| Salt | Concentration | Molar conductivity |
|---|---|---|
| (M) | (S cm2 mol−1) | |
| NaNO3 | 0.01 | 111 |
| 0.04 | 101 | |
| NaCl | 0.01 | 117 |
| 0.04 | 107 | |
| AgNO3 | 0.01 | 125 |
| 0.04 | 116 |
Click an option to check it.
A pair of platinised-Pt electrodes dips into the electrolyte. The meter drives a small AC signal and reads the conductance G; the conductivity is κ = G × Gcell and the molar conductivity is Λm = 1000κ/c. Change the salt and the concentration, then record points: the solution model is the Debye–Hückel–Onsager law Λm = Λ°m − A√c, with Λ° and A taken from the paper's own data.
Ion count scales with concentration; drift speed is drawn proportional to the solution's molar conductivity (schematic — the paper's data fix the salt totals, not the individual ionic values).
| Salt | c (M) | √c | κ (S cm⁻¹) | Λm |
|---|
For a strong electrolyte Λm falls linearly in √c, so the intercept at √c = 0 is the limiting molar conductivity Λ°m. Solid markers are the two tabulated points per salt; the dashed violet line is AgCl, which is never measured directly — it is constructed in the next panel. Hollow markers are your own recorded points, and their least-squares fit is drawn when you have two or more for one salt.
| Salt | Λm at 0.01 M | Λm at 0.04 M | Slope A | Λ°m (intercept) |
|---|---|---|---|---|
| NaNO3 | 111 | 101 | 100 | 121 |
| NaCl | 117 | 107 | 100 | 127 |
| AgNO3 | 125 | 116 | 90 | 134 |
| AgCl | not measurable (insoluble) | — | 140 | |
At infinite dilution each ion migrates independently, so Λ° of a salt is just the sum of its two ionic contributions. Combine the three measured salts so that Na+ and NO3− cancel and only Ag+ + Cl− survives.
A saturated AgCl solution is so dilute that its molar conductivity is already the limiting value. Rearranging Λm = 1000κ/c gives the solubility directly. Drag κ to see how the answer responds — the paper's value is 1.40×10−6 S cm−1.
NaNO3, NaCl and AgNO3 are strong electrolytes, so over this dilute range the Debye–Hückel–Onsager relation holds:
Two concentrations per salt are given, which is exactly what a straight line needs.
With c₁ = 0.01 M (√c = 0.1) and c₂ = 0.04 M (√c = 0.2), the √c values differ by exactly 0.1, so the extrapolation collapses to a one-line formula:
Na+ and NO3− appear once with a plus sign and once with a minus sign, so they cancel identically — no individual ionic conductivity is ever needed.
The problem states that for the saturated solution Λm = Λ°m = 140 S cm² mol⁻¹ (legitimate: at ~10⁻⁵ M the A√c correction is only about 0.3 S cm² mol⁻¹, i.e. 0.2 %).
Answer: (C) 5. As a by-product, Ksp(AgCl) = X² = 1.0×10⁻¹⁰ at 300 K, which matches the accepted value closely.
| Simulation ID | ADV-2026-P2-CHE-Q01 |
| Exam / Year / Paper | JEE Advanced · 2026 · Paper 2 |
| Subject | Chemistry (Physical) |
| Chapter | Electrochemistry |
| Topic | Conductance of electrolytic solutions |
| Subtopics | Molar & limiting molar conductivity · Kohlrausch's law of independent migration · Solubility of a sparingly soluble salt from conductance |
| Question type | Single correct MCQ (+3 / 0 / −1) |
| Difficulty | Moderate |
| Answer | (C) 5 |