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Consider the reaction

2POCl3(g)2PCl3(g)+O2(g)

  1. Calculate ΔGofor this reaction. The ΔGR0values for 2POCl3(g)and 2PCl3(g)are \(-502kJ/mol\)and \(-270kJ/mol\), respectively.
  2. Is this reaction spontaneous under standard conditions at 298K?
  3. The value of ΔSofor this reaction is 179J/K . At what temperatures is this reaction spontaneous at standard conditions? Assume that ΔHo and ΔSodo not depend on temperature.

Short Answer

Expert verified

ΔGr°=464kJ/mol, non-spontaneous and temperature more than T=2890Kare the solutions.

Step by step solution

01

 Calculation for ∆G0 for a

In the calculation,

2POCl3(g)2PCl3(g)+O2(g)ΔGR°=2ΔGf°(PCl3(g))+1ΔGf°(O2(g))-1ΔGf°(POCl3(g))=2mol-270kJ/mol + 1mol×0kJ/mol-2mol×-502kJ/molΔGR°=464KJ

02

 Calculation for b

The chemical reaction is an example of a non-spontaneous reaction

03

 Calculation for C

ΔT°ForthereactionT>2890K

From part aΔGR0=53kJ,ΔH0=100kJ

T=(25+273)K=298K

In the calculation,

ΔHo=ΔG0+TΔSo=464kJ+(298K)(179kJ/K)=517.34kJΔH0=TΔS0=ΔH0ΔS0=1000.1577ΔH0=634K

Equilibrium at ΔG°=0

ΔH0=TΔSoT=ΔHoΔS0=517.34kJ0.179kJ/KT=2890K

04

Conclusion

Therefore, ΔGr°=464kJ/mol, non-spontaneous and temperature more thanT=2890K are the solutions.

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Most popular questions from this chapter

It is quite common for a solid to change from one structure to another at a temperature below its melting point. For example, sulphur undergoes a phase change from the rhombic crystal structure to the monoclinic crystal form at temperatures above 95°C

  1. Predict the signs of HandSfor the processSrhombicSmonoclinic
  2. Which form of sulphur has the more ordered crystalline structure (has the smaller positional probability)?

Consider the dissociation of a weak acid HA(Ka=4.5×10-3)in water:
HA(aq)H+(aq)+A-(aq)
Calculate Go for this reaction at 25°C.

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.)

Consider the system

AgBgat25oC

a. Assuming that GA=8996Jmoland localid="1649245009617" GB=11,718Jmol, calculate the value of the equilibriumconstant for this reaction.
b. Calculate the equilibrium pressures that result if 1.00 mole of Agat 1.00 atm and 1.00 mole ofBgat 1.00 atm are mixed at 25°C.
c. Show by calculations that ΔG=0at equilibrium.

128. For rubidium Hvapo=69.0kJ/molat 686°C, its boilingpoint. Calculate So,q,w,andE for the vaporization of 1.00 mole of rubidium at 686°C and 1.00 atm pressures.

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