Q.At equilibrium the rate of dissolution of a solid solute in a volatile liquid solvent is __________.
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.
Concept: Dynamic equilibrium in a saturated solution.
When a solid dissolves in a solvent, two opposing processes occur simultaneously: dissolution (solid → solution) and crystallization (solution → solid). Initially, the dissolution rate exceeds crystallization because the solution is unsaturated.
As more solute dissolves, the solution concentration increases, which accelerates the crystallization rate. Equilibrium is reached when the solution becomes saturated — at this point, the rate at which solute particles leave the solid phase exactly matches the rate at which they return to it.
This is a dynamic equilibrium: both processes continue, but their rates are equal, so the net concentration remains constant. Neither process stops (rate ≠ zero), and neither dominates the other.
At equilibrium, the rate of dissolution equals the rate of crystallization. The answer is (iii).
At equilibrium, opposing processes occur at equal rates; dissolution and crystallisation balance perfectly, giving (iii).
Understanding Dynamic Equilibrium
Equilibrium in chemistry is not a static, frozen state - it's a dynamic balance. When a solid dissolves in a liquid, two processes compete:
- Dissolution: solid particles leave the crystal lattice and enter the solution
- Crystallisation: dissolved particles return to the solid phase
Initially, only dissolution occurs. As concentration rises, crystallisation begins too.
Reaching Equilibrium
- Early stage: Rate of dissolution > rate of crystallisation - net dissolution continues.
- Equilibrium: Rate of dissolution = rate of crystallisation - the solution becomes saturated; concentration stays constant, but particles continuously exchange between phases.
- The key insight: equilibrium does not mean nothing is happening - forward and reverse processes proceed at identical rates, so no net change occurs.
A common mistake is thinking equilibrium means "everything stops." In reality both dissolution and crystallisation continue - they just cancel out macroscopically.
Ratedissolution=Ratecrystallisation
The correct option is (iii): equal to the rate of crystallisation.
Concept: Dynamic Equilibrium in Solutions
When a solid solute dissolves in a volatile liquid solvent, two opposing processes occur simultaneously:
- Dissolution — solute particles leave the solid surface and enter the solvent.
- Crystallisation — dissolved solute particles return to the solid surface and re-form the solid.
At equilibrium, these processes do not stop — they continue at the same rate. This is called dynamic equilibrium.
Method: Dynamic Equilibrium Principle
Steps:
-
Identify the two opposing processes
- Dissolution (solid → solution)
- Crystallisation (solution → solid)
-
Recall the definition of dynamic equilibrium
At equilibrium, the rates of the forward and reverse processes become equal, not zero.
-
Apply to the given situation
- Rate of dissolution = Rate of crystallisation
- The system appears static (no net change in amount of solid or concentration), but both processes are ongoing.
-
Eliminate incorrect options
- (i) and (ii) imply unequal rates — not possible at equilibrium.
- (iv) implies both rates are zero — incorrect, as equilibrium is dynamic.
Final Answer:
(iii) equal to the rate of crystallisation
Common Mistakes & How to Avoid Them
Mistake 1: Confusing “equilibrium” with “no change” → Choosing (iv) zero
Why it happens:
Students often think “at equilibrium, nothing happens.” They see the word equilibrium and assume the rate must be zero.
How to avoid:
Remember: Equilibrium is dynamic, not static.
- At equilibrium, the net change is zero, but the forward and reverse processes continue at equal rates.
- For dissolution: solid particles leave the surface (dissolve) and dissolved particles return to the surface (crystallise) at the same speed.
- So the rate is not zero — it is equal to the rate of crystallisation.
Correct choice: (iii) equal to the rate of crystallisation.
Mistake 2: Thinking dissolution stops when solution is saturated
Why it happens:
Students believe that once a solution is saturated, no more solid can dissolve, so the dissolution rate becomes zero.
How to avoid:
- Saturation means the concentration of dissolved solute is at its maximum at that temperature.
- But molecules are still moving: some solid leaves the surface, some dissolved solute returns.
- At saturation, the two rates are equal — dissolution continues, but crystallisation matches it exactly.
Key takeaway:
“Saturated” ≠ “dissolution stopped.” It means dissolution rate = crystallisation rate.
Mistake 3: Misreading “volatile liquid solvent” and overcomplicating
Why it happens:
The phrase “volatile liquid solvent” distracts students. They think volatility changes the equilibrium behaviour.
How to avoid:
- Volatility of the solvent affects vapour pressure and boiling, but not the dissolution–crystallisation equilibrium of a solid solute.
- The principle of dynamic equilibrium for dissolution is the same regardless of solvent volatility.
- Ignore the “volatile” label — it’s a red herring. Focus on the solid–solution interface.
Mistake 4: Picking (i) or (ii) — thinking one rate is always higher
Why it happens:
Students confuse the direction of net change before equilibrium with the state at equilibrium.
How to avoid:
- Before equilibrium (unsaturated solution): dissolution rate > crystallisation rate → net dissolving.
- At equilibrium: rates are equal.
- After equilibrium (supersaturated): crystallisation rate > dissolution rate → net crystallisation.
The question asks at equilibrium — so only (iii) is correct.
Quick Summary Table
| Mistake | Wrong choice | Why it’s wrong | Correct reasoning |
|---|---|---|---|
| Equilibrium = no activity | (iv) zero | Equilibrium is dynamic | Rates are equal, not zero |
| Saturation = dissolution stops | (iv) zero | Saturation is dynamic | Dissolution continues at same rate as crystallisation |
| Distracted by “volatile” | Any | Volatility irrelevant here | Focus on solid–solution equilibrium |
| Confusing before/at equilibrium | (i) or (ii) | Those describe net change before equilibrium | At equilibrium, rates are equal |
Final answer: (iii) equal to the rate of crystallisation.
Showing the 12 most recent of 33 on this concept.
- TG EAPCET 2026Set eng-2026-05-09-AN1 markMCQQ.The difference in bond angles between SO2 and H2O is (A) 12.5∘ (B) 17.5∘ (C) 15.0∘ (D) 13.0∘
›Reveal solutionSolution
The bond angle in SO₂ is about 119∘ (due to VSEPR: trigonal planar with one lone pair), and in H₂O it is about 104.5∘ (tetrahedral with two lone pairs). The difference is 119∘−104.5∘=14.5∘, which rounds to 15.0∘, so the correct option is (C).
The key to this question is understanding how molecular geometry and lone pairs affect bond angles. Both SO₂ and H₂O are bent molecules, but their central atoms have different numbers of lone pairs, which changes the repulsion pattern and the angle.
In VSEPR theory, lone pairs repel more strongly than bonding pairs. The more lone pairs you have, the more the bonding pairs are squeezed together, reducing the bond angle. Let’s apply this to each molecule.
-
SO₂ (sulfur dioxide)
Sulfur has 6 valence electrons. In SO₂, it forms two double bonds with oxygen atoms (using 4 electrons) and retains one lone pair. That gives a steric number of 3 (two bonds + one lone pair). The electron geometry is trigonal planar, with ideal angles of 120∘. But the lone pair repels the bonding pairs more than they repel each other, so the O–S–O bond angle is slightly less than 120∘ — experimentally, it is 119∘.
-
H₂O (water)
Oxygen has 6 valence electrons. It forms two single bonds with hydrogen atoms (using 2 electrons) and has two lone pairs. The steric number is 4 (two bonds + two lone pairs), so the electron geometry is tetrahedral, with ideal angles of 109.5∘. The two lone pairs exert stronger repulsion, compressing the H–O–H bond angle to 104.5∘.
-
Finding the difference
Subtract the smaller angle from the larger:
119∘−104.5∘=14.5∘
Among the given options, 14.5∘ is closest to 15.0∘.
Watch outA common mistake is to take the ideal angles (120∘ and 109.5∘) and subtract them, getting 10.5∘, which is not an option. You must use the actual experimental bond angles, which account for lone-pair repulsion.
TipFor quick recall: SO₂ bond angle ≈ 119∘, H₂O bond angle ≈ 104.5∘. The difference is always around 14−15∘ in such problems.
✓Final answerThe correct option is (C), with a difference of 15.0∘.
-
- TG EAPCET 2026Set eng-2026-05-09-FN1 markMCQQ.2.9 g of a gas (molar mass 40gmol−1) at T(K) occupied the same volume as 0.184 g of dihydrogen at 17∘C at the same pressure. The value of T(K) is (A) 568 (B) 368 (C) 468 (D) 268
›Reveal solutionSolution
Using the ideal gas law under identical pressure and volume, the number of moles of each gas must be equal; solving gives T=368K, which corresponds to option (B).
Concept & Intuition
The problem gives two gases at the same pressure and occupying the same volume. The ideal gas law, PV=nRT, tells us that when P and V are fixed, the product nT is constant. But here the gases are different, so we must compare their moles. Since P and V are identical for both, the number of moles of each gas must be the same. That’s the key: equal P and V implies equal n (because R is universal). So we can set the moles of the unknown gas equal to the moles of dihydrogen (H2) and solve for the unknown temperature.
Step-by-step solution
- Find moles of dihydrogen (H2) Mass of H2=0.184g. Molar mass of H2=2.0gmol−1.
nH2=2.00.184=0.092mol
- Find moles of the unknown gas Mass = 2.9g, molar mass = 40gmol−1.
ngas=402.9=0.0725mol
- Apply the condition of equal pressure and volume For the unknown gas at temperature T: PV=ngasRT For H2 at 17∘C (which is 17+273=290K): PV=nH2R(290) Since P and V are the same, the right-hand sides are equal:
ngasRT=nH2R(290)
Cancel R:
ngasT=nH2×290
- Solve for T
T=ngasnH2×290=0.07250.092×290
Calculate stepwise:
0.092×290=26.68
26.68÷0.0725=368 (since 0.0725×368=26.68 exactly).
So T=368K.
Watch outA common mistake is to forget converting Celsius to Kelvin. The temperature of hydrogen is given as 17∘C, which is 290K, not 17K. Always use Kelvin in gas law calculations.
TipNotice that the molar masses are different, but the equality of moles is what matters here. If you mistakenly set masses equal, you’d get a wrong answer. Always go through moles when P and V are fixed.
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2026Set eng-2026-05-10-AN1 markMCQQ.Which of the following is not correctly matched with the example mentioned in brackets? (A) Solid dispersed in gas (Smoke) (B) Solid dispersed in liquid (Paint) (C) Liquid dispersed in solid (Butter) (D) Gas dispersed in liquid (Cloud)
›Reveal solutionSolution
The question asks which colloid type is mismatched with its example. The key is to classify each example by the physical state of the dispersed phase and the dispersion medium. The mismatched pair is Cloud — it is a liquid-in-gas colloid, not gas-in-liquid. The correct option is (D).
The concept here is colloidal classification by phase. A colloid is a mixture where one substance (the dispersed phase) is finely distributed throughout another (the dispersion medium). The trick is to identify the state of matter of each part — solid, liquid, or gas — and then match it to the given example.
Let’s check each option step by step:
-
Option (A): Solid dispersed in gas (Smoke)
- Smoke consists of tiny solid particles (e.g., carbon or ash) suspended in air (a gas).
- Dispersed phase: solid; dispersion medium: gas.
- This matches perfectly. ✓
-
Option (B): Solid dispersed in liquid (Paint)
- Paint is a mixture of solid pigment particles dispersed in a liquid binder (like oil or water).
- Dispersed phase: solid; dispersion medium: liquid.
- Correct match. ✓
-
Option (C): Liquid dispersed in solid (Butter)
- Butter is a water-in-oil emulsion where tiny droplets of water (liquid) are trapped in a solid fat matrix.
- Dispersed phase: liquid; dispersion medium: solid.
- This is correct. ✓
-
Option (D): Gas dispersed in liquid (Cloud)
- A cloud is made of tiny water droplets (liquid) suspended in air (gas).
- So the dispersed phase is liquid, and the dispersion medium is gas.
- The given description says “gas dispersed in liquid” — that would be something like foam (e.g., whipped cream or shaving cream).
- Therefore, this is incorrectly matched. ✗
Watch outA common mistake is to think of clouds as “gas in liquid” because they look like floating gas. But clouds are actually liquid droplets (or ice crystals) in air — a liquid-in-gas colloid (aerosol). The classic gas-in-liquid colloid is a foam, like soap bubbles.
TipTo avoid confusion, remember: the first word in the description is the dispersed phase, the second is the medium. For “Gas dispersed in liquid,” the gas is inside the liquid — think of fizzy soda or foam.
✓Final answerThe correct option is (D).
ANSWER: D
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- TG EAPCET 2026Set eng-2026-05-10-FN1 markMCQQ.The following graph is obtained by taking partial pressure of HCl(g) on y-axis and mole fraction of HCl(g) in cyclohexane on x-axis. The slope (m) of the graph is [FIGURE] (A) Henry constant (KH) of cyclohexane (B) KH of HCl(g) (C) Square root of KH of HCl(g) (D) KH(HCl)1
›Reveal solutionSolution
The graph plots partial pressure of HCl (y-axis) vs. mole fraction of HCl in cyclohexane (x-axis). According to Henry’s law, the slope equals Henry’s constant for HCl in cyclohexane, so the correct option is (B).
The key here is Henry’s law, which describes the solubility of a gas in a liquid. For a dilute solution, the partial pressure of the gas above the liquid is directly proportional to its mole fraction in the liquid:
PHCl=KH⋅xHCl
where KH is the Henry’s law constant. The constant is specific to the gas–solvent pair. In this graph, the y-axis is PHCl and the x-axis is xHCl, so the slope m is exactly KH.
Now, which substance does this KH belong to? The graph is for HCl gas dissolved in cyclohexane. The constant describes how much HCl partitions between the gas phase and the liquid phase. That is the Henry’s constant of HCl in cyclohexane — not of cyclohexane itself.
Let’s walk through the reasoning step by step.
- Identify the axes and the law The y-axis is partial pressure of HCl gas, PHCl. The x-axis is mole fraction of HCl in the liquid, xHCl. Henry’s law states:
PHCl=KH⋅xHCl
This is a linear relation through the origin (for dilute solutions). The slope is KH.
-
Interpret the slope
The slope m=ΔxHClΔPHCl. Since the graph is a straight line through the origin, the slope is constant and equals the proportionality constant in Henry’s law.
-
Assign the constant to the correct species
Henry’s constant is always defined for the solute (the gas being dissolved), not the solvent. Here, HCl is the solute; cyclohexane is the solvent. So KH is the Henry’s constant of HCl in cyclohexane.
-
Match with the options
- (A) says “Henry constant of cyclohexane” — incorrect, because cyclohexane is the solvent.
- (B) says “KH of HCl (g)” — correct.
- (C) says “square root of KH of HCl” — no square root appears in Henry’s law.
- (D) says “1/KH(HCl)” — that would be the reciprocal, not the slope.
Watch outA common mistake is to think the slope is the reciprocal of Henry’s constant, or to confuse which substance the constant refers to. Remember: the graph’s slope is directly KH for the gas whose pressure is plotted.
TipIf the axes were swapped (mole fraction on y, pressure on x), the slope would be 1/KH. Always check which variable is on which axis.
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2026Set eng-2026-05-11-FN1 markMCQQ.Identify the correct statements from the following I. Hydrogen bonding is present in liquid water and solid water (ice) II. Hydrogenation of vegetable oils give a fat called vanaspati III. Water present in BaCl2.2H2O belongs to the type "interstitial water" (A) I, III only (B) I, II, III (C) I, II only (D) II, III only
›Reveal solutionSolution
All three statements are correct: hydrogen bonding is present in both liquid and solid water, hydrogenation of vegetable oils produces vanaspati, and the water in BaCl2.2H2O is interstitial. The correct option is (B).
Let's analyze each statement to determine its correctness.
Concept and Intuition
This question tests your understanding of fundamental concepts in chemistry:
- Hydrogen Bonding: A strong intermolecular force crucial for the properties of water.
- Hydrogenation: A chemical reaction used to modify the properties of fats and oils.
- Water of Crystallization: The different ways water molecules can be incorporated into crystal structures.
We will evaluate each statement based on these principles.
Step-by-Step Evaluation
1. Statement I: Hydrogen bonding is present in liquid water and solid water (ice)
- Reasoning: Hydrogen bonding is a special type of dipole-dipole interaction that occurs when a hydrogen atom covalently bonded to a highly electronegative atom (like oxygen, nitrogen, or fluorine) is attracted to another highly electronegative atom in a different molecule.
- In water (H2O), oxygen is highly electronegative and forms covalent bonds with two hydrogen atoms. This creates a strong partial positive charge on the hydrogen atoms and a strong partial negative charge on the oxygen atom.
- Liquid Water: In liquid water, molecules are constantly moving, but they form a dynamic network of hydrogen bonds. Each water molecule can form up to four hydrogen bonds with neighboring water molecules (two through its hydrogen atoms and two through the lone pairs on its oxygen atom). These bonds are continuously breaking and reforming.
- Solid Water (Ice): In ice, water molecules arrange themselves into a highly ordered, open, hexagonal crystalline structure. Each water molecule is tetrahedrally hydrogen-bonded to four other water molecules. This rigid, extensive network of hydrogen bonds is responsible for ice being less dense than liquid water.
- Conclusion: Statement I is correct.
2. Statement II: Hydrogenation of vegetable oils give a fat called vanaspati
- Reasoning: Vegetable oils are typically unsaturated fats, meaning their fatty acid chains contain one or more carbon-carbon double bonds (C=C). These double bonds give them a bent structure, preventing close packing and making them liquid at room temperature.
- Hydrogenation is a chemical process where hydrogen gas (H2) is added across these carbon-carbon double bonds in the presence of a catalyst (commonly nickel, palladium, or platinum). This converts the unsaturated fatty acids into saturated fatty acids (containing only C−C single bonds).
- Product: The resulting saturated fats have straighter chains, allowing them to pack more closely. This changes their physical state from liquid oil to a solid or semi-solid fat at room temperature. This product is commonly known as vanaspati ghee (or hydrogenated vegetable oil), which is used as a cooking medium and in the production of margarine.
- Conclusion: Statement II is correct.
3. Statement III: Water present in BaCl2.2H2O belongs to the type "interstitial water"
- Reasoning: Water of crystallization refers to water molecules that are an integral part of the crystal structure of a compound. There are different types based on how the water molecules are incorporated:
- Coordinated water: Water molecules directly bonded to the metal ion in the coordination sphere (e.g., in [Cu(H2O)4]SO4⋅H2O, four water molecules are coordinated to copper).
- Lattice or Interstitial water: Water molecules that occupy specific positions within the crystal lattice, filling voids or interstitial spaces. They are not directly bonded to the metal ion but are held by hydrogen bonds to other water molecules, anions, or cations in the lattice.
- Hydrogen-bonded water: Water molecules held by hydrogen bonds to other water molecules or to anions/cations, but not necessarily occupying specific interstitial sites or being coordinated to a metal ion. This category often overlaps with interstitial water.
- In BaCl2.2H2O (barium chloride dihydrate), the water molecules are not directly coordinated to the Ba2+ ion. Instead, they are located in the spaces (interstices) within the crystal lattice and are held there by hydrogen bonds to the chloride ions and other water molecules. This arrangement is characteristic of interstitial water.
- Conclusion: Statement III is correct.
Since all three statements (I, II, and III) are correct, the option that includes all of them is the correct answer.
✓Final answerAll three statements are correct, so the correct option is (B).
- TG EAPCET 2026Set eng-2026-05-11-AN1 markMCQQ.At T(K), the pressure of two ideal gases A and B is in 2:5 ratio (pA:pB=2:5). At this temperature, their density is same. Molar mass ratio (MA:MB) is (A) 5:2 (B) 1:2 (C) 5:1 (D) 25:4
›Reveal solutionSolution
Using the ideal gas law in density form pM=ρRT, with equal densities and given pressure ratio, the molar mass ratio is the inverse of the pressure ratio, giving MA:MB=5:2.
The key concept is the density form of the ideal gas law. For an ideal gas, pV=nRT. Since n=Mm (mass over molar mass), we can write pV=MmRT. Rearranging gives pM=VmRT=ρRT, where ρ is density. This form directly links pressure, molar mass, and density at a fixed temperature — perfect for comparing two gases when density is the same.
-
Write the relation for each gas.
For gas A: pAMA=ρART
For gas B: pBMB=ρBRT
Since the temperature T and the gas constant R are identical, and the problem states ρA=ρB, we can set the right-hand sides equal.
-
Equate the two expressions.
Because ρART=ρBRT, we have:
pAMA=pBMB
- Use the given pressure ratio. The ratio pA:pB=2:5 means pBpA=52. From pAMA=pBMB, we get:
MBMA=pApB=25
So MA:MB=5:2.
Watch outA common mistake is to think that higher pressure means higher molar mass when density is equal. Actually, from pM=ρRT, pressure and molar mass are inversely proportional at constant density and temperature. So the gas with lower pressure has the higher molar mass.
TipYou can also think of it as: if two gases have the same density at the same temperature, the one with lower pressure must have heavier molecules to pack the same mass into the same volume.
✓Final answerThe correct option is (A).
ANSWER: A
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- TG EAPCET 2026Set eng-2026-05-11-AN1 markMCQQ.If two liquids A and B have PA∘:PB∘=1:2 and have mole fraction in solution as 1:2, then mole fraction of B in vapour phase is (A) 0.2 (B) 0.8 (C) 0.4 (D) 0.6
›Reveal solutionSolution
Using Raoult’s law and Dalton’s law, the mole fraction of B in the vapour phase is found to be 0.8, so the correct option is (B).
Concept & Intuition
This problem is about the relationship between the composition of a liquid mixture and the composition of the vapour above it. The key idea: in an ideal solution, the partial pressure of each component in the vapour is given by Raoult’s law (Pi=xiPi∘), and the total pressure is the sum of these partial pressures. The mole fraction of a component in the vapour phase is then the ratio of its partial pressure to the total pressure. So we just need to compute these pressures from the given ratios.
Step-by-step solution
-
Assign variables from the given ratios
The ratio of pure vapour pressures is PA∘:PB∘=1:2. Let PA∘=p and PB∘=2p for some p.
The mole fraction ratio in the liquid is xA:xB=1:2. Since xA+xB=1, we have xA=31 and xB=32.
-
Apply Raoult’s law to find partial pressures
Raoult’s law: PA=xAPA∘ and PB=xBPB∘.
So
PA=31⋅p=3p,PB=32⋅2p=34p.
-
Find total vapour pressure
Total pressure Ptotal=PA+PB=3p+34p=35p.
-
Compute mole fraction of B in vapour
By Dalton’s law, the mole fraction of B in the vapour phase is
yB=PtotalPB=5p/34p/3=54=0.8.
TipNotice that the p cancels out — you never need the actual vapour pressures, only their ratio. This is a common shortcut in such problems.
Watch outA common mistake is to confuse the liquid mole fraction xB with the vapour mole fraction yB. Here xB=2/3≈0.667, but yB=0.8 — the vapour is richer in the more volatile component (B has higher P∘).
✓Final answerThe correct option is (B).
ANSWER: B
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- TG EAPCET 2025Set eng-2025-05-02-FN1 markMCQQ.A substance has a density of 2 g cm−3. It crystallizes in the fcc crystal with an edge length of 600 pm. The molar mass of the substance (in g mol−1) is (NA=6×1023 mol−1) (A) 54.8 (B) 64.8 (C) 74.8 (D) 84.7
›Reveal solutionSolution
Using the density formula for a crystal, we relate density, number of atoms per unit cell, molar mass, and edge length. For fcc, Z=4; solving gives molar mass ≈ 64.8 g mol⁻¹, matching option (B).
The key idea is that the density of a crystalline solid is given by
ρ=NA⋅a3Z⋅M
where Z is the number of atoms per unit cell, M is the molar mass, NA is Avogadro’s number, and a is the edge length. For an fcc lattice, Z=4. We are given ρ=2 gcm−3, a=600 pm, and NA=6×1023 mol−1. We solve for M.
- Convert edge length to cm The edge length is 600 pm. Since 1 pm=10−12 m and 1 m=100 cm, we have
a=600×10−12 m=600×10−10 cm=6×10−8 cm.
- Write the density formula
ρ=NA⋅a3Z⋅M
Rearranging for M:
M=Zρ⋅NA⋅a3.
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Substitute the known values
- ρ=2 gcm−3
- NA=6×1023 mol−1
- a=6×10−8 cm → a3=(6×10−8)3=216×10−24=2.16×10−22 cm3
- Z=4 (fcc)
So
M=42×(6×1023)×(2.16×10−22).
- Simplify step by step First, multiply the numerator:
2×6×1023=12×1023
Then multiply by 2.16×10−22:
12×1023×2.16×10−22=12×2.16×101=25.92×10=259.2
Now divide by 4:
M=4259.2=64.8 gmol−1.
TipA common mistake is forgetting to convert pm to cm. Since density is in g cm⁻³, the edge length must be in cm. Also, note that 1 pm=10−10 cm, so 600 pm=6×10−8 cm.
Watch outSome students use Z=1 (simple cubic) or Z=2 (bcc) by accident. For fcc, always remember Z=4.
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2025Set eng-2025-05-03-AN1 markMCQQ.Diborane on hydrolysis gives a compound X. The correct statements about X are I. It is a tribasic acid II. It is a weak monobasic acid III. It has a layer structure IV. It is highly soluble in water (A) I & III (B) II & III (C) II & IV (D) I & IV
›Reveal solutionSolution
Diborane hydrolysis yields boric acid (H₃BO₃), which is a weak monobasic acid (not tribasic) and has a layered crystal structure; thus the correct statements are II and III, corresponding to option (B).
Concept & Intuition
Diborane (B₂H₆) reacts violently with water to give boric acid (H₃BO₃) and hydrogen gas. The key is understanding the actual acidic behavior of boric acid: despite having three hydroxyl groups, it does not donate three protons. Instead, it acts as a Lewis acid, accepting an OH⁻ from water to form [B(OH)₄]⁻, releasing only one H⁺. That makes it a weak monobasic acid, not a tribasic one. Also, boric acid crystallizes in a layered structure held together by hydrogen bonds, which explains its slippery feel and certain physical properties.
- Hydrolysis reaction Diborane reacts with water:
B2H6+6H2O→2H3BO3+6H2
So compound X is boric acid, H3BO3.
- Acidic nature – why it’s monobasic, not tribasic Boric acid does not ionize by losing H⁺ from its O–H bonds. Instead, it accepts a hydroxide ion from water:
B(OH)3+H2O⇌[B(OH)4]−+H+
Only one H⁺ is produced per molecule. Hence it is a weak monobasic acid (statement II is true, statement I is false).
Watch outA common mistake is to count the three OH groups and assume three acidic protons. But boron’s electron deficiency makes it a Lewis acid, not a Brønsted acid.
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Structure – layered crystal
In the solid state, boric acid molecules form hydrogen-bonded sheets (layers) with a hexagonal arrangement. These layers stack on top of each other with weak van der Waals forces. This layer structure gives boric acid its characteristic flaky, slippery feel (statement III is true).
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Solubility in water
Boric acid is moderately soluble in water (about 5.7 g/100 mL at 25°C). It is not “highly soluble” like, say, sugar or NaCl. Statement IV (“highly soluble”) is therefore false.
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Matching the options
- True statements: II (weak monobasic acid) and III (layer structure).
- This corresponds to option (B).
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2025Set eng-2025-05-03-AN1 markMCQQ.Two liquids ‘A’ and ‘B’ form an ideal solution. At 300 K, the vapour pressure of a solution containing 1 mole of ‘A’ and 3 moles of ‘B’ is 550 mm Hg. At the same temperature, if one more mole of ‘B’ is added to the solution, the vapour pressure of solution increases to 560 mm Hg. Then the ratio of vapour pressures of A and B in their pure state is (A) 1 : 3 (B) 3 : 1 (C) 2 : 3 (D) 3 : 2
›Reveal solutionSolution
Solving the two Raoult's-law equations gives PA0=400 and PB0=600 mm Hg, so PA0:PB0=2:3 — option (C).
Concept
For an ideal solution, the total vapour pressure is the mole-fraction-weighted sum of the pure vapour pressures:
P=xAPA0+xBPB0
Two different compositions give two equations in the two unknowns.
Solution
First solution — 1 mol A, 3 mol B, so xA=41, xB=43:
41PA0+43PB0=550⇒PA0+3PB0=2200(1)
Second solution — add 1 mol B: 1 mol A, 4 mol B, so xA=51, xB=54:
51PA0+54PB0=560⇒PA0+4PB0=2800(2)
Subtract (1) from (2):
PB0=600 mm Hg
Back-substitute into (1):
PA0=2200−3(600)=400 mm Hg
Ratio:
PA0:PB0=400:600=2:3
✓Final answer(C) 2 : 3.
- TG EAPCET 2025Set eng-2025-05-03-AN1 markMCQQ.Noble gas ‘X’ is used as a diluent for oxygen in modern diving apparatus and noble gas ‘Y’ is used mainly to provide an inert atmosphere in high temperature metallurgical processes. ‘Y’ and ‘X’ are respectively? (A) He, Ar (B) Ar, He (C) He, Kr (D) Ar, Kr
›Reveal solutionSolution
The key is matching each noble gas to its specific industrial use: helium (He) is the diluent for oxygen in diving, and argon (Ar) provides the inert atmosphere in high‑temperature metallurgy. Thus the pair is Ar, He — option (B).
Concept & Intuition
Noble gases are prized for their chemical inertness, but each has unique physical properties that suit particular applications.
- Helium (He) is extremely light (low density) and has very low solubility in blood. This makes it ideal as a diluent for oxygen in deep‑sea diving, replacing nitrogen to avoid decompression sickness (“the bends”) and reducing breathing resistance.
- Argon (Ar) is denser than air, cheap, and readily available. It is the most common inert gas used in welding and high‑temperature metallurgy (e.g., arc welding of aluminium, titanium processing) because it forms a protective blanket that prevents oxidation without reacting with molten metals.
Now let’s confirm step by step.
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Identify noble gas ‘X’ (diluent for oxygen in diving)
- In standard compressed air, nitrogen dissolves under pressure and can cause narcosis and decompression sickness.
- Helium is used to replace nitrogen because it is much less soluble in blood and diffuses quickly, reducing these risks.
- Neon and krypton are too expensive or have undesirable properties; argon is denser than air and would increase breathing resistance.
- Therefore, X = He.
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Identify noble gas ‘Y’ (inert atmosphere in high‑temperature metallurgy)
- Argon is the most widely used shielding gas in arc welding, casting, and heat treatment of reactive metals (titanium, zirconium).
- Helium is also used in welding but is less common for metallurgy because it is lighter and escapes more easily; argon’s higher density provides a better blanket.
- Krypton is too rare and costly for bulk industrial use.
- Therefore, Y = Ar.
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Match the order in the question
- The question asks: “Y and X are respectively?”
- So Y = Ar, X = He → the pair is Ar, He.
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Check the options
- (A) He, Ar → wrong order.
- (B) Ar, He → correct.
- (C) He, Kr → both wrong.
- (D) Ar, Kr → Y correct, X wrong.
Watch outA common mistake is to reverse the order: the question explicitly says “Y and X are respectively”, so the first answer is Y, the second is X. Option (A) gives He, Ar — that would be X, Y, not Y, X.
TipRemember: Helium for diving (light, low solubility), Argon for welding (dense, cheap, inert). This pairing is a classic fact in chemistry of noble gases.
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2025Set eng-2025-05-03-FN1 markMCQQ.Which of the following is a lung irritant that can lead to an acute respiratory disease in children? (A) CO (B) SO2 (C) CO2 (D) NO2
›Reveal solutionSolution
NO2 is the textbook lung irritant that can cause acute respiratory disease in children — option (D).
Concept. Oxides of nitrogen, especially NO2, are key air pollutants formed in high-temperature combustion and in photochemical smog. NO2 is a reddish-brown, highly reactive gas that attacks respiratory tissue.
Reasoning through the options.
- CO (A): toxic because it binds haemoglobin to form carboxyhaemoglobin, impairing oxygen transport — a blood-level poison, not primarily a lung irritant.
- SO2 (B): irritates eyes and the respiratory tract and aggravates asthma, but the specific textbook statement about acute respiratory disease in children is attached to NO2.
- CO2 (C): not a lung irritant at ambient levels; its concern is the greenhouse effect.
- NO2 (D): per the standard (NCERT) environmental chemistry text, elevated NO2 damages the lungs — it "is a lung irritant that can lead to an acute respiratory disease in children." It also injures plant leaves and retards photosynthesis.
✓Final answerThe lung irritant that can lead to an acute respiratory disease in children is NO2 — the correct option is (D).
ANSWER: D
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