energy, or power, of electron beam induced in the flue gas is divided and absorbed by their gas components roughly depending on their electron fraction. Therefore almost all the energy is absorbed by the main components of the flue gas, namely, N2, O2, CO2, and H2O. Table 2 shows a typical concentration of the components in coal-fired flue gas in Japan. The ratio of the total number of electrons in each gas components is also listed in the same table. The energy absorbed directly by the toxic components (SO2 and NO) is negligibly small. For electron beam treatment of flue gas, ammonia gas is added to the flue gas before the irradiation. The amount of ammonia is usually set as stoichiometrically, i.e., 2A[S02] + A[NO], where A[S02] and A[NO] are the concentrations of SO2 and NO intended to be treated, respectively. The concentration of ammonia is usually higher than the initial concentration of SO2 and NO however, it is still far lower than that of the main components. 

Step 3 List Stoichiometric Coefficients, Exponents, and Charges List stoichiometric coefficients, exponents, and charges in equations based on the previously identified reaction equations and equilibria. Most of them are listed in an array form. For any two-dimensional (notone-dimensional) array, for example, AR(I,J), the I index is in rows, and the J index is in columns. The orders of elements and fluid species must be the same as those in which their names are listed in the EQBATCH input file, EQIN. However, there are several exceptions in the example presented in Appendix C of the UTCHEM Technical Manual. For the exchange equilibrium constants (Table C.13), exponents (Table C.14), and valence differences on the matrix (Table C.1S), the order is Ca-Na, Mg-Na, and H-Na. 

As a matter of record. Table 3.2 lists vitamins, chemical names, and stoichiometric chemical formulas. In many or most cases, however, the vitamin structure is too complicated for any kind of simplified representation. 

Stoichiometric relationship of these components, the hydroxyl number of the bark used had to be determined. Results of the analysis of the two bark materials studied, namely, Ponderosa Pine and Douglas Fir are given Table II. The amount of diiso-... 

This Cu complex has spectroscopic characteristics similar to those of GOase, such as the EPR spectrum, but it is only able to perform the stoichiometric oxidation of benzyl alcohol to benzaldehyde (76). Two years later. Stack and co-workers reported a significant improvement of the activities High turnover numbers (TON) were reached for reactions carried out at latm of O2 and room temperature (73). Two N2O2 donors, namely BSP (Fig. 9, Ri = SPh and R2 = Bu ) and BDB (Fig. 9, Ri = Bu and R2 = Bu ), were used as copper ligands to generate catalysts that can efficiently convert neat benzylic and allylic alcohols to their respective aldehydes or ketones in the presence of a basic co-catalyst, i.e., lithium or sodium methoxide (Table IV) (73). 

Solution We determined that only two of the four reactions are independent. We may choose any two independent reactions to describe the system, namely, any two of the four in R1-R6, or any linear combination of these, such as reactions R5 and R6 in Example m.iq. We choose reactions Ri and R2 and build the stoichiometric table shown below using the gas standard state for all components. 

TABLE 1 Structure, name, abbreviation used terpenephenois, their stoichiometric factor (i) and rate constants of TP with ethylbenzene peroxy radical k). 

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