Physical Chemistry
2nd Edition
ISBN: 9781133958437
Author: Ball, David W. (david Warren), BAER, Tomas
Publisher: Wadsworth Cengage Learning,
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Chapter 4, Problem 4.64E
Interpretation Introduction
Interpretation:
The value of
Concept introduction:
The chemical potential is the energy absorbed or released in a
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Under what conditions will the quantities q and w be negative numbers?
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P2D.2 Starting from the expression Cp − CV = T(∂p/∂T)V(∂V/∂T)p, use theappropriate relations between partial derivatives (The chemist’s toolkit 9 inTopic 2A) to show thatC CT V TV p( / )( / ) p VpT2− = ∂ ∂∂ ∂
Use this expression to evaluate Cp − CV for a perfect gas.
Chapter 4 Solutions
Physical Chemistry
Ch. 4 - List the sets of conditions that allow dS, dU, and...Ch. 4 - Explain why conditions for using S>0 as a strict...Ch. 4 - Explain how the equation dU+pdVTdS0 is consistent...Ch. 4 - Explain why the spontaneity conditions given in...Ch. 4 - Prove that the adiabatic free expansion of an...Ch. 4 - Derive equation 4.6 from equation 4.5.Ch. 4 - Derive equation 4.8 from equation 4.7.Ch. 4 - The third part of equation 4.9 mentions a...Ch. 4 - Calculate A for a process in which 0.160mole of an...Ch. 4 - What is the maximum amount of non-pV work that can...
Ch. 4 - Consider a piston whose compression ratio is 10:1;...Ch. 4 - When one dives, water pressure increases by 1atm...Ch. 4 - Calculate G(25C) for this chemical reaction, which...Ch. 4 - Thermodynamic properties can also be determined...Ch. 4 - Calculate G in two different ways for the...Ch. 4 - Calculate G in two different ways for the...Ch. 4 - For the reaction C(graphite)C(diamond) at 25C,...Ch. 4 - Determine G for the following reaction at 0C and...Ch. 4 - What is the maximum amount of electrical that is,...Ch. 4 - When a person performs work, it is non-pV work....Ch. 4 - Can non-pV work be obtained from a process for...Ch. 4 - Can pV work be obtained from a process for which...Ch. 4 - Batteries are chemical systems that can be used to...Ch. 4 - The value of G for any phase change at constant p...Ch. 4 - The value of G for any phase change at constant p...Ch. 4 - Under what conditions is A=0 for a phase change?...Ch. 4 - Example 4.2 calculated A for one step of a Carnot...Ch. 4 - Can CV and Cp be easily defined using the natural...Ch. 4 - Analogous to equation 4.26, what is the expression...Ch. 4 - Prob. 4.30ECh. 4 - Prob. 4.31ECh. 4 - Prob. 4.32ECh. 4 - Although ideally, U=H=0 for a gas-phase process at...Ch. 4 - Use equations 4.21 and 4.25 to explain why H and G...Ch. 4 - Prob. 4.35ECh. 4 - Which of the following functions are exact...Ch. 4 - Prob. 4.37ECh. 4 - Prob. 4.38ECh. 4 - Prob. 4.39ECh. 4 - Equation 4.19 says that (UV)S=p If we are...Ch. 4 - For an isentropic process, what is the approximate...Ch. 4 - Use the ideal gas law to demonstrate the cyclic...Ch. 4 - Prob. 4.43ECh. 4 - Prob. 4.44ECh. 4 - Evaluate (U/V)T for an ideal gas. Use the...Ch. 4 - Evaluate (U/V)T for a van der Waals gas. Use the...Ch. 4 - Repeat the previous exercise for a gas that...Ch. 4 - Determine an expression for (p/S)T for an ideal...Ch. 4 - Determine the value of the derivative {[(G)]/T}p...Ch. 4 - Prob. 4.50ECh. 4 - Prob. 4.51ECh. 4 - A 0.988-mole sample of argon expands from 25.0L to...Ch. 4 - A 3.66-mol sample of He contracts from 15.5L to...Ch. 4 - Prob. 4.54ECh. 4 - Prob. 4.55ECh. 4 - Use the Gibbs-Helmholtz equation to demonstrate...Ch. 4 - For the equation 2H2(g)+O2(g)2H2O(g)...Ch. 4 - Use equation 4.46 as an example and find an...Ch. 4 - What is the value of G when 1.00mol of water at...Ch. 4 - Prob. 4.60ECh. 4 - Prob. 4.61ECh. 4 - Prob. 4.62ECh. 4 - Prob. 4.63ECh. 4 - Prob. 4.64ECh. 4 - What is the change in the chemical potential of a...Ch. 4 - Prob. 4.66ECh. 4 - Prob. 4.67ECh. 4 - Prob. 4.68ECh. 4 - Prob. 4.69ECh. 4 - Can equation 4.62 be used to calculate for an...Ch. 4 - Prob. 4.71ECh. 4 - Of helium and oxygen gases, which one do you...Ch. 4 - Prob. 4.73ECh. 4 - Use equation 4.39 to determine a numerical value...Ch. 4 - Prob. 4.75ECh. 4 - Prob. 4.76E
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- Under what conditions will U be exactly zero for a process whose initial conditions are not thesame as its final conditions?arrow_forwardWith regard to exercise 2.50, how accurate do you think your answer is, and why?arrow_forwardUse the data in Table 2.2 to determine PH T for N2 at 50C and 20atm. Make any reasonable assumptions necessary.arrow_forward
- Physical Chemistry Plot the Pxy for the following systems at 90 degrees celsius:a. Benzene(1)/ethylbenzene(2)b. 1-chlorobutane(1)/chlorobenzene(2)arrow_forwardA 0.250 mol nitrogen initially at 50 °C with a volume of 8.00 L is allowed to expand reversibly and adiabatically until its volume has doubled. Calculate the value of ΔH when Cp = 7/2Rarrow_forwardSketch two plot of pressure (p) vs. volume (V): one for irreversible expansion and one for reversible expansion. Is the work in each case the same? Explain why or why not.arrow_forward
- Since we will be dealing with partial derivatives later in the semester, this is a good opportunity to review this topic (see appendix C). Then evaluate the following partial derivatives (a) PV = nRT; (∂ P/∂V)T (b) r = (x2 + y2 + z 2 )1/2; (∂ r/∂y)x,zarrow_forwardA 0.250 mol nitrogen initially at 50 °C with a volume of 8.00 L is allowed to expand reversibly and adiabatically until its volume has doubled. Calculate the value of ΔHwhen Cp = 7/2R.arrow_forwardAbsolute zero is _____________________ K.arrow_forward
- Why is equation2.37 written interms of CV and Cp and not c-v and c-p ?arrow_forwardDescribe why it is easier to use Gto determine the spontaneity of a process rather than S uarrow_forwardDetermine an expression for V/T p, n in terms of and . Does the sign on the expression make sense in terms of what you know happens to volume as temperature changes?arrow_forward
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