Heat and Thermodynamics

JEE Physics · 315 questions · Page 27 of 32 · Click an option or "Show Solution" to reveal answer

Q261
Given below are two statements. One is labelled as Assertion (A) and the other is labelled as Reason (R).Assertion (A) : With the increase in the pressure of an ideal gas, the volume falls off more rapidly in an isothermal process in comparison to the adiabatic process.Reason (R) : In isothermal process, PV = constant, while in adiabatic process PVγPV^{\gamma} = constant. Here γ\gamma is the ratio of specific heats, P is the pressure and V is the volume of the ideal gas.In the light of the above statements, choose the correct answer from the options given below:
A (A) is true but (R) is false
B Both (A) and (R) are true but (R) is NOT the correct explanation of (A)
C (A) is false but (R) is true
D Both (A) and (R) are true and (R) is the correct explanation of (A)
Correct Answer
Option D
Solution

We know, ideal gas equation, Pv=nRT\mathrm{Pv = nRT} For isothermal process, T = constant PV=const.\mathrm{\Rightarrow PV = const.} P1V\mathrm{\Rightarrow P \propto \dfrac{1}{V}} For an adiabatic process, PVr=constant\mathrm{PV^r=constant} We can see, for the same pressure incresement,

P2P1{P_2} - {P_1}

,

(v4v3)>(v2v1)\left( {{v_4} - {v_3}} \right) > \left( {{v_2} - {v_1}} \right)

i.e. the volume falls off more rapidly in an isothermal process in comparison to the adiabatic process.

Hence, option 4 is corret.

Q262
A cup of coffee cools from 90°C to 80°C in t minutes when the room temperature is 20°C. The time taken by the similar cup of coffee to cool from 80°C to 60°C at the same room temperature is:
A 135t\dfrac{13}{5}t
B 1013t\dfrac{10}{13}t
C 513t\dfrac{5}{13}t
D 1310t\dfrac{13}{10}t
Correct Answer
Option A
Solution

Here, we will use the Newton's law of cooling. We know,

T1T2Δt=k(T1+T22Ts){{{T_1} - {T_2}} \over {\Delta t}} = k\left( {{{{T_1} + {T_2}} \over 2} - {T_s}} \right)

.... (1) where, T1_1 and T2_2 are initial and final temperatures respectively. Ts\mathrm{T_s} = surrounding temperature Δt\Delta t = time taken kk = positive constant Given, Ist case :

T1=90C{T_1} = 90^\circ C
T2=80C{T_2} = 80^\circ C
Δt=t\Delta t = t

,

Ts=20C{T_s} = 20^\circ C

IInd case :

T1=80C{T_1} = 80^\circ C
T2=60C{T_2} = 60^\circ C
Ts=20C{T_s} = 20^\circ C

,

Δt=?\Delta t = ?

Now, for Ist case,

9080t=k(90+80220){{90 - 80} \over t} = k\left( {{{90 + 80} \over 2} - 20} \right)

...... (from (1))

10t=k(8520)\Rightarrow {{10} \over t} = k\left( {85 - 20} \right)
10t=65k\Rightarrow {{10} \over t} = 65k

.... (2) For IInd case,

8060Δt=k(80+60220){{80 - 60} \over {\Delta t}} = k\left( {{{80 + 60} \over 2} - 20} \right)

.... (From (1))

20Δt=k(7020)\Rightarrow {{20} \over {\Delta t}} = k\left( {70 - 20} \right)
20Δt=50k\Rightarrow {{20} \over {\Delta t}} = 50k

.... (3) Now, by (2) ÷\div (3),

10t20Δt=1310{{{{10} \over t}} \over {{{20} \over {\Delta t}}}} = {{13} \over {10}}
Δtt(12)=135\Rightarrow {{\Delta t} \over t}\left( {{1 \over 2}} \right) = {{13} \over 5}
Δt=135t\Rightarrow \Delta t = {{13} \over 5}t
Q263
The work done in an adiabatic change in an ideal gas depends upon only :
A change in its pressure
B change in its temperature
C change in its specific heat
D change in its volume
Correct Answer
Option B
Solution

ΔW=ΔU=nCvΔT\Delta \mathrm{W}=-\Delta \mathrm{U}=-\mathrm{nC}_{\mathrm{v}} \Delta \mathrm{T}

Q264
Two spherical bodies of same materials having radii 0.2 m and 0.8 m are placed in same atmosphere. The temperature of the smaller body is 800 K and temperature of the bigger body is 400 K . If the energy radiated from the smaller body is E, the energy radiated from the bigger body is (assume, effect of the surrounding temperature to be negligible),
A 64 E
B 16 E
C E
D 256 E
Correct Answer
Option C
Solution

To determine the energy radiated by two spherical bodies, both made of the same material but with different radii and temperatures, we can use the Stefan-Boltzmann law.

This law states that the energy radiated by a black body per unit time is proportional to the product of the surface area A A and the fourth power of its temperature T T .

The formula for power P P is given by: P=σeAT4 P = \sigma e A T^4 Where: σ \sigma is the Stefan-Boltzmann constant e e is the emissivity of the material A A is the surface area of the sphere T T is the temperature in Kelvin Expressing this relationship as a proportionality: PAT4 P \propto A T^4 For a sphere, the surface area A A is: A=4πR2 A = 4\pi R^2 Hence, the power radiated is proportional to: PR2T4 P \propto R^2 T^4 For two bodies with radii R1 R_1 and R2 R_2 , and temperatures T1 T_1 and T2 T_2 , the ratio of their powers is: P1P2=(R1R2)2(T1T2)4 \dfrac{P_1}{P_2} = \left( \dfrac{R_1}{R_2} \right)^2 \left( \dfrac{T_1}{T_2} \right)^4 Given: R1=0.2m R_1 = 0.2 \, \text{m} , T1=800K T_1 = 800 \, \text{K} R2=0.8m R_2 = 0.8 \, \text{m} , T2=400K T_2 = 400 \, \text{K} Substituting into the formula: EE=(0.20.8)2(800400)4 \dfrac{E}{E'} = \left( \dfrac{0.2}{0.8} \right)^2 \left( \dfrac{800}{400} \right)^4 Calculating each part: (0.20.8)2=(14)2=116\left( \dfrac{0.2}{0.8} \right)^2 = \left( \dfrac{1}{4} \right)^2 = \dfrac{1}{16} (800400)4=24=16\left( \dfrac{800}{400} \right)^4 = 2^4 = 16 Combining these calculations: EE=116×16=1 \dfrac{E}{E'} = \dfrac{1}{16} \times 16 = 1 This implies that the energy radiated by the bigger body E E' equals the energy radiated by the smaller body E E .

Thus, E=E E' = E .

Q265
An amount of ice of mass 103 kg10^{-3} \mathrm{~kg} and temperature 10C-10^{\circ} \mathrm{C} is transformed to vapour of temperature 110C110^{\circ} \mathrm{C} by applying heat. The total amount of work required for this conversion is, (Take, specific heat of ice =2100Jkg1 K1=2100 \mathrm{Jkg}^{-1} \mathrm{~K}^{-1}, specific heat of water =4180Jkg1 K1=4180 \mathrm{Jkg}^{-1} \mathrm{~K}^{-1}, specific heat of steam =1920Jkg1 K1=1920 \mathrm{Jkg}^{-1} \mathrm{~K}^{-1}, Latent heat of ice =3.35×105Jkg1=3.35 \times 10^5 \mathrm{Jkg}^{-1} and Latent heat of steam =2.25×106=2.25 \times 10^6 Jkg1\mathrm{Jkg}^{-1} )
A 3022 J
B 3043 J
C 3003 J
D 3024 J
Correct Answer
Option B
Solution
ΔQ1=msiΔT2,ΔQ2=mLi\Delta {Q_1} = m{s_i}\Delta {T_2},\,\Delta {Q_2} = m{L_i}
ΔQ3=mSwΔT3,ΔQ4=mLs,ΔQ5=mSsΔT5\Delta {Q_3} = m{S_w}\Delta {T_3},\,\Delta {Q_4} = m{L_s},\,\Delta {Q_5} = m{S_s}\Delta {T_5}
ΔQnet=m(SiΔT1+Li+SwΔT3+Ls+SsΔTs)\Delta {Q_{net}} = m({S_i}\Delta {T_1} + {L_i} + {S_w}\Delta {T_3} + {L_s} + {S_s}\Delta {T_s})
=103(2100×10+335000+4180×100+2250000+1920×10)= {10^{ - 3}}(2100 \times 10 + 335000 + 4180 \times 100 + 2250000 + 1920 \times 10)
=103(3043200)=3043.2J= {10^{ - 3}}(3043200) = 3043.2\,J

So,

ΔQnet3043J\Delta {Q_{net}} \approx 3043\,J
Q266
Given are statements for certain thermodynamic variables, (A) Internal energy, volume (V)(\mathrm{V}) and mass (M)(\mathrm{M}) are extensive variables. (B) Pressure (P), temperature ( T ) and density ( ρ\rho ) are intensive variables. (C) Volume (V), temperature (T) and density ( ρ\rho ) are intensive variables. (D) Mass (M), temperature (T) and internal energy are extensive variables. Choose the correct answer from the options given below :
A (C) and (D) Only
B (A) and (B) Only
C (D) and (A) Only
D (B) and (C) Only
Correct Answer
Option B
Solution

Check Statement (A): “Internal energy (U), volume (V), and mass (M) are extensive variables.”

Internal energy is extensive.

Volume is extensive.

Mass is extensive.

Hence, statement (A) is correct.

Check Statement (B): “Pressure (P), temperature (T), and density (ρ) are intensive variables.”

Pressure is intensive.

Temperature is intensive.

Density is intensive.

Hence, statement (B) is correct.

Check Statement (C): “Volume (V), temperature (T), and density (ρ) are intensive variables.”

Volume is not intensive; it is an extensive property.

(T) and (ρ) are indeed intensive.

Since volume is miscategorized here, (C) is incorrect.

Check Statement (D): “Mass (M), temperature (T), and internal energy are extensive variables.”

Mass is extensive.

Temperature is not extensive (it is intensive).

Internal energy is extensive.

Because temperature is miscategorized, (D) is incorrect.

Only (A) and (B) are correct statements.

Therefore, the correct choice is: Option B: (A) and (B) Only.

Q267
For a diatomic gas, if γ1=(CpCv)\gamma_1=\left(\dfrac{C p}{C v}\right) for rigid molecules and γ2=(CpCv)\gamma_2=\left(\dfrac{C p}{C v}\right) for another diatomic molecules, but also having vibrational modes. Then, which one of the following options is correct? (Cp and Cv are specific heats of the gas at constant pressure and volume)
A γ2<γ1\gamma_2<\gamma_1
B γ2>γ1\gamma_2>\gamma_1
C γ2=γ1\gamma_2=\gamma_1
D 2γ2=γ12 \gamma_2=\gamma_1
Correct Answer
Option A
Solution

Let's analyze the problem step by step: For a rigid diatomic molecule (without vibrational modes): Degrees of freedom: Translation: 3 Rotation: 2 Total: 5 The molar specific heat at constant volume is given by:

Cv=52RC_v = \frac{5}{2}R

At constant pressure, it is:

Cp=Cv+R=52R+R=72RC_p = C_v + R = \frac{5}{2}R + R = \frac{7}{2}R

Therefore, the ratio is:

γ1=CpCv=72R52R=751.4\gamma_1 = \frac{C_p}{C_v} = \frac{\frac{7}{2}R}{\frac{5}{2}R} = \frac{7}{5} \approx 1.4

For the diatomic molecule that also has vibrational modes (assuming the vibrational mode is fully excited): Additional vibrational mode contributions: Each vibrational mode contributes 2 degrees of freedom (one kinetic and one potential).

Therefore, the degrees of freedom become:

3 (translation)+2 (rotation)+2 (vibration)=73\ (\text{translation}) + 2\ (\text{rotation}) + 2\ (\text{vibration}) = 7

The molar specific heat at constant volume now is:

Cv=72RC_v = \frac{7}{2}R

And at constant pressure:

Cp=Cv+R=72R+R=92RC_p = C_v + R = \frac{7}{2}R + R = \frac{9}{2}R

Thus, the ratio is:

γ2=CpCv=92R72R=971.2857\gamma_2 = \frac{C_p}{C_v} = \frac{\frac{9}{2}R}{\frac{7}{2}R} = \frac{9}{7} \approx 1.2857

Comparison: For the rigid molecule,

γ11.4\gamma_1 \approx 1.4

. For the molecule with vibrational modes,

γ21.2857\gamma_2 \approx 1.2857

. Clearly,

γ2Therefore,thecorrectoptionis:OptionA:\gamma_2 Therefore, the correct option is: Option A:

\gamma_2

Q268
The ratio of vapour densities of two gases at the same temperature is 425 \dfrac{4}{25} , then the ratio of r.m.s. velocities will be :
A 52 \dfrac{5}{2}
B 254 \dfrac{25}{4}
C 425 \dfrac{4}{25}
D 25 \dfrac{2}{5}
Correct Answer
Option A
Solution

We are given that the ratio of the vapour densities of the two gases is

425.\frac{4}{25}.

Since vapour density is proportional to the molecular mass, we can write

M1M2=425,\frac{M_1}{M_2} = \frac{4}{25},

where M1M_1 and M2M_2 are the molecular masses of the gases. The root mean square (r.m.s.) velocity of a gas is given by

vrms=3RTM,v_{\text{rms}} = \sqrt{\frac{3RT}{M}},

where: RR is the universal gas constant, TT is the temperature, MM is the molecular mass of the gas.

Since both gases are at the same temperature, the ratio of their r.m.s. velocities is

vrms,1vrms,2=M2M1.\frac{v_{\text{rms,1}}}{v_{\text{rms,2}}} = \sqrt{\frac{M_2}{M_1}}.

Substitute the ratio of molecular masses:

vrms,1vrms,2=254=52.\frac{v_{\text{rms,1}}}{v_{\text{rms,2}}} = \sqrt{\frac{25}{4}} = \frac{5}{2}.

Thus, the ratio of their r.m.s. velocities is

52.\frac{5}{2}.

The correct answer is Option A:

52.\frac{5}{2}.
Q269
A gun fires a lead bullet of temperature 300 K into a wooden block. The bullet having melting temperature of 600 K penetrates into the block and melts down. If the total heat required for the process is 625 J , then the mass of the bullet is _______ grams. (Latent heat of fusion of lead =2.5×104JKg1=2.5 \times 10^4 \mathrm{JKg}^{-1} and specific heat capacity of lead =125JKg1=125 \mathrm{JKg}^{-1} K1)\left.\mathrm{K}^{-1}\right)
A 20
B 15
C 5
D 10
Correct Answer
Option D
Solution

Let's determine the mass step by step: The bullet is heated from 300 K to 600 K, so the increase in temperature is:

ΔT=600K300K=300K.\Delta T = 600\, \text{K} - 300\, \text{K} = 300\, \text{K}.

The heat required to raise the temperature of the bullet (using the specific heat capacity of lead) is:

Q1=m×c×ΔT=m×125J/kg K×300K=37500mJ,Q_1 = m \times c \times \Delta T = m \times 125\, \text{J/kg K} \times 300\, \text{K} = 37500\, m \, \text{J},

where m m is the mass in kilograms.

After reaching 600 K, the bullet melts.

The heat required for the phase change (melting) is given by:

Q2=m×L=m×2.5×104J/kg=25000mJ.Q_2 = m \times L = m \times 2.5 \times 10^4\, \text{J/kg} = 25000\, m \, \text{J}.

The total heat required for the process is:

Q=Q1+Q2=37500m+25000m=62500mJ.Q = Q_1 + Q_2 = 37500\, m + 25000\, m = 62500\, m \, \text{J}.

We are given that the total heat is 625 J, so:

62500m=625.62500\, m = 625.

Solving for m m :

m=62562500=0.01kg.m = \frac{625}{62500} = 0.01\, \text{kg}.

Finally, converting the mass from kilograms to grams:

0.01kg=0.01×1000g=10g.0.01\, \text{kg} = 0.01 \times 1000\, \text{g} = 10\, \text{g}.

Thus, the mass of the bullet is 10 grams. This corresponds to Option D.

Q270
Water of mass mm gram is slowly heated to increase the temperature from T1T_1 to TγT_\gamma. The change in entropy of the water, given specific heat of water is 1Jkg1 K11 \mathrm{Jkg}^{-1} \mathrm{~K}^{-1}, is :
A m(T2T1)\mathrm{m}\left(\mathrm{T}_2-\mathrm{T}_1\right)
B zero
C mln(T1 T2)\mathrm{m} \ln \left(\dfrac{\mathrm{T}_1}{\mathrm{~T}_2}\right)
D mln(T2 T1)\mathrm{m} \ln \left(\dfrac{\mathrm{T}_2}{\mathrm{~T}_1}\right)
Correct Answer
Option D
Solution

To determine the change in entropy when water is heated from temperature

T1T_1

to

T2T_2

(here,

TγT_\gamma

is equivalent to

T2T_2

), we use the definition of entropy change for a reversible process:

ΔS=T1T2dQT\Delta S = \int_{T_1}^{T_2} \frac{dQ}{T}

Since the water is being heated slowly, the process is reversible, and the heat added is given by:

dQ=mcdTdQ = mc\,dT

where: •

mm

is the mass of the water, •

cc

is the specific heat capacity (given as

1Jkg1K11\,\mathrm{J\,kg^{-1}\,K^{-1}}

). Substitute

dQdQ

into the integral:

ΔS=T1T2mcdTT=mcT1T2dTT.\Delta S = \int_{T_1}^{T_2} \frac{mc\,dT}{T} = mc\, \int_{T_1}^{T_2} \frac{dT}{T}.

Since

c=1c = 1

, the equation simplifies to:

ΔS=mT1T2dTT.\Delta S = m \int_{T_1}^{T_2} \frac{dT}{T}.

Evaluating the integral, we have:

T1T2dTT=lnTT1T2=ln(T2T1).\int_{T_1}^{T_2} \frac{dT}{T} = \ln{T}\Big|_{T_1}^{T_2} = \ln\left(\frac{T_2}{T_1}\right).

Thus, the change in entropy is:

ΔS=mln(T2T1).\Delta S = m \ln\left(\frac{T_2}{T_1}\right).

Comparing with the options provided, the correct answer is: Option D:

mln(T2T1).m \ln\left(\frac{T_2}{T_1}\right).
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