Direction (Q. Nos. 1-10) This section contains 10 multiple choice questions. Each question has four choices (a), (b), (c) and (d), out of which ONLY ONE option is correct.
Q. Entropy change for the following reversible process is 1 mole H2O
(l, 1 atm, 100°C ) 1 mole H2O (g , 1 atm, 100°C)(ΔHvap = 40850 J mol-1)
∆S=Change in energy/Absolute temp =∆H/(100+273)K =40850/373 = 109.52 J/K/mol
Entropy change when 2 moles of an ideal gas expands reversibly from an initial volume of 1 dm3 to a final volume of 10 dm3 at a constant temperature of 298 K is
∆S= 2.303nR × log(V2/V1)Here n=2, R=8.314, V2= 10, V1= 1
3 moles of a diatomic gas are heated from 127° C to 727° C at a constant pressure of 1 atm. Entropy change is (log 2.5 = 0 .4)
∆S = nCplnT2/T1 + nRlnP1/P2
Since pressure is constant, so the second term will be zero.
Or ∆S = 3×7/2×8.314×2.303×log(1000/400)
= 80.42 JK-1
10 dm3 of an ideal monoatomic gas at 27° C and 1.01 x 105 Nm-2 pressure are heated at constant pressure to 127°C. Thus entropy change is
For isobaric process, we have ∆S =nCpln(T2/T1)
T2 = 273+127 = 400K and T1 = 273+227 = 300K
Applying pV = nRT at initial condition,
1×10 = n×0.0821×300
n = 0.40
Applying ∆S =nCpln(T2/T1)
∆S =0.40×5/2R×ln(400/300) = 2.38 JK-1
Exactly 100 J of heat was transferred reversibly to a block of gold at 25.00° C from a thermal reservoir at 25.01 °C, and then exactly 100 J of heat was absorbed reversibled from the block of gold by a thermal reservoir at 24.99° C. Thus entropy change of the system is
Given
I. C (diamond) + O2(g) → CO2(g) ; ΔH° = - 91.0 kcdl mol-1
II. C(graphite) + O2(g) → CO2(g) ; ΔH° = - 94.0 kcal mol-1
Q. At 298 K, 2.4 kg of carbon (diamond) is converted into graphite form. Thus, entropy change is
The reaction is
C(diamond) → C(graphite) ∆H = (94-91) = 3 kcal mol-1
∆S = ∆H/T
∆H = (94-91)×2.4×103/12
= 600 kcal
∆S = 600/298 = 2.013 kcal K-1
Consider a reversible isentropic expansion of 1.0 mole of an ideal monoatomic gas from 25°C to 75°C. If the initial pressure was 1.0 bar, final pressure is
Isentropic process means that entropy is constant. This is true only for reversible adiabatic process.
Applying P11-γ T1γ = P21-γ T2γ (for monatomic species, γ = 5/3)
(1/P)-⅔ = (75+273/25+273)5/3
Or (1/P)-2 = (348/298)5
Or P = 1.474 bar
Consider the following figure representing the increase in entropy of a substance from absolute zero to its gaseous state at some temperature
Q. ΔS° (fusion) and ΔS° (vaporisation) are respectively indicated by
You can co-relate both graph and the result will be option c.
ΔHvap = 30 kJ mol-1 and ΔSvap = 75 J mol-1 K-1. Thus, temperature of the vapour at 1 atm is
[IIT JEE 2004]
Vapour pressure is equal to atmospheric pressure ,it means the substance is at boiling point
At boiling point, liquid and Gas are in equilibrium. Therefore dG=0
dG = H - TdS
dG = 0
⇒H = TdS
⇒T = H/dS
⇒ T = 30 103/75 = 400K
For the process, and 1 atmosphere pressure, the correct choice is
[JEE Advanced 2014]
At 100°C and 1 atmosphere pressure H2O (l) ⇋ H2O(g) is at equilibrium. For equilibrium
Direction (Q. Nos. 11-14) This section contains 4 multiple choice questions. Each question has four choices (a), (b), (c) and (d), out of which ONE or MORE THANT ONE is correct.
Q. For an ideal gas, consider only (p -V) work in going from initial state X to the final state Z. The final state Z can be reached either of the two paths shown in the figure. Which of the following choice (s) is (are) correct?
(Take ΔS as change in entropy and W as work done)
[IIT JEE 2012]
∆SX→Z = ∆SX→Y + ∆SY→Z(Entropy is a state function, so it is additive)
WX→Y→Z = WX→Y (work done in y→z is zero as the process is isochoric)
Benzene and naphthalene form an ideal solution at room temperature. For this process, the true statement(s) is (are)
[JEE Advanced 2013]
When an ideal solution is formed process is spontaneous
According to Raoult's law, for an ideal solution
ΔH=0
ΔVmix=0
Since there is no exchange of heat energy between system and surroundings
ΔSsurroundings=0
ΔSsys.=+ve
∴ From the relation
ΔG=ΔH–TΔS
ΔG=−ve
Hence, the correct options are B, C and D
Consider the following process
Select correct choices(s)
∆SX→Y = ∆SX→Z + ∆SZ→Y(Entropy is a state function, so it is additive)
However, ∆SX→Z is zero. As for adiabatic process. There is no change in entropy.
∆SX→Y = ∆SZ→Y = 2.303 5 8.314 log(10/1) = 95.7 JK-1
In which of the following cases, entropy of I is larger than that of II?
a) More molar mass, more entropy. So ∆SN2O4 > ∆SNO2
b) CO2 has more entropy than dry ice at -78°C
c) Pure alumina iss crystalline solid while ruby is amorphous. And ∆Samorphous > ∆SCrystalline. So alumina has less entropy than ruby.
d) At lower pressure, entropy be higher as gas particles are far from each other. So (∆SN2)1 bar > (∆SN2)5 bar
Direction (Q. Nos. 15 and 18) This section contains 2 paragraphs, each describing theory, experiments, data etc. Four questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d)
Passage I
Consider a series of isotherms and adiabates as shown
AB, CD and EF are isotherms.
AC, CE, BD and D F are adiabates.
Q.
AB, CD and EF are isotherms.
AC, CE, BD and D F are adiabates.
For adiabatic process, we have change n entropy = 0
So EntropyA→B = EntropyC→D = EntropyE→F and EntropyA→C = EntropyA→C = EntropyC→E = EntropyF→D = EntropyD→B
By this, all options are correct.
Passage I
Consider a series of isotherms and adiabates as shown
AB, CD and EF are isotherms.
AC, CE, BD and D F are adiabates.
Q. Select incorrect relationship
Passage II
The stopcock connecting A and B is of negligible volume. Stopcock is opened and gases are allowed to mix isothermally.
Q. Final pressure set up is
Volume in (I) = nRT/P1 = 1× 0.0821× 298/4 = 6.11 L
Volume in (II) = nRT/P2 = 1× 0.0821× 298/2 = 12.23 L
Total volume = 18.34 L
Applying PV = nRT at final condition,
P = 2× 0.0821× 298/18.34 = 2.66
Passage II
The stopcock connecting A and B is of negligible volume. Stopcock is opened and gases are allowed to mix isothermally.
Q. Entropy change for the system is
Direction (Q. Nos. 19 and 20) This section contains 2 questions. Each question, when worked out will result in an integer from 0 fo 9 (both inclusive).
Q. Consider two Carnot engines (1) and (2)
Efficiency η2
Derive the value of η2 η1
η1 = 1-273/298 = 25/298
η2 = 1-248/298 = 50/298
η2/η1 = (50/298)/25/298 = 2
A cyclic heat engine operates between a source temperature of 927 oC and a sink temperature of 27 oC. What will be the maximum efficiency of the heat engine?
Heat engine is operated between the temperatures
T1 = 927 0C = 927 + 273 = 1200 K and
T2 = 27 0C = 27 + 273 = 300 K
The maximum efficiency of a heat engine is given by,
ηmax = 1 – (T2/T1)
ηmax = 1 – (300/1200)
ηmax = 0.75
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