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 27 on this concept.
- AP EAPCET 2026Set eng-2026-05-12-AN1 markMCQQ.Equal amounts of a diatomic ideal gas are contained in two separate cylinders, P and Q. Cylinder P has a movable piston, while cylinder Q has a fixed piston. Both gases are initially at 273 K, and the same amount of heat is supplied to each. If the gas in cylinder P shows a temperature rise of 20 K, then the increase in temperature of the gas in cylinder Q is (A) 38 K (B) 20 K (C) 42 K (D) 28 K
›Reveal solutionSolution
Equal heat causes a larger temperature rise at constant volume than at constant pressure (since some heat at constant pressure goes into expansion work); for a diatomic gas the ratio is exactly Cp/Cv=7/5, giving 28 K.
Concept and Intuition
At constant pressure, part of the supplied heat does work pushing the piston outward, so less heat is 'left over' to raise the gas's internal energy/temperature — the effective heat capacity is Cp (larger). At constant volume, no work is done, so all the heat raises the internal energy — the effective heat capacity is Cv (smaller). Since Cv<Cp, the same amount of heat produces a larger temperature rise at constant volume than at constant pressure.
Step-by-Step Solution
- Cylinder P has a movable piston ⇒ constant-pressure process: Q=nCpΔTP.
- Cylinder Q has a fixed piston ⇒ constant-volume process: Q=nCvΔTQ.
- Both cylinders receive the same heat Q and contain the same amount (n) of the same diatomic gas, so:
nCpΔTP=nCvΔTQ⇒ΔTQ=CvCpΔTP.
- For a diatomic ideal gas, Cv=25R, Cp=27R, so CvCp=57=1.4.
- ΔTQ=1.4×20 K=28 K.
Common Mistakes
- Inverting the ratio (using Cv/Cp instead of Cp/Cv) — remember the constant-volume rise must be larger, since none of its heat is 'spent' on work.
- Using the monatomic ratio (5/3) instead of the diatomic ratio (7/5) by forgetting the gas is diatomic.
✓Final answerThe correct option is (D) — 28 K.
ANSWER: D
- AP EAPCET 2026Set ap-2026-05-19-AN1 markMCQQ.When some amount of heat energy is supplied to a monoatomic gas at constant pressure P, the volume of the gas is increased by 42%. If the same amount of heat is supplied to a rigid diatomic gas at constant pressure 2P, then the percentage increase in the volume of the diatomic gas is (A) 63% (B) 15% (C) 21% (D) 30%
›Reveal solutionSolution
The key is to relate heat input to volume change via the molar specific heat at constant pressure and the ideal gas law. For the monatomic gas, a 42% volume increase at pressure P corresponds to a certain heat input; applying the same heat to a diatomic gas at pressure 2P yields a 15% volume increase, so the correct option is (B).
Concept and Intuition
When heat is supplied at constant pressure, the gas expands and does work. The amount of heat needed to raise the temperature by ΔT is Q=nCpΔT, where Cp is the molar specific heat at constant pressure. For an ideal gas, the volume change at constant pressure is directly proportional to the temperature change: V∝T (from PV=nRT). So the fractional volume increase VΔV=TΔT.
We are given that for a monatomic gas at pressure P, the volume increases by 42% when a certain heat Q is supplied. For a diatomic gas at pressure 2P, the same Q is supplied. We need the new percentage volume increase. The trick: different gases have different Cp values, and the pressure difference affects the initial volume but not the fractional change (since V∝T at constant P). We’ll compare the temperature rises and then the volume changes.
Step-by-step solution
-
Recall molar specific heats
For a monatomic ideal gas: Cv=23R, so Cp=Cv+R=25R.
For a rigid diatomic ideal gas (no vibration): Cv=25R, so Cp=27R.
-
Express the heat supplied for the monatomic case
Let n be the number of moles (same gas amount in both cases).
Heat supplied: Q=nCp,monoΔT1=n⋅25R⋅ΔT1.
At constant pressure P, the volume change is V1ΔV1=T1ΔT1.
Given V1ΔV1=42%=0.42, so ΔT1=0.42T1.
-
Find Q in terms of T1
Substitute ΔT1:
Q=n⋅25R⋅(0.42T1)=nRT1⋅25⋅0.42=nRT1⋅1.05.
- Apply the same heat to the diatomic gas at pressure 2P For the diatomic gas: Q=nCp,diΔT2=n⋅27R⋅ΔT2. Set equal to the previous Q:
n⋅27R⋅ΔT2=nRT1⋅1.05.
Cancel nR:
27ΔT2=1.05T1⇒ΔT2=72⋅1.05T1=0.3T1.
-
Relate ΔT2 to the volume change
For the diatomic gas at constant pressure 2P, the initial state obeys 2PV2=nRT2.
But we don’t know T2 directly. However, the fractional volume increase at constant pressure is still V2ΔV2=T2ΔT2.
We need T2 in terms of T1. The initial conditions: the monatomic gas had pressure P and volume V1 at temperature T1. The diatomic gas has pressure 2P and some volume V2 at temperature T2. The problem doesn’t specify that the initial volumes or temperatures are the same, but we can assume the same number of moles n and that the gases start at the same temperature? Actually, careful: The problem only says “when some amount of heat is supplied… at constant pressure P” and then “the same amount of heat is supplied to a rigid diatomic gas at constant pressure 2P”. It does not state that the initial temperatures are equal. However, the percentage increase in volume depends only on the ratio ΔT/T for the given initial state. We need to find T2 relative to T1 from the ideal gas law using the given pressures and the fact that the heat input is the same. But wait — the initial volumes are not given, so we must assume the initial temperatures are the same? Let’s check: If the gases are initially at the same temperature T0, then for the monatomic gas: PV1=nRT0. For the diatomic gas: 2PV2=nRT0, so V2=V1/2. That is plausible. But does the problem imply that? Usually in such problems, the initial temperature is taken as the same unless stated otherwise. Let’s verify with the numbers: If T2=T1, then ΔT2=0.3T1 gives V2ΔV2=0.3=30%. That would be option (D). But we got 0.3 from the equation, so is it 30%? Wait, we must check: The calculation gave ΔT2=0.3T1. If T2=T1, then percentage increase = 30%. But the answer choices include 30% as (D). However, we need to be careful: The initial temperature of the diatomic gas might not be the same as that of the monatomic gas. Let’s re-examine.
Actually, the problem does not specify initial temperatures. But we can deduce them from the fact that the same amount of heat is supplied. The heat Q is fixed. For the monatomic gas, we expressed Q in terms of T1. For the diatomic gas, we have Q=n27RΔT2. So ΔT2=7nR2Q. But we also have Q=1.05nRT1, so ΔT2=72⋅1.05T1=0.3T1. That is correct. Now, the fractional volume increase is ΔV2/V2=ΔT2/T2. We need T2. The initial state of the diatomic gas is at pressure 2P and some volume V2. But we don’t know V2 or T2. However, we can relate T2 to T1 if we assume the gases are initially at the same temperature? That is a common hidden assumption in such problems. Let’s test: If T2=T1, then answer is 30%. But let’s see if there’s another relation.
Alternatively, perhaps the initial volumes are the same? No, that would give different pressures. The problem likely intends that the initial conditions (temperature and number of moles) are the same for both gases, only the pressure differs because the container is different. So we set T1=T2=T (initial). Then:
V2ΔV2=T0.3T=0.3=30%.
That gives option (D). But wait, the answer choices include 15%, 21%, 30%, 63%. Let’s double-check the calculation: For monatomic, Cp=5R/2, 42% volume increase means ΔT/T=0.42, so Q=n(5R/2)(0.42T)=nRT⋅1.05. For diatomic, Cp=7R/2, so ΔT=n(7R/2)Q=3.5nR1.05nRT=0.3T. So if initial T same, volume increase = 30%. That seems straightforward. But why is 15% an option? Perhaps I missed that the diatomic gas is rigid (no vibration) so Cv=5R/2 is correct. Let’s check if the pressure difference affects the initial volume? The fractional change doesn’t depend on initial volume, only on temperature change. So 30% seems correct.
However, let’s re-read the problem: “When some amount of heat energy is supplied to a monoatomic gas at constant pressure P, the volume of the gas is increased by 42%. If the same amount of heat is supplied to a rigid diatomic gas at constant pressure 2P, then the percentage increase in the volume of the diatomic gas is” — note that the pressures are different. Could it be that the initial volumes are the same? If the initial volumes are the same, then from PV=nRT, for monatomic: PV=nRT1, for diatomic: 2PV=nRT2, so T2=2T1. Then the fractional volume increase for diatomic would be ΔV2/V2=ΔT2/T2. We have ΔT2=0.3T1 from the heat equation, so ΔV2/V2=(0.3T1)/(2T1)=0.15=15%. That gives option (B). That makes sense: the initial temperature of the diatomic gas is higher because at the same volume, higher pressure means higher temperature. So the same temperature rise gives a smaller fractional increase. This is a classic pitfall: assuming initial temperatures are equal when pressures differ.
Watch outA common mistake is to assume the initial temperatures are the same. But the problem states different constant pressures, and if the initial volumes are not specified, one might implicitly assume they are equal. However, the phrase “at constant pressure P” and “at constant pressure 2P” does not specify initial volumes. In such problems, it is typical to assume the same initial volume for both gases, because the heat is supplied to the gas in a container; the pressure is different because the container’s piston loading is different. So we should assume the same initial volume V0. Let’s verify: If the initial volumes are the same, then the initial temperatures are different: Tmono=nRPV0, Tdi=nR2PV0=2Tmono. That yields the 15% result.
Let’s confirm with the numbers: For monatomic, ΔV1/V0=0.42, so ΔT1=0.42Tmono. Then Q=n(5R/2)(0.42Tmono)=1.05nRTmono. For diatomic, Q=n(7R/2)ΔT2, so ΔT2=(2/7)∗1.05Tmono=0.3Tmono. Now, initial volume V0 for diatomic, so ΔV2/V0=ΔT2/Tdi=(0.3Tmono)/(2Tmono)=0.15=15%. So the answer is 15%.
TipWhen pressures differ, always check if initial volumes or temperatures are implicitly the same. Here, the natural assumption is same initial volume (the gas is in a container of fixed size before heating), leading to different initial temperatures.
- Final answer The percentage increase in volume for the diatomic gas is 15%.
✓Final answerThe correct option is (B).
ANSWER: B
-
- AP EAPCET 2025Set eng-2025-05-22-AN1 markMCQQ.When an ideal diatomic gas is heated at constant pressure, the fraction of the heat utilised to increase the internal energy of the gas is (A) 52 (B) 53 (C) 73 (D) 75
›Reveal solutionSolution
This tests the split of heat between internal energy and work at constant pressure — the fraction going into internal energy is always Cv/Cp. For a diatomic ideal gas this is 5/7.
Concept and Intuition
When a gas is heated at constant pressure, it must expand (since P is fixed and T rises, V must rise by the ideal gas law). Some of the supplied heat raises the internal energy (temperature) of the gas, and the rest is spent doing work pushing back the surroundings as it expands. The internal energy rise for ANY process (not just constant pressure) is ΔU=nCvΔT, since U depends only on T for an ideal gas. But the heat SUPPLIED specifically at constant pressure is Q=nCpΔT. So the fraction of heat that becomes internal energy is Cv/Cp, a fixed number for a given gas — for diatomic gases with 5 degrees of freedom (3 translational + 2 rotational), Cv=25R and Cp=Cv+R=27R.
Step-by-Step Solution
- At constant pressure, heat supplied: Q=nCpΔT.
- Internal energy is a state function depending only on T: ΔU=nCvΔT (true regardless of the path).
- Fraction of heat going to internal energy: QΔU=CpCv.
- For a diatomic gas: Cv=25R, Cp=27R.
- Fraction =7/2R5/2R=75.
Common Mistakes
- Confusing this with the fraction going to WORK, which would be 1−5/7=2/7 (using R/Cp), not 2/5.
- Using the monatomic values (Cv=3/2R) instead of diatomic (Cv=5/2R).
✓Final answerThe correct option is (D) — 75.
ANSWER: D
- AP EAPCET 2025Set ap-2025-05-19-AN1 markMCQQ.At constant pressure, if the work done by a gas is 40% of the increase in the internal energy of the gas, then the specific heat capacity of the gas at constant volume is (Universal gas constant = 8.3 J mol−1 K−1) (A) 29.05 J mol−1 K−1 (B) 25.35 J mol−1 K−1 (C) 20.75 J mol−1 K−1 (D) 32.55 J mol−1 K−1
›Reveal solutionSolution
Comparing the constant-pressure work (nRΔT) to the internal energy change (nCvΔT) via the given 40% ratio pins down Cv=2.5R=20.75 J mol−1K−1.
Concept and Intuition
At constant pressure, a gas expanding does work W=PΔV=nRΔT (ideal gas law), while its internal energy changes by ΔU=nCvΔT regardless of the process. The ratio W/ΔU=R/Cv is therefore a fixed property of the gas, independent of how much it's heated.
Step-by-Step Solution
- W=nRΔT (constant pressure); ΔU=nCvΔT.
- Given W=0.4ΔU: nRΔT=0.4×nCvΔT.
- The nΔT cancels: R=0.4Cv⇒Cv=0.4R=2.5R.
- Cv=2.5×8.3=20.75 J mol−1K−1.
Common Mistakes
- Confusing Cv with Cp in the ratio (the work here is compared to ΔU, which uses Cv, not Cp).
- Forgetting that n and ΔT cancel out, and trying to solve for them separately using leftover given data.
✓Final answerThe correct option is (C) — 20.75 J mol−1 K−1.
ANSWER: C
- AP EAPCET 2025Set ap-2025-05-19-FN1 markMCQQ.When a polyatomic gas is heated at constant pressure, the percentage of heat given to the gas that is converted into external work is (Ratio of the specific heat capacities of the gas =34) (A) 30 (B) 25 (C) 20 (D) 45
›Reveal solutionSolution
The fraction of heat converted to external work at constant pressure is the universal formula (γ−1)/γ; for a polyatomic gas with γ=4/3 this comes out to exactly 25%.
Concept and Intuition
At constant pressure, the first law gives Q=ΔU+W, where for an ideal gas Q=nCpΔT, ΔU=nCvΔT, and the external work done by the expanding gas is W=PΔV=nRΔT (ideal gas law at constant P). The fraction of the supplied heat that goes into external work is therefore
QW=nCpΔTnRΔT=CpR.
Using Cp−Cv=R and γ=Cp/Cv, one can show Cp=γ−1γR, so CpR=γγ−1 — a clean, gas-independent formula in terms of γ alone.
Step-by-Step Solution
- Fraction of heat converted to work at constant pressure: QW=CpR=γγ−1.
- Substitute γ=34: γ−1=31.
- Fraction =4/31/3=31×43=41.
- As a percentage: 41×100%=25%.
Common Mistakes
- Confusing this with the fraction of heat that becomes internal energy (ΔU/Q=1/γ, which would give 75% here, not what's asked).
- Using γ for a diatomic gas (7/5) instead of the given polyatomic value (4/3).
✓Final answerThe correct option is (B) — 25.
ANSWER: B
- AP EAPCET 2025Set ap-2025-05-20-AN1 markMCQQ.If the relation between the absolute temperature (T) and volume (V) of an ideal gas which expands adiabatically is T∝V1, then the ratio of the specific heat capacities of the gas is (A) 1.3 (B) 1.5 (C) 1.4 (D) 2.0
›Reveal solutionSolution
For an adiabatic process, matching the given T–V power law to TVγ−1= const gives γ=1.5.
Concept and Intuition
For a reversible adiabatic process of an ideal gas, PVγ=const. Using PV=nRT, this can be rewritten purely in terms of T and V:
TVγ−1=const
So whenever a problem gives you T as some power of V in an adiabatic process, you can read off γ−1 directly as (minus) that power.
Step-by-Step Solution
- Given: T∝V−1/2, i.e. TV1/2=const.
- Compare exponents with the adiabatic relation TVγ−1=const.
- Matching powers of V: γ−1=21.
- Hence γ=1+21=1.5.
Common Mistakes
- Confusing the adiabatic relation between T,V with the one between P,V (PVγ= const) and mismatching the exponent sign.
- Forgetting that γ−1 is the magnitude of the power on V in the T–V form.
✓Final answerThe correct option is (B) — 1.5.
ANSWER: B
- AP EAPCET 2025Set ap-2025-05-20-AN1 markMCQQ.If the differences between the specific heat capacities at constant pressure and constant volume of hydrogen and another gas are in the ratio 16 : 1, then the other gas is (A) nitrogen (B) oxygen (C) carbon (D) argon
›Reveal solutionSolution
Since specific heat differences scale as 1/M, a ratio of 16 between hydrogen and another gas means the other gas has 16 times hydrogen's molar mass — oxygen (M=32).
Concept and Intuition
Mayer's relation for one mole is Cp−Cv=R. But when working with specific heat capacities (per unit mass, i.e. cp=Cp/M), dividing through by molar mass M gives
cp−cv=MR
So the difference between the specific heats is inversely proportional to the molar mass of the gas — a heavier gas has a smaller specific-heat difference.
Step-by-Step Solution
- Write the specific heat difference for hydrogen and for the unknown gas:
(cp−cv)H2=MH2R,(cp−cv)gas=MgasR
- Take the given ratio:
(cp−cv)gas(cp−cv)H2=MH2Mgas=116
- With MH2=2 g/mol:
Mgas=16×2=32 g/mol
- A diatomic gas of molar mass 32 g/mol is oxygen, O2.
Common Mistakes
- Inverting the ratio (forgetting that the specific-heat-difference ratio is inversely, not directly, proportional to the molar-mass ratio).
- Using MH2=1 (atomic mass of H) instead of 2 (molecular mass of H2 gas).
✓Final answerThe correct option is (B) — oxygen.
ANSWER: B
- AP EAPCET 2025Set ap-2025-05-20-FN1 markMCQQ.The heat to be supplied to 20 g of oxygen to increase its temperature from 27 °C to 59 °C at constant pressure is (Universal gas constant = 8.3 Jmol−1K−1) (A) 1162 J (B) 423 J (C) 934 J (D) 581 J
›Reveal solutionSolution
Oxygen is diatomic, so Cp=27R; plugging in the given moles and temperature change gives Q≈581 J.
Concept and Intuition
At constant pressure, part of the heat supplied to a gas goes into internal energy (raising temperature) and part into work done during expansion — captured together by the molar heat capacity at constant pressure, Cp. For a diatomic ideal gas (like O2), Cp=27R (5 degrees of freedom: 3 translational + 2 rotational, plus the R from the pV=nRT work term).
Step-by-Step Solution
- Moles of oxygen: n=32 g/mol20 g=0.625 mol.
- Temperature change: ΔT=59−27=32 K.
- Molar heat capacity at constant pressure (diatomic): Cp=27R=3.5×8.3=29.05 Jmol−1K−1.
- Heat supplied: Q=nCpΔT=0.625×29.05×32≈581 J.
Common Mistakes
- Using Cv=25R (constant volume) instead of Cp=27R since the process here is explicitly at constant pressure.
- Using the wrong molar mass for oxygen (it's O2, molar mass 32 g/mol, not atomic oxygen at 16 g/mol).
✓Final answerThe correct option is (D) — 581 J.
ANSWER: D
- AP EAPCET 2025Set ap-2025-05-20-FN1 markMCQQ.If four moles of hydrogen and two moles of helium form a gaseous mixture, then the molar specific heat capacity of the mixture at constant pressure is (A) 716R (B) 167R (C) R (D) 619R
›Reveal solutionSolution
The molar Cp of a gas mixture is the mole-weighted average of the individual Cp values; combining diatomic H2 (7R/2) and monatomic He (5R/2) in the given proportions gives 19R/6.
Concept and Intuition
When two ideal gases are mixed (and don't react), the total internal energy and total enthalpy of the mixture are just the sums of the individual gases' contributions. Dividing by the total number of moles gives the mixture's molar heat capacities as mole-fraction-weighted averages of the pure-gas values.
Step-by-Step Solution
- H2 is diatomic: Cp,H2=27R. Moles n1=4.
- He is monatomic: Cp,He=25R. Moles n2=2.
- Mixture's molar Cp:
Cp,mix=n1+n2n1Cp,H2+n2Cp,He=4+24(27R)+2(25R)=614R+5R=619R
Common Mistakes
- Simply averaging the two Cp values without weighting by the number of moles of each gas.
- Using Cv values for one gas and Cp for the other, or mixing up which gas is diatomic vs monatomic.
✓Final answerThe correct option is (D) — 619R.
ANSWER: D
- AP EAPCET 2025Set eng-2025-05-24-FN1 markMCQQ.When 80 J of heat is supplied to a gas at constant pressure, if the work done by the gas is 20 J, then the ratio of the specific heat capacities of the gas is (A) 34 (B) 35 (C) 57 (D) 79
›Reveal solutionSolution
This tests extracting the ratio of specific heats γ from the first law of thermodynamics at constant pressure; the answer is (A) 34.
Concept and Intuition
At constant pressure, the heat supplied equals nCpΔT, while the internal energy change (which depends only on temperature for an ideal gas) equals nCvΔT regardless of the process. The first law Q=ΔU+W then lets us find ΔU from the given Q and W, and the ratio Q/ΔU directly gives Cp/Cv=γ.
Step-by-Step Solution
- First law: ΔU=Q−W=80−20=60 J.
- Q=nCpΔT=80 J and ΔU=nCvΔT=60 J.
- Ratio: γ=CvCp=nCvΔTnCpΔT=ΔUQ=6080=34.
Common Mistakes
- Computing Q/W instead of Q/ΔU for the ratio of specific heats.
- Forgetting that W here is the work done BY the gas, which subtracts from Q to give ΔU (sign confusion).
✓Final answerThe correct option is (A) — 34.
ANSWER: A
- AP EAPCET 2025Set eng-2025-05-27-FN1 markMCQQ.The change in internal energy of given mass of a gas, when its volume changes from V to 3V at constant pressure P is (γ - Ratio of the specific heat capacities of the gas) (A) γ−1PV (B) γ−12PV (C) γ−13PV (D) 2γ−1PV
›Reveal solutionSolution
This tests the relation ΔU=γ−1PΔV for an ideal gas undergoing an isobaric change; the answer is (B) γ−12PV.
Concept and Intuition
For an ideal gas, the change in internal energy depends only on the temperature change, ΔU=nCvΔT, regardless of the process. At constant pressure, the ideal gas law gives PΔV=nRΔT, which lets us trade ΔT for the more directly known quantity ΔV. Combining these with Cv=γ−1R gives a compact formula purely in terms of P and ΔV.
Step-by-Step Solution
- Internal energy change: ΔU=nCvΔT.
- At constant pressure, nRΔT=PΔV, so nCvΔT=RCv(PΔV).
- Since Cv=γ−1R, we get ΔU=γ−1PΔV.
- Given V→3V at constant P: ΔV=3V−V=2V.
- Substituting: ΔU=γ−1P(2V)=γ−12PV.
Common Mistakes
- Forgetting that ΔU depends only on ΔT (state function), and trying to use W=PΔV directly as ΔU (that's the work done, not the internal energy change).
- Using ΔV=3V instead of 2V (forgetting to subtract the initial volume).
✓Final answerThe correct option is (B) — γ−12PV.
ANSWER: B
- AP EAPCET 2024Set ap-2024-05-16-FN1 markMCQQ.Heat is supplied at constant pressure to a diatomic gas. The part of this heat, that was utilized to increase its internal energy is (A) 4/5 (B) 5/7 (C) 3/5 (D) 5/6
›Reveal solutionSolution
This tests knowing the degrees-of-freedom-based specific heats of a diatomic gas (Cv=25R, Cp=27R) and using them to split constant-pressure heat between internal-energy increase and work done.
Concept and Intuition
At constant pressure, supplied heat dQ splits into two parts: raising internal energy (dU) and doing work on the surroundings as the gas expands (dW=PdV), per the first law dQ=dU+dW. Since dU=nCvdT always (regardless of process) while dQ=nCpdT at constant pressure, the fraction of heat that goes into internal energy at constant pressure is simply the ratio Cv/Cp — a fixed number depending only on the gas's degrees of freedom.
Step-by-Step Solution
- For a diatomic ideal gas (5 degrees of freedom: 3 translational + 2 rotational), Cv=25R and Cp=Cv+R=27R.
- At constant pressure, dQ=nCpdT and dU=nCvdT, so the fraction going to internal energy is dQdU=CpCv.
- Substituting: CpCv=7R/25R/2=75.
Common Mistakes
- Using the monoatomic values (Cv=23R, giving 3/5) instead of diatomic.
- Confusing this ratio with Cv/Cp=1/γ written the wrong way round.
✓Final answerThe correct option is (B) — 5/7.
ANSWER: B
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