Q.What amount of heat must be supplied to 2.0×10−2 kg of nitrogen (at room temperature) to raise its temperature by 45∘C at constant pressure? (Molecular mass of N2=28; R=8.3 J mol−1 K−1.)
Concept understanding — Heat Capacity at Constant Pressure
Heat Capacity at Constant Pressure — From Intuition to Precision
Imagine you have a pot of water on a stove. You turn the burner on, and the water gets hotter. How much heat does it take to raise its temperature by, say, 10°C? That depends on two things: how much water you have, and whether the pot is open to the air or sealed tight.
If the pot is open (constant pressure — the air above it is always at atmospheric pressure), the water can expand as it heats. Some of the energy you supply goes into pushing the atmosphere aside — doing work against the outside air. So you need to put in more heat than if the pot were sealed (constant volume), where no expansion work is possible.
That extra heat is the key idea behind heat capacity at constant pressure, denoted Cp.
The Intuition First
Heat capacity tells you: "How much heat must I add to raise the temperature of this substance by 1°C (or 1 K)?"
- At constant volume (Cv): All the heat goes into increasing the internal energy (the kinetic and potential energy of the molecules). No work is done because the volume doesn't change.
- At constant pressure (Cp): Some heat goes into internal energy, but some also goes into the work of expansion against the constant external pressure. So Cp is always larger than Cv for gases (and for most solids/liquids, the difference is tiny because they barely expand).
For an ideal gas, the difference is exactly Cp−Cv=nR, where n is the number of moles and R is the universal gas constant. This is a direct consequence of the first law of thermodynamics.
The Precise Statement
Heat capacity at constant pressure is defined as the amount of heat required to raise the temperature of a substance by 1 K (or 1°C) while keeping the pressure constant.
Mathematically:
Cp=(dTδQ)p
The subscript p means "at constant pressure." The δQ (not dQ) reminds us that heat is a path-dependent quantity, not a state function.
But we can rewrite this in terms of a state function — enthalpy (H). At constant pressure, the heat added equals the change in enthalpy:
δQp=dH
Therefore:
Cp=(∂T∂H)p
This is the working definition you'll use in problems: Cp is the partial derivative of enthalpy with respect to temperature at constant pressure.
Molar vs. Specific Heat Capacity
You'll encounter two common forms:
- Molar heat capacity at constant pressure (Cp,m): heat capacity per mole (units: J mol⁻¹ K⁻¹)
- Specific heat capacity at constant pressure (cp): heat capacity per unit mass (units: J kg⁻¹ K⁻¹)
The total heat capacity of a sample is:
Cp=n⋅Cp,m=m⋅cp
Why It Matters
In most chemical reactions and physical processes, the system is open to the atmosphere — constant pressure. So Cp is the relevant quantity for:
- Calculating enthalpy changes (ΔH=nCp,mΔT)
- Designing calorimeters (like coffee-cup calorimeters that operate at constant pressure)
- Understanding why gases heat up when compressed (and cool when expanded)
Do not confuse Cp with Cv. For gases, the difference is significant. For solids and liquids, the difference is often negligible (typically less than 1%), so many textbooks treat them as approximately equal for condensed phases.
A Quick Example
How much heat is needed to raise the temperature of 2 moles of an ideal gas from 300 K to 400 K at constant pressure? (Given Cp,m=29.1 J mol−1K−1)
Qp=nCp,mΔT=(2)(29.1)(100)=5820 J
If the same gas were heated at constant volume, you'd need less heat — about 5820−nRΔT=5820−(2)(8.314)(100)=4157 J — because no expansion work is done.
Final takeaway: Cp is the heat capacity you measure when the system is free to expand against a constant external pressure. It's always larger than Cv for gases, and the difference comes from the work of expansion.
Students searching for "Heat Capacity at Constant Pressure: Definition, Formula & Real-World Examples" or "Heat Capacity at Constant Pressure 11 physics" will find this explanation directly aligned with the Class 11 Physics curriculum prescribed under NCERT/CBSE. It is also a recurring theme in JEE Main, NEET and state engineering/medical entrance exams, so working through it carefully pays off well beyond board exams.
Concept: Heat capacity at constant pressure for an ideal gas.
For a diatomic gas like nitrogen at room temperature, the molar heat capacity at constant pressure is Cp=27R. The heat required is given by:
Q=nCpΔT
where n is the number of moles.
Step 1: Calculate the number of moles.
n=Mm=28×10−3 kg mol−12.0×10−2 kg=2820=0.714 mol
Step 2: Substitute into the heat equation with ΔT=45 K (since a change in Celsius equals a change in Kelvin).
Q=0.714×27×8.3×45
Q=0.714×3.5×8.3×45=933 J
The heat required is 933 J or approximately 0.93 kJ.
For an ideal gas at constant pressure, heat supplied is Q=nCpΔT. Using Cp=27R for diatomic nitrogen, the heat required is 933J.
When we heat a gas at constant pressure, it not only gains internal energy but also does work by expanding against the external pressure. This is why the heat capacity at constant pressure, Cp, is always larger than at constant volume, Cv. For an ideal gas, the relationship is Cp=Cv+R.
Nitrogen is a diatomic molecule. At room temperature, it has three translational and two rotational degrees of freedom (vibrational modes are not excited). By the equipartition theorem, each degree of freedom contributes 21R per mole to the molar heat capacity at constant volume:
Cv=25R
Therefore, the molar heat capacity at constant pressure is:
Cp=Cv+R=25R+R=27R
Cp=27R=27×8.3=29.05J mol−1K−1
Now let's calculate the heat required step by step:
-
Find the number of moles of nitrogen.
Given mass m=2.0×10−2kg=20g and molecular mass M=28g mol−1:
n=Mm=2820=75mol
-
Identify the temperature change.
The temperature rise is ΔT=45∘C=45K (since a change in Celsius equals a change in Kelvin).
-
Apply the heat capacity formula at constant pressure.
The heat supplied at constant pressure is:
Q=nCpΔT
Substituting the values:
Q=75×27×8.3×45
-
Simplify the calculation.
Notice that 75×27=25:
Q=25×8.3×45=2.5×8.3×45
Q=2.5×373.5=933.75J
A common mistake is to use Cv instead of Cp when the problem specifies constant pressure. Always check whether the process is isobaric (constant P) or isochoric (constant V).
The amount of heat that must be supplied is 933J (or 934J if rounded).
A quick cross-check: nitrogen's tabulated specific heat at constant pressure is about cp≈1.04 J g−1K−1, so Q=mcpΔT=20 g×1.04×45≈936 J — matching the kinetic-theory answer to within rounding. This is a useful shortcut whenever you have a handy tabulated specific heat: it lets you skip converting mass to moles and multiplying by Cp=27R entirely, and it's also a good way to sanity-check that the molar route was set up correctly.
Showing the 12 most recent of 36 on this concept.
- TG EAPCET 2026Set eng-2026-05-09-AN1 markMCQQ.5 moles of monoatomic gas and one mole of rigid diatomic gas are mixed. The internal energy (in kJ) of the gaseous mixture at a temperature of 127 ∘C is (Universal gas constant = 8.31 J mol−1 K−1) (A) 66.48 (B) 49.86 (C) 16.62 (D) 33.24
›Reveal solutionSolution
Total internal energy U=(23n1+25n2)RT=10RT=33.24kJ.
For n1=5 moles monoatomic gas, CV=23R; for n2=1 mole rigid diatomic gas, CV=25R. Temperature T=127∘C=400K.
U=(n1⋅23R+n2⋅25R)T=(215+25)RT=10RT
U=10×8.31×400=33240J=33.24kJ
✓Final answerU=33.24kJ — option (D).
- TG EAPCET 2026Set eng-2026-05-11-FN1 markMCQQ.If Q1 is the heat required to convert 2 g of ice at a temperature of 0∘C to water at a temperature of 40∘C and Q2 is the heat required to convert 4 g of ice at a temperature of 0∘C to water at a temperature of 80∘C, then Q1:Q2= (Latent heat of fusion of ice =80calg−1 and specific heat capacity of water =1calg−1∘C−1) (A) 3:8 (B) 1:2 (C) 1:4 (D) 3:4
›Reveal solutionSolution
The ratio Q1:Q2 is found by calculating the total heat (latent + sensible) for each case and simplifying. The result is 3:8.
The problem asks for the ratio of two heats, each involving two stages: melting ice at 0∘C into water at 0∘C (latent heat), then heating that water to a final temperature (sensible heat). The key is to treat each stage separately and sum them.
Latent heat depends only on mass, not on temperature change. Sensible heat depends on mass, specific heat, and the temperature rise. So for each case, we compute Q=mLf+mcΔT, then take the ratio.
-
For Q1 (2 g ice to 40∘C water):
Mass m1=2g.
Latent heat: Qlatent,1=m1Lf=2×80=160cal.
Sensible heat (heating water from 0∘C to 40∘C): Qsensible,1=m1cΔT1=2×1×40=80cal.
Total: Q1=160+80=240cal.
-
For Q2 (4 g ice to 80∘C water):
Mass m2=4g.
Latent heat: Qlatent,2=4×80=320cal.
Sensible heat (heating from 0∘C to 80∘C): Qsensible,2=4×1×80=320cal.
Total: Q2=320+320=640cal.
-
Find the ratio:
Q2Q1=640240=83.
So Q1:Q2=3:8.
Watch outA common mistake is to forget the latent heat part and only compare the sensible heats, which would give 1:4 — option (C). Always account for the phase change first.
TipNotice that both masses and temperature changes are in simple multiples. You could write Q1=m1(Lf+cΔT1) and Q2=m2(Lf+cΔT2), then take the ratio directly: 4(80+80)2(80+40)=4×1602×120=640240=83.
✓Final answerThe ratio is 3:8, which corresponds to option (A).
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- TG EAPCET 2026Set eng-2026-05-11-AN1 markMCQQ.Ice of mass 80 g at a temperature of −10∘C is mixed with water of mass 100 g at a temperature of 20∘C. The ratio of the masses of ice and water in the mixture in equilibrium is (Latent heat of fusion of ice =80calg−1, specific heat capacities of water and ice are 1calg−1∘C−1 and 0.5calg−1∘C−1 respectively) (A) 4:5 (B) 1:2 (C) 2:3 (D) 3:4
›Reveal solutionSolution
The key idea is to check whether all the ice melts or not by comparing the heat needed to warm and melt the ice with the heat the water can supply. The final equilibrium mixture has ice and water in the ratio 1:2, so the correct option is (B).
Concept and Intuition
When ice and water at different temperatures are mixed, heat flows from the warmer water to the colder ice. The ice first warms to 0 °C, then may melt if enough heat remains. The water cools to 0 °C. The final state depends on whether the water’s available heat is enough to melt all the ice. We calculate the heat required to bring the ice to 0 °C and then melt it, and compare it with the heat the water can give up by cooling to 0 °C. If the water’s heat is insufficient, only part of the ice melts, and the mixture stays at 0 °C with both ice and water present.
Step-by-step solution
- Heat needed to warm the ice from –10 °C to 0 °C Mass of ice mi=80 g, specific heat of ice ci=0.5 cal g−1°C−1.
Q1=miciΔT=80×0.5×(0−(−10))=80×0.5×10=400 cal.
- Heat needed to melt all the ice at 0 °C Latent heat of fusion L=80 cal g−1.
Q2=miL=80×80=6400 cal.
Total heat required to turn all ice into water at 0 °C:
Qice, total=Q1+Q2=400+6400=6800 cal.
- Heat the water can supply by cooling from 20 °C to 0 °C Mass of water mw=100 g, specific heat of water cw=1 cal g−1°C−1.
Qwater=mwcwΔT=100×1×(20−0)=2000 cal.
-
Compare the heat available with the heat needed
The water can supply only 2000 cal, but melting all the ice requires 6800 cal. Clearly, not all ice melts. The mixture will end at 0 °C with some ice remaining.
-
How much ice actually melts?
First, the ice must be warmed to 0 °C, which uses 400 cal. The remaining heat from the water is
2000−400=1600 cal.
This remaining heat goes into melting ice. Mass of ice melted:
mmelted=801600=20 g.
- Final masses in the mixture
- Ice remaining: 80−20=60 g.
- Water originally: 100 g, plus the 20 g of melted ice gives 100+20=120 g of water. Ratio of ice to water (by mass) in the final mixture:
12060=21.
So the ratio is 1:2.
Watch outA common mistake is to forget that the ice must first be warmed to 0 °C before any melting can occur. Skipping that step gives a wrong melted mass and a different ratio.
TipAlways check whether the water can supply enough heat to both warm and melt the ice. If not, the final temperature is 0 °C and you only partially melt the ice.
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2025Set eng-2025-05-02-FN1 markMCQQ.The heat required to convert 8 g of ice at a temperature of −20∘C to steam at 100∘C is [Specific heat capacity of ice =2100Jkg−1K−1, specific heat capacity of water =4200Jkg−1K−1, latent heat of fusion of ice =336×103Jkg−1 and latent heat of steam =2.268×106Jkg−1] (A) 5400 cal (B) 5840 cal (C) 5760 cal (D) 5120 cal
›Reveal solutionSolution
Sum the four stages — warming ice, melting, warming water, boiling — to get 24528 J, which is 5840 cal — option (B).
Concept
Taking 8 g=0.008 kg from ice at −20∘C to steam at 100∘C needs four heat inputs: raising ice to 0∘C, melting it, raising water to 100∘C, and vaporising it.
Solution
Q1=mciceΔT=0.008×2100×20=336 J.
Q2=mLf=0.008×336×103=2688 J.
Q3=mcwaterΔT=0.008×4200×100=3360 J.
Q4=mLv=0.008×2.268×106=18144 J.
Total:
Q=336+2688+3360+18144=24528 J.
Converting with 1 cal=4.2 J:
Q=4.224528=5840 cal.
✓Final answerThe heat required is 5840 cal — option (B).
- TG EAPCET 2025Set eng-2025-05-02-AN1 markMCQQ.A gas is suddenly compressed such that its absolute temperature is doubled. If the ratio of the specific heat capacities of the gas is 1.5, then the percentage decrease in the volume of the gas is (A) 30 (B) 50 (C) 25 (D) 75
›Reveal solutionSolution
For an adiabatic process, TVγ−1=constant. With γ=1.5 and T2=2T1, the volume ratio is V2/V1=1/22≈0.3536, so the percentage decrease is about 64.6% — but the given options suggest a different interpretation: the problem likely intends a sudden compression as an adiabatic process where T∝V1−γ, leading to a 75% decrease, matching option (D).
Concept & Intuition
The phrase “suddenly compressed” is the key. In thermodynamics, a sudden change means there is no time for heat exchange with the surroundings — the process is adiabatic. For an ideal gas undergoing a reversible adiabatic process, the relation between temperature and volume is
TVγ−1=constant,
where γ=Cp/Cv is the ratio of specific heats. Here γ=1.5, and the temperature doubles. We can directly find how the volume changes.
Step-by-step solution
- Write the adiabatic relation For an adiabatic process:
T1V1γ−1=T2V2γ−1.
Given T2=2T1 and γ=1.5, so γ−1=0.5.
- Substitute and solve for the volume ratio
T1V10.5=(2T1)V20.5.
Cancel T1 (non-zero):
V10.5=2V20.5.
Square both sides:
V1=4V2⇒V1V2=41.
- Interpret the result The final volume is one-fourth of the initial volume. That means the volume decreases by
V1V1−V2×100%=(1−41)×100%=75%.
Watch outA common mistake is to use the relation PVγ=constant and then try to connect temperature via the ideal gas law, but that leads to the same result if done correctly. Another pitfall: forgetting that γ−1=0.5 and accidentally using γ directly.
TipWhen γ=1.5, the exponent γ−1=1/2, so the relation T∝V−1/2 is easy to invert: doubling T means V must become 1/4 of its original value.
✓Final answerThe correct option is (D).
ANSWER: D
- TG EAPCET 2025Set eng-2025-05-04-AN1 markMCQQ.A Carnot engine uses diatomic gas as a working substance. During the adiabatic expansion part of the cycle, if the volume of the gas becomes 32 times its initial volume, then the efficiency of the engine is (A) 100% (B) 75% (C) 50% (D) 25%
›Reveal solutionSolution
The efficiency of a Carnot engine depends only on the temperatures of the reservoirs. For a diatomic gas undergoing adiabatic expansion with a volume ratio of 32, the temperature ratio is found using the adiabatic relation TVγ−1=constant, with γ=7/5. This gives an efficiency of 75%, so the correct option is (B).
The key idea is that in a Carnot cycle, efficiency is η=1−ThotTcold. The adiabatic expansion step connects the hot and cold temperatures via the volume change. For a diatomic gas, the adiabatic index γ=Cp/Cv=7/5. Using the relation TVγ−1=constant, we can find the temperature ratio from the given volume ratio, and then compute the efficiency.
-
Recall the Carnot efficiency formula
The efficiency of a Carnot engine is η=1−ThTc, where Th is the temperature of the hot reservoir and Tc is the temperature of the cold reservoir. The adiabatic expansion in the cycle connects these two temperatures.
-
Apply the adiabatic relation for an ideal gas
For a reversible adiabatic process, TVγ−1=constant. Let the initial volume before expansion be V1 and the final volume after expansion be V2=32V1. The temperatures at these points are Th (start of adiabatic expansion) and Tc (end of adiabatic expansion). Thus:
ThV1γ−1=TcV2γ−1
Rearranging:
ThTc=(V2V1)γ−1
- Substitute the volume ratio and γ for a diatomic gas For a diatomic gas, γ=57, so γ−1=52. The volume ratio V2/V1=32, so V1/V2=1/32. Therefore:
ThTc=(321)2/5
Now, 32=25, so 322/5=(25)2/5=22=4. Hence:
ThTc=41
- Compute the efficiency
η=1−ThTc=1−41=43=75%
TipNotice that 32=25 and the exponent 2/5 cancels neatly, giving a simple ratio of 1/4. This is a common trick in such problems — always express the volume ratio as a power of 2 when the exponent is a fraction.
Watch outA common mistake is to use γ=5/3 (for monatomic gas) instead of 7/5 (for diatomic). That would give (1/32)2/3=1/8, leading to an efficiency of 87.5%, which is not among the options. Always check the gas type.
✓Final answerThe correct option is (B).
ANSWER: B
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- TG EAPCET 2025Set eng-2025-05-04-FN1 markMCQQ.A Carnot engine uses diatomic gas as a working substance. During the adiabatic expansion part of the cycle, if the volume of the gas becomes 32 times its initial volume, then the efficiency of the engine is (A) 100% (B) 50% (C) 75% (D) 25%
›Reveal solutionSolution
For a Carnot engine with a diatomic gas, the adiabatic relation TVγ−1=constant links the temperature drop to the volume expansion. Using γ=7/5 for a diatomic gas and a 32‑fold volume increase in the adiabatic expansion, the efficiency comes out to 75%.
The key idea is that a Carnot engine’s efficiency depends only on the temperatures of the two reservoirs: η=1−TC/TH. In the adiabatic expansion step, the gas cools from TH to TC as its volume increases. For an ideal gas undergoing a reversible adiabatic process, temperature and volume are related by TVγ−1=constant. So the ratio TC/TH can be found directly from the volume ratio, without needing any other data.
A diatomic gas at ordinary temperatures has γ=Cp/Cv=7/5=1.4. That’s a standard result: Cv=25R, Cp=27R, so γ−1=2/5=0.4.
Now let’s work through the calculation.
- Adiabatic relation for the expansion For a reversible adiabatic process, TVγ−1=constant. If the gas starts at temperature TH and volume V1, and ends at TC and volume V2, then
THV1γ−1=TCV2γ−1.
Rearranging gives
THTC=(V2V1)γ−1.
- Plug in the given numbers The volume becomes 32 times its initial value, so V2/V1=32, hence V1/V2=1/32. For a diatomic gas, γ−1=2/5=0.4. Therefore
THTC=(321)0.4.
- Simplify the exponent Write 32=25. Then
(251)0.4=2−5×0.4=2−2=41.
So TC/TH=1/4.
- Efficiency of the Carnot engine
η=1−THTC=1−41=43=75%.
Watch outA common mistake is to use γ=5/3 (monatomic gas) instead of 7/5 (diatomic). That would give TC/TH=(1/32)2/3=1/8, leading to η=87.5%, which is not among the options. Always check the gas’s atomicity.
TipNotice that 32=25 and γ−1=2/5 for a diatomic gas. The exponents cancel neatly: 5×2/5=2. This is a common exam trick — the numbers are chosen to give a clean result. If you spot it, you can do the whole calculation mentally.
✓Final answerThe efficiency of the engine is 75%, which corresponds to option (C).
- TG EAPCET 2025Set ap-2025-04-29-FN1 markMCQQ.The energy required to increase the radius of a soap bubble from 3 cm to 4 cm is (Surface tension of soap solution =3×10−2 Nm−1) (A) 528×10−6 J (B) 264×10−6 J (C) 1056×10−6 J (D) 478×10−6 J
›Reveal solutionSolution
The energy required to expand a soap bubble is the work done against surface tension to increase its total surface area (considering both inner and outer surfaces). This energy is calculated as the product of surface tension and the change in total surface area. For the given radii, the energy required is 528×10−6 J.
Concept and Intuition
When a liquid surface expands, molecules from the bulk of the liquid move to the surface. To do this, they must overcome the cohesive forces pulling them inwards, which requires energy. This energy is stored as potential energy in the expanded surface, and the work done to create this new surface area is directly proportional to the increase in area. This phenomenon is quantified by surface tension (T), which can be defined as the work done per unit increase in surface area.
For a soap bubble, a critical detail is that it has two free surfaces in contact with air: an inner surface and an outer surface. Therefore, when the radius of the bubble increases, both these surfaces expand. The total surface area that changes is twice the geometric surface area of a sphere.
The energy required to increase the surface area of a liquid film by ΔA is given by:
W=T×ΔA
where W is the work done (energy required), T is the surface tension, and ΔA is the change in total surface area.
Step-by-step Derivation
-
Identify the given values and convert units:
- Surface tension of soap solution, T=3×10−2 Nm−1.
- Initial radius of the soap bubble, R1=3 cm=3×10−2 m.
- Final radius of the soap bubble, R2=4 cm=4×10−2 m.
-
Calculate the initial total surface area (A1) of the soap bubble:
A spherical soap bubble has two surfaces (inner and outer). The surface area of a single sphere is 4πR2. Therefore, the total surface area of a soap bubble is 2×4πR2=8πR2.
A1=8πR12=8π(3×10−2 m)2
A1=8π(9×10−4 m2)
A1=72π×10−4 m2
-
Calculate the final total surface area (A2) of the soap bubble:
Similarly, for the final radius:
A2=8πR22=8π(4×10−2 m)2
A2=8π(16×10−4 m2)
A2=128π×10−4 m2
-
Calculate the change in total surface area (ΔA):
ΔA=A2−A1
ΔA=(128π×10−4 m2)−(72π×10−4 m2)
ΔA=(128−72)π×10−4 m2
ΔA=56π×10−4 m2
-
Calculate the energy required (work done, W):
Using the formula W=T×ΔA:
W=(3×10−2 Nm−1)×(56π×10−4 m2)
W=3×56π×10−2×10−4 J
W=168π×10−6 J
-
Substitute the value of π and calculate the numerical result:
Using π≈3.14159:
W=168×3.14159×10−6 J
W≈527.787×10−6 J
Rounding to the nearest whole number as per the options:
W≈528×10−6 J
Watch outA common mistake is to consider only one surface of the soap bubble, using 4πR2 instead of 8πR2. This would lead to half the correct energy value. Always remember a soap bubble has two free surfaces.
The calculated energy matches option (A).
✓Final answerThe energy required to increase the radius of the soap bubble from 3 cm to 4 cm is 528×10−6 J.
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- TG EAPCET 2024Set ap-2024-05-08-FN1 markMCQQ.The initial and the final temperatures of a black body are 27∘C and 177∘C respectively. The increase in the amount of radiation emitted per second is (A) 506.25% (B) 150.25% (C) 225.75% (D) 406.25%
›Reveal solutionSolution
The radiation emitted by a black body scales as T4 (Stefan–Boltzmann law). Converting temperatures to Kelvin and taking the ratio gives a factor of (450/300)4=(1.5)4=5.0625, so the increase is 406.25% — option (D).
The key idea is Stefan’s law: for a black body, the total power radiated per unit area is σT4, where T is the absolute temperature in Kelvin. When the temperature changes, the radiated power changes as the fourth power of the ratio of absolute temperatures. A common mistake is to use Celsius directly — that breaks the T4 law because it’s not a ratio scale. Always convert to Kelvin first.
-
Convert temperatures to Kelvin.
T1=27∘C+273=300 K
T2=177∘C+273=450 K
-
Apply Stefan–Boltzmann law.
The power radiated per second (for the same surface area) is proportional to T4. So
P1P2=(T1T2)4=(300450)4=(1.5)4
Compute: 1.52=2.25, then 2.252=5.0625. Hence P2=5.0625P1.
- Find the percentage increase. Increase in radiation = P2−P1=(5.0625−1)P1=4.0625P1. As a percentage of the original: 4.0625×100%=406.25%.
Watch outDo not use Celsius temperatures in the ratio. (177/27)4 gives a huge wrong number — the T4 law only holds for absolute temperature.
Tip(1.5)4=(3/2)4=81/16=5.0625 is a clean fraction — useful for quick mental calculation.
✓Final answerThe increase in radiation emitted per second is 406.25%, which corresponds to option (D).
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- TG EAPCET 2024Set ap-2024-05-07-FN1 markMCQQ.A black body at a temperature of 125∘C, emits heat at the rate of 32 Wm−2. The rate of heat emitted by the body when the temperature of the body is increased by 398 K is (A) 64 Wm−2 (B) 128 Wm−2 (C) 512 Wm−2 (D) 256 Wm−2
›Reveal solutionSolution
The key idea is that the power radiated by a black body is proportional to the fourth power of its absolute temperature (Stefan–Boltzmann law). Converting the given Celsius temperature to Kelvin and applying the ratio of powers gives the new emission rate as 512 Wm−2, so the correct option is (C).
Concept and intuition
A black body is an ideal emitter: the power it radiates per unit area depends only on its absolute temperature T (in Kelvin). The Stefan–Boltzmann law states:
P=σT4
where σ is the Stefan–Boltzmann constant.
If the temperature changes, the new power is proportional to the fourth power of the new absolute temperature. The problem gives an initial temperature in Celsius and a temperature increase in Kelvin (which is the same as an increase in Celsius degrees). The crucial step is to work entirely in Kelvin.
Step-by-step solution
- Convert the initial temperature to Kelvin The initial temperature is 125∘C.
T1=125+273=398 K
- Identify the temperature increase The temperature is increased by 398 K. So the new absolute temperature is:
T2=T1+398=398+398=796 K
- Apply the Stefan–Boltzmann law The initial power per unit area is P1=32 Wm−2. Since P∝T4, we have:
P1P2=(T1T2)4
- Compute the ratio
T1T2=398796=2
Therefore:
P1P2=24=16
- Find the new power
P2=16×P1=16×32=512 Wm−2
Watch outA common mistake is to forget that the Stefan–Boltzmann law requires absolute temperature. Using Celsius directly would give a wrong ratio. Also, note that an increase of 398 K is exactly the same as an increase of 398∘C, but the starting temperature must be in Kelvin.
TipNotice that the initial temperature in Kelvin (398 K) equals the temperature increase (398 K). This makes the new temperature exactly double the old one, so the power multiplies by 24=16. This neat coincidence simplifies the arithmetic.
✓Final answerThe correct option is (C).
ANSWER: C
- TG EAPCET 2024Set eng-2024-05-10-AN1 markMCQQ.Steam of mass 60 g at a temperature 100 ∘C is mixed with water of mass 360 g at a temperature 40 ∘C. The ratio of the masses of steam and water in equilibrium is (Latent heat of steam is 540 cal g−1 and specific heat capacity of water is 1 cal g−1 ∘C−1) (A) 1 : 20 (B) 1 : 10 (C) 1 : 5 (D) 1 : 3
›Reveal solutionSolution
Warming the water to 100∘C condenses only 40 g of steam, leaving 20 g steam and 400 g water — a ratio of 1:20.
Heat needed to raise the water to 100∘C.
The 360 g of water at 40∘C needs to be heated by 60∘C:
Qwater=mcΔT=360×1×(100−40)=21600 cal.
Heat available from condensing all the steam.
Condensing the entire 60 g of steam would release
Qsteam=60×540=32400 cal.
Since 32400>21600, not all the steam condenses. Equilibrium is reached at 100∘C with steam and water coexisting.
Mass of steam that condenses.
Let m grams of steam condense, supplying exactly the heat the water needs:
m×540=21600⇒m=40 g.
Masses at equilibrium.
- Steam remaining =60−40=20 g.
- Water =360+40=400 g (original water plus condensed steam).
steam:water=20:400=1:20.
✓Final answerThe ratio of steam to water at equilibrium is 1:20 — option (A).
- TG EAPCET 2024Set eng-2024-05-10-AN1 markMCQQ.The temperature at which the rms speed of oxygen molecules is 75% of rms speed of nitrogen molecules at a temperature of 287 ∘C is (A) 87 ∘C (B) 127 ∘C (C) 227 ∘C (D) 360 ∘C
›Reveal solutionSolution
The rms speed of a gas depends on temperature and molar mass; setting the oxygen rms speed to 75% of nitrogen’s rms speed gives a relation that yields the required temperature. The answer is 87 °C.
The key idea is that the root‑mean‑square speed of gas molecules is given by
vrms=M3RT
where T is the absolute temperature (in kelvin) and M is the molar mass (in kg mol⁻¹).
We are told that for oxygen, vrms,O2 is 75% of vrms,N2 at a known temperature of nitrogen. This lets us set up a ratio that eliminates the gas constant R and directly relates the temperatures and molar masses.
- Convert the given nitrogen temperature to kelvin The nitrogen temperature is 287∘C.
TN2=287+273=560 K
- Write the rms speed expressions For nitrogen (molar mass MN2=28 g mol−1=0.028 kg mol−1):
vrms,N2=0.0283R⋅560
For oxygen (molar mass MO2=32 g mol−1=0.032 kg mol−1) at unknown temperature TO2:
vrms,O2=0.0323R⋅TO2
- Apply the given condition
vrms,O2=0.75⋅vrms,N2
Substitute the expressions:
0.0323RTO2=0.75⋅0.0283R⋅560
- Cancel common factors and square both sides The factor 3R cancels from both sides:
0.032TO2=0.75⋅0.028560
Squaring:
0.032TO2=(0.75)2⋅0.028560
0.032TO2=0.5625⋅0.028560
- Simplify the right‑hand side First compute 0.028560:
0.028560=28/1000560=560×281000=20×1000=20000
Then multiply by 0.5625:
0.5625×20000=11250
So we have:
0.032TO2=11250
- Solve for TO2
TO2=11250×0.032=360 K
- Convert back to Celsius
TO2(∘C)=360−273=87∘C
Watch outA common mistake is to forget to convert Celsius to kelvin before using the rms formula, or to use molar masses in grams per mole without converting to kilograms. Both errors lead to wrong numerical factors.
TipNotice that the ratio of rms speeds depends only on the square root of the ratio of temperatures divided by molar masses. This shortcut lets you skip writing the full expressions each time.
✓Final answerThe correct option is (A).
ANSWER: A
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