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Ch.18 - Thermodynamics: Entropy, Free Energy & Equilibrium
Chapter 18, Problem 106

What is the relationship between the free-energy change under nonstandard-state conditions, ∆G, the free-energy change under standard-state conditions, ∆G°, and the reaction quotient, Q?

Verified step by step guidance
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Step 1: Understand the concept of free energy change (∆G) in a chemical reaction, which indicates the spontaneity of the reaction. A negative ∆G means the reaction is spontaneous, while a positive ∆G means it is non-spontaneous.
Step 2: Recognize that ∆G° is the free energy change under standard-state conditions, which are typically 1 atm pressure for gases, 1 M concentration for solutions, and pure solids or liquids for other phases at a specified temperature (usually 298 K).
Step 3: Learn about the reaction quotient, Q, which is a measure of the relative amounts of products and reactants present during a reaction at a given point in time. It is calculated using the same expression as the equilibrium constant, K, but for non-equilibrium conditions.
Step 4: Use the relationship between ∆G, ∆G°, and Q, which is given by the equation: ∆G = ∆G° + RT ln(Q), where R is the universal gas constant (8.314 J/mol·K) and T is the temperature in Kelvin.
Step 5: Analyze how this equation shows that the free energy change under nonstandard conditions (∆G) depends on both the standard free energy change (∆G°) and the reaction quotient (Q). When Q = 1, ∆G = ∆G°. When Q < K, ∆G is negative, indicating the reaction will proceed forward. When Q > K, ∆G is positive, indicating the reaction will proceed in reverse.
Related Practice
Textbook Question
Use the values of of ∆G°f in Appendix B to calculate the stan-dard free-energy change for the synthesis of dichloroethane from ethylene and chlorine: C2H41g2 + Cl21g2S CH2ClCH2Cl1l2 Is it possible to synthesize dichloroethane from gaseous C2H4 and Cl2, each at 25 °C and 1 atm pressure?
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Textbook Question
Ethanol is manufactured in industry by the hydration of ethylene: Using the data in Appendix B, calculate ∆G° and show that this reaction is spontaneous at 25 °C. Why does this reaction become nonspontaneous at higher temperatures? Estimate the temperature at which the reaction becomes nonspontaneous.
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Textbook Question
Consider the conversion of 1,2-dichloroethane to vinyl chloride, the starting material for manufacturing poly(vinyl chloride) (PVC) plastics: Is this reaction spontaneous under standard-state conditions? Would it help to carry out the reaction in the presence of base to remove HCl? Explain. Is it possible to synthesize vinyl chlo-ride from graphite, gaseous H2, and gaseous Cl2 at 25 °C and 1 atm pressure?
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Textbook Question
Compare the values of ∆G and ∆G° when: (a) Q < 1. (b) Q = 1. (c) Q > 1. Does the thermodynamic tendency for the reaction to occur increase or decrease as Q increases?
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Textbook Question
Use the data in Appendix B to calculate ∆G for the decom-position of nitrosyl chloride at 25 °C when the partial pressures are 2.00 atm of NOCl, 1.00 * 10^-3 atm of NO, and 1.00 * 10^-3 atm of Cl2: Is the reaction spontaneous in the forward or the reverse direction under these conditions?
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Textbook Question
Urea (NH2CONH2), an important nitrogen fertilizer, is produced industrially by the reaction Given that ∆G° = -13.6 kJ, calculate ∆G at 25 °C for the following sets of conditions. . (a) 10 atm NH3, 10 atm CO2, 1.0 M NH2CONH2 (b) 0.10 atm NH3, 0.10 atm CO2, 1.0 M NH2CONH2 Is the reaction spontaneous for the conditions in part (a) and/or part (b)?
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