Stoichiometrically equivalent

The point in a titration where stoichiometrically equivalent amounts of analyte and titrant react. 

For a titration to be accurate we must add a stoichiometrically equivalent amount of titrant to a solution containing the analyte. We call this stoichiometric mixture the equivalence point. Unlike precipitation gravimetry, where the precipitant is added in excess, determining the exact volume of titrant needed to reach the equivalence point is essential. The product of the equivalence point volume, Veq> and the titrant s concentration, Cq, gives the moles of titrant reacting with the analyte. 

The equivalence point of a redox titration occurs when stoichiometrically equivalent amounts of analyte and titrant react. As with other titrations, any difference between the equivalence point and the end point is a determinate source of error. 

The combined liquors, which comprise an aqueous hydrochloric acid solution of 3-amino-methyl-pyridine hydrochloride, are then heated to a temperature of 60° to 65°C, and ethyl nitrite gas is passed into the heated solution. The ethyl nitrite is generated by placing 20 liters of 90% ethyl alcohol in a suitable vessel, diluting with 200 liters of water, and, while stirring, adding to the dilute alcohol 18.3 kg of nitrosyl chloride at the rate of 2.25 kg per hour. (The process using methyl nitrite is carried out by substituting a stoichiometrically equivalent quantity of methyl alcohol for the ethyl alcohol.)... 

When the titration curve is symmetrical about the equivalence point the end point, defined by the maximum value of AE/AV, is identical with the true stoichiometrical equivalence point. A symmetrical titration curve is obtained when the indicator electrode is reversible and when in the titration reaction one mole or ion of the titrant reagent reacts with one mole or ion of the substance titrated. Asymmetrical titration curves result when the number of molecules or ions of the reagent and the substance titrated are unequal in the titration reaction, e.g. in the reaction... 

In such reactions, even though the indicator electrode functions reversibly, the maximum value of AE/AV will not occur exactly at the stoichiometric equivalence point. The resulting titration error (difference between end point and equivalence point) can be calculated or can be determined by experiment and a correction applied. The titration error is small when the potential change at the equivalence point is large. With most of the reactions used in potentiometric analysis, the titration error is usually small enough to be neglected. It is assumed that sufficient time is allowed for the electrodes to reach equilibrium before a reading is recorded. 

Faraday s law of electrolysis The amount of product formed or reactant consumed by an electric current is stoichiometrically equivalent to the amount of electrons supplied. 

Illustrative Procedure 2 Poly(iminocarbonates) by Solution Polymerization (46) Under argon, 1 g of a diphenol and an exact stoichiometric equivalent of a dicyanate were dissolved in 5 ml of freshly distilled THF. 1 mol% of potassium tert-butoxide was added, and the reaction was stirred for 4 hr at room temperature. Thereafter, the poly(iminocarbonate) was precipitated as a gumUke material by the addition of acetone. The crude poly(iminocarbonate) can be purified by extensive washings with an excess of acetone. The molecular weight (in chloroform, relative to polystyrene standards by GPC) is typically in the range of 50,000-80,000. 

Different yields, mainly of the oxidizing species, were found by Koulkes-Pujo and Berthou who studied the system Fe /DMSO in the presence of high concentration of H2SO4. They found that the yields of the primary species in acidic media are Gh = 2.1 + 0.3 and Gqx (for the oxidizing species) = 3.8 + 0.4. These results are supported by studies of the system Ce /DMSO in the presence of H2SO4 . Assuming that the radicals have stoichiometric equivalence to those found in water-DMSO mixtures, we may write the observed G(-Ce ) = 13.9 + 0.4 as equal to = 3Gqx + Gh = 13.5. The difference between the yields in acidic media and for pure DMSO is due to reaction of H with the precursors of these species. 

Cationic polyacrylamide may be used in the initial treatment stages to promote rapid polymer adsorption (201). Adjustment of the pH may allow deeper penetration of the fluids in an aluminate crosslinking system prior to gelation (202). A process involving injection of alternate slugs of stoichiometrically equivalent amounts of partially hydrolyzed polyacrylamide and Al O ) has been evaluated in the laboratory permeability of sana packs were reduced by more than 96% (203). Mixtures of Al(IIl) and Zr(IV) have also been evaluated as partially hydrolyzed polyacrylamide crosslinkers (204). 

Real-Time FTIR. For our IR studies, we utilized a stoichiometrically equivalent amount of a trifunctional thiol, trimethylolpropane tris(2-mercaptoacetate), with a difunctional allyl, trimethylolpropane diallyl ether. The thiols were protected from oxidative polymerization by the addition of hydroquinone. The monomers and hydroquinone were purchased from Aldrich Chemicals and were used as received. This formulation was mixed for five minutes and then a commercial photoinitiator, Esacure TZT (Sartomer Inc.), which contained a blend of methyl benzophenones, was added at a level of 1.0% by weight of monomers to the formulation. Stirring was maintained for a further five minutes following the addition of the photoinitiator. The final formulation contained 2.0% by weight of hydroquinone. The samples were prepared prior to each experiment in order to ensure reproducibility of sample history. 

Thus, a semilogarithmic plot of the gel time as a function of 1/T should be linear, with the slope corresponding to the apparent activation energy. We have determined the gel times for a temperature range of 25°-50° C for a thiol-ene system consisting of stoichiometrically equivalent amounts of a trifunctional thiol, trimethylolpropane tris(2-mercaptoacetate), and a trifiinctional allyl monomer, triallyl isocyanurate. In this system, we also added 0.31% by weight of hydroquinone, to prevent premature polymerization, and 1.0% by weight of a commercial photoinitiator, Esacure TZT. 

The abatement of chlorine vents and the subsequent destruction of the resulting sodium hypochlorite has been the subject of many studies. There are a variety of approaches to the waste hypochlorite destruction including chemical dosing, homogeneous and slurry catalysis as well as fixed-bed catalysis. For the most part these processes treat the hypochlorite at its natural strength the stoichiometric equivalent strength of the caustic soda fed to the scrubber. 

If the reaction mixture contains er .-oxonium ions (V) (reactions 6a, b), or oxycarbenium ions (VI) (reaction 6c), or any other oxygen-containing cations which are stoichiometrically equivalent to these (see for example, (X) and (XI) below), the ethoxide ions combine with them and are thus incorporated in the polymer ... 

Since electron transfer (log kE) represents the adiabatic counterpart to the photochemical process (hvcr), the triad in (87) is (stoichiometrically) equivalent to that in (63) and its collapse to the Wheland intermediate will lead to nitration products that are the same as those formed in charge-transfer nitration. When such a comparison of electrophilic and charge-transfer nitrations is carried out in quantitative detail, the aromatic donors fall roughly into two categories. 

A noticeable difference occurring between the stoichiometric equivalence point of a reaction and the observed end-point. 4. Volatalization of weighing forms on ignition, and... 

Cyclic voltammograms were recorded after progressively adding stoichiometric equivalents of K+, Na+ and Li+ cations to solutions of the receptors. Disappointingly, with all metal cations only relatively small anodic... 

The stratified gaseous layer established over the liquid fuel surface varies from a fuel-rich mixture to within the lean flammability limits of the vaporized fuel and air mixture. At some point above the liquid surface, if the fuel temperature is high enough, a condition corresponds to a stoichiometric equivalence ratio. For most volatile fuels this stoichiometric condition develops. Experimental evidence indicates that the propagation rate of the curved flame front that develops is many times faster than the laminar flame speed discussed earlier. There are many less volatile fuels, however, that only progress at very low rates. 

Asymmetric hydrogenation of vinyl ether alcohols proceeded in better selectivity than the ester counterparts, but acid sensitivity was observed for 66a-d, and a stoichiometric equivalent of potassium carbonate relative to the substrate was... 

From the equation showing the mechanism it is evident that 1 mol of lithium aluminum hydride can reduce as many as four molecules of a carbonyl compound, aldehyde or ketone. The stoichiometric equivalent of lithium aluminum hydride is therefore one fourth of its molecule, i.e. 9.5 g/mol, as much as 2 g or 22.4 liters of hydrogen. Decomposition of 1 mol of lithium aluminum hydride with water generates four molecules of hydrogen, four hydrogens from the hydride and four from water. 

Stoichiometric Equivalence Purity of reactants Equipment Pressure... 

Reaction that occurs when stoichiometrically equivalent amounts of an acid and a base are mixed. 

The solution behavior of poly(amic acids) was until recently, probably the least understood aspect of the soluble polyimide precursor. However, the advent of sophisticated laser light scattering and size exclusion chromatography instrumentation has allowed elucidation of the solution behavior of poly(amic adds). In the early days of polyimide chemistry, when most molecular weight characterization was based on viscosity determinations, a decrease in viscosity was associated with molecular weight degradation [15, 28, 29]. Upon combination of the two monomers an increase in the viscosity to the stoichiometric equivalence point is observed, followed by a decrease in the solution viscosity as a... 

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