The free energy change, ∆ G , for a process at constant temperature and pressure is related to ∆ S univ and reflects the spontaneity of the process. How is ∆ G related to ∆ S univ ? 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 − T∆S 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?
The free energy change, ∆ G , for a process at constant temperature and pressure is related to ∆ S univ and reflects the spontaneity of the process. How is ∆ G related to ∆ S univ ? 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 − T∆S 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?
Solution Summary: The author explains the terms associated with thermodynamics, such as system, surrounding, entropy, spontaneity, and many more.
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 − T∆S 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?
Draw the product of the reaction shown below. Ignore inorganic
byproducts.
+
H
CH3CH2OH
HCI
Drawing
please explain this in simple terms
K
Most Reactive
Na
(3 pts) Can the metal activity series (shown on the right) or a
standard reduction potential table explain why potassium metal
can be prepared from the reaction of molten KCI and Na metal but
sodium metal is not prepared from the reaction of molten NaCl and
K metal? Show how (not).
Ca
Mg
Al
с
Zn
Fe
Sn
Pb
H
Cu
Ag
Au
Least Reactive
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The Laws of Thermodynamics, Entropy, and Gibbs Free Energy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=8N1BxHgsoOw;License: Standard YouTube License, CC-BY