Stoichiometry production

The stoichiometry product does not agree with that used in the experiment, as Ni and B compounds are mixed in diethylether in a 1 1 mole ratio. The (Ph3P)2NiBPh2 0.5 OEt2 product is a dimer with a Ni — B—Ni multicentered bond. ... 

From the reaction stoichiometry, product B is formed at exactly the same rate as that at which reactant A, is decomposed. 

Cytochrome P 450. The mechanism of P-450 catalysis is outlined in Figure 2 (3, 4). The mechanism is based on the stoichiometry, product analysis, and labeling experiments, quenching experiments, spectral evidence for the structures of intermediates involved, and model studies (enzyme models as well as oxidant models) of P-450 catalysis. 

Table 7-1 Stoichiometries, Products, and Apparent Second-Order Rate Constants (ki/[S]) for the Reaction of Excess 02 - with Halogenated Hydrocarbons in Dimethylformamide (0.1 M Tetraethylammonium Perchlorate) at 25°C ...

The reaction stoichiometries, product profiles, and apparent second-order rate constants for the combination of perfluoroaromatic molecules (and several hydro and dihydro derivatives) with excess superoxide ion in dimethylformamide are summarized in Table 7-1. The primary product from the combination of C6F6 with 2 equivalents of O2-- is CeEgOO on the basis of the F-NMR spectrum of the product solution and the mass spectrum for the major peak from the capillary GC of the product solution.24 Similar analyses of the product solutions for the other fluoro substrates are consistent with a peroxide product from the displacement of a fluoride ion. A reasonable first step for these oxygenations is nucleophilic addition of O2 - to the polyfluoroaromatic. Subsequent loss of fluoride ion will give an aryl peroxy radical, which will be reduced by a second O2-- to the aryl peroxide product. This reaction sequence (with the initial nucleophilic displacement the rate-determining step) is analogous to that observed for chlorohydrocarbons and polychlorobenzenes (Scheme 7-8). However, the peroxo product of the latter systems is an effective nucleophile that attacks a second substrate molecule (or an adjacent aryl chlorine... 

Unfortunately, in most cases not all the available information on a reaction is given in the reaction equation in a publication, and even less so in reaction databases. To obtain a fuller picture of the reaction that was performed, the text describing the experimental procedure in the publication or a lab journal) would have to be consulted. Reaction products that are considered as trivial, such as water, alcohol, ammonia, nitrogen, etc., are generally not included in the reaction equation or mentioned in the text describing the experimental work. This poses serious problems for the automatic identification of the reaction center. It is highly desirable to have the full stoichiometry of a reaction specified in the equation. 

Stoichiometric relationships and calculations are important in many quantitative analyses. The stoichiometry between the reactants and products of a chemical reaction is given by the coefficients of a balanced chemical reaction. When it is inconvenient to balance reactions, conservation principles can be used to establish the stoichiometric relationships. 

The accuracy of a standardization depends on the quality of the reagents and glassware used to prepare standards. For example, in an acid-base titration, the amount of analyte is related to the absolute amount of titrant used in the analysis by the stoichiometry of the chemical reaction between the analyte and the titrant. The amount of titrant used is the product of the signal (which is the volume of titrant) and the titrant s concentration. Thus, the accuracy of a titrimetric analysis can be no better than the accuracy to which the titrant s concentration is known. 

An additional problem is encountered when the isolated solid is non-stoichiometric. For example, precipitating Mn + as Mn(OH)2, followed by heating to produce the oxide, frequently produces a solid with a stoichiometry of MnO ) where x varies between 1 and 2. In this case the nonstoichiometric product results from the formation of a mixture of several oxides that differ in the oxidation state of manganese. Other nonstoichiometric compounds form as a result of lattice defects in the crystal structure. ... 

In a gravimetric analysis a measurement of mass or change in mass provides quantitative information about the amount of analyte in a sample. The most common form of gravimetry uses a precipitation reaction to generate a product whose mass is proportional to the analyte. In many cases the precipitate includes the analyte however, an indirect analysis in which the analyte causes the precipitation of another compound also is possible. Precipitation gravimetric procedures must be carefully controlled to produce precipitates that are easily filterable, free from impurities, and of known stoichiometry. 

In Example 13.1 the initial concentration of analyte is determined by measuring the amount of unreacted analyte at a fixed time. Sometimes it is more convenient to measure the concentration of a reagent reacting with the analyte or the concentration of one of the reaction s products. The one-point fixed-time integral method can still be applied if the stoichiometry is known between the analyte and the species being monitored. For example, if the concentration of the product in the reaction... 

Several important points about the rate law are shown in equation A5.4. First, the rate of a reaction may depend on the concentrations of both reactants and products, as well as the concentrations of species that do not appear in the reaction s overall stoichiometry. Species E in equation A5.4, for example, may represent a catalyst. Second, the reaction order for a given species is not necessarily the same as its stoichiometry in the chemical reaction. Reaction orders may be positive, negative, or zero and may take integer or noninteger values. Finally, the overall reaction order is the sum of the individual reaction orders. Thus, the overall reaction order for equation A5.4 isa-l-[3-l-y-l-5-l-8. 

As with other problems with stoichiometry, it is the less abundant reactant that limits the product. Accordingly, we define the extent of reaction p to be the fraction of A groups that have reacted at any point. Since A and B groups... 

Octabromodiphenyl Oxide. Octabromodiphenyl oxide [32536-52-0] (OBDPO) is prepared by bromination of diphenyl oxide. The degree of bromination is controlled either through stoichiometry (34) or through control of the reaction kinetics (35). The melting poiat and the composition of the commercial products vary somewhat. OBDPO is used primarily ia ABS resias where it offers a good balance of physical properties. Poor uv stabiUty is the primary drawback and use ia ABS is being supplanted by other brominated flame retardants, primarily TBBPA. 

Coproductioa of ammonium sulfate is a disadvantage of the formamide route, and it has largely been supplanted by processes based on the direct hydrolysis of methyl formate. If the methanol is recycled to the carbonylation step the stoichiometry corresponds to the production of formic acid by hydration of carbon monoxide, a reaction which is too thermodynamicaHy unfavorable to be carried out directly on an iadustrial scale. 

Prior to methanation, the gas product from the gasifier must be thoroughly purified, especially from sulfur compounds the precursors of which are widespread throughout coal (23) (see Sulfurremoval and recovery). Moreover, the composition of the gas must be adjusted, if required, to contain three parts hydrogen to one part carbon monoxide to fit the stoichiometry of methane production. This is accompHshed by appHcation of a catalytic water gas shift reaction. 

MPD-1 fibers may be obtained by the polymeriza tion of isophthaloyl chloride and y -phenylenediamine in dimethyl acetamide with 5% lithium chloride. The reactants must be very carefully dried since the presence of water would upset the stoichiometry and lead to low molecular weight products. Temperatures in the range of 0 to —40° C are desirable to avoid such side reactions as transamidation by the amide solvent and acylation of y -phenylenediamine by the amide solvent. Both reactions would lead to an imbalance in the stoichiometry and result in forming low molecular weight polymer. Fibers are dry spun direcdy from solution. 

The stoichiometry (4 mol lithium hydride to 1 mol LiAlH ) makes this an inherently expensive process, even though high yields of pure product are obtained. For large-scale production, metathesis from NaAlH is economically preferred. 

Butane-Based Fixed-Bed Process Technology. Maleic anhydride is produced by reaction of butane with oxygen using the vanadium phosphoms oxide heterogeneous catalyst discussed earlier. The butane oxidation reaction to produce maleic anhydride is very exothermic. The main reaction by-products are carbon monoxide and carbon dioxide. Stoichiometries and heats of reaction for the three principal reactions are as follows ... 

The main by-pioducts of this type of reaction are sulfides. By exercising careful control of stoichiometry, these can be rninimized quite readily. By-products are disposed of by incineration or by reprocessing for fuel value. 

Excess alkylating reagent is required if the tetraorganotin is desired as the exclusive product. In commercial practice, the stoichiometry is kept at or below 4 1, since the cmde product is usually redistributed to lower organotin chlorides in a subsequent step and an ether is used as the solvent (86). The use of diethyl ether in the Grignard reaction has been generally replaced with tetrahydrofuran. 

The perhydrolysis reaction could theoretically continue to give four moles of peracid per mole of TAED but stops at this stoichiometry because of the substantial increase in the conjugate acid pify of the leaving group going from an amide (p-R = 17) to an amine (pif = 35) (94,95). Nonanoyloxybenzene sulfonate (NOBS) [101482-85-3] is used in detergent products in the United States and Japan. The NOBS perhydrolysis reaction is shown in equation 20 (96). 

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