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General Physics III Practice Exam I Solutions Fall 2007

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<strong>General</strong> <strong>Physics</strong> <strong>III</strong> <strong>Practice</strong> <strong>Exam</strong> I <strong>Solutions</strong> <strong>Fall</strong> <strong>2007</strong><br />

PROBLEM SCORE<br />

1. _______/ 20<br />

2. _______/ 38<br />

3. _______/ 22 TOTAL SCORE ______________ / 100<br />

4. _______/ 20<br />

______________________________________________________________________________<br />

PROBLEMS<br />

1. Determine the latent heat of fusion of mercury (Hg) using the following calorimetric data: 1.00 kg of solid Hg<br />

at its melting point of -39°C is placed in a 0.62 kg aluminum calorimeter with 0.43 kg of water at 12.80°C; the resulting<br />

equilibrium temperature is 5.06°C.<br />

The specific heat of aluminum is c Al = 900 J/kg°C, of water is c water = 4186 J/kg°C and of mercury is c Hg = 138 J/kg°C.<br />

Solution:<br />

(20 points)<br />

Heat lost = Heat gained:<br />

(m Al c Al + m water c water ) ΔT water = m Hg (L Hg + c Hg ΔT Hg )<br />

[(0.620 kg)(900 J/kg · °C) + (0.430 kg)(4186 J/kg · °C)](12.80°C – 5.06°C) =<br />

(1.00 kg){L Hg + (138 J/kg · °C)[5.06°C – (– 39.0°C)]},<br />

which gives L Hg = 1.22x10 4 J/kg


2. A heat engine uses 1.00 mol of a monatomic gas and follows the cycle shown in the diagram below. The<br />

temperature of state 1 is 300 K. The energy transferred by heat to the gas during the process 1 to 2 is 3750<br />

J.<br />

(a) Calculate the volume of the gas for state 1, and the pressures, volumes and temperatures for the gas<br />

at states 2, 3 and 4. Show your work and list the values in the table below.<br />

State P (kPa) V (m 3 ) T (K)<br />

1 300 8.31 x10 -3 300<br />

2 601 8.31 x10 -3 601<br />

3 601 1.66 x10 -2 1202<br />

4 300 1.66 x10 -2 600<br />

(a) 12 points<br />

(1pt for V 1 ,V 2 , V 3 ,V 4 , P 2 , P 3 )<br />

(2 pts. for T 2 , T 3 , T 4 )<br />

(a) The first law of thermodynamics is Q =Δ Eth + WS<br />

. For the isochoric process 1 → 2, W S 1 → 2 = 0 J. Thus,<br />

Q = 1 2<br />

3750 J = Δ E = th<br />

nC Δ<br />

→ V<br />

T<br />

3750 J 3750 J 3750 J<br />

⇒Δ T = = = = 301 K<br />

3 3<br />

nCV ( 1.0 mol)( 2<br />

R) ( 1.0 mol)( 2)( 8.31 J/mol K)<br />

⇒T − T = 300.8 K ⇒ T = 300.8 K + 300 K = 601 K<br />

To find volumes V 2 and V 1 ,<br />

V<br />

2 1 2<br />

( 1.0 mol )( 8.31 J/mol K)( 300 K) −3 3<br />

nRT<br />

= V = = = 8.31×<br />

10 m<br />

3.0 10 Pa<br />

1<br />

2 1 5<br />

p1<br />

×<br />

The pressure p 2 can be obtained from the isochoric condition as follows:<br />

p p T ⎛<br />

= ⇒ p = p = ( )<br />

T T T<br />

⎜<br />

× = ×<br />

300 K<br />

⎟<br />

⎝ ⎠<br />

2 1 2<br />

2 1<br />

2 1 1<br />

601 K ⎞ 3.00 10<br />

5 Pa 6.01 10<br />

5 Pa<br />

With the above values of p 2 , V 2 and T 2 , we can now obtain p 3 , V 3 and T 3 . We have<br />

The value of p 4 = p 3 , and V 4 = V 1 ; and<br />

V = 2V = 1.662 × 10 m p = p = 6.01×<br />

10 Pa<br />

−2 3 5<br />

3 2 3 2<br />

T T V<br />

= ⇒ T = T = 2T<br />

= 1202 K<br />

V V V<br />

3 2<br />

3<br />

3 2 2<br />

3 2 2<br />

T T V<br />

= ⇒ T = T = 2T<br />

= 600 K<br />

V V V<br />

4 1 4<br />

4 1 1<br />

4 1 1


(b)<br />

Determine the work done by the gas system W S , the heat Q, and the change in<br />

internal energy for each of the four processes in the cycle. Show your work and<br />

list your answers in the table below.<br />

Process W S (J) Q (J) ΔE int (J)<br />

1 → 2 0 3750 3750<br />

2 → 3 4990 12,480 7490<br />

3 → 4 0 –7500 –7500<br />

4 → 1 –2490 –6230 –3740<br />

(b) (17 Points) (1 pt. for W 12 , W 34 , Q 34, ΔE int12. ΔE int34 ), (2 pts. for W 23 , W 41 , Q 13 , Q 41 , ΔE int23. ΔE int41 )<br />

For the isochoric process 1 → 2,<br />

W S 1 → 2 = 0 J. Thus, ΔE th = Q 12 = 3750 J<br />

For the isobaric process 2 → 3,<br />

5 5<br />

( )( )( ) ( )( )( )( )<br />

Q = nC Δ T = 1.0 mol R T − T = 1.0 mol 8.31 J/mol K 601 K = 12,480 J<br />

2→3 P 2 3 2<br />

2<br />

S 2→3 3 3 2<br />

We are now able to obtain p 4 , V 4 and T 4 . We have<br />

5 −3 3<br />

( ) ( )( )<br />

W = p V − V = 6.01× 10 Pa 8.31× 10 m = 4990 J<br />

Δ E = Q − W = 12,480 J − 4990 J = 7490 J<br />

th 2→3 S 2→3<br />

V = V = 1.662 × 10 m p = p = 3.00 × 10 Pa<br />

−2 3 5<br />

4 3 4 1<br />

5<br />

T4 T3<br />

p ⎛<br />

4<br />

3.00 × 10 Pa ⎞<br />

= ⇒ T4 = T3 = ⎜<br />

5 ⎟( 1202 K)<br />

= 600 K<br />

p4 p3 p3<br />

⎝ 6.01×<br />

10 Pa ⎠<br />

For isochoric process 3 → 4,<br />

3 3<br />

( )( )( ) ( )( )( )( )<br />

Q = nC Δ T = 1.0 mol R T − T = 1.0 mol 8.31 J/mol K − 602 = −7500 J<br />

3→4 V 2 4 3<br />

2<br />

W = 0 J ⇒ Δ E = Q − W = −7500 J<br />

S 3→4 th 3→4 S 3→4<br />

For isobaric process 4 → 1,<br />

Q = nC Δ T = 1.0 mol<br />

5<br />

8.31 J/mol K 300 K − 600 K = −6230 J<br />

4→1 P 2<br />

S 4→1 4 1 4<br />

( ) ( )( )<br />

5 −3 3 −2 3<br />

( ) ( ) ( )<br />

W = p V − V = 3.00 × 10 Pa × 8.31× 10 m − 1.662 × 10 m = −2490 J<br />

th 4→1 S 4→1<br />

( )<br />

Δ E = Q − W = −6230 J − − 2490 J = −3740 J<br />

(c) Calculate the efficiency of this heat engine and compare it to the efficiency of a Carnot heat engine<br />

operating between the same maximum and minimum temperatures as this cycle.<br />

(5 points)<br />

The thermal efficiency of this heat engine is<br />

η<br />

W W<br />

2500 J<br />

Q Q + Q 3750 J + 12,480 J<br />

out<br />

out<br />

= = = = =<br />

H 1→2 2→3<br />

0.154 15.4%<br />

The efficiency of a Carnot heat engine operating between the same maximum and minimum temperatures<br />

would be (4 points)<br />

TC<br />

300K<br />

e = 1 − C<br />

1 1 0.25 0.75 75%<br />

T<br />

= − 1200K<br />

= − = =<br />

H


3. Two samples of an ideal gas are initially at the same temperature and pressure. They are each compressed<br />

reversibly from volume V to volume V/2, one isothermally, the other adiabatically.<br />

(a) In which sample is the final pressure greater?<br />

(b) Determine the change in entropy of the gas for each process.<br />

(c) What is the entropy change of the environment for each process?<br />

(22 points)<br />

Solution:<br />

(a) For the isothermal process we find the ratio of pressures from the ideal gas equation:<br />

(P 2 V 2 /P 1 V 1 ) = T 2 /T 1 = 1, so P 2 /P 1 = V 1 /V 2 = 2.<br />

(4 points)<br />

For the adiabatic process,<br />

P 1 V γ 1 = P 2 V γ 2 , so P 2 /P 1 = (V 1 /V 2 ) γ = 2 γ .<br />

(4 points)<br />

Because γ > 1, P2/P1 > 2 in the adiabatic case, so the final pressure is greater for the adiabatic process.<br />

(b)<br />

For the isothermal process we have<br />

ΔE int = 0; Q = -W.<br />

Thus ΔS = -W/T = [nRT ln(V 2 /V 1 )]/T = nR ln(1/2) = – nR ln 2.<br />

(4 points)<br />

For the adiabatic process we have<br />

Q = 0.<br />

Thus ΔS a = 0. (3 points)<br />

(c)<br />

Because each process is reversible, the energy change of the universe is zero.<br />

For the isothermal process we have<br />

ΔS surr = – ΔSi = nR ln 2. (4 points)<br />

For the adiabatic process we have<br />

ΔS surr = –ΔS = 0. (3 points)


4A. This P-V diagram represents a system consisting of a fixed amount of ideal gas that undergoes two<br />

different processes in going from state A to state B:<br />

A. Process #1<br />

A. State B<br />

Pressure<br />

II. State A<br />

B. Process #2<br />

<strong>III</strong>. Volume<br />

[In these questions, W represents the work done by the system during a process; Q represents the heat transfer to<br />

the system during a process.]<br />

1. Is W for Process #1 greater than, less than, or equal to that for Process #2? Explain.<br />

Answer: (5 points)<br />

The work done by the system in Process #1 is greater than the work done by the system in Process #2 because this work is<br />

V<br />

given by the integral ∫ B PdV , equivalent to the area under the curve, and this is greater for Process #1.<br />

VA<br />

2. Is Q for Process #1 greater than, less than, or equal to that for Process #2? Please explain your answer.<br />

Answer: (5 points)<br />

Q = ΔU + W; since ΔU is defined as U final state – U initial state , ΔU will be the same for both processes. The work done by the<br />

system in Process #1 is greater than that in Process #2, therefore the heat transfer in Process #1 is greater than the heat<br />

transfer in Process #2.<br />

3. Which would produce the largest change in the total energy (kinetic plus potential) of all the atoms in the<br />

system: Process #1, Process #2, or both processes produce the same change?<br />

Answer: (5 points)<br />

Both processes would have the same change in total energy since they have the same initial and final states.<br />

4B. A subsystem A is in thermal contact with its environment B and they together comprise an isolated<br />

system that is undergoing an irreversible process. Consider the following situations:<br />

I. Entropy of subsystem A increases by 5 J/K; entropy of the environment B decreases by 5 J/K.<br />

II. Entropy of subsystem A increases by 5 J/K; entropy of the environment B decreases by 3 J/K.<br />

<strong>III</strong>. Entropy of subsystem A increases by 3 J/K; entropy of the environment B decreases by 5 J/K.<br />

IV. Entropy of subsystem A decreases by 3 J/K; entropy of the environment B increases by 5 J/K.<br />

Which of the above four situations can actually occur?<br />

(Circle the correct answer listed below)<br />

a. I only<br />

b. II only<br />

c. <strong>III</strong> only<br />

d. II and IV only<br />

e. I, II, and IV only<br />

Answer: d. II and IV only. (5 points)<br />

The total entropy of an isolated system (i.e. system + environment) must increase during any irreversible<br />

process. There is no separate constraint on the entropy of a subsystem or of its environment.

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