For the given reaction, the ratio of partial pressure of water vapor to the partial pressure of hydrogen sulfide and its assumptions has to be given. Concept introduction: Standard free energy change: Standard free energy change is measured by subtracting the product of temperature and standard entropy change from the standard enthalpy change of a system. ΔG o = ΔH o - TΔS o where, ΔG o - standard free energy change ΔH o - standard enthalpy change ΔS o - standard entropy change and T - temperature . Relationship between Δ G o a n d K : The relationship between free energy change and equilibrium constant is given by ΔG o = -RTlnK where, ΔG o - standard free energy change R - gas constant T - temperature and K - equilibrium constant . To calculate: The value of P H 2 O /P H 2 S
For the given reaction, the ratio of partial pressure of water vapor to the partial pressure of hydrogen sulfide and its assumptions has to be given. Concept introduction: Standard free energy change: Standard free energy change is measured by subtracting the product of temperature and standard entropy change from the standard enthalpy change of a system. ΔG o = ΔH o - TΔS o where, ΔG o - standard free energy change ΔH o - standard enthalpy change ΔS o - standard entropy change and T - temperature . Relationship between Δ G o a n d K : The relationship between free energy change and equilibrium constant is given by ΔG o = -RTlnK where, ΔG o - standard free energy change R - gas constant T - temperature and K - equilibrium constant . To calculate: The value of P H 2 O /P H 2 S
Solution Summary: The author explains the relationship between free energy change and equilibrium constant.
For the given reaction, the ratio of partial pressure of water vapor to the partial pressure of hydrogen sulfide and its assumptions has to be given.
Concept introduction:
Standard free energy change:
Standard free energy change is measured by subtracting the product of temperature and standard entropy change from the standard enthalpy change of a system.
If we assume a system with an anodic overpotential, the variation of n as a function
of current density:
1. at low fields is linear 2. at higher fields, it follows Tafel's law
Obtain the range of current densities for which the overpotential has the same value
when calculated for 1 and 2 cases (maximum relative difference of 5% compared to
the behavior for higher fields).
To which overpotential range does this correspond?
Data: i = 1.5 mA cm², T = 300°C, B = 0.64, R = 8.314 J K1 mol-1 and F = 96485 C mol-1.
Answer by equation please
Some of the theories used to describe interface structure can be distinguished by:1. the measured potential difference.2. the distribution of ions in solution.3. the calculation of charge density.4. the external Helmoltz plane.
Chapter 18 Solutions
OWLv2 for Ebbing/Gammon's General Chemistry, 11th Edition, [Instant Access], 1 term (6 months)
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.