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Consider1.00moleofCO2(g)at300Kand5.00atm.The gas expands until the final pressure is1.00atm. For each of the following conditions describing the expansion, calculateΔS,ΔSsurr,andΔSuniv.CpforCO2is37.1JK-1mol-1, and assume that the gas behaves ideally.

  1. The expansion occurs isothermally and reversibly.
  2. The expansion occurs isothermally against a constant external pressure of1.00atm
  3. The expansion occurs adiabatically and reversibly

Short Answer

Expert verified

a.ΔSuniv=0ΔSsys=13.4 J/KΔSsurr=13.4 J/K

b.ΔSuniv=6.77  J/KΔSsys=13.4 J/KΔSsurr=6.63 J/K

c.

ΔSuniv=0ΔSsys=0ΔSsurr=0

Step by step solution

01

Definition of isothermal expansion

Isothermal expansion is defined as keeping the gas at a constant temperature.

02

Calculations

a.ΔSuniv=0(reversible)

role="math" localid="1663759404643" ΔSsys=nRlnP1P2ΔSsys=1.00mol×8.314 J/mol×ln5.001.00ΔSsys=13.4 J/KΔSuniv=ΔSsys+ΔSsurrΔSsurr=ΔSsysΔSsurr=13.4 J/K

b.ΔSsys=13.4 J/KVi=4.92 LVf=24.6 L

q=PexΔVq=1990 JΔSsurr=6.63 J/KΔSuniv=ΔSsys+ΔSsurr              =13.46.63ΔSuniv=6.77 J/K

c.

ΔSuniv=0qrev=0ΔSsys=0ΔSsurr=-qactualTΔSsurr=0

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Most popular questions from this chapter

Question: Consider the following reaction at

N2(g)+3F2(g)2NF3

An equilibrium mixture contains the following partial pressures

PN2=0.021atm,PF2=0.063atm,andPNF3=0.48atm.

Calculate ΔGofor the reaction at 800 K.

Consider the reaction

2NO2(g)N2O4(g)

For each of the mixtures of reactants andproducts at 25°C, predict the direction in which the reaction will shift to reach equilibrium. Use thermodynamic data in Appendix 4.

  1. PNO2=PN2O4=1.0atm
  2. PNO2=0.21atm,PN2O4=0.50atm
  3. PNO2=0.29atm,PN2O4=1.6atm

Impure nickel, refined by smelting sulfide ores in a blast furnace, can be converted into metal from 99.90% to 99.99% purity by the Mond process. The primary reaction involved in the Mond process is
Ni(s)+4CO(g)Ni(CO)4(g)
a. Without referring to Appendix 4, predict the sign ofS° for the preceding reaction. Explain.
b. The spontaneity of the preceding reaction is temperature-dependent. Predict the sign of SSUIT for this reaction. Explain.
c. For, Ni(CO)4(g),Ht°=-607kj/moland S°=417J-1mol-1 at 298 K. Using these values and data in Appendix 4, calculate H°andS° for the preceding reaction.
d. Calculate the temperature at which G°=0(K=1) for the preceding reaction, assuming that H°andS° do not depend on temperature.
e. The first step of the Mond process involves equilibrating impure nickel with COgandNiCO4gatabout 50°C. The purpose of this step is to convert as much nickel as possible into the gas phase. Calculate the equilibrium constant for the preceding reaction at 50.°C.
f. In the second step of the Mond process, the gaseousNiCO4g is isolated and heated at 227°C. The purpose of this step is to deposit as much nickel as possible as pure solid (the reverse of the preceding reaction). Calculate the equilibrium constant for the preceding reaction at 227°C.
g. Why is temperature increased for the second step of the Mond process?

h. The Mond process relies on the volatility of NiCO4 for its success. Only pressures and temperatures at which NiCO4, is a gas are useful. A recently developed variation of the Mond process carries out the first step at higher pressures and a temperature of 152°C. Estimate the maximum pressure of NiCO4gthat can be attained before the gas will liquefy at 152°C. The boiling point for NiCO4is 42°C, and the enthalpy of vaporization is29.0kJ/mol . (Hint: The phase-change reaction and the corresponding equilibrium expression are
NiCO4INiCO4gK=PNiCO4
NiCO4gwill liquefy when the pressure of role="math" NiCO4is greater than the K value.)

Given the following data:

2C6H6(l)+15O2(g)12CO2(g)+6H2O(l)C(s)+O2(g)CO2(g)H2(g)+12O2(g)H2O(l)

Calculate ΔGo for the reaction 6C(s)+3H2(g)C6H6(l)

ΔGo=-6399kJΔGo=-394kJΔGo-237kJd

The equilibrium constant K for the reaction

2Cl(g)Cl2(g)

was measured as a function of temperature (in Kelvins). A graph of In( ) versus 1T for this reaction gives a straight line with a slope of 1.352×104K and y intercept of -14.51. Determine the value of ΔHoand ΔSofor this reaction. (See Exercise 88)

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