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Question 15 Marks
A geyser heats water flowing at the rate of 3.0 litres per minute from 27°C to 77°C. If the geyser operates on a gas burner, what is the rate of consumption of the fuel if its heat of combustion is 4.0 × 104J/g?
Answer
Water is flowing at a rate of 3.0 litre/min.

The geyser heats the water, raising the temperature from 27°C to 77°C.

Initial temperature, T1 = 27°C

Final temperature, T2 = 77°C

$\therefore$ Rise in temperature, ΔT = T2 - T1

= 77 – 27= 50°C

Heat of combustion = 4 × 104J/g

Specific heat of water, c = 4.2J g-1°C-1

Mass of flowing water, m = 3.0 litre/min = 3000g/min

Total heat used, $\Delta\text{Q} =\text{mc}\Delta\text{T}$

= 3000 × 4.2 × 50

= 6.3 × 105J/min

$\therefore$ Rate of consumption $=\frac{6.3\times0^5}{4\times10^4}=15.75\text{g/min}$

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Question 25 Marks
A cylinder with a movable piston contains 3 moles of hydrogen at standard temperature and pressure. The walls of the cylinder are made of a heat insulator, and the piston is insulated by having a pile of sand on it. By what factor does the pressure of the gas increase if the gas is compressed to half its original volume?
Answer
The cylinder is completely insulated from its surroundings. As a result, no heat is exchanged between the system (cylinder) and its surroundings. Thus, the process is adiabatic.

Initial pressure inside the cylinder = P1

Final pressure inside the cylinder = P2

Initial volume inside the cylinder = V1

Final volume inside the cylinder = V2

Ratio of specific heats, γ = 1.4

For an adiabatic process, we have:

P1V1γ = P2V2γ

The final volume is compressed to half of its initial volume.

$\therefore$ V2 = V1/2

P1V1γ = P2(V1/2)γ

P2/P1 = V1γ/(V1/2)γ

= 2γ = 21.4 = 2.639

Hence, the pressure increases by a factor of 2.639.

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Question 35 Marks
In changing the state of a gas adiabatically from an equilibrium state A to another equilibrium state B, an amount of work equal to 22.3J is done on the system. If the gas is taken from state A to B via a process in which the net heat absorbed by the system is 9.35 cal, how much is the net work done by the system in the latter case? (Take 1 cal = 4.19J)
Answer
The work done (W) on the system while the gas changes from state A to state B is 22.3J.

This is an adiabatic process. Hence, change in heat is zero.

$\therefore\Delta\text{Q} = 0$

$\Delta\text{W} = -22.3\text{ J}$ (Since the work is done on the system)

From the first law of thermodynamics, we have:

$\Delta\text{Q}=\Delta\text{U}+\Delta\text{W}$

Where,

ΔU = Change in the internal energy of the gas

$\therefore\ \Delta\text{U}=\Delta\text{Q}-\Delta\text{W}=-(-22.3\text{ J})$

$\Delta\text{U} = +22.3\text{ J}$

When the gas goes from state A to state B via a process, the net heat absorbed by the system is:

$\Delta\text{Q} = 9.35\text{ cal}$

= 9.35 × 4.19 = 39.1765J

Heat absorbed, $\Delta\text{Q}=\Delta\text{U}+\Delta\text{Q}$

$\therefore\ \Delta\text{W}=\Delta\text{Q}-\Delta\text{U}$

= 39.1765 - 22.3

= 16.8765 

Therefore, 16.88J of work is done by the system.

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Question 45 Marks
What amount of heat must be supplied to 2.0 × 10-2kg of nitrogen (at room temperature) to raise its temperature by 45°C at constant pressure? (Molecular mass of N2 = 28; R = 8.3J mol-1 K-1.)
Answer
Mass of nitrogen, m = 2.0 × 10-2kg = 20g

Rise in temperature, $\Delta\text{T}=45^\circ\text{C}$

Molecular mass of N2, M = 28

Universal gas constant, R = 8.3J mol-1 K-1

Number of moles, $\text{n}=\frac{\text{m}}{\text{M}}$

$=\frac{20.\times10^{-2}\times10^3}{28}=0.714$

Molar specific heat at constant pressure for nitrogen Cp = (7/2)R

= 7/2 × 8.3

= 29.05J mol-1 K-1

The total amount of heat to be supplied is given by the relation:

$\Delta\text{Q}=\text{nC}_\text{p}\Delta\text{T}$

$=0.714\times29.05\times45$

$=933.38\text{ J}$

Therefore, the amount of heat to be supplied is 933.38J.

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Question 55 Marks
Two Carnot engines A and B are operated in series. The first one A receives heat at 900K and rejects it to a reservoir at temperature T. The second engine B operates on this reservoir and rejects heat to a reservoir at 400K. Calculate temperature T when,
  1. Efficiencies of both A and B are equal.
  2. The work outputs of both A and B are equal.
Answer
  1. Efficiency of A = efficiency of B

$\eta_\text{A}=\eta_\text{B}$

$\Rightarrow1-\frac{\text{T}}{900}=1-\frac{400}{\text{T}}$

$\Rightarrow\text{T}^2=900\times400$

$\Rightarrow\text{T}=600\text{K}$

  1. Let the first engine take Q1 heat as input at temperature, T1 = 800 K and gives out heat Q2 at temperature T0. The second engine receive Q2 as input and ive is out heat Q3 at temprature T3 = 300K to the sink.

Work done by first (A) engine = work done by second (B) engine.

Thus, Q1 - Q2 = Q2 - Q3

Dividing both sides by Q1

$1-\frac{\text{Q}_2}{\text{Q}_1}=\frac{\text{Q}_2}{\text{Q}_1}-\frac{\text{Q}_3}{\text{Q}_1}$

$\Rightarrow1-\frac{\text{T}}{\text{T}_1}=\frac{\text{Q}_2}{\text{Q}_1}\Big(1-\frac{\text{Q}_3}{\text{Q}_2}\Big)$

$\Rightarrow1-\frac{\text{T}}{\text{T}_1}=\frac{\text{T}}{\text{T}_1}\Big(1-\frac{\text{T}_3}{\text{T}}\Big)$

$\Rightarrow\frac{\text{T}_1}{\text{T}}-1=1-\frac{\text{T}_3}{\text{T}}$

$\Rightarrow\frac{\text{T}_1}{\text{T}}+\frac{\text{T}_3}{\text{T}}=2$

$\Rightarrow\frac{1}{\text{T}}\Big(\text{T}_1+\text{T}_3)=2$

$\Rightarrow\text{T}=\frac{\text{T}_1+\text{T}_3}{2}$

$\Rightarrow\text{T}=\frac{900+400}{2}=650\text{K}$

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Question 65 Marks
A gas undergoes reduction in volume (i) adiabatically, (ii) isothermally. Find the work done in the process.
Answer
  1. For an adiabatic process of thermodynamics,

dQ = 0

Since dU = n Cv dT irrespective of the process, from 1st law, we get,

dW = -dU = -n CV dT

So work done,

W = -nCV(Tf - Ti)

$=-\frac{\text{C}_\text{V}}{\text{R}}(\text{P}_\text{f}\text{V}_\text{f}-\text{P}_\text{i}\text{V}_\text{i})$

  1. For an isothermal process, dT = 0

So, $\text{dW}\int\limits{\text{PdV}}=\int\limits\frac{\text{nRT}}{\text{V}}\text{dV}$

Work done $=\text{W}=\text{nRT}|\log_\text{e}\text{V}|_{\text{V}_\text{i}}^{\text{V}_\text{f}}$

$\text{W}=\text{n}\text{RT}\log_\text{e}\Big(\frac{\text{V}_\text{f}}{\text{V}_\text{i}}\Big)$

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Question 75 Marks
Consider one mole of perfect gas in a cylinder of unit cross section with a piston attached (Fig.) A spring (spring constant k) is attached (unstretched length L) to the piston and to the bottom of the cylinder. Initially the spring is unstretched and the gas is in equilibrium. A certain amount of heat Q is supplied to the gas causing an increase of volume from Vo to V1.

  1. What is the initial pressure of the system.
  2. What is the final pressure of the system.
  3. Uing the first law of thermodynamics, write down a relation between Q, Pa, V, Vo and k.
Answer
  1. It is considered that piston is mass less and piston is balanced by atmospheric pressure (Pa). So the initial pressure of system inside the cylinder = Pa,
  2. On supply heat Q. Volume of gas increase from V0 to Vand spring stretched also.So increase in volume = V1 - V0

If displacement of piston is x then volume increase in cylinder ) 

= Aera of base × height = A × x

A × x = V1 - V0 (A = area of cross section of cylinder)

$\therefore\ \text{x}=\frac{\text{V}_1-\text{V}_0}{\text{A}}$

Force exerted by spring $\text{F}_\text{s}=\text{K}_\text{x}=\frac{\text{K}(\text{V}_1-\text{V}_0)}{\text{A}}$

As the piston is of unit area of cross - section $\therefore\ \text{A}=1$

Force due to spring =$\text{K}(\text{V}_1-\text{V}_0)$ on unit area can be say press due to spring = $\text{K}(\text{V}_1-\text{V}_0)$

Final total pressure on gas $\text{P}_\text{f}=\text{P}_\text{a}+\text{K}(\text{V}_1-\text{V}_0)$

  1. by 1st law of thermodynamics $\text{dQ}=\text{dU}+\text{dW}$

Now $\text{DQ}=\text{dU}+\text{dW}$

$=\text{c}_\text{v}(\text{T}-\text{T}_0)+\text{P}_\text{a}(\text{V}_1-\text{V}_0)+\frac{1}{2}\text{kx}^2$

$\text{dQ}=\text{C}_\text{V}(\text{T}-\text{T}_0)+\text{P}_\text{a}(\text{V}_1-\text{V}_0)+\frac{1}{2}\text{k}(\text{V}_1-\text{V}_0)^2$

It is required relation.

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Question 85 Marks
A geyser heats water flowing at the rate of 3.0 litres per minute from 27°C to 77°C. If the geyser operates on a gas burner, what is the rate of consumption of the fuel if its heat of combustion is 4.0 × 104J/g?
Answer
Water is flowing at a rate of 3.0 litre/min.
The geyser heats the water, raising the temperature from 27°C to 77°C.
Initial temperature, T1 = 27°C
Final temperature, T2 = 77°C
$\therefore$ Rise in temperature, ΔT = T2 - T1
= 77 – 27= 50°C
Heat of combustion = 4 × 104J/g
Specific heat of water, c = 4.2J g-1°C-1
Mass of flowing water, m = 3.0 litre/min = 3000g/min
Total heat used, $\Delta\text{Q} =\text{mc}\Delta\text{T}$
= 3000 × 4.2 × 50
= 6.3 × 105J/min
$\therefore$ Rate of consumption $=\frac{6.3\times0^5}{4\times10^4}=15.75\text{g/min}$
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Question 95 Marks
Specific heat capacity of argon at constant pressure is 0.125 cal/ g/ k and at constant volume is 0.075 cal/ g/ k. Calculate the density of argon at STP. Given J = 4.18 J/ cal and the normal pressure = 1.01 × 105 Nm-2.
Answer
Here, Cp = 0.125 cal/ g/ K
CV = 0.075 cal/ g/ K
J = 4.18 J/ cal or 4.18 × 107 erge/ cal
Normal pressure = 1.01 × 105 N/ m2 or 1.01 × 106 dyne/ cm2
Absolute temprerature T = 273K
Let p be the density of argon at S.T.P. for one mole
$\therefore\ \text{PV}=\text{RT}$ (gas equation)
or $\text{R}=\frac{\text{PV}}{\text{T}}=\frac{\text{P}}{\rho\text{T}}$ for a 1 mole of gas
Now $\text{C}_\text{p}-\text{C}_\text{V}=\frac{\text{R}}{\text{J}}$
$\text{R}=\text{J}(\text{C}_\text{P}-\text{C}_\text{V})$
$\frac{\text{P}}{\rho\text{T}}=4.18\times10^7(0.125-0.075)$
$\Rightarrow\ \frac{1.01\times10^6}{\rho\times273}$
$=4.18\times10^7\times0.05$
$\therefore\ \rho=\frac{1.01\times10^6}{273\times4.18\times10^7\times0.05}$
Hence $\rho=1.77\times10^{-3}\text{g}/\text{cm}^3$ or $1.77\times10^3\ \text{Kg}/\text{m}^3$
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Question 105 Marks
There is a layer of ice 10cm thick over the surface of a pond. Temperature above the surface is -5°C. How long will it take for the next 1mm of ice to form? The thermal conductivity of ice is 0.008 CGS units and its latent heat is 80 cal/g. Density of ice = 0.9 g/cc.
Answer
Thickness of layer = 10cm,
Temperature = -5°C, K = 0.008 CCS units,
$\text{L}=80\text{cal g}^{-1},\rho=0.9\text{ gcc}^{-1}$
Suppose the area of the surface of ice to be 1 sq. cm.
Volume of 1 mm thickness of layer
= Area × Thickness = 1 × 0.1
= 0.1cm3
Mass of the new layer formed
= Volume × Density = 0.1 × 0.9
= 0.09g
Amount of heat radiated by the water to freeze 0.09g of ice = 0.09 × 80 = 7.2 cal.
We know that,
$\frac{\text{Q}}{\text{t}}=\text{KA}\frac{\Delta\text{T}}{\Delta\text{x}}$
Here, $\text{Q}=7.2\text{ cal},\text{K}=0.008,$
$\Delta\text{T}=0-(-5)=5^\circ\text{C},\text{A}=1\text{sq. cm}$
$\Delta\text{x}=\frac{10+10.1}2=10.05\text{cm}$
Putting these value, we have,
$\frac{7.2}{\text{t}}=0.008\times\frac{1\times5}{10.05}$
$\text{t}=\frac{7.2\times10.05}{0.008\times5}=30\text{min 9s.}$
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Question 115 Marks
A carnot engine works between ice point and steam point. It is desired to increase the efficiency by 20% by (a) making temperature of the source as constant (b) making temperature of the sink as constant. Calculate the change in temperature in the two cases. Which one of these will you prefer and why?
Answer
$\eta=1-\frac{\text{T}_1}{\text{T}_1}=1-\frac{273}{373}=\frac{100}{373}$

Adding 20% i.e. $\big(\frac15\big)$ to the existing $\eta,$

$\eta=\frac{100}{3+3}+20\%=\frac{100}{373}+\frac15=\frac{873}{1865}$

  1. If the temperature of the sink corresponding to $\eta'$ be $\text{T}'_2$ (source at 373k), then,

Thus, $\eta'=1-\frac{\text{T}_2'}{373}$

$\frac{\text{T}_2'}{373}=1-\eta'=1-\frac{873}{1865}=\frac{992}{1865}$

$\text{T}'_2=198.4\text{K}$

$\text{T}_2'-\text{T}_2=198.4\text{K}-273\text{K}=-74.6\text{K}$

  1. If the temperature of the source corresponding to $\eta'$ be $\text{T}'_2$ (sinkb at 273K), then

$\eta'=1-\frac{\text{T}'_2}{\text{T}'_1}$ or $\frac{873}{1865}=1-\frac{273}{\text{T}'_1}$

$\frac{273}{\text{T}'_1}=1-\frac{873}{1865}=\frac{992}{1865}$

$\text{T}'_2=513\text{K}$

$\text{T}'_1-\text{T}_1=513\text{K}-373\text{K}$

$=149.25\text{K}=140^\circ\text{C}$

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Question 125 Marks
The P-V diagram for a cyclic process is a triangle ABC drawn in order. The co-ordinates of A, B, C are (4, 1), (2, 4) and (2, 1). The co-ordinates are in the order (P-V). Pressure is in Nm-2 and volume is in litre. Calculate work done during the process from A to B, B to C and C to A. Also, calculate work done in the complete cycle.

Answer
The P-V diagram drawn as per the question is show in figure (adjacent).

  1. Work done during the process from A to B (expansion),

$\text{W}_{\text{AB}}=+\text{area ABKLA}$

= area of $\Delta\text{ABC}+\text{area or rectangle BCLK}$

$\text{W}_{\text{AB}}=\frac{1}{2}\text{BC}\times\text{AC}+\text{KL}\times\text{LC}$

Now, BC = KC = 4 - 1 = 3 litre

= 3 × 10-3m3

AC = 4 - 2 = 2 Nm-2

LC = 2 - 0 = 2 Nm-2

$\therefore\text{W}_{\text{AB}}=\frac{1}{2}\times3\times10^{-3}\times2+3\times10^{-3}\times2$

$\text{W}_{\text{AB}}=9\times10^{-3}\text{J}$

  1. Work done during the process from B to C (compression) is,

$\text{W}_{\text{BC}}=-\text{area BCLK}=-\text{KL}\times\text{LC}$

$=-3\times10^{-3}\times2=-6\times10^{-3}\text{J}$

  1. Work done during the process from C to A. As there is no change in volume of the gas in this process, therefore,

$\text{W}_{\text{CA}}=0.$

Net work done in the complete cycle,

$\text{W}=\text{W}_{\text{AB}}+\text{W}_\text{BC}+\text{W}_\text{CA}$

$=9\times10^{-3}+(-6\times10^{-3})+0$

$=3\times10^{-3}\text{J}$

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Question 135 Marks
Explain with the suitable example that a reversible process must be carried slowly and a fast process is necessarily irreversible.
Answer
A reversible process must pass through equilibrium states which are very close to each other so that when process is reversed, it passes back through these equilibrium states.
Then, it is again decompressed or it passes through same equilibrium states, system can be restored to its initial state without any change in surroundings. e.g. If a gas is compressed as shown

But a reversible process can proceeds without reaching equilibrium in intermediate states.

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Question 145 Marks
Define molar specific heat capacities at constant volume and pressure. Considering thermodynamical process in a cylinder with parameters P, V and T, derive the Mayer's relation.
Answer
Molar specific heat capacity is the heat energy required to raise the temperature of 1 mole of a substance by 1K and expressed in J mol-1 K-1.
$\text{C}=\frac{\text{Q}}{1\text{mole 1}\text{K}}$
Depending on the condition that whether volume or pressure is constant, molar specific heat is written as Cv and Cp.
Relation between Cp and CvSuppose one mole of a gas is heated so that its temperature rises by dT.
Heat supplied $=1\times\text{C}_\text{V}\times\text{C}_\text{V}\text{dT}\dots(\text{i})$
Since the volume is constant, the gas will not perform external work in accordance with the first law of thermodynamics and the heat supplied will be just equal to the increase in the internal energy of the gas.
$\therefore\text{dU}=\text{C}_{\text{V}}\text{dT}\dots\text{(ii)}$
Let the gas be heated at constant pressure to again increase its temperature by dT, and dQ be the amount of heat supplied, therefore,
dQ = 1 × CP × dT = CPdT ...(iii)
The heat supplied at a constant pressure increases the temperature by dT hence increases its internal energy by dU = CvdT as well as enables the gas to perform work dW.
dW = PdV ...(iv)
From the first law of thermodynamics, we have
dQ = dU + dW
Substituting the values, we get,
$\text{C}_\text{P}\text{dT}=\text{C}_\text{v}\text{dT}+\text{PdV}$
But PV = RT (For one mole of the gas)
or PdV = RdT
$\therefore\text{C}_\text{P}\text{dT}=\text{C}_\text{V}\text{dT}$
$\text{C}_\text{P}-\text{C}_\text{V}=\text{R}$
This is the relation between two principal specific heats of the gas when Cp, Cv and R are measured in the units of either heat or of work.
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Question 155 Marks
  1. What is an adiabatic process? Derive expression for the work done during such process.
  2. A refrigerator is to maintain eatable kept inside at 9°C. If the room temperature is 36°C. Calculate the co-efficient of performance.
Answer
  1. Adiabatic process: A change in pressure and volume of a gas in which temperature also changes is called an adiabatic change. In such a change, no heat is allowed to enter into or escape from the gas (i.e., there is no exchange of heat between the gas and its surroundings).

Derivation: Consider one gram mole of an ideal gas enclosed in a cylinder with perfectly non-conducting walls, and fitted with a perfectly frictionless, non-conducting piston. P1 = Let be the initial pressure, v1 be the volume and T1 be the temperature of the gas.

Force exerted by the gas on the piston of area of cross-section ‘A’ is given by

F = P × A ...(i)

Where P is the pressure at any instant during expansion.

If we assume that pressure of the gas during an infinitesimally small outward displacement dx of the piston remains constant, then small amount of work done during expansion,

dW = F × dx = (P × A)dx

dW = PdV ...(ii)

Where dV = A(dx) = small increase in the volume of the gas. Total work done by the gas in adiabatic expansion from volume v1 to v2 is

$\text{W}=\int\limits^{\text{V}_2}_{\text{V}_1}\text{P dV}\dots\text{(iii)}$

The equation of adiabatic changes is 

PV' = K, a constant ...(iv)

Where, $\gamma=\frac{\text{C}_\text{P}}{\text{C}_\text{V}}$

$=\frac{\text{Specific heat of gas at constant pressure}}{\text{Specific heat of gas at constant volume}}$

For equation (iv)

$\text{P}=\frac{\text{K}}{\text{V}^\gamma}=\text{KV}^{-\gamma},$ put in equation (iii)

$\text{W}=\int\limits^{\text{V}_2}_{\text{v}_1}\text{KV}^{-\gamma}\text{dV}=\text{K}\Big[\frac{\text{V}^{(1-\gamma)}}{1-\gamma}\Big]^{\text{v}_2}_{\text{v}_1}$

$\text{W}=\frac{\text{K}}{1-\gamma}\Big[\text{K}\nu^{(1-\gamma)}_2-\text{K}\nu^{(1-\gamma)}_1\Big]$

$\text{W}=\frac{1}{1-\gamma}\Big[\text{K}\nu^{(1-\gamma)}_2-\text{K}\nu^{(1-\gamma)}_1\Big]\dots\text{(v)}$

From standard gas equation P1 V1 = RT, P2V2 = RT2

$\text{W}=\frac{1}{1-\gamma}[\text{RT}_2-\text{RT}_1]$

[Putting above in equation (v)]

$\text{W}=\frac{\text{R}(\text{T}_2-\text{T}_1)}{1-\gamma}$

  1. Here, T2 = 9°C = 9 + 273K = 282K,

T1 = 36°C = 36 + 273 = 309K

Coeffiecient of performance

$=\frac{\text{T}_2}{\text{T}_1-\text{T}_2}=\frac{282}{309-282}=\frac{282}{27}=10.4$

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Question 165 Marks
  1. Define isothermal process. Derive an expression for work done during isothermal process.
  2. A refrigerator is to remove heat from the eatables kept inside at 10°C. Calculate the coefficient of performance if room temperature is 36°C.
Answer
  1. Isothermal process is a change in pressure and volume of a gas without any change in its temperature. In such a change, there is a free exchange of heat between the gas and its surroundings.

For a small change in volume, work done is given by

dW = PdV

We know, PV = nRT

$\therefore\text{P}=\frac{\text{nRT}}{\text{V}}$

For T = constant,

$\text{dW}=\text{nRT}\frac{\text{dV}}{\text{V}}$

Net work done under isothermal condition to change the volume from Vi to Vf is,

$\text{W}=\int\limits^{\text{V}_\text{f}}_{\text{V}_\text{i}}\text{dW}=\text{nRT}\int\limits^{\text{V}_\text{f}}_{\text{V}_\text{i}}\frac{\text{dV}}{\text{V}}$

$=\text{nRT}\big|\log_\text{e}\text{V}\big|^{\text{V}_\text{f}}_{\text{V}_\text{i}}$

$\text{W}=\text{nRT }\log_\text{e}\Big(\frac{\text{V}_\text{f}}{\text{V}_\text{i}}\Big)$

$\therefore\text{W}=2.3026\text{ nRT }\log_\text{10}\Big(\frac{\text{V}_\text{f}}{\text{V}_\text{i}}\Big)$

Where n is the number of moles. If Pf and Pi are the pressures, we can also write,

$\text{W}=2.3026\ \text{nRT }\log_{10}\Big(\frac{\text{P}_\text{i}}{\text{P}_\text{f}}\Big)$

  1. Coefficient of performance, $\beta=\frac{\text{T}_2}{\text{T}_1-\text{T}_2}$

$\because\text{T}_1=36 +273=309\text{K}$

and $\text{T}_2=10+273=283\text{K}$

$\therefore\beta=\frac{283}{309-283}=\frac{283}{26}=10.8$

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Question 175 Marks
  1. In a carnot engine, temperature of sink is increased. What will happen to its efficiency?
  2. A carnot engine absorbs 1000J of heat from a reservoir at 127°C and rejects 600J of heat during each cycle. Calculate the
  1. Efficiency of engine.
  2. Temperature of the sink.
  3. Amount of the useful work done during each cycle.
Answer
  1. Since $\eta=1-\frac{\text{T}_2}{\text{T}_1}$ On increasing T2, effieciecy drops.
  2. Q1 = 1000J, T1 = 127 + 273 = 400K, Q2 = 600J.
  1. Effciency $=\eta=\frac{\text{Q}_1-\text{Q}_2}{\text{Q}_1}=1-\frac{\text{T}_2}{\text{T}_1}$

$=\frac{400}{1000}=0.4\text{ or }40\%$

  1. Using $\eta=\frac{\text{Q}_1-\text{Q}_2}{\text{Q}_1}=1-\frac{\text{T}_2}{\text{T}_1}$

We get $\frac{400}{1000}=1-\frac{\text{T}_2}{\text{T}_1}$

$\Rightarrow\text{T}_2=400\times\frac{600}{1000}=240\text{K}$

  1. Work done = Q1 - Q2 = 400J
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Question 185 Marks
  1. State first law of thermodynamics. What are its limitations? Why Cp > Cv?
  2. An electric heater supplies heat to a system at a rate 100W. If the system performs work at a rate of 75 joules per second at what rate is the internal energy increases.

OR

  1. Derive an expression for the work done during the isothermal expression of x mole of an ideal gas.
  2. A steam engine delivers 5.4 × 108J of work per minute and services 3.6 × 109J of heat per minute from its boiler. What is the efficiency of the engine? How much heat is wasted per minute?
Answer
  1. According to the first law of thermodynamics, the total heat energy change dQ is the sum of the internal energy change dU and work done dW,

i.e. dQ = dU + dW

Limitations of the first law of thermodynamics:

  1. The first law does not indicate the direction in which the heat change can occur.
  2. The first law does not give any idea about the extent of heat change.
  3. The first law of thermodynamics gives no information about the source of heat, i.e. whether it is a hot or cold body.

The relation between two specific heats of a gas, i.e. Cp and Cv is given by Cp - Cv = R where, R is the molar gas constant and is equal to 8.31J mole-1K-1.

Cp > Cv because a part of the energy supplied in the isobaric process goes to increase the volume of the gas and the remaining increases the temperature.

  1. According to first law of thermodynamics,

dQ = dU + dW

Differentiating w.r.t., time (t)

$\frac{\text{dQ}}{\text{dt}}=\frac{\text{dU}}{\text{dt}}+\frac{\text{dW}}{\text{dt}}$

$100\text{W}=\frac{\text{dU}}{\text{dt}}+75$

$[\because$ Given, system performs work at a rate of 75J/ sec.$]$

$\frac{\text{dU}}{\text{dt}}\rightarrow$ Rate of change of internal energy

$\frac{\text{dU}}{\text{dt}}=100-75=25\text{W}$

Alternate Answer

  1. For a small change in volume, work done is given by dW = PdV.

We know, PV = nRT

For T = Constant

$\text{dW}=\text{nRt}\cdot\frac{\text{dV}}{\text{V}}$

$\therefore\text{P}=\frac{\text{nRT}}{\text{V}}$

Net work done under isothermal condition to change the volume from Yi to Vf is,

$\text{W}=\int\limits^{\text{V}_\text{f}}_{\text{V}_\text{i}}\text{dW}$

$=\text{nRT}\int\limits^{\text{V}_\text{f}}_{\text{V}_\text{i}}\frac{\text{dV}}{\text{V}}=\text{nRT}|\log_\text{e}\text{V}|^{\text{V}_\text{f}}_{\text{V}_\text{i}}$

$=\text{nRT }\log_\text{e}\Big(\frac{\text{V}_\text{f}}{\text{V}_\text{i}}\Big)$

$\therefore\text{W}=2.3026\text{ nRT }\log_{10}\Big(\frac{\text{V}_\text{f}}{\text{V}_\text{i}}\Big)$

  1. Work done by a steam energy,

W = 5.4 × 108J, Q1 = 3.6 × 109J

Efficiency of the engine, $\eta=?,\text{Q}_2=?$

$\eta=\frac{\text{W}}{\text{Q}_1}=\frac{5.4\times10^8\text{J}} {3.6\times10^9\text{J}}$

$=\frac{54}{36}\times10^{-1}=\frac{3}{20}=0.15$ or 15%

Heat wasted per minute,

$\text{Q}_2=\text{Q}_1-\text{W}$

$\text{Q}_2=3.6\times10^9\text{J}-5.4\times10^8\text{J}$

$=36\times10^8\text{J}-5.4\times10^8\text{J}$

$=10^8(36-5.4)\text{J}=30.6\times10^9\text{J}$

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Question 195 Marks
Three moles of an ideal gas of 300K are isothermally expanded to five times its volume and heated at this constant volume so that the pressure is raised to its initial value before expansion. In the whole process 83.14 kJ heat is required. Calculate the ratio $\frac{\text{C}_\text{P}}{\text{C}_\text{V}}$ of gas $(\log_\text{e}5=1.61).$
Answer
For isothermal expansion P1V1 = P2V2
$\therefore\frac{\text{P}_1}{\text{P}_2}=\frac{\text{V}_2}{\text{V}_1}=\frac{\text{5V}_1}{\text{V}_1}=5$
From gas law at constant volume
$\frac{\text{P}_2}{\text{T}_2}=\frac{\text{P}_3}{\text{T}_3}=\frac{\text{P}_1}{\text{P}_3}(\because\text{P}_3=\text{P}_1)$
$\therefore\frac{\text{P}_2}{\text{P}_1}=\frac{\text{T}_2}{\text{T}_3}=\frac{\text{T}_1}{\text{T}_3}$ or $\frac{\text{T}_3}{\text{T}_1}=\frac{\text{P}_1}{\text{P}_2}=5$
Now $\text{T}_3=5\text{T}_1=5\times300$
$=1500\text{K}$
We know that $\text{dQ}=\text{dU}+\text{dW}$
$\therefore\text{dQ}=\text{nC}_\upsilon\Delta\text{T}+\int\limits^{\text{V}_2}_{\text{V}_1}\text{PdV}$ where, $\text{P}=\frac{\text{nRT}_1}{\text{V}}$
$\text{dQ}=\text{nC}_\upsilon\Delta\text{T}+\text{nRT}_1\log_\text{e}\Big(\frac{\text{V}_2}{\text{V}_1}\Big)$
$\text{C}_\text{P}-\text{C}_\upsilon=\text{R}$ and $\frac{\text{C}_\text{P}}{\text{C}_\upsilon}=\gamma\ $ $\therefore\text{C}_\upsilon=\Big(\frac{\text{R}}{\gamma}-1\Big)$
$\therefore\text{dQ}=\frac{\text{nR}}{\gamma-1}\Delta\text{T}+\text{nRT}_1\log_\text{e}\Big(\frac{\text{V}_2}{\text{V}_1}\Big)$
$83.14\times10^3=\frac{3\times8.3}{\gamma-1}\times(1500-300)+3\times8.3\times\log_\text{e}5$
Solving we get $\gamma=1.42$
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Question 205 Marks
Write Kelvin-Planck and Clausius statements for second law of thermodynamics. Define coefficient of efficiency and coefficient of performance. Show the heat flow in case of an engine and refrigerator using schematic diagrams.
Answer
Kelvin-Planck Statement of Second Law of Thermodynamics: It is impossible to realise a heat engine which works in a cyclic process performing the single job of taking heat from a body at a constant temperature and converting it completely into mechanical work. The law stresses the fact that work done on the system can facilitate to convert heat into work, however with some unavoidable loss.
Clausius Statement: It is impossible for a self-acting machine, unaided by any external agency, to transfer heat from a body at lower temperature to another at higher temperature.

Efficiency in forward cycle,
$=\frac{\text{Work done}}{\text{Heat supplied}}=\frac{\text{Q}_1-\text{Q}_2}{\text{Q}_2}=1-\frac{\text{Q}_2}{\text{Q}_1}=1-\frac{\text{T}_2}{\text{T}_1}$
Coeffiecient of performance,
$=\frac{\text{Heat drawn from sink}}{\text{Work on the system}}=\frac{\text{Q}_2}{\text{Q}_1-\text{Q}_2}=\frac{\text{T}_2}{\text{T}_1-\text{T}_2}$
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Question 215 Marks
Define 1st law of thermodynamics. By using this law, derive relationship between Cp and Cv.
Answer
First Law of Thermodynamics: It is based on the conservation of energy. The total heat energy change in any system is the sum of the internal energy change and the work done, i.e.,
dQ = dU + dW
where dU → internal energy change and dW = PdV is the work done by/ on the system, dU is a state function and depends on dT. (dU = nCvdT). dW depends on the path followed and so, is different in various processes.
Relationship between Cp and Cv: Suppose one mole of a gas is heated at constant volume so that its temperature rises by dT.
Heat supplied = 1 × CV × dT = CVdT .,.(i)
Since the volume is costant, the gas will not perform external work in accordance with the first law of thermodynamics and the heat supplied will be just equal to the increase in the internal energy of the gas.
$\therefore\text{dU}=\text{C}_\text{V}\text{dT}\dots\text{(ii)}$
Let the gas be heated at constant pressure to again increase its temperature by dT, and dQ be the amount of heat supplied, therefore,
$\text{dQ}=1\times\text{C}_\text{P}\times\text{dT}=\text{C}_\text{P}\text{dT}\dots\text{(iii)}$
The heat supplied at a constant pressure increases the temperature by dT hence increases its internal energy by dU=CvdT as well as enables the gas to perform work dW.
dW = PdV ...(iv)
From the first law of thermodynamics, we have
dQ = dU + dw S
Substituting the values, we get,
$\text{C}_\text{P}\text{dT}=\text{C}_\text{V}\text{dT}+\text{PdV}$
But
PV = RT (For one mole of an ideal gas)
or PdV = RdT,
$\therefore\text{C}_\text{P}\text{dT}=\text{C}_\text{V}\text{dT}+\text{RdT}$
$\text{C}_\text{P}-\text{C}_\text{V}=\text{R}\dots\text{(v)}$
This is the relationship between two principal specific heats of the gas when Cp, Cv and R are measured in the units of either heat or of work.
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Question 225 Marks
Consider a cycle tyre being filled with air by a pump. Let V be the volume of the tyre (fixed) and at each stroke of the pump $\Delta\text{V}(<<\text{V})$ of air is transferred to the tube adiabatically. What is the work done when the pressure in the tube is increased from P1 to P2?
Answer
Air is transferred into tyre adiabatically let initial volume of air in tyre V and after pumping one stroke it become (V + dV) and pressure increase from P to (P + dP) then 
$\text{P}_{1}\text{V}_{1}^\gamma=\text{P}_{2}\text{V}_{2}^\gamma$
$\text{P}(\text{d}+\text{dv})^\gamma=(\text{P}+\text{dp})\text{V}^\gamma$
$\text{PV}\Big[1+\frac{\text{dV}}{\text{V}}\Big]^\gamma=\text{P}\Big[1+\frac{\text{dP}}{\text{P}}\Big]\text{V}^\gamma$
As volume of tyre V remains constant 
$\text{PV}^\gamma\Big[1+\gamma\frac{\text{dV}}{\text{V}}\Big]=\text{PV}^\gamma\Big[1+\frac{\text{dP}}{\text{P}}\Big]$
$\big[$on expanding by binomial theorm neglecting the higher terms of $\Delta\text{V}$ as $\Delta\text{V}<<\text{V}\big]$
$1+\gamma\frac{\text{dV}}{\text{V}}=1+\frac{\text{dP}}{\text{P}}$
$\text{dV}=\frac{\text{VdP}}{\gamma\text{P}}$
Integrating both side in limits W1 to W2 and P→ P2
$\int\text{pdV}=\int\limits^{\text{p}_2}_{\text{p}_1}\frac{\text{VdP}}{\gamma}$
$\int\limits^{\text{w}_2}_{\text{w}_1}\text{dw}=\frac{\text{V}}{\gamma}(\text{P}_{2}-\text{P}_{1})(\text{V}=\text{constant})$
$\text{W}=\frac{(\text{P}_{2}-\text{P}_{1})\text{V}}{\gamma}$
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Question 235 Marks
Calculate the heat required to convert 0.6kg of ice at -20°C, kept in a calorimeter to steam at 100°C at atmospheric pressure. Given the specific heat capacity of ice = 2100J kg-1K-1, specific heat capacity of water is 4186J kg -1K-1, latent heat of ice = 3.35 × 105J kg-1, and latent heat of steam = 2.256 × 106J kg-1.
Answer
Heat required to convert ice at -20°C to 0°C
$\text{Q}_1=\text{m s}_\text{ice}\Delta\text{T}_1=0.6\times2100\times[0-(-20)]$
$=25200\text{J}$
Heat required to melt ice at 0°C to water at 0°C
$\text{Q}_2=\text{m L}_\text{ice}=0.6\times(3.35\times10^5)$
$=201000\text{J}$
Heat required to convert water at 0°C to water at 100°C
$\text{Q}-3=\text{ms}_\text{w}\Delta\text{T}-2=0.6\times4186\times(100-0)$
$=251160\text{J}$
Heat required to convert water at 100°C to steam at 100°C.
$\text{Q}_4=\text{m L}_\text{steam}=0.6\times2.256\times10^6$
$=1353600\text{J}$
Total heat spent $\text{Q}_1+\text{Q}_2+\text{Q}_3+\text{Q}_4$
$=1830960=1.8\times10^6\text{J}$
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Question 245 Marks
A cylinder fitted with a movable piston contains hydrogen at a pressure of 3.5 × 105N-m2 and temperature 366K. Hydrogen expands adiabatically until the pressure in the cylinder falls to 0.7 × 105 N-m-2. The piston is then fixed and the gas is heated until the temperature becomes 366K. The pressure in the cylinder is now found to be 1.1 × 105N-m-2. Determine the specific heats of hydrogen. (R = 8.3 J mol-1 K-1).
Answer

The processes are shown in Fig.
The process B to C is at constant volume, hence
$\frac{\text{P}_3}{\text{P}_2}=\frac{\text{T}_3}{\text{T}_2}$
or $\text{T}_2=\text{T}_3\times\frac{\text{P}_2}{\text{P}_3}$
$=366\times\frac{7\times10^4}{1.1\times10^5}$
$=233\text{K}$
The process A to B is adiabatic, hance
$\frac{\text{T}_1}{\text{T}_2}=\Big(\frac{\text{P}_1}{\text{P}_2}\Big)^{\frac{(\gamma-1)}{\gamma}}$ or $\frac{366}{233}=\Big(\frac{3.5\times10^5}{7\times10^4}\Big)^{\frac{(\gamma-1)}{\gamma}}$
Solving we get $\gamma=1.39$
Now, $\frac{\text{C}_\text{P}}{\text{C}_\text{V}}=1.39\Big(\because\gamma=\frac{\text{C}_\text{P}}{\text{C}_\text{V}}\Big)\dots\text{(i)}$
Again $\text{C}_\text{P}-\text{C}_\text{V}=\text{R}\text{}$ or $\text{C}_\text{P}-\text{C}_\text{V}=8.3\dots\text{(ii)}$
From equation (i) $\text{C}_\text{P}=1.39\text{C}_\text{V}$
Substituting the value of CP in equation (2), we have
$1.39\text{C}_\text{V}-\text{C}_\text{V}=8.3$ or $0.39\text{C}_\text{V}=8.3$
$\therefore\text{C}_\text{V}=\frac{8.3}{0.39}$
$=21.28\text{J mol}^{-1}\text{K}^{-1}$
Now $\text{C}_\text{P}=8.3+\text{C}_\text{V}$
$=8.3+21.28$
$=29.58\text{J}\text{ mol}^{-1}\text{K}^{-1}$
Hence, $\text{C}_\text{P}=29.58\text{J mol}^{-1}\text{K}^{-1}$ and $\text{C}_\text{V}=21.28\text{J mol}^{-1}\text{K}^{-1}$
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Question 255 Marks
When a system is taken from state i to state f along the path iaf (see fig. below), it is found that the heat Q absorbed by the system is 50 cal. and work done W by the system is equal to 20 cal. along the path ibf; Q = 36 cal.
  1. What is W along the path ibf?
  2. If W = -13 cal. for the curved return path fi, what is for this path?
  3. Take Ui = 10 cal, what is Uf?
  4. If Ub = 22 cal. what are Q for the processes bf and ib?
​​​​​​​
Answer
According to first law of thermdynamics,

dQ = dU + dW or Q = Uf - Ui + W

Uf = internal energy

In final state and Ui internal energy in initial state.

For path i a f,

Q = +50cal. and W = 20cal

$\because\text{U}_\text{f}-\text{U}_\text{i}=\text{Q}-\text{W}$

$=50-20=30\text{cal}$

Here it should be remembered that the change in internal energy between i and f state remains the same i.e., 20 cal. whatever path is followed.

  1. For path ibf,

Q = 36cal. and dU = Uf - Ui = 30cal

$\therefore\text{W}=\text{Q}-(\text{U}_\text{f}-\text{U}_\text{i})$

$=36-30=6\text{cal}$

  1. For path fi.

$\text{W}=-13\text{cal}\text{ dU}=30\text{cal}$

$\therefore\text{Q}=\text{W}+(\text{U}_\text{f}-\text{U}_\text{i})$

  1. $\text{U}_\text{i}=10\text{cal}$

$\text{dU}=\text{U}_\text{f}-\text{U}_\text{i}=30$

$\therefore\text{U}_\text{f}=30+\text{U}_\text{i}$

$=30+10=40\text{cal}$

  1. For process bf, volume is constant i.e., work done is zero.

$\therefore\text{Q}=\text{dU}=\text{U}_\text{f}-\text{U}_\text{b}$

$=40-22=18\text{cal}$

For path ib,

$\therefore\text{Q}=\text{Q}_{\text{ibf}}-\text{Q}_\text{bf}$

$=36-18=18\text{cal}$

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Question 265 Marks
A lead bullet penetrates into a solid object and melts. Assuming that 50% of the K.E. was used to heat it, calculate the initial speed of the bullet. The initial temperature of bullet is 27°C and its melting point is 327°C. Latent heat of fusion of lead = 2.5 × 104J kg-1 and specific heat capacity of lead = 125J kg-1K-1.
Answer
Here, let m be the mass of the bullet. Heat required to raise its temperature fiom 27°C to 327°C.
$\because372^\circ\text{C}=600\text{K}$
$27^\circ\text{C}=300\text{K}$
$\Delta\text{Q}_1=\text{mc}\Delta\text{T}=125\times\text{m}\times(600-300)$
$=(3.75\times10^4)\text{m J}$
If v is initial velocity of the bullet, then K.E. of bullet $=\frac12\text{mv}^2$
As heat developed $=\frac12\text{K.E.}=\frac12\times\frac12\text{mv}^2$
$\therefore3.75\times10^4\text{m}+2.5\times10^4\text{m}=\frac14\text{mv}^2$
$6.25\times10^4\text{m}=\frac{1}{4}\text{mv}^2$
$\Rightarrow\text{v}=\sqrt{4\times6.25\times10^4}$
$\Rightarrow\text{v}=5\times10^2\text{m/s}$
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Question 275 Marks
The motor in a refrigerator has power output 250 watt. The freezing compartment is at 270K and outside air at 300K. Assuming ideal efficiency, what is the amount of heat that can be extracted from the freezing compartment in 10 minutes? What is the shortest time in which 10kg of water at 273K can be converted into ice? J = 4.2 × 103 kcal-1.
Answer
We know that

$\beta=\frac{\text{Q}_2}{\text{W}}=\frac{\text{Q}_2}{\text{Q}_1-\text{Q}_2}=\frac{\text{T}_2}{\text{T}_1-\text{T}_2}$

Here, $\text{T}_1=300\text{K},\ \text{T}_2=270\text{K}$

$\text{W}=250\text{W}=250\text{Js}^{-1}$

$\text{Q}=?,\text{t}=?$

$\therefore\text{Q}_2=\text{W}\beta=\text{W}\Big(\frac{\text{T}_2}{\text{T}_1-\text{T}_2}\Big)$

$=250\Big(\frac{270}{300-270}\Big)$

$=250\times\frac{270}{30}=2250\text{Js}^{-1}$

  1. Let Q be the heat etracted from the freezing compertment in 10 minutes

$\therefore\text{Q}=\text{Q}_2\times10\text{min}$

$=2250\times10\times60$

$=1350000\text{J}$

$=\frac{135\times10^4}{4.2\times10^3}\text{kcal}$

$=321.4\text{ kcal}$

  1. Heat required to convert 1kg of water at 273K into ice,

$\text{Q}'=\text{m}\times\text{L}$

$=1\times80\text{ kcal}$

$=80\times4.2\times10^3\text{J}$

Let Q' be etraction of heat from freezing compartment

$=\frac{80\times4.2\times10^3}{\text{t}}\text{Js}^{-1}$

This rate must be equal to Q2.

i.e., $2250=\frac{80\times1.2\times10^3}{\text{t}}$

$\therefore\text{t}=\frac{80\times4.2\times10^3}{2250}=149.33\text{s}.$

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Question 285 Marks
A Carnot engine is working between ice point and steam point. It is desired to increase its efficiency by 20% (a) by changing temperature of hot reservoir alone, (b) by changing temperature of colder reservoir only. Calculate the change in temperature in each case.
Answer
Here, T1 = 100°C = 373K and T2 = 0°C = 273K

$\eta=\frac{\text{T}_1-\text{T}_2}{\text{T}_1}=\frac{373-273}{373}$

$=\frac{100}{373}=0.268$

As we want to increase its efficiency by 20%, hence new efficiency is,

$\eta'=26.\%+20\%=46.8\%$

  1. If keeping temperature of colder reservoir fixed the temperature of hot reservoir is changed to $\text{T}_1'$ then

$46.8=\frac{\text{T}_1'-273}{\text{T}'_1}\times100$

$\Rightarrow46.8\text{T}_1'=100$

$\text{T}_1'-27300$

$\Rightarrow53.2\text{T}'_2=27300$ or $\frac{27300}{53.2}=\text{513.2}\text{K}$

$\therefore\text{T}_1'-\text{T}_1=513.2-373=140.2\text{K}$

It means that temprature of hot resevoir be raised by 140.2K

  1. If keeping temperature of hot reservoir fixed, the temperature of colder reservoir is changed to $\text{T}_2',$ then

$46.8=\frac{\text{T}_1-\text{T}_2'}{\text{T}_1}\times100$

$=\frac{373-\text{T}'_2}{373}\times100$

$\therefore373\times46.8=373\times100-100\text{T}_2'$

$\Rightarrow100\text{T}_2'=373\times(100-46.8)$

$=373\times53.2$

$\Rightarrow\text{T}'_2=\frac{373-53.2}{100}=198.4\text{K}$

$\therefore\text{T}_2-\text{T}_2'=273-198.4$

$=74.6\text{K}=74.6^\circ\text{C.}$

It means that temparture of colder reservoir be lowered by 74.6°C.

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Question 295 Marks
The difference between the two specific heat capacities (at constant pressure and volume) of a gas is 5000J kg-1 k-1 and the ratio of these specific heat capacities is 1.6. Find the two specific heat capacities i.e. Cp and Cv.
Answer
We Know that,
$\text{C}_\text{P}-\text{C}_\text{V}=\text{R}$
$\text{C}_\text{P}-\text{C}_\text{V}=5000$
Dividing by CV we get,
$\frac{\text{C}_\text{P}}{\text{C}_\text{V}}-1=\frac{5000}{\text{C}_\text{V}}$
$1.6-1=\frac{5000}{\text{C}_\text{V}}$
$0.6=\frac{5000}{\text{C}_\text{V}}$
$\therefore\text{C}_\text{V}=\frac{5000}{\text{0.6}}$
$=8333.33\text{J/}\ \text{Kg}^{-1}\text{K}^{-1}$
Now, $\text{C}_\text{P}-\text{C}_\text{V}=5000$
$\text{C}_\text{P}-8333.33+5000$
$=13333.33\ \text{J}\ \text{Kg}^{-1}\text{K}^{-1}$
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Question 305 Marks
0.32g of oxygen is kept in a rigid container and is heated. Find the amount of heat needed to raise the temperature from 25°C to 35°C. The molar heat capacity of oxygen at constant volume is 20J mole-1K-1.
Answer
Here, molecular wt. of oxygen = 32g/ mole
$\therefore$ Amount of oxygen in moles (n)
$=\frac{0.32}{32}=0.01\text{mole}$
$\therefore$ Amount of heat required
$\Delta\text{Q}=\text{n}\text{C}_\nu\Delta\text{T}=0.01\times20(35-25)=2.0\text{J}$
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Question 315 Marks
Explain how Carnot's cycle works with the heat flow diagram. Using the same, explain the working of a refrigerator. Also, give its coefficient of performance.
Answer
Refrigerator absorbs heat from the body at a low temperature and liberates it to a body at a high temperature by doing work. It can be shown by the given diagram.
Q2→ Energy absorbed from sink.
Q1 → Energy liberated to source.
W → Work done on the system.

Coefficient of performance $=\frac{\text{Q}_2}{\text{Q}_1-\text{Q}_2}$
Q1 – Q2 refers to the work done on the system/refrigerator.
Coefficient of performance (COP) $=\frac{\text{Q}_2}{\text{Q}_1-\text{Q}_2}=\frac{\text{T}_2}{\text{T}_1-\text{T}_2}$
Refrigerator: It works in the reverse Carnot's cycle. Heat is absorbed from sink at low temperature T2 and given to the source at higher temperature T1 with the help of an external agency doing work on the system. (W = Q1 - Q2).

The compressor in the refrigerator uses electrical energy and does work on the system. The coefficient of performance is defined as the heat energy absorbed from low temperature sink Q2 to the amount of work done.
$\text{W}=\text{Q}_1-\text{Q}_2$
$\text{COP}=\frac{\text{Q}_2}{\text{Q}_1-\text{T}_2}=\frac{\text{T}_2}{\text{T}_1-\text{T}_2}$
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Question 325 Marks
Show analytically that work done by one mole of an ideal gas during isothermal expansion from volume V1 to volume V2 is given by,
$\text{W}=\text{RT}\log_\text{e}\Big(\frac{\text{V}_2}{\text{V}_1}\Big)$
Answer
Consider 1 g mole of an ideal gas enclosed in a cylinder with perfectly conducting Walls and fitted with a perfectly frictionless and conducting piston.
Let P1 ,V1 T be the initial pressure, volume and temperature of the gas. Let the gas expand to a volume V2 when pressure reduces to P2 and temperature remains constant at T. At any instant during expansion, let the pressure of the gas be P. If A is the area of cross-section of the piston, then force exerted by the gas on the piston is,
F = P × A ...(i)
If we assume that pressure of the gas during an infinitestimally small outward displacement dx of the piston remains constant, then small amount of work done during expansion
dW = F × dx = P × A × dx
dW = P(dv)
where dV = A(dx) = Small increase in volume of the gas
Total work done by the gas in expansion from initial volume.
Volume V1 to final volume V2 is,
$\text{W}=\int\limits^{\text{V}_2}_{\text{V}_1}\text{P}(\text{dV})$
From standard gas equation, PV = RT or $\text{P}=\frac{\text{RT}}{\text{V}}$
$\text{W}=\int\limits^{\text{V}_2}_{\text{V}_1}\frac{\text{RT}}{\text{V}}\text{dV}$
$=\text{RT}\int\limits^{\text{V}_2}_{\text{V}_1}\frac{1}{\text{V}}\text{dV}=\text{RT}[\log_s\text{V}]^{\text{V}_2}_{\text{V}_1}$
$\text{W}=\text{RT}[\log_\text{e}\text{V}_2-\log\text{V}_1]$
$\text{W}=\text{RT}\log_\text{e}\Big(\frac{\text{V}_2}{\text{V}_1}\Big)$
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Question 335 Marks
A cylinder with a movable piston contains 3 moles of hydrogen at standard temperature and pressure. The walls of the cylinder are made of a heat insulator, and the piston is insulated by having a pile of sand on it. By what factor does the pressure of the gas increase if the gas is compressed to half its original volume?
Answer
The cylinder is completely insulated from its surroundings. As a result, no heat is exchanged between the system (cylinder) and its surroundings. Thus, the process is adiabatic.
Initial pressure inside the cylinder = P1
Final pressure inside the cylinder = P2
Initial volume inside the cylinder = V1
Final volume inside the cylinder = V2
Ratio of specific heats, γ = 1.4
For an adiabatic process, we have:
P1V1γ = P2V2γ
The final volume is compressed to half of its initial volume.
$\therefore$ V2 = V1/2
P1V1γ = P2(V1/2)γ
P2/P1 = V1γ/(V1/2)γ
= 2γ = 21.4 = 2.639
Hence, the pressure increases by a factor of 2.639.
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Question 345 Marks
State first law of thermodynamics. On the basis of this establish the relation between two molar specific heats for an ideal gas.
Answer
First Law of Thermodynamics: We know that the internal energy U of a system can change through two modes of energy transfer : heat and work.
Let dQ = a small amount of heat supplied to the system by the surrounding.
dW = a small amount of work done by the system on the surrounding
According to the general principle of conservation of energy dQ = dU + dW is known as the first law of thermodynamics. U- Internal energy of the system is a state variable depends only on the final and the initial state of the system. dQ, dW depend upon the path taken by the gas to go from one state to the other.
Derivation: Consider 1g mole of an ideal gas enclosed in a cylinder fitted with a piston, which is perfectly frictionless. Let P, V, T be the pressure, volume and temperature of the gas.
Let the gas be heated at constant volume through a small range of temperature dT.
$\therefore$ Amount of heat energy supplied to the gas
dQ = Cv . 1. dT ...(i)
Cv = Molar specific heat of the gas at constant volume
 As volume remains constant dV = 0
$\therefore$ dW = P(dV) = 0
According to the first law of thermodynamics,
dQ = dU + DW
CvdT = DU + 0
⇒ dU = CvdT ….(ii)
Let the gas be now heated at constant pressure through the same range of temperature dt, when its volume increases by a small amount dV.
Amount of heat energy supplied to the gas,
dQ' = Cp.1. dT ...(iii)
Where, Cp is molar specific heat of the gas at constant pressure.
dW' = P(dV)) ...(iv)
According to the first law of thermodynamics,
dQ' = dU' + dW’
CpdT = dU' + PdV ...(v)
As rise in temperature of the gas in the two cases is the same (= dT), therefore increase in its internal energy (which depends only on temperature in case of ideal gas) must be the same in the two cases; i.e.
dU' = dU
Using (ii), dU' = dU = CvdT ....(vi)
Putting in (v),
CpdT = Cv dT + PdV
(Cp- Cv)dt = PdV ...(vii)
According to the standard equation of gas,
PV = RT
PDV = RDT [by differentiating on both sides]
Where, P and R are constants.
$\therefore(\text{C}_\text{P}-\text{C}_\text{V})\text{dT}=\text{RdT}$ [Putting PdV = RdT in (vii)]
⇒ CP - CV = R
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Question 355 Marks
In an experiment on the specific heat of a metal, a 0.20kg block of the metal at 150°C is dropped in a copper calorimeter (of water equivalent 0.025kg) containing 150 c.c. of water at 27°C. The final temperature is 40°C. Calculate the specific heat of the metal. If heat losses to the surroundings are not negligible, is your answer greater or smaller than the actual value of specific heat of the metal?
Answer
Here, mass of metal,
m = 0.20kg = 200g
Fall in temperature of metal,
$\Delta\text{T}=150-40=110^\circ\text{C}$
If C is specific heat of the metal, then heat lost by the metal,
$\Delta\text{Q}=\text{mC}\Delta\text{T}=200\times\text{C}\times110\dots\text{(i)}$
Volume of water = 150 c.c.
$(\because$ density of water is 1g/ cc$)$
$\therefore$ Mass of water, m' = 150g
Water equivalent of calorimete
W = 0.025kg = 25g
Rise in temperature of water and calorimeter
$\Delta\text{T}'=40-27=13^\circ\text{C}$
Heat gained by water and calorimeter,
$\Delta\text{Q}'=(\text{m}'+\text{W})\Delta\text{T}'$
$=(150+25)\times13$
$=175\times13\dots\text{(ii)}$
As $\Delta\text{Q}=\text{Q}'$
$\therefore$ From (i) and (ii), 200 × C × 110
= 175 × 13
$\text{C}=\frac{175\times13}{200\times110}=0.1$
If some heat is lost to the surroundings, value of C so obtained will be less than the actual value of C.
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Question 365 Marks
In a refrigerator one removes heat from a lower temperature and deposits to the surroundings at a higher temperature. In this process, mechanical work has to be done which is provided by an electric motor. If the motor is of 1KW power, and heat is transferred from –3°C to 27°C, find the heat taken out of the refrigerator per second assuming its efficiency is 50% of a perfect engine.
Answer
Carton's engine is perfect heat engine operating between two tempreature T1  and  T(source and sink). Refrigerator is aiso carnot's engine working in reverse order its efficiency in $\eta$
$\eta=1-\frac{\text{T}_{2}}{\text{T}_{2}}=1-\frac{273-3}{273+27}=1-\frac{270}{300}=-.9=1=\frac{1}{10}$
Efficiency of refrigerator's 50 % of perfect engine
$\therefore$ Efficiency of refrigerator = 50% of 1 = 0.5
Net efficiency = $\eta'$ = 0.5 × 0.1 = 0.05
$\therefore$ Cofficient of performence $\beta=\frac{\text{Q}_{2}}{\text{W}}=\frac{1-\eta'}{\eta'}$
$\beta=\frac{1-0.05}{0.05} =\frac{0.95}{0.05}=19$
Q2 = 19% W .D. by motor on refrigerator
= 19 × 1KW =19KJ/ s
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Question 375 Marks
In changing the state of a gas adiabatically from an equilibrium state A to another equilibrium state B, an amount of work equal to 22.3J is done on the system. If the gas is taken from state A to B via a process in which the net heat absorbed by the system is 9.35 cal, how much is the net work done by the system in the latter case? (Take 1 cal = 4.19J)
Answer
The work done (W) on the system while the gas changes from state A to state B is 22.3J.

This is an adiabatic process. Hence, change in heat is zero.

$\therefore\Delta\text{Q} = 0$

$\Delta\text{W} = -22.3\text{ J}$ (Since the work is done on the system)

From the first law of thermodynamics, we have:

$\Delta\text{Q}=\Delta\text{U}+\Delta\text{W}$

Where,

ΔU = Change in the internal energy of the gas

$\therefore\ \Delta\text{U}=\Delta\text{Q}-\Delta\text{W}=-(-22.3\text{ J})$

$\Delta\text{U} = +22.3\text{ J}$

When the gas goes from state A to state B via a process, the net heat absorbed by the system is:

$\Delta\text{Q} = 9.35\text{ cal}$

= 9.35 × 4.19 = 39.1765J

Heat absorbed, $\Delta\text{Q}=\Delta\text{U}+\Delta\text{Q}$

$\therefore\ \Delta\text{W}=\Delta\text{Q}-\Delta\text{U}$

= 39.1765 - 22.3

= 16.8765 

Therefore, 16.88J of work is done by the system.

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Question 385 Marks
What amount of heat must be supplied to 2.0 × 10-2kg of nitrogen (at room temperature) to raise its temperature by 45°C at constant pressure? (Molecular mass of N2 = 28; R = 8.3J mol-1 K-1.)
Answer
Mass of nitrogen, m = 2.0 × 10-2kg = 20g
Rise in temperature, $\Delta\text{T}=45^\circ\text{C}$
Molecular mass of N2, M = 28
Universal gas constant, R = 8.3J mol-1 K-1
Number of moles, $\text{n}=\frac{\text{m}}{\text{M}}$
$=\frac{20.\times10^{-2}\times10^3}{28}=0.714$
Molar specific heat at constant pressure for nitrogen Cp = (7/2)R
= 7/2 × 8.3
= 29.05J mol-1 K-1
The total amount of heat to be supplied is given by the relation:
$\Delta\text{Q}=\text{nC}_\text{p}\Delta\text{T}$
$=0.714\times29.05\times45$
$=933.38\text{ J}$
Therefore, the amount of heat to be supplied is 933.38J.
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Question 395 Marks
A person of mass 60kg wants to lose 5kg by going up and down a 10m high stairs. Assume he burns twice as much fat while going up than coming down. If 1kg of fat is burnt on expending 7000 kilo calories, how many times must he go up and down to reduce his weight by 5kg?
Answer
Gravitational potential energy (PE) of an object at height (h) is mgh. The energy losses by person in the form of fat will be utilised to increase PE of the person. As it is given that he burns twice as much fat while going up than coming down. Thus, the calorie consumed by the person in going up is mgh, and calorie consumed by the person in comming down is 1/ 2 mgh
According to the problem, height of the stairs  = h = 10 m 
Work done to burn 5kg of fat 
= (5kg) (7000 × 103 cal) (4.2J/ cal)
= 147 × 106J
Work done towards burning of fat in one trip (up and down the stairs )
$=\text{mgh}+\frac{1}{2}\text{mgh}=\frac{3}{2}\text{mgh}$
$=\frac{3}{2}(60\text{kg})(10\text{m/ s}^2)(10m)=9\times10^3\text{J}$
(as only half the work done while coming down is useful in burning fat ) 
$\therefore$ Number of times, the person has to go up and  down the stairs (no. of trips required)
$\text{N}=\frac{147\times10^6\text{J}}{9\times10^3\text{J}}=16.3\times10^3\text{times}$
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Question 405 Marks
Describe the working of Carnot engine. Obtain an expression for its efficiency.
Answer
Carnot used a set of four devices—a source at a high temperature (say T1), a sink at a low temperature (say T2), a non-conducting base and a cylinder with a working substance, frictionless piston made of conducting base and non-conducting walls and piston.
He carried the system through a step of four processes to complete a cycle as shown here.
Process I-HW is an isothermal expansion. Q1 energy flows in and temperature is maintained at T1 by placing the cylinder over the source.

Process II-WN is an adiabatic processes at a temperature flow from T1 to T2 conducted with cylinder over (NCB = Non conducting base).
Process III-NF is an isothermal process at T2 which gives out an energy Q2 with cylinder over sink
Process IV-FH is an adiabatic process which changes the temperature from T2 to T1 conducted with the cylinder placed over (NCB = Non conducting base).

In the process, a net work equalling the area HWNFH is done with the net heat intake,
Q1 - Q2 So, Efficiency $=\frac{\text{Work done}}{\text{heat supplied}}$
$=\frac{\text{Q}_1-\text{Q}_2}{\text{Q}_1}=1-\frac{\text{Q}_2}{\text{Q}_1}=1-\frac{\text{T}_2}{\text{T}_1}$
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Question 415 Marks
Calculate the work done for adiabatic expansion of a gas.
Answer
Consider (say u mole) an ideal gas, which is undergoing an adiabatic expansion. Let the gas expands by an infinitesimally small volume dV, at pressure p, then the infinitesimally small work done given by dW = pdV
The net work done from an initial volume V1 to final volume V2 is given by,
$\text{W}=\int\limits^{\text{V}_2}_{\text{V}_1}\text{pdV}$
For an adiabatic process, $\text{pV}^\gamma=\text{constant}=\text{K}$
$\text{p}=\frac{\text{K}}{\text{V}^\gamma}=\text{KV}^{-\gamma}$
$\therefore\text{W}=\int\limits^{\text{V}_2}_{\text{V}_1}(\text{KV}^{-\gamma})\text{dV}=\text{K}\Big[\frac{\text{V}^{-\gamma+1}}{-\gamma+1}\Big]^{\text{V}_2}_{\text{V}_2}$
$=\frac{\text{KV}^{-\gamma+1}_2-\text{KV}_1^{-\gamma+1}}{(1-\gamma)}$
For an adiabatic process,
$\text{K}=\text{p}_1\text{V}_1^\gamma=\text{p}_2\text{V}_2^\gamma$
$\Rightarrow\text{W}=\frac{\text{p}_2\text{V}_2^\gamma\cdot\text{V}^{-\gamma+1}-\text{p}_1\text{V}_1^\gamma\cdot\text{V}_2^{-\gamma+1}}{(1-\gamma)}$
$=\frac{1}{(1-\gamma)}(\text{p}_2\text{V}_2-\text{p}_1\text{V}_1)$
For an ideal gas, $\text{p}_1\text{V}_1=\mu\text{RT}_1$ and $\text{p}_2\text{V}_2=\mu\text{RT}_2.$
So, we have
$\text{W}=\frac{1}{(1-\gamma)}[\mu\text{RT}_2-\mu\text{RT}_1]$
$=\frac{\mu\text{R}}{(\gamma-1)}[\text{T}_1-\text{T}_2]$
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Question 425 Marks
Consider that an ideal gas (n moles) is expanding in a process given by P = f( V ), which passes through a point (V0, P0 ). Show that the gas is absorbing heat at (P0, V0 ) if the slope of the curve P = f(V ) is larger than the slope of the adiabat passing through (P0, V0 ).
Answer
slope of graph at  $\big(\text{V}_0,\text{P}_0\big)=\Big(\frac{\text{dP}}{\text{dV}}\Big)_{(\text{V}_0\text{P}_0)}$
$\text{P}=\text{f}(\text{V})$ for adiabatic process $\text{PV}^\gamma$ = constant (K)
 $\text{Or}\ \text{P}=\frac{\text{K}}{\text{V}^\gamma}\ \text{or}\ \frac{\text{dP}}{\text{dV}}=\text{K}\big(-\gamma\big)\text{V}^{-\gamma-1}$
$\frac{\text{dP}}{\text{dV}}=-\gamma\text{PV}^\gamma\text{V}^{-\gamma}\text{V}^{-1}=-\frac{\gamma\text{P}}{\text{V}}$
$\Big(\frac{\text{dP}}{\text{dV}}\Big)_{\text{(P}_0\text{V}_0)}=\frac{-\gamma\text{P}_0}{\text{V}_0}$ Heat absorbed by in the process $$$\text{P}=\text{f}(\text{V})$
$\text{dQ}=\text{dU}+\text{dW}$
$\text{dQ}=\text{n}\text{C}_\text{V}\text{dT}+\text{PdV}\ .....(\text{i})$
$\text{PV}=\text{nRT}$
$\text{T}=\frac{\text{PV}}{\text{nR}}=\frac{\text{V}}{\text{nR}}\text{f}(\text{V})$
$\frac{\text{dT}}{\text{dV}}=\frac{1}{\text{nR}}\big[\text{f}(\text{V})+\text{Vf}\ '(\text{V})\big]$
$\frac{\text{dQ}}{\text{dV}}=\text{nC}_\text{V}\frac{\text{dT}}{\text{dV}}+\text{P}.\frac{\text{dV}}{\text{dV}}=\frac{\text{nC}_\text{V}}{\text{nR}}$$\big[\text{f(V)}+\text{Vf}\ '\text{(V)}\big]+\text{P}$
$\Big(\frac{\text{dQ}}{\text{dV}}\Big)_{\text{V}-\text{V}_0}=\frac{\text{C}_\text{V}}{\text{R}}$$\big[\text{f}(\text{V}_0)+\text{V}_0\text{f}\ '(\text{V}_0)\big]+\text{f}_0\text{V})$$\big[\because\text{P}=\text{f}(\text{V})\text{ given}\big]$
$=\text{f}(\text{V}_0)\Big[\frac{\text{C}_\text{V}}{\text{R}}+1\Big]+\text{V}_0\text{f}\ '(\text{V}_0)\frac{\text{C}_\text{V}}{\text{R}}$
$\text{C}_\text{P}-\text{C}_\text{V}=\text{R}\Rightarrow\frac{\text{C}_\text{P}}{\text{C}_\text{V}}-1=\frac{\text{R}}{\text{C}_\text{V}}$
$\therefore\gamma-1=\frac{\text{R}}{\text{C}_\text{V}}\Rightarrow\text{C}_\text{V}=\frac{\text{R}}{\gamma-1}\Rightarrow\frac{\text{C}_\text{V}}{\text{R}}=\frac{1}{\gamma-1}$
$\Big(\frac{\text{dQ}}{\text{dV}}\Big)_{\text{V-V}_0}=\text{f}(\text{V}_0)\Big[\frac{1}{\gamma-1}\Big]+\text{V}_0\text{f}\ '(\text{V}_0)\frac{1}{\gamma-1}$
$=\text{f}(\text{V}_0)\Big[\frac{1+\gamma-1}{\gamma-1}\Big]+\frac{\text{V}_0\text{f}\ '(\text{V}_0)}{\gamma-1}$
$=\frac{\gamma}{(\gamma-1)}\text{f}(\text{V}_0)+\text{V}_0\frac{\text{f}\ '(\text{V}_0)}{\gamma-1}$
$=\frac{1}{(\gamma-1)}\big[\gamma\ \text{f}(\text{V}_0)+\text{V}_0\text{f}\ '(\text{V}_0)\big]$$\big(\because\ \text{f}(\text{V}_0)=\text{P}_0\big)$
$\Big(\frac{\text{dQ}}{\text{dV}}\Big)_{\text{V}-\text{V}_0}=\frac{1}{\gamma-1}$$\big[\gamma\ \text{P}_0+\text{V}_0\text{f}\ '(\text{V}_0)\big]$
$\therefore\ \Big(\frac{\text{dQ}}{\text{dV}}\Big)_{\text{V}-\text{V}_0}>1\therefore\ \text{and}\ \gamma>1\ \text{so}\ \frac{1}{\gamma-1}\text{is}+\text{ve}$
$\therefore\ \gamma\text{P}_0+\text{V}_0\text{f}\ '(\text{V}_0)>0$
$\text{V}_0\text{f}\ '(\text{V}_0)>-\gamma\text{P}_0$
$\text{f}\ '(\text{V}_0)>\frac{-\gamma\text{P}_0}{\text{V}_0}$
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Question 435 Marks
1 gram of water at 373K is converted into steam at the same temperature. The volume of 1cm3 of water becomes 1671cm3 on boiling. Calculate change in internal energy of the system, if heat of vapourisation is 540cal g-1. Given standard atmospheric pressure is 1.013 × 10% Nm-2.
Answer
Here, mass of water,
m = 1g
$\therefore$ Initial volume of water,
V1 = 1cm3
Volume of steam,
V2 = 1671cm3
$\therefore$ Change in volume,
dV = V2 - V1
1671 - 1 = 1670cm3 = 1670 × 10-6m3
standard atmospheric pressure
P = 1.013 × 105Nm-2
As change of state is invoved,
$\therefore\text{dQ}=\text{mL}=1\times4.18\text{J}$
$=2257\text{J}$
Change in internal energy, dU is aked.
dW = PdV
= 1.013 × 105 × 1670 × 10-6
= 169.17J
From dQ = dU + dW
⇒ dU = dQ - dW = 2257 - 169.17
dU = 2087.83J
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Question 445 Marks
A cycle followed by an engine (made of one mole of an ideal gas in a cylinder with a piston) is shown in Fig. Find heat exchanged by the engine, with the surroundings for each section of the cycle. (Cv = (3/2) R)

AB : constant volume

BC : constant pressur

CD : adiabati

DA : constant pressure

Answer
  1. : For A → B, dV = 0 

so,$\text{dW}=\int\text{P}.\text{dV}=\int\text{p}\times0=0$

$\text{dW}=0$

By $1^\text{st}$ law of thermodynamics

$\text{dQ}=\text{dU}+\text{dW}=\text{dU}+0$

$\therefore\ \text{dQ} =\text{dU}$

$\big(\text{dQ}=\text{n}\text{C}_\text{V}\text{dT}\big)$

So, $\text{dQ}-1\frac{3}{2}\text{R}\big(\text{T}_\text{B}-\text{T}_\text{A}\big).....(\text{i})$

$\text{dU}=\text{dQ}=\frac{3}{2}\big(\text{R}\text{T}_\text{}B-\text{R}\text{T}_\text{A}\big)=\frac{3}{2}\big(\text{P}_\text{B}\text{V}_\text{B}-\text{P}_\text{A}\text{}V_\text{A}\big)$

$\therefore$  Heat exchange [to system]

$\text{dQ}_1=\text{dU}=\frac{3}{2}\big(\text{P}_\text{s}\text{V}_\text{s}-\text{P}_\text{A}\text{V}_\text{A}\big)$

  1. For B to C, $\Delta\text{P}=0\ \text{n}=1$

$\text{dQ}=\text{dU}+\text{dW}=\text{C}_\text{V}\text{(dT)}+\text{P}_\text{S}\text{dV}$

$\text{dQ}_2=\frac{3}{2}\text{R}\big(\text{T}_\text{C}-\text{T}_\text{B}\big)+\text{P}_\text{B}\big(\text{V}_\text{C}-\text{V}_\text{B}\big)$

$=\frac{3}{2}\big(\text{T}_\text{C}\text{R}-\text{RT}_\text{B}\big)+\text{P}_\text{B}\text{V}_\text{C}-\text{P}_\text{B}\text{V}_\text{B}$

$=\frac{3}{2}[\text{P}_\text{C}\text{V}_\text{C}]-\frac{3}{2}[\text{P}_\text{B}\text{V}_\text{B}]-\text{P}_\text{B}\text{V}_\text{B}-\text{P}_\text{B}\text{V}_\text{C}$

$\text{V}_\text{A}=\text{V}_\text{B}\ \text{and}\ \text{P}_\text{B}=\text{P}_\text{C}$

$\therefore\text{dQ}_2=\frac{3}{2}\text{P}_\text{B}\text{V}_\text{C}-\frac{3}{2}\text{P}_\text{B}\text{V}_\text{A}-\text{P}_\text{B}\text{V}_\text{A}+\text{P}_\text{B}\text{V}_\text{C}$

$=\frac{5}{2}\text{P}_\text{B}\text{V}_\text{C}-\frac{5}{2}\text{P}_\text{B}\text{V}_\text{A}$

$\text{dQ}_2=\frac{5}{2}\text{P}_\text{B}[\text{V}_\text{C}-\text{V}_\text{A}]$

  1.  For diagram C → B,  adiabatic change

$\text{dQ}_3=0$  (No exchange of heat )

  1.  For diagram D  →  A, $\Delta\text{P}=0$ Compression of gas from volume VD to VA  pressure hence heat exchange similar to part (b) i.e. Heat exchange$\text{dQ}_3=\frac{5}{2}\text{P}_\text{A}\big(\text{V}_\text{A}-\text{V}_\text{D}\big)$
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Question 455 Marks
A cycle followed by an engine (made of one mole of perfect gas in a cylinder with a piston) is shown in Fig.

A to B : volume constant

B to C : adiabatic

C to D : volume constant

D to A : adiabatic

V= V= 2V= 2VB

  1. In which part of the cycle heat is supplied to the engine from outside?
  2. In which part of the cycle heat is being given to the surrounding by the engine?
  3. What is the work done by the engine in one cycle? Write your answer in term of PA, PB, VA.
  4. What is the efficiency of the engine?[$\gamma=\frac{5}{3}$ for the gas], $\big(\text{C}_\text{v}=\frac{3}{2}\text{R for one mole}\big)$
Answer

(a) A to B

(b) C to D

(c) $\text{W}_\text{AB}=\int\limits^\text{B}_\text{A}\text{pdV}=0;\text{W}_\text{CD}=0.$

Simillarly. $\text{W}_\text{BC}=\Big[\int\limits^\text{C}_\text{B}\text{pdV}=\text{k}\int\limits^\text{C}_\text{B}\frac{\text{dV}}{\text{V}^\text{r}}=\text{k}\frac{\text{V}^\text{-r+1}}{-\text{R}+1}\Big]^{\text{V}_{\text{C}}}_{\text{V}_\text{B}}$

$= \frac{1}{1-\gamma}(\text{P}_\text{c}\text{V}_\text{c}-\text{P}_\text{B}\text{V}_\text{B})$

Simillarly, $\text{W}_\text{DA}=\frac{1}{1-\gamma}(\text{P}_\text{A}\text{V}_\text{A}-\text{P}_\text{D}\text{V}_\text{D})$

Now $\text{P}_\text{C}=\text{P}_\text{B}\Big(\frac{\text{V}_\text{B}}{\text{V}_\text{C}}\Big)^\gamma=2^{-\gamma}\text{P}_\text{B}$

Simillarly, $\text{P}_\text{D}=\text{P}_\text{A}2^{-\gamma}$

Total work done $=\text{W}_\text{BC}+\text{W}_\text{DA}$

$=\frac{1}{1-\gamma}\big[\text{P}_\text{B}\text{V}_\text{B}\big(2^{-\gamma+1}-1\big)-\text{P}_\text{A}\text{V}_\text{A}\big(2^{-\gamma+1}-1\big)\big]$

$=\frac{1}{1-\gamma}\big(2^{1-\gamma}-1\big)\big(\text{P}_\text{B}-\text{P}_\text{A}\big)\text{V}_\text{A}$

$=\frac{3}{2}\big(1-\Big(\frac{1}{2}\Big)^\frac{2}{3}\big)\big(\text{P}_\text{B}-\text{P}_\text{A}\big)\text{V}_\text{A}$

  1. Heat supplied during process A, B 

$\text{d}\text{Q}_\text{AB}=\text{d}\text{U}_\text{AB}$

$\text{Q}_\text{AB}=\frac{3}{2}\text{n}\text{R}\big(\text{T}_\text{B}-\text{T}_\text{A}\big)\text{V}_\text{A}$

$\text{Efficiency}=\frac{\text{Net Work done }}{\text{Heat Supplied}}=\Big[1-\Big(\frac{1}{2}\Big)^\frac{2}{3}\Big]$

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