Calculate AS,rxnthe reaction.for the following reaction. The S° for each species is shown belowC2H2(g) +2 H2(8) → C2H6(8)C2H2(g) H2(g)C2H6(8)S°(J/mol.K)200.9130.7229.2-303.3 J/K+560.8 J/K-233.1 J/K-229.2 J/K-102.4 J/K

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Answered: Calculate AS, rxn the reaction. for the…

Chemistry for Engineering Students

4th Edition

ISBN:9781337398909

Author:Lawrence S. Brown, Tom Holme

Publisher:Lawrence S. Brown, Tom Holme

Chapter10: Entropy And The Second Law Of Thermodynamics

Section: Chapter Questions

Problem 10.7PAE: On the basis of your experience, predict which of the following reactions are spontaneous. (a)...

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For the reaction C2H2(g)+4F2(g)2CF4(g)+H2(g) S is equal to 358 J/K. Use this value and data from Appendix 4 to calculate the value of S for CF4(g).
For the reaction NO(g)+NO2(g)N2O3(g) , use tabulated thermodynamic data to calculate H and S. Then use those values to answer the following questions. (a) Is this reaction spontaneous at 25°C? Explain your answer. (b) If the reaction is not spontaneous at 25°C, will it become spontaneous at higher temperatures or lower temperatures? (c) To show that your prediction is accurate, choose a temperature that corresponds to your prediction in part (b) and calculate G . (Assume that both enthalpy and entropy are independent of temperature.)
9.96 Most first aid "cold packs" are based on the endothermic dissolution of ammonium nitrate in water: NH4NO3(s)NH4+(aq)+NO3(aq) H= 25.69 kJ A particular cold pack contains 50.0 g of NH4NO3 and 125.0 g of water. When the pack is squeezed, the NH4NO3dissolves in the water. If the pack and its contents are initially at 24.0°C, what is the lowest temperature that this bag could reach? (Assume that the ammonium nitrate solution has a specific heat of 4.25J g-l K-l, and that the heat capacity of the bag itself is small enough to be neglected.)
Given the following information at 25C, calculate G at 25C for the reaction 2A(g)+B(g)3C(g) Substance Hf(kJ/mol) S(J/molK) A(g) 191 244 B(g) 70.8 300 C(g) 197 164 a 956 kJ b 956 kJ c 346 kJ d 346 kJ e 1.03 103 kJ
Thermodynamics provides a way to interpret everyday occurrences. If you live in northern climates, one common experience is that during early winter, snow falls but then melts when it hits the ground. Both the formation and the melting happen spontaneously. How can thermodynamics explain both of these seemingly opposed events?
For the reaction at 298 K, 2NO2(g)N2O4(g) the values of H and S are 58.03 kJ and 176.6 J/K, respectively. What is the value of G at 298 K? Assuming that H and S do not depend on temperature, at what temperature is G = 0? Is G negative above or below this temperature?
For the reaction TiCl2(s) + Cl2(g) TiCl4(), rG = 272.8 kj/mol-txn. Using this value and other data available in Appendix L, calculate the value of fG for TiCl2(s).
The free energy change, G, for a process at constant temperature and pressure is related to Suniv and reflects the spontaneity of the process. How is G related to Suniv? When is a process spontaneous? Nonspontaneous? At equilibrium? G is a composite term composed of H, T, and S. What is the G equation? Give the four possible sign combinations for H and S. What temperatures are required for each sign combination to yield a spontaneous process? If G is positive, what does it say about the reverse process? How does the G = H TS equation reduce when at the melting-point temperature of a solid-to-liquid phase change or at the boiling-point temperature of a liquid-to-gas phase change? What is the sign of G for the solid-to-liquid phase change at temperatures above the freezing point? What is the sign of G for the liquid-to-gas phase change at temperatures below the boiling point?
When solid sodium acetate crystallizes from a supersaturated solution, can you accurately predict the sign of H for the crystallization? Why or why not?
Consider the system shown in Figure 16.9. What is the change in entropy for the process where the energy is initially associated with particles A and B, and the energy is distributed between two particles in different boxes (one in A-B, the other in C-D)?
The decomposition of diamond to graphite [C(diamond) C(graphite)] is thermodynamically favored, but occurs slowly at room temperature. a. Use fG values from Appendix L to calculate rG and Keq for the reaction under standard conditions and 298.15 K. b. Use fH and S values from Appendix L to estimate rG and Keq for the reaction at 1000 K. Assume that enthalpy and entropy values are valid at these temperatures. Does heating shift the equilibrium toward the formation of diamond or graphite? c. Why is the formation of diamond favored at high pressures? d. The phase diagram shows that diamond is thermodynamically favored over graphite at 20,000 atmospheres pressure (about 2 GPa) at room temperature. Why is this conversion actually done at much higher temperatures and pressures?
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Calculate AS, rxn the reaction. for the following reaction. The S° for each species is shown below C2H2(g) +2 H2(8) → C2H6(8) C2H2(g) H2(g) C2H6(8) S°(J/mol.K) 200.9 130.7 229.2 -303.3 J/K +560.8 J/K -233.1 J/K -229.2 J/K -102.4 J/K