Q.H2S, a toxic gas with rotten egg like smell, is used for the qualitative analysis. If the solubility of H2S in water at STP is 0.195 m, calculate Henry's law constant.
Concept understanding — Henrys Law
Henry's Law: The Physics of "Fizz"
Imagine you open a cold bottle of soda. You hear that familiar psshhht sound. Bubbles rush out. Now think: why were those bubbles inside the bottle in the first place? The liquid wasn't boiling. The answer is Henry's Law.
The Intuition: Gas Wants to Dissolve
Gases are just molecules flying around. When a gas touches a liquid, some of those molecules get "trapped" inside the liquid — they dissolve. But here's the key: the more you push on the gas, the more of it gets forced into the liquid.
Think of a crowded bus. If you push more people toward the door (higher pressure), more people get squeezed inside. If you let the pressure off (open the bottle), people rush out. That's exactly what happens with gas and liquid.
In the soda bottle, carbon dioxide gas is pumped in at high pressure. That pressure forces a huge amount of CO₂ to dissolve into the liquid. When you open the bottle, the pressure above the liquid drops to normal air pressure. Suddenly, the liquid can't hold all that CO₂ anymore — so it escapes as bubbles. That's the fizz.
The Precise Statement
Henry's Law says:
C=kH⋅P
Where:
- C = concentration of the dissolved gas in the liquid (usually mol/L or g/L)
- P = partial pressure of that gas above the liquid (usually atm or kPa)
- kH = Henry's law constant — a number that depends on the specific gas, the liquid, and the temperature
In words: At a constant temperature, the amount of gas that dissolves in a liquid is directly proportional to the partial pressure of that gas above the liquid.
What the Constant kH Tells You
kH is not universal. It's different for every gas-liquid pair. For example:
- CO₂ in water has a certain kH
- O₂ in water has a different kH (smaller — oxygen doesn't dissolve as easily)
Temperature matters too. Higher temperature means lower kH — gases become less soluble in hot liquids. That's why a warm soda goes flat faster than a cold one.
Henry's Law works only for dilute solutions and non-reacting gases. If the gas reacts chemically with the liquid (like HCl gas dissolving in water to form hydrochloric acid), Henry's Law does not apply — the concentration will be much higher than predicted.
Real-Life Examples
| Situation | What Henry's Law explains |
|---|---|
| Soda fizz | High pressure forces CO₂ in; releasing pressure lets it out |
| Scuba diving | At depth, high pressure forces more N₂ into blood; rising too fast causes decompression sickness ("the bends") |
| Fish breathing | Oxygen dissolves in water at the surface (where partial pressure is highest); deeper water has less dissolved O₂ |
| Altitude sickness | At high altitude, lower atmospheric pressure means less O₂ dissolves in your blood |
The Key Takeaway
Henry's Law is a proportionality: double the pressure above the liquid → double the gas dissolved in the liquid (at constant temperature). It's why carbonated drinks are bottled under pressure, why deep-sea divers must ascend slowly, and why a warm drink loses its carbonation faster.
The law is simple, but its consequences are everywhere — from the soda in your hand to the air you breathe at different altitudes.
Henry's law is a key quantitative concept in the NCERT/CBSE Class 12 Chemistry chapter on Solutions, and ‘Henry's law formula’ or ‘Henry's law numericals’ are common important-question searches for board exams, JEE Main and NEET. Its real-world applications, like gas solubility in carbonated drinks and blood at altitude, make it a favourite for application-based competitive-exam questions.
Why this formula?
Henry's Law: Why the Formula Holds
Henry's Law describes the solubility of a gas in a liquid at a constant temperature. The key formula is:
P=kH⋅x
Where:
- P = partial pressure of the gas above the liquid
- x = mole fraction of the gas dissolved in the liquid
- kH = Henry's constant (depends on gas, liquid, and temperature)
Why This Linear Relationship Exists
1. Dynamic Equilibrium at the Interface
Imagine a gas above a liquid. At the molecular level:
- Gas molecules constantly strike the liquid surface and dissolve
- Dissolved molecules constantly escape back into the gas phase
At equilibrium, the rate of dissolution equals the rate of escape. This is a dynamic balance, not a static one.
2. The Driving Force for Dissolution
The rate at which gas molecules enter the liquid depends on:
- How many gas molecules hit the surface — this is proportional to the partial pressure P of the gas
- How easily they dissolve — this is captured by kH
So:
Ratedissolve∝P
3. The Driving Force for Escape
The rate at which dissolved molecules leave the liquid depends on:
- How many dissolved molecules are near the surface — this is proportional to the mole fraction x of the gas in the liquid
- How easily they escape — also captured by kH
So:
Rateescape∝x
4. Equating the Two Rates
At equilibrium:
Ratedissolve=Rateescape
Therefore:
P∝x
Introducing the proportionality constant kH:
P=kH⋅x
Why It's Linear (Not Exponential or Logarithmic)
The linearity arises because:
- No saturation effects at low concentrations — the molecules don't "crowd" each other
- Ideal behavior is assumed — gas molecules don't interact strongly with each other or with the solvent
- Temperature is constant — kH doesn't change
This is analogous to Raoult's Law for ideal solutions, but for a solute gas rather than a solvent.
Key Exam Points
- Henry's Law works best for dilute solutions (low x)
- kH increases with temperature — gases become less soluble as temperature rises
- kH is different for each gas-liquid pair — e.g., CO2 in water vs O2 in water
- The law fails if the gas reacts chemically with the solvent (e.g., HCl in water)
Quick Example
If kH=3.0×104 atm for O2 in water at 25°C, and the partial pressure of O2 in air is 0.21 atm:
x=kHP=3.0×1040.21=7.0×10−6
This tiny mole fraction explains why fish need gills to extract enough oxygen from water!
Bottom line: Henry's Law is a direct consequence of dynamic equilibrium at the gas-liquid interface, where the rates of dissolution and escape balance each other linearly.
The key idea is Henry’s Law: at constant temperature, the partial pressure of a gas above a liquid is proportional to its mole fraction dissolved in the liquid, p=KH⋅x.
Step 1: Convert the given solubility (0.195 molal) to a mole fraction.
Moles of water in 1 kg: nwater=1000/18=55.56mol.
xH2S=0.195+55.560.195=55.7550.195≈0.0035
Step 2: At STP, the partial pressure of H2S is p=1bar.
Step 3: Solve for KH.
KH=xp=0.00351≈286bar
The Henry's law constant is 286 bar (approximately).
Convert the solubility (0.195 m) to a mole fraction of H2S, then apply Henry's law p=KHx at STP (taking p=1bar, the standard STP pressure). The result is KH≈286 bar.
Henry's law states p=KHx, where p is the partial pressure of the gas above the solution, x is the mole fraction of the dissolved gas, and KH is Henry's law constant.
1. Moles of solute and solvent.
A solubility of 0.195 m means 0.195 mol of H2S dissolved per 1 kg of water.
nwater=181000=55.56 mol
2. Mole fraction of H2S.
x=nH2S+nwaternH2S=0.195+55.560.195=55.7550.195≈0.0035
3. Apply Henry's law.
At STP the partial pressure of H2S above the (dilute, near-pure) solvent is taken as p=1bar (the standard reference pressure), so
KH=xp=0.00351≈286 bar
Henry's law constant for H2S in water at STP is KH≈286 bar (equivalently, about 286 atm if pressure is taken as 1 atm).
Method: Henry's Law (mole-fraction form)
Henry's Law states that at constant temperature, the partial pressure of a gas above a liquid is directly proportional to its mole fraction dissolved in the liquid:
p=KH⋅x
where:
- p = partial pressure of the gas above the solution
- KH = Henry's law constant (same units as pressure)
- x = mole fraction of the gas in solution
Steps
- Convert molality to mole fraction. Solubility m=0.195mol/kg means 0.195 mol H2S per 1 kg (55.56 mol) of water.
xH2S=0.195+55.560.195=55.7550.195≈0.0035
-
Identify the pressure at STP.
P=1bar (standard STP pressure).
-
Apply Henry's Law and solve for KH.
KH=xP=0.00351≈286bar
Key Exam Point
For this chapter, Henry's Law is always applied in its mole-fraction form, p=KHx - never in a 'per kg of solvent' (molal) form. Always convert a given molality to a mole fraction before applying Henry's Law.
This question is a direct application of Henry's Law in terms of molality, and it's a classic trap for students.
✓ The Core Concept First
Henry's Law states:
At constant temperature, the solubility of a gas in a liquid is directly proportional to the partial pressure of the gas above the liquid.
Mathematically:
p=KH⋅x
where:
- p = partial pressure of the gas (in bar or atm)
- KH = Henry's law constant (same units as pressure)
- x = mole fraction of the gas in the solution
✗ Common Mistake #1: Using molality (m) directly as mole fraction
The error:
Students see "0.195 m" and plug it directly into p=KH⋅m.
Why it's wrong:
Henry's law uses mole fraction, not molality. Molality is moles of solute per kg of solvent — a different quantity.
How to avoid:
Always convert molality to mole fraction first.
Correct method:
- At STP, take p=1 bar (see Mistake #2).
- 0.195 m means 0.195 moles of H2S in 1 kg of water.
- Moles of water in 1 kg = 181000≈55.56 mol.
- Mole fraction of H2S:
xH2S=0.195+55.560.195≈55.7550.195≈0.003497
- Then:
KH=xp=0.0034971≈286 bar
Key takeaway: Always compute x first.
✗ Common Mistake #2: Fumbling the pressure at STP
The error:
Students either ignore pressure entirely or assume some unrelated value.
Why it's wrong:
STP (Standard Temperature and Pressure) on the modern IUPAC definition — the one NCERT uses — is 273.15 K and 1 bar, so here p=1 bar. (Older texts defined STP with 1 atm; since the mole fraction is unchanged, the numerical answer is ≈ 286 either way — only the unit label follows your pressure convention.)
How to avoid:
Memorise:
- STP → T=273.15 K, p=1 bar (older convention: 1 atm)
- NTP → T=293 K, p=1 atm
- SATP → T=298 K, p=1 bar
✗ Common Mistake #3: Using molarity instead of molality
The error:
Students treat "0.195 m" as 0.195 M (moles per litre).
Why it's wrong:
The unit "m" means molality (mol/kg solvent), not molarity (mol/L solution). They are not interchangeable, especially when density is not given.
How to avoid:
- "m" = molality
- "M" = molarity
- If the problem says "0.195 m", it's molality — use mass of solvent, not volume.
✗ Common Mistake #4: Ignoring the "negligible" approximation
The error:
Students write x=55.560.195 and forget to add 0.195 in the denominator.
Why it's wrong:
Mole fraction = nsolute+nsolventnsolute. If you omit nsolute in the denominator, you get a slightly larger x and a smaller KH.
How to avoid:
Always include both terms in the denominator. For dilute solutions, the error is small — but in exams, full accuracy is expected.
✓ Final Correct Answer (for reference)
KH≈286 bar
(≈ 286 atm on the older 1-atm STP convention — same number, different unit label.)
📌 Quick Checklist to Avoid Mistakes
| Mistake | How to Avoid |
|---|---|
| Using molality as mole fraction | Convert m → x using nwater=181000 |
| Wrong pressure at STP | Use p=1 bar (modern IUPAC / NCERT convention) |
| Confusing molality & molarity | "m" = molality, use mass of solvent |
| Omitting solute moles in denominator | Always use x=nsolute+nsolventnsolute |
Showing the 12 most recent of 16 on this concept.
- KCET 2025Set D-41 markMCQQ.Variation of solubility with temperature T for a gas in liquid is shown by the following graphs. The correct representation is: (A)
(B)
(C)
(D)
›Reveal solutionSolution
Henry's law makes gas solubility fall as temperature rises — a straight line sloping DOWNWARD, not up, flat, or a hump.
Why solubility decreases with temperature for a gas. Dissolving a gas in a liquid is generally exothermic. As temperature rises, the dissolved gas molecules gain kinetic energy and increasingly escape back into the gas phase, so less gas stays dissolved at equilibrium — the everyday example is a fizzy drink going flat faster when warm.
Ruling out the other shapes: an upward line (A) or hump (C) would mean solubility rises with heating, which is the opposite of the real gas-solubility trend; a flat line (B) would mean no temperature dependence at all, which contradicts the well-established Henry's-law relationship.
✓Final answerOption (D) — the downward-sloping line.
- KCET 2025Set D-41 markMCQQ.If N2 gas is bubbled through water at 293 K, how many moles of N2 gas would dissolve in 1 litre of water? Assume that N2 exerts a partial pressure of 0.987 bar. [Given KH for N2 at 293 K is 76.48 K bar] (A) 0.716×10−3 (B) 7.16×10−5 (C) 7.16×10−4 (D) 7.16×10−3
›Reveal solutionSolution
Use Henry's law to get the mole fraction of dissolved N2, then convert that mole fraction to moles using the ≈55.5 mol of water in 1 litre.
Step 1 — Henry's law.
The solubility of a gas in a liquid at a given temperature is proportional to its partial pressure above the liquid:
p=KH⋅x
where x is the mole fraction of the gas in solution and KH is the Henry's-law constant. Rearranged:
x=KHp
Step 2 — Substitute (watch the units on KH).
The constant is given as 76.48 Kbar, i.e. 76.48 kilobar =76.48×103 bar=76,480 bar (this is the standard NCERT value for N2 at 293 K).
xN2=76,480 bar0.987 bar=1.29×10−5
A very small number — nitrogen is only sparingly soluble in water, as expected.
Step 3 — Moles of water in 1 litre.
nH2O=18 gmol−11000 g=55.5 mol
Step 4 — Convert mole fraction to moles of N2.
By definition
xN2=nN2+nH2OnN2≈nH2OnN2
The approximation is excellent because nN2⋘nH2O (we are about to find nN2∼10−4 against 55.5). Hence
nN2=xN2×nH2O=(1.29×10−5)(55.5)
nN2=7.16×10−4 mol
Step 5 — Check the options.
7.16×10−4 is option (C). Option (A), 0.716×10−3, is numerically the same number (0.716×10−3=7.16×10−4) — but the standard NCERT-printed form of this answer, and the form matching the option set's convention, is (C). Options (B) and (D) are out by a factor of ten either way, which is what you get by mishandling the kbar in KH or forgetting the 55.5.
(Physical note: the everyday consequence of this small solubility is decompression sickness — divers breathing high-pressure air dissolve extra N2 in their blood, and it bubbles out if they surface too fast.)
✓Final answerThe correct option is (C) — 7.16×10−4 mol.
ANSWER: C
- COMEDK 2025Set 2025-E1 markMCQQ.The ratio of N2 and O2 gases in the atmosphere is 4:1. The ratio of the mole fractions of the dissolved gases N2 : O2 in rain water will be approximately ........ (At 293 K, KH for Nitrogen and Oxygen in kbar units are 76.48 and 34.86 respectively.) (A) 3:1 (B) 2:1 (C) 4:1 (D) 1:4
›Reveal solutionSolution
Henry’s law says the mole fraction of a dissolved gas is proportional to its partial pressure times its Henry’s constant. Using the given atmospheric ratio and Henry’s constants, the dissolved N₂:O₂ ratio comes out to about 2:1, so option (B) is correct.
Concept & Intuition
Rainwater is in contact with air, so gases dissolve according to Henry’s law:
xgas=KHpgas
where xgas is the mole fraction in the liquid, pgas is the partial pressure in the gas phase, and KH is Henry’s constant (here given in kbar). The atmospheric ratio N₂:O₂ is 4:1 by volume, which means the partial pressures are in the same ratio (since total pressure ≈ 1 atm, but we only need the ratio). The dissolved ratio is not simply 4:1 because O₂ dissolves more readily (lower KH). We must compute the ratio of p/KH for each gas.
Step-by-step
- Set up partial pressures In dry air, N₂ and O₂ are in volume ratio 4:1. Since partial pressure is proportional to mole fraction in the gas,
pN2:pO2=4:1
Let pO2=P, then pN2=4P.
- Apply Henry’s law for each gas Henry’s law:
xN2=KH,N2pN2,xO2=KH,O2pO2
Given KH,N2=76.48 kbar and KH,O2=34.86 kbar.
- Find the ratio of dissolved mole fractions
xO2xN2=pO2/KH,O2pN2/KH,N2=pO2pN2⋅KH,N2KH,O2
Substitute the partial pressure ratio 4/1:
xO2xN2=4×76.4834.86
- Calculate numerically
76.4834.86≈0.4558
Then
4×0.4558≈1.823
So the ratio is roughly 1.823:1, which is very close to 2:1.
- Select the closest option Among (A) 3:1, (B) 2:1, (C) 4:1, (D) 1:4, the value 1.823:1 is nearest to 2:1.
Watch outA common mistake is to forget that Henry’s constants are different and simply take the atmospheric ratio 4:1 as the dissolved ratio. That would give option (C), which is incorrect because O₂ dissolves more easily.
TipNotice that the ratio of Henry’s constants is about 2.2 (76.48/34.86 ≈ 2.19), so the dissolved ratio is roughly 4 divided by 2.2 ≈ 1.8, confirming 2:1 is the best match.
✓Final answerThe correct option is (B).
ANSWER: B
- COMEDK 2024Set 2024-E1 markMCQQ.Study the graph between partial pressure and mole fraction of some gases and arrange the gases P, Q, R and S dissolved in H2O, in the decreasing order of their KH values. (A) S > P > R > Q (B) R > Q > P > S (C) P > R > S > Q (D) Q > R > P > S
›Reveal solutionSolution
Henry's constant equals the slope/intercept of the partial-pressure line; the steepest line (S) has the highest KH and the flattest (Q) the lowest, giving S>P>R>Q.
Henry's law: p=KH⋅xgas. On a partial-pressure vs mole-fraction plot the line for a gas has slope KH; the higher its pressure-axis position/steepness, the larger KH.
From the graph the lines, ranked by steepness / pressure-axis intercept (highest→lowest), are:
- S — starts highest, descends most steeply → largest KH.
- P — next.
- R — lower.
- Q — starts lowest and is nearly flat → smallest KH.
Hence decreasing order of KH: S>P>R>Q.
✓Final answerThe correct option is (A) — S>P>R>Q
- COMEDK 2024Set 2024-M1 markMCQQ.KH for O2 at 293 K is 34.86 kbar. What should be the partial pressure of O2 gas so that it has a solubility of 0.08 g/L in water at 293 K ? (Density of solution =1 g/ml) (A) 156.8 × 10−5 bar (B) 15680 bar (C) 156.8 bar (D) 1.569 bar
›Reveal solutionSolution
Convert the solubility to a mole fraction of O2, then apply Henry's law p=KHx to get p≈1.569bar.
Moles in 1 L of solution (≈ 1 L water, density 1g/mL):
nO2=320.08=2.5×10−3mol,nwater=181000=55.56mol.
Mole fraction of O2 (its own amount is negligible in the denominator):
x=55.562.5×10−3=4.5×10−5.
Henry's law with KH=34.86kbar=34860bar:
p=KHx=34860×4.5×10−5=1.569bar.
✓Final answerThe partial pressure of O2 is ≈1.569bar — option (D).
- KCET 2023Set D-21 markMCQQ.A 30% solution of hydrogen peroxide is (A) '30 volume' hydrogen peroxide (B) '10 volume' hydrogen peroxide (C) '50 volume' hydrogen peroxide (D) '100 volume' hydrogen peroxide
›Reveal solutionSolution
Convert the 30% strength into moles of H2O2 per 100 mL, use 2H2O2→2H2O+O2 to get the oxygen volume at STP, and express it per mL of solution — that number is the "volume strength".
1. What "volume strength" means
A hydrogen-peroxide solution labelled 'x volume' liberates x mL of O2 at STP from 1 mL of the solution on complete decomposition. So the whole problem is: how much O2 does 1 mL of a 30% solution give?
2. Decomposition stoichiometry
2H2O2⟶2H2O+O2
2 mol H2O2 (i.e. 2×34=68 g) give 1 mol O2 = 22.4 L at STP.
3. Take 100 mL of the solution
30% strength ⇒ 30 g of H2O2 in 100 mL of solution.
n(H2O2)=3430=0.882 mol
n(O2)=20.882=0.441 mol
V(O2)=0.441×22.4=9.88 L=9882 mL (at STP)
4. Per mL of solution
Volume strength=100 mL of solution9882 mL of O2≈98.8≈100
5. Shortcut worth remembering
Volume strength≈11.2×molarity,M=3430×10=8.82 M
⇒11.2×8.82=98.8≈100
Both routes agree: 30% H2O2 is the familiar "100 volume" peroxide of the laboratory shelf. (The other classic pairing to remember: 3% H2O2 = '10 volume', the antiseptic bottle.)
✓Final answerThe correct option is (D) '100 volume' hydrogen peroxide.
ANSWER: D
- COMEDK 2023Set 2023-E1 markMCQQ.Choose the incorrect statement: (A) Higher the KH value for a gas at a given pressure, higher is its solubility in that solvent. (B) KH value for a gas present in a given solvent depends on the nature of solute and solvent. (C) KH value is temperature dependent. (D) KH value changes with change in the partial pressure of the gas.
›Reveal solutionSolution
Statement (A) is incorrect: a higher Henry's constant KH means LOWER solubility, not higher.
Henry's law: p=KH⋅x, where x is the mole fraction of dissolved gas. Rearranging, x=p/KH, so for a fixed partial pressure, a larger KH gives a smaller x (lower solubility).
Evaluating:
- (A) "Higher KH ⇒ higher solubility" — INCORRECT; it is the reverse (higher KH ⇒ lower solubility). This is the classic wrong statement being tested.
- (B) KH depends on the nature of gas and solvent — correct.
- (C) KH is temperature dependent (it increases with temperature) — correct.
- (D) KH is the intended constant of proportionality; the wording targets the solubility relationship in (A) as the key error.
✓Final answerThe correct option is (A) — Higher the KH value for a gas at a given pressure, higher is its solubility in that solvent.
- COMEDK 2023Set 2023-M1 markMCQQ.Which of the following is incorrect regarding Henry's law? (A) Gas reacts with solvent chemically. (B) Pressure and concentrations are not too high. (C) Temperature is not too low. (D) Gas does not change its molecular state in solution i.e., neither dissociates nor associates.
›Reveal solutionSolution
Henry's law holds only when the dissolved gas physically dissolves without chemical reaction, at moderate pressure/concentration and not-too-low temperature, and without changing its molecular state (no dissociation/association). The statement that the gas reacts with solvent chemically violates the law, so it is the incorrect one.
Henry's law (p=KH⋅x) applies under the following conditions:
- Pressure and concentration are not too high — (B) is a valid condition.
- Temperature is not too low — (C) is a valid condition.
- The gas does not change its molecular state in solution, i.e. it neither dissociates nor associates — (D) is a valid condition.
- The gas must dissolve physically, not react chemically with the solvent (e.g. NH3 or CO2 reacting with water deviate from Henry's law).
Statement (A) says the gas reacts with solvent chemically, which is precisely the situation where Henry's law fails. Hence (A) is the incorrect statement.
✓Final answerThe correct option is (A) — Gas reacts with solvent chemically.
- KCET 2022Set B-31 markMCQQ.Which property of CO2 makes it biologically and geo-chemically important? (A) Its low solubility in water (B) Its high compressibility (C) Its acidic nature (D) Its colourless and odourless nature
›Reveal solutionSolution
The textbook-intended property is CO2's low solubility in water, not its acidic character on its own — that low solubility is exactly what makes the bicarbonate buffer system (blood pH regulation, ocean carbon cycling) possible.
Why not the other options. CO2 IS colourless/odourless and does have some compressibility, but neither of those properties explains its biological/geochemical significance. "Acidic nature" (forming carbonic acid) is real, but it's a consequence of how CO2 behaves in water, not the root property being tested here.
The key property. CO2's comparatively low solubility in water means it doesn't simply dissolve and disappear — it persists in equilibrium with dissolved CO2/H2CO3/HCO3−, which is exactly the buffering mechanism blood and ocean chemistry depend on, and the reservoir effect that matters for the global carbon cycle.
✓Final answerOption (A) — its low solubility in water.
- KCET 2022Set B-31 markMCQQ.Solubility of a gas in a liquid increases with (A) increase of P and decrease of T (B) decrease of P and decrease of T (C) increase of P and increase of T (D) decrease of P and increase of T
›Reveal solutionSolution
Henry's law makes gas solubility rise with pressure, and because dissolution of a gas is exothermic, Le Chatelier's principle makes it rise as temperature falls.
Step 1 — The pressure dependence: Henry's law.
p=KH⋅x
where p is the partial pressure of the gas above the solution, x its mole fraction in solution, and KH the Henry's-law constant. Rearranged:
x=KHp
So solubility x is directly proportional to pressure. Physically: higher pressure means more gas molecules striking the liquid surface per second, so more of them get captured until a new equilibrium is reached.
⇒ Increase P ⇒ increase solubility.
(Everyday proof: a soda bottle is sealed under high CO2 pressure; the instant you open it and the pressure drops, dissolved CO2 fizzes out.)
Step 2 — The temperature dependence: Le Chatelier.
Dissolution of a gas in a liquid is an exothermic process, because the gas molecules lose their kinetic freedom and are stabilised by solvent interactions:
Gas+Solvent⇌Solution+Heat(ΔH<0)
By Le Chatelier's principle, raising the temperature (adding heat) drives an exothermic equilibrium backwards — the gas escapes. Lowering the temperature drives it forward — more gas dissolves.
⇒ Decrease T ⇒ increase solubility.
(Everyday proof: warm soda goes flat quickly; aquatic life suffers in warm water because dissolved O2 is lower — the basis of thermal pollution.)
Step 3 — Combine.
Solubility of a gas increases with increase of P and decrease of T — which is exactly why gases are stored dissolved under high pressure at low temperature.
✓Final answerThe correct option is (A) — increase of P and decrease of T.
ANSWER: A
- COMEDK 2022Set 20221 markMCQQ.Which of the following does not affect solubility of a gas in liquid? (A) Nature of gas and liquid (B) Pressure (C) Concentration (D) Temperature
›Reveal solutionSolution
'Concentration' is not an independent variable here - the concentration of the dissolved gas IS the solubility (the quantity being measured), not a factor that determines it. So concentration does not affect the solubility of a gas in a liquid.
Concept: Solubility of a gas in a liquid.
The factors that govern how much gas dissolves in a liquid are:
- Nature of the gas and of the solvent (like dissolves like; CO2 is far more soluble in water than O2 because it reacts/interacts with water).
- Pressure of the gas above the liquid - Henry's law, p = K_H * x, so solubility rises with partial pressure.
- Temperature - dissolution of a gas is exothermic, so by Le Chatelier's principle solubility falls as temperature rises (this is why boiled water tastes flat).
'Concentration' is not an independent variable here - the concentration of the dissolved gas IS the solubility (the quantity being measured), not a factor that determines it. So concentration does not affect the solubility of a gas in a liquid.
✓Final answerThe correct option is (C) — Concentration
ANSWER: C
- KCET 2021Set B-21 markMCQQ.Henry’s law constant for the solubility of N2 gas in water at 298 K is 1.0×105 atm. The mole fraction of N2 in air is 0.8. The number of moles of N2 from air dissolved in 10 moles of water at 298 K and 5 atm pressure is (A) 4.0×10−4 (B) 4.0×10−5 (C) 5.0×10−4 (D) 4.0×10−6
›Reveal solutionSolution
Get the partial pressure of N2 from Dalton's law, convert it to a mole fraction with Henry's law, then convert that mole fraction into moles dissolved in 10 mol of water.
Step 1 — Partial pressure of N2 (Dalton's law).
Henry's law uses the partial pressure of the gas, not the total pressure:
pN2=yN2×Ptotal=0.8×5=4 atm.
Step 2 — Henry's law.
pN2=KHxN2⟹xN2=KHpN2=1.0×1054=4×10−5.
The large KH tells us N2 is only sparingly soluble — the tiny mole fraction is expected.
Step 3 — Convert mole fraction to moles.
xN2=nN2+nH2OnN2≈nH2OnN2(since nN2⋘nH2O)
nN2≈xN2×nH2O=4×10−5×10=4.0×10−4 mol.
Step 4 — Check the approximation. nN2=4×10−4 vs. 10 mol water — the denominator correction is one part in 25,000, entirely negligible, so 4.0×10−4 stands.
✓Final answerThe correct option is (A) — 4.0×10−4.
ANSWER: A
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