2H6 g( ) . - Department of Chemistry at Illinois State University

Chemistry 360
Dr. Jean M. Standard
Spring 2015
March 18, 2015
Name __________________________________
Exam 2 – 100 points
Note: You must show your work on problems in order to receive full credit for any answers. You must turn in
your equation sheet along with this exam in order to receive full credit for the exam. Please turn off cell phones
and store them during the exam.
1.) (14 points) Using the values in the table below reported at 25°C, determine ΔGR! at 300ºC for the
hydrogenation of acetylene to ethane,
C2 H 2 ( g) + 2 H 2 (g) → C2 H 6 (g) .
ΔH !f (kJ/mol)
C2H2 (g)
C2H6 (g)
H2 (g)
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ΔG !f (kJ/mol)
227.4
209.2
–84.0
–32.0
0
0
2
2.) (14 points) Consider a classroom that is 5 m × 10 m × 3 m in size. Initially, the temperature in the room is
20°C and the pressure is 1 bar. There are 20 people in the class. Each person gives off heat to the room at an
average rate of 150 Watts [1 Watt = 1 Joule/second]. Assume that the walls, ceiling, floor, and furniture are
perfectly insulating and do not absorb any heat; that is, all the heat from the people in the classroom is absorbed
by the air in the room.
a.) Determine the heat (in Joules) required to raise the room temperature to 37°C. Assume that the pressure
remains constant at 1 bar, the air behaves ideally, and the molar constant pressure heat capacity of air is
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C p,m = R .
2
b.) How long in minutes will it take for the air in the classroom to reach 37°C?
c.)
Determine the change in entropy (in J/K) of the air in the classroom.
3
3.) (14 points) Consider the following standard molar entropies at 298 K.
!
Sm
(J/molK)
Compound
CO (g)
CO2 (g)
C2H4 (g)
C2H6 (g)
197.7
213.8
€
219.3
229.2
Explain why we are able to obtain absolute molar entropies of substances; that is, what is the theoretical
foundation that allows the determination of absolute molar entropies? Discuss and explain any trends observed
in the molar entropies of the substances given in the table above.
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4.) (15 points) True/false, short answer, multiple choice.
a.) True or False: The reaction 2 H 2 (g) + O 2 (g) → 2 H 2O ( ℓ) is an example of a formation reaction.
b.) True or False: In the statistical definition of entropy, S = kB lnW , the quantity W corresponds to the
energy.
c.) Short answer
The _______________________________
equals H − TS .
d.) Short answer
The ____________________________________ states that that ΔS ≥ 0 for an isolated system.
e.) Multiple Choice: A spontaneous process at constant temperature and pressure must have:
1) ΔU < 0 .
2) ΔH < 0 .
3) ΔA < 0 .
4) ΔG < 0 .
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5.) (14 points) Determine ΔS for the isothermal compression at 300 K from 100 L to 10 L of two moles of a real
gas obeying the equation of state given by
€
Z = 1 + B
,
Vm
where Z is the compression factor and B is a constant. Assume that B = −0.122 L/mol .
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6
6.) (14 points) The standard molar enthalpy of combustion of graphite is
molar enthalpy of combustion of C2H2 (g) is
ΔH R!
ΔH R!
= − 393.51 kJ/mol and the standard
= −1299.58 kJ/mol , both at 298 K. Use this information,
along with the standard molar enthalpy changes for the following reactions at 298 K,
(1)
CaC 2 (s) +
(2)
Ca (s)
(3)
CaO (s)
2 H 2O (ℓ)
1
2
+
+
O 2 (g)
H 2O (ℓ)
→
→
→
Ca(OH) 2 (s)
+ C 2 H 2 (g)
CaO (s)
Ca(OH) 2 (s)
to determine the standard molar enthalpy of formation of CaC2 (s) at 298 K.
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ΔH 1" = − 127.9 kJ/mol
ΔH 2" = − 635.1 kJ/mol
ΔH 3" =
− 65.2 kJ/mol ,
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7.) (15 points) True/false, short answer, multiple choice.
a.) True or False: For the reaction 2 CO (g) + O2 (g) → 2 CO2 (g), the entropy change is expected to be
negative.
!∂ G $
b.) True or False: The expression – #
& is equal to the volume V.
" ∂ P %T
c.) Short answer
The ______________________________ is equivalent to the isothermal work under reversible
conditions.
d.) Short answer
The differential dH = T dS + V dP corresponds to one of four _________________________________ .
e.) Multiple Choice: The molar constant pressure heat capacity of a crystalline solid at very low temperatures
is given by the expression:
1) C p,m = aT 2 .
T1
2) C p,m = ∫ 0
aT 2
dT .
T
3) C p,m = aT 3.
T1
4) C p,m = ∫ 0
aT 3
dT .
T
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PHYSICAL CONSTANTS, CONVERSION FACTORS, AND EQUATIONS
R = 0.08206 L atm mol–1 K–1 = 8.314 J mol–1 K–1 = 0.08314 L bar mol–1 K–1
1 atm = 101325 Pa = 1.013 bar = 760 torr
1 bar = 105 Pa = 0.98692 atm
1 L atm = 101.3 J; 1 L bar = 100 J
1 cal = 4.184 J
1 L = 1000 mL = 1000 cm3 = 1×10–3 m3
Fundamental Equations
dU = T dS − P dV
dH = T dS + V dP
dA = − S dT − P dV
dG = − S dT + V dP
Maxwell€Relations
#∂ T &
#∂ P &
%
( = −%
(
$ ∂ V 'S
$ ∂ S 'V
#∂ T &
#∂ V &
%
( = %
(
$ ∂ P 'S
$ ∂ S 'P
#∂ S &
#∂ P &
%
( = %
(
$ ∂ V 'T
$ ∂ T 'V
#∂ S &
#∂ V &
%
( = −%
(
$ ∂ P 'T
$ ∂ T 'P
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