Conductometric Titration Virtual Lab G vs V
Electrochemical Analysis & Ionic Mobilities for JEE & NEET
1. Titration Parameter
2. Flow Controllers
3. Live Microscopic Ion Watcher
Adding Na⁺ + OH⁻ to H⁺ + Cl⁻
4. Live Lab Log & Mechanism
5. Conductance Plotter
Equivalence Calculator
Verify stoichiometry using $N_1V_1 = N_2V_2$. Leave one parameter blank to solve.
JEE/NEET Quick Quiz
๐ Qualitative Chemistry: Ionic Mobilities & Conductance Curves Explained
Theoretical Foundation
Conductometric titrations are governed by Ohm’s Law. The measured electrical conductance ($G$) of an electrolyte solution depends directly on the concentration and individual mobilities of dissolved ions:
Where $C_i$ represents concentrations and $\lambda_i$ indicates equivalent ionic conductivities.
Relative Ionic Mobilities (S cm² mol⁻¹)
At $25^\circ\text{C}$, the molar conductivities at infinite dilution exhibit highly unequal values due to different charge densities and proton-hopping mechanisms:
- $\text{H}^+$ (349.6) - Extremely fast (Grothuss hopping).
- $\text{OH}^-$ (198.3) - Highly conducting.
- $\text{NH}_4^+$ (73.5) / $\text{Cl}^-$ (76.3) - Moderate.
- $\text{Na}^+$ (50.1) / $\text{CH}_3\text{COO}^-$ (40.9) - Slower.
Slope Mechanism Analysis
- HCl vs NaOH: Initial drop is highly steep because ultra-fast $\text{H}^+$ ions are systematically neutralized and replaced by slower $\text{Na}^+$ ions. After equivalence, excess $\text{OH}^-$ addition causes a sharp rise.
- CH₃COOH vs NaOH: Initial small drop due to common ion suppression. Then conductance rises as highly ionized sodium acetate salt replaces poorly dissociated acetic acid.
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