Thermodynamics MCQ Questions & Answers in Heat and Thermodynamics | Physics
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131.
If $$\Delta U$$ and $$\Delta W$$ represent the increase in internal energy and work done by the system respectively in a thermodynamical process, which of the following is true?
A
$$\Delta U = - \Delta W,$$ in an adiabatic process
B
$$\Delta U = \Delta W,$$ in an isothermal process
C
$$\Delta U = \Delta W,$$ in an adiabatic process
D
$$\Delta U = - \Delta W,$$ in an isothermal process
Answer :
$$\Delta U = - \Delta W,$$ in an adiabatic process
From first law of thermodynamics $$\Delta Q = \Delta U + \Delta W$$
For adiabatic process, $$\Delta Q = 0$$
$$\eqalign{
& \because \Delta Q = 0 \cr
& {\text{So,}}\,\,\Delta U = - \Delta W \cr} $$
132.
One mole of an ideal gas goes from an initial state $$A$$ to final state $$B$$ via two processes : It first undergoes isothermal expansion from volume $$V$$ to $$3V$$ and then its volume is reduced from $$3V$$ to $$V$$ at constant pressure. The correct $$P-V$$ diagram representing the two processes is :
A
B
C
D
Answer :
1st process is isothermal expansion which is only correct shown in option (D)
2nd process is isobaric compression which is correctly shown in option (D)
133.
An ideal gas is subjected to cyclic process involving four thermodynamic states, the amounts of heat $$\left( Q \right)$$ and work $$\left( W \right)$$ involved in each of these states
$${Q_1} = 6000\,J;{Q_2} = - 5500\,J;{Q_3} = - 3000\,J;{Q_4} = + 3500\,J$$
$${W_1} = 2500\,J;{W_2} = - 1000\,J;{W_3} = - 1200\,J;{W_4} = xJ$$
The ratio of the net work done by the gas to the total heat absorbed by the gas is $$\eta .$$ The values of $$x$$ and $$\eta $$ respectively are
135.
Figure shows the variation of internal energy $$\left( U \right)$$ with the pressure $$\left( P \right)$$ of $$2.0\,mole$$ gas in cyclic process $$abcda.$$ The temperature of gas at $$c$$ and $$d$$ are $$300\,K$$ and $$500\,K.$$ Calculate the heat absorbed by the gas during the process.
A
$$400\,R\ln 2$$
B
$$200\,R\ln 2$$
C
$$100\,R\ln 2$$
D
$$300\,R\ln 2$$
Answer :
$$400\,R\ln 2$$
Change in internal energy for cyclic process $$\left( {\Delta U} \right) = 0.$$
For process $$a \to b,\,\left( {P{\text{ - constant}}} \right)$$
$$\eqalign{
& {W_{a \to b}} = P\Delta V \cr
& = nR\Delta T = - 400\,R \cr} $$
For process $$b \to c,\,\,\left( {T{\text{ - constant}}} \right)$$
$${W_{b \to c}} = - 2R\left( {300} \right)\ln 2$$
For process $$c \to d,\,\left( {P{\text{ - constant}}} \right)$$
$${W_{c \to d}} = + 400\,R$$
For process $$d \to a,\,\left( {T{\text{ - constant}}} \right)$$
$${W_{d \to a}} = + 2R\left( {500} \right)\ln 2$$
Net work $$\left( {\Delta W} \right) = {W_{a \to b}} + {W_{b \to c}} + {W_{c \to d}} + {W_{d \to a}}$$
$$\eqalign{
& \Delta W = 400\,R\ln 2 \cr
& \therefore dQ = dU + dW,\,{\text{first law of thermodynamics}} \cr
& \therefore dQ = 400\,R\ln 2. \cr} $$
136.
An engine takes heat from a reservoir and converts its $$\frac{1}{6}$$ part into work. By decreasing temperature of sink by $${62^ \circ }C,$$ its efficiency becomes double. The temperatures of source and sink must be
A
$${90^ \circ }C,{37^ \circ }C$$
B
$${99^ \circ }C,{37^ \circ }C$$
C
$${372^ \circ }C,{37^ \circ }C$$
D
$${206^ \circ }C,{37^ \circ }C$$
Answer :
$${99^ \circ }C,{37^ \circ }C$$
If $${T_1}$$ is temperature of source and $${T_2}$$ the temperature of sink, the efficiency of engine
$$\eqalign{
& \eta = \frac{{{\text{Work done}}\left( W \right)}}{{{\text{Heat taken}}\left( {{Q_1}} \right)}} = 1 - \frac{{{T_2}}}{{{T_1}}} \cr
& \therefore 1 - \frac{{{T_2}}}{{{T_1}}} = \frac{1}{6}\,......\left( {\text{i}} \right) \cr} $$
When temperature of sink is reduced by $${62^ \circ }C,$$ then temperature of sink
$$\eqalign{
& {{T'}_2} = {T_2} - 62 \cr
& \therefore \eta ' = 1 - \frac{{{{T'}_2}}}{{{T_1}}} \cr} $$
As according to question efficiency becomes double
So, $$\eta ' = 2\eta = \frac{2}{6} = \frac{1}{3}$$
$$\therefore \frac{1}{3} = 1 - \frac{{{T_2} - 62}}{{{T_1}}}\,......\left( {{\text{ii}}} \right)$$
From Eq. (i) $$\frac{{{T_2}}}{{{T_1}}} = \frac{5}{6}\,......\left( {{\text{iii}}} \right)$$
From Eq. (ii) $$\frac{{{T_2} - 62}}{{{T_1}}} = \frac{2}{3}\,......\left( {{\text{iv}}} \right)$$
Dividing Eq. (iii) by Eq. (iv)
$$\eqalign{
& \frac{{{T_2}}}{{{T_2} - 62}} = \frac{5}{4} \cr
& \Rightarrow 4{T_2} = 5{T_2} - 310 \cr
& \Rightarrow {T_2} = 310\,K \cr} $$
and from Eq. (iii), we have
$$\frac{{310}}{{{T_1}}} = \frac{5}{6} \Rightarrow {T_1} = 372\,K$$
Hence, $${T_1} = 372\,K = 372 - 273 = {99^ \circ }C$$
and $${T_2} = 310\,K = 310 - 273 = {37^ \circ }C$$
As kinetic energy of a gas depends on its atomicity.
137.
Consider an ideal gas confined in an isolated closed chamber. As the gas undergoes an adiabatic expansion, the average time of collision between molecules increases as $${V^q},$$ where $$V$$ is the volume of the gas. The value of $$q$$ is: $$\left( {\gamma = \frac{{{C_p}}}{{{C_v}}}} \right)$$
138.
Thermodynamics is concerned in part with transformations between
A
different forms of heat energy
B
internal energy at various temperatures
C
one form of mechanical energy into other forms
D
heat, internal energy and mechanical work
Answer :
heat, internal energy and mechanical work
Thermodynamics concerned with $$\Delta H,\Delta U$$ and $$\Delta W.$$
139.
One mole of an ideal monatomic gas undergoes a process described by the equation $$p{V^3} = $$ constant. The heat capacity of the gas during this process is
A
$$\frac{3}{2}R$$
B
$$\frac{5}{2}R$$
C
$$2R$$
D
$$R$$
Answer :
$$R$$
As we know that for polytropic process of index $$\alpha $$ specific heat capacity $$ = {C_V} + \frac{R}{{1 - \alpha }}$$
$$\eqalign{
& \because {\text{Process,}}\,\,p{V^3} = {\text{constant}} \Rightarrow \alpha = 3 \cr
& \therefore C = {C_V} + \frac{R}{{1 - \alpha }} = \frac{{fR}}{2} + \frac{R}{{1 - 3}} \cr
& {\text{where,}}\,\,{C_V} = \frac{{fR}}{2} = \frac{{3R}}{2} \cr} $$
For monatomic gas, $$f = 3 = \frac{{3R}}{2}$$
$$ \Rightarrow C = \frac{{3R}}{2} - \frac{R}{2} = R$$
140.
$${C_P}$$ and $${C_V}$$ are specific heats at constant pressure and constant volume respectively. It is observed that
$${C_P} - {C_V} = a$$ for hydrogen gas
$${C_P} - {C_V} = b$$ for nitrogen gas
The correct relation between $$a$$ and $$b$$ is:
A
$$a = 14\,b$$
B
$$a = 28\,b$$
C
$$a = \frac{1}{{14}}\,b$$
D
$$a = b$$
Answer :
$$a = 14\,b$$
As we know, $${C_P} - {C_V} = R$$ where $${C_P}$$ and $${C_V}$$ are molar specific heat capacities
or, $${C_P} - {C_V} = \frac{R}{M}$$
For hydrogen $$\left( {M = 2} \right){C_P} - {C_V} = a = \frac{R}{2}$$
For nitrogen $$\left( {M = 28} \right){C_P} - {C_V} = b = \frac{R}{28}$$
$$\therefore \,\,\frac{a}{b} = 14\,\,{\text{or, }}a = 14\,b$$