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Enthalpy values for the

Using these data and the enthalpy value for the reaction... [Pg.549]

Drago and coworkers have also calculated the enthalpy values for the formation of many complexes or hydrogen bonds by NMR and calorimetric techniques. For example, in a series of phenols or t-BuOH, they observed the IR frequency shifts (Avqh) of the hydroxyl compounds and found that a linear relationship exists between bases and individual acids. In Table 7 shows some AH values calculated by equation 2, and Avqh values of t-BuOH" " while in Table 8 frequency data Avq of various substituted phenols and the AH values are given. [Pg.549]

Vanadium forms numerous oxides, the most important of which are vanadium monoxide, vanadium sesquioxide, vanadium dioxide and vanadium pentoxide. In the earlier examples (e.g., oxides of chromium and of niobium) the enthalpy values for the aluminothermic reduction of each of the oxides was given for the purpose of illustration. Normally, the consideration can be restricted to only those oxides which are readily obtained and which can be handled freely without any special or cumbersome precautions. In the case of vanadium for example, it is sufficient to consider the reduction of the sesquioxide (V203) and the pentoxide (V2Os). The pertinent reactions are ... [Pg.395]

Practically, all the hydrocarbons have BDE of C—H bonds higher than 300 kJ mol-1, and this method of calculation can be used for them. The enthalpy of reaction was calculated as AH= D(R—H)—220 (kJ mol-1). The weakest bonds participate in this reaction. The pre-exponential factor depends on the reaction enthalpy value for the reactions with high enthalpy [18]. [Pg.167]

In the first case, where the repressor protein is cut in half, the binding enthalpy for each part would be essentially half the enthalpy value for the intact repressor. The entropy would be less favorable (less positive) because of the chelation effect. As a result, the free energy would be less favorable (less negative). [Pg.888]

K. Using the enthalpy value for the liquid at the melting point as determined by Treverton and Margrave ( ) and the enthalpy value of the crystal at the melting point as determined by our adopted functions, we calculate A, H 7.264... [Pg.1510]

Steps 8 and 9 (Continued) Enthalpy data have been taken from Table 4.3. The heat of reaction at 25°C (77°F) and 1 atm from Example 4.31 after conversion of units is — 121,672 Btu/lb mol of CO. We can assume that the slightly higher pressure than SC of 2 atm has no effect on the heat of reaction or the enthalpy values. Figure E4.40b shows the sensible heat (enthalpy) values for the entering and exiting materials. [Pg.462]

The adiabatic cooling lines are lines of almost constant enthalpy for the entering air-water mixture, and you can use them as such without much error (1 or 2%). However, if you want to correct a saturated enthalpy value for the deviation which exists for a less-than-saturated air-water vapor mixture, you can employ the enthalpy deviation lines which appear on the chart and which can be used as illustrated in the examples below. Any process that is not a wet-bulb process or an adiabatic process with recirculated water can be treated by the usual material and energy balances, taking the basic data for the calculation from the humidity charts. If there is any increase or decrease in the moisture content of the air in a psychrometric process, the small enthalpy effect of the moisture added to the air or lost by the air may be included in the energy balance for the process to make it more exact as illustrated in Examples 4.47 and 4.49. [Pg.487]

The convention of arbitrarily assigning a zero enthalpy value for the most stable form of each element in the standard state of 25°C is a convenient way of dealing with enthalpies of reactions. Explain why this convention cannot be applied to nuclear reactions. [Pg.235]

Several complexes of cuprous halides with acrylonitrile 69> and acrolein 70> have been investigated. The enthalpies of complexing have been found from vapour pressure measurements the enthalpy of formation of the complex from solid copper chloride and liquid acrylonitrile was -29.3 kJ mole-1, while with copper bromide this was -1.3 kJ mole-1. The corresponding value for the acrolein complex was -17.3 kJ mole-1 the enthalpy values for the formation from the gaseous olefinic compounds were -62.3, -34.3 and -49.2 kJ mole-1 respectively. [Pg.103]

Table V-33 Experimental reaction enthalpy values for the formation of Ni(II)-thiocyanate complexes. Table V-33 Experimental reaction enthalpy values for the formation of Ni(II)-thiocyanate complexes.
Table V-32 Experimental equilibrium data for the Ni(ll) - thiocyanate system. .. 233 Table V-33 Experimental reaction enthalpy values for the formation... Table V-32 Experimental equilibrium data for the Ni(ll) - thiocyanate system. .. 233 Table V-33 Experimental reaction enthalpy values for the formation...
Table 7.4 Approximate enthalpy values for the formation and movement of vacancies in alkali halide crystals... Table 7.4 Approximate enthalpy values for the formation and movement of vacancies in alkali halide crystals...
A comparison of enthalpy values for the LE/LC phase transition of both acids at equivalent temperatures above T (17.9°C for TCDA and 29.0°C for PCDA) using a modified two dimensional analog of the Qapeyron equation ... [Pg.703]

Strategy We basically follow the same procedure as that in Example 9.13. Note, however, that H2O is a polyatomic molecule, and so we need to use the average bond enthalpy value for the O—H bond. [Pg.398]


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