Skip to main content
Ch.18 - Thermodynamics: Entropy, Free Energy & Equilibrium
Chapter 18, Problem 107

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?

Verified Solution

Video duration:
2m
This video solution was recommended by our tutors as helpful for the problem above.
Was this helpful?

Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Gibbs Free Energy (∆G)

Gibbs Free Energy (∆G) is a thermodynamic potential that measures the maximum reversible work obtainable from a thermodynamic process at constant temperature and pressure. It indicates the spontaneity of a reaction: if ∆G is negative, the reaction is spontaneous; if positive, it is non-spontaneous. The value of ∆G changes based on the reaction's conditions, including the concentrations of reactants and products.
Recommended video:
Guided course
01:51
Gibbs Free Energy of Reactions

Standard Gibbs Free Energy Change (∆G°)

Standard Gibbs Free Energy Change (∆G°) refers to the change in Gibbs Free Energy under standard conditions (1 bar pressure, 1 M concentration for solutes, and a specified temperature, usually 298 K). It provides a reference point for predicting the direction of a reaction. Unlike ∆G, which varies with the reaction's progress, ∆G° remains constant for a given reaction at specified conditions.
Recommended video:
Guided course
00:32
Standard Gibbs Free Energy and Temperature

Reaction Quotient (Q)

The Reaction Quotient (Q) is a dimensionless number that reflects the ratio of the concentrations of products to reactants at any point in a reaction. It is used to determine the direction in which a reaction will proceed to reach equilibrium. When Q < 1, the reaction favors products; when Q = 1, the system is at equilibrium; and when Q > 1, the reaction favors reactants, indicating that as Q increases, the tendency for the reaction to occur decreases.
Recommended video:
Guided course
00:49
Reaction Quotient Q
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?
396
views
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.
612
views
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?
501
views
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?
327
views
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)?
2195
views
Textbook Question
Ammonium nitrate is dangerous because it decomposes (sometimes explosively) when heated: (a) Using the data in Appendix B, show that this reaction is spontaneous at 25 °C.
334
views