Stoichiometry moles

See also Molal Concentration Molar Concentration Mole (Stoichiometry) Mole Fraction and Mole Volume,... 

See also Denial Solution Gram-Equivalent Gram-Molecular Weight Molal Concentration Molar Concentration Mole Fraction Mole (Stoichiometry) Mnle Volume and Normal Concentration. 

Mole-to-Mole Stoichiometry One disadvantage of burning propane (CsHg) is that carbon dioxide (CO2) is one of the products. The reieased carbon dioxide increases the concentration of CO2 in the atmosphere. How many moies of CO2 is produced when 10.0 moi of C3H8 is burned in excess oxygen in a gas griii ... 

Techniques responding to the absolute amount of analyte are called total analysis techniques. Historically, most early analytical methods used total analysis techniques, hence they are often referred to as classical techniques. Mass, volume, and charge are the most common signals for total analysis techniques, and the corresponding techniques are gravimetry (Chapter 8), titrimetry (Chapter 9), and coulometry (Chapter 11). With a few exceptions, the signal in a total analysis technique results from one or more chemical reactions involving the analyte. These reactions may involve any combination of precipitation, acid-base, complexation, or redox chemistry. The stoichiometry of each reaction, however, must be known to solve equation 3.1 for the moles of analyte. 

Knowing the stoichiometry of the titration reaction(s), we can calculate the moles of analyte. 

Almost any chemical reaction can serve as a titrimetric method provided that three conditions are met. The first condition is that all reactions involving the titrant and analyte must be of known stoichiometry. If this is not the case, then the moles of titrant used in reaching the end point cannot tell us how much analyte is in our sample. Second, the titration reaction must occur rapidly. If we add titrant at a rate that is faster than the reaction s rate, then the end point will exceed the equivalence point by a significant amount. Finally, a suitable method must be available for determining the end point with an acceptable level of accuracy. These are significant limitations and, for this reason, several titration strategies are commonly used. 

Where Is the Equivalence Point In discussing acid-base titrations and com-plexometric titrations, we noted that the equivalence point is almost identical with the inflection point located in the sharply rising part of the titration curve. If you look back at Figures 9.8 and 9.28, you will see that for acid-base and com-plexometric titrations the inflection point is also in the middle of the titration curve s sharp rise (we call this a symmetrical equivalence point). This makes it relatively easy to find the equivalence point when you sketch these titration curves. When the stoichiometry of a redox titration is symmetrical (one mole analyte per mole of titrant), then the equivalence point also is symmetrical. If the stoichiometry is not symmetrical, then the equivalence point will lie closer to the top or bottom of the titration curve s sharp rise. In this case the equivalence point is said to be asymmetrical. Example 9.12 shows how to calculate the equivalence point potential in this situation. 

A procedure for determining the stoichiometry between two reactants by preparing solutions containing different mole fractions of one reactant also known as Job s method. 

Mole-ratio plots used to determine the stoichiometry of a metal-ligand complexation reaction. 

Both the method of continuous variations and the mole-ratio method rely on an extrapolation of absorbance data collected under conditions in which a linear relationship exists between absorbance and the relative amounts of metal and ligand. When a metal-ligand complex is very weak, a plot of absorbance versus Ay or n-J m may be curved, making it impossible to determine the stoichiometry by extrapolation. In this case the slope ratio may be used. 

This experiment describes the use of FIA for determining the stoichiometry of the Fe +-o-phenanthroline complex using the method of continuous variations and the mole-ratio method. Directions are also provided for determining the stoichiometry of the oxidation of ascorbic acid by dichromate and for determining the rate constant for the reaction at different pH levels and different concentration ratios of the reactants. 

The essential information implied by the chemical equation is the stoichiometry at the macroscopic level, ie, if a moles of M react, then b moles of B do also p moles of P are formed, etc. No inference should be made about behavior at the microscopic or atomic level, ie, there is no implication thatp molecules of P appear simultaneously. There may or may not be intermediates that appear and disappear in the course of the reaction. 

Some moisture must be present to promote these reactions. Dry carbon dioxide does not react with the superoxides. One mole of MO2 yields 1.5 mol oxygen and then absorbs one mole of carbon dioxide to form carbonate, or two moles to form bicarbonate. Thus, if only carbonate is formed, an RQ of 0.67 is reached if only bicarbonate is formed, an RQ of 1.33 results. The required stoichiometry for an RQ of 0.82 is. 

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). 

Methanol synthesis will be used many times as an example to explain some concepts, largely because the stoichiometry of methanol synthesis is simple. The physical properties of all compounds are well known, details of many competing technologies have been published and methanol is an important industrial chemical. In addition to its relative simplicity, methanol synthesis offers an opportunity to show how to handle reversible reactions, the change in mole numbers, removal of reaction heat, and other engineering problems. 

Since the volume depends on conversion or time in a constant pressure batch reactor, consider the mole balance in relation to the fractional conversion X. From the stoichiometry. 

The fixation of carbon dioxide to form hexose, the dark reactions of photosynthesis, requires considerable energy. The overall stoichiometry of this process (Eq. 22.3) involves 12 NADPH and 18 ATP. To generate 12 equivalents of NADPH necessitates the consumption of 48 Einsteins of light, minimally 170 kj each. However, if the preceding ratio of l ATP per NADPH were correct, insufficient ATP for COg fixation would be produced. Six additional Einsteins would provide the necessary two additional ATP. Prom 54 Einsteins, or 9180 kJ, one mole of hexose would be synthesized. The standard free energy change, AG°, for hexose formation from carbon dioxide and water (the exact reverse of cellular respiration) is +2870 kj/mol. 

Stoichiometry in Reactive Systems. The use of molar units is preferred in chemical process calculations since the stoichiometry of a chemical reaction is always interpreted in terms of the number of molecules or number of moles. A stoichiometric equation is a balanced representation that indicates the relative proportions in which the reactants and products partake in a given reaction. For example, the following stoichiometric equation represents the combustion of propane in oxygen ... 

Strategy First (1), write the chemical equation for the reaction that occurs when strong acid or base is added. Then (2), apply the principles of stoichiometry to find the numbers of moles of weak acid and weak base remaining after reaction. Finally (3), apply the relation [H+] = X mhb/mb to find [H+] and then the pH. 

Strategy Part (a) is essentially a stoichiometry problem of the type discussed in Chapter 4. For parts (b) and (c), start by calculating (1) the number of moles of OH added and then (2) the number of moles of H+ or OH- in excess. Finally, calculate (3) [H+] and pH. Remember to use the total volume of the solution at that point... 

From the reaction stoichiometry, for each mole of acetic acid one mole of oxygen was used. So the equal molar oxygen consumption is ... 

The absolute rate constants for attack of carbon-centered radicals on p-benzoquinone (38) and other quinones have been determined to be in the range I0M08 M 1 s 1.1 -04 This rate shows a strong dependence on the electrophilicity of the attacking radical and there is some correlation between the efficiency of various quinones as inhibitors of polymerization and the redox potential of the quinone. The complexity of the mechanism means that the stoichiometry of inhibition by these compounds is often not straightforward. Measurements of moles of inhibitor consumed for each chain terminated for common inhibitors of this class give values in the range 0.05-2.0.176... 

P the total pressure, aHj the mole fraction of hydrogen in the gas phase, and vHj the stoichiometric coefficient of hydrogen. It is assumed that the hydrogen concentration at the catalyst surface is in equilibrium with the hydrogen concentration in the liquid and is related to this through a Freundlich isotherm with the exponent a. The quantity Hj is related to co by stoichiometry, and Eg and Ag are related to - co because the reaction is accompanied by reduction of the gas-phase volume. The corresponding relationships are introduced into Eqs. (7)-(9), and these equations are solved by analog computation. 

The a—time curves for the oxidation reactions [60] of both nickel maleate (534—568 K) and nickel fumarate (548—583 K) were similar to those characteristic of each reactant in vacuum, though E values were reduced to 150 10 kJ mole-1. It was concluded that the distributions of nucleation sites and subsequent patterns of product development were little altered by the change in composition of product from Ni/C (and Ni3C) to NiO. This difference, however, significantly changed the temperature coefficient and stoichiometry of the interface processes, since all carbonaceous material in the reactants was converted to CO2. A constant value of E (150 kJ mole-1) was thus found for the oxidations of the four nickel salts studied [60], the maleate, fumarate, formate and malonate. 

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