Advanced Ionic Equilibrium
60 lessons, pages 2481–2540.
- Advanced Ionic Equilibrium: The Species View — Simultaneous acid-base, charge-balance and solubility equilibria
- Activities Versus Concentrations — Why equilibrium constants are defined with activities
- Ionic Strength and Effective Activity — Background electrolyte effects and qualitative activity coefficients
- Mass Balance in Aqueous Systems — Conservation equations across dissolved chemical species
- Charge Balance in Aqueous Systems — Electroneutrality and including spectator ions
- Choosing Equations for Ionic Equilibrium — Independent equilibria, balances and unknown species
- Approximations and Their Verification — Small-x tests and error checks in acid-base calculations
- Water Autoionisation in Dilute Solutions — When water's H⁺ and OH⁻ contributions cannot be ignored
- Temperature Dependence of Kw and pH — Neutrality, temperature and avoiding a fixed-pH slogan
- Monoprotic Acid Speciation — Fraction protonated and deprotonated as pH varies
- Polyprotic Acids and Stepwise Ka Values — Sequential proton loss and distinct equilibrium constants
- Diprotic Acid Species and Charge — H₂A, HA⁻ and A²⁻ mass and charge accounting
- First-Dissociation Approximation for Diprotic Acids — Conditions under which Ka1 controls initial pH
- Second Dissociation and Its Contribution — Estimating A²⁻ and testing neglected proton release
- Diprotic Distribution Fractions — Alpha fractions as functions of H⁺, Ka1 and Ka2
- Triprotic Acid Speciation — Four protonation states and three stepwise equilibria
- Phosphoric Acid as a Triprotic Example — H₃PO₄ family and pH-dependent dominant species
- Carbonate System Equilibria — Carbonic-acid family, dissolved CO₂ and bicarbonate
- Amphiprotic Intermediate Ions — Species that can both donate and accept a proton
- pH of Amphiprotic Salt Solutions — Approximate midpoint relation and its assumptions
- Polyprotic Acid Titration Stages — Successive equivalence points and species changes
- Overlapping Polyprotic Equilibria — When similar stepwise Ka values obscure separate stages
- Buffer Action Revisited — Conjugate-pair consumption of added H⁺ and OH⁻
- Henderson–Hasselbalch from Ka — Derivation, activities and ratio interpretation
- Selecting a Buffer Pair — Target pH, pKa and chemically compatible components
- Buffer Ratio Design — Choosing acid-to-base proportions for target pH
- Buffer Capacity — Resistance to added acid or base and total concentration
- Buffer Capacity Near pKa — Why equal conjugate-pair amounts balance acid and base response
- Preparing Buffers by Partial Neutralisation — Stoichiometry before equilibrium for weak acid and strong base
- Preparing Buffers from Weak Base and Strong Acid — Controlled protonation and remaining base accounting
- Response of a Buffer to Strong Acid — Mole ledger before revised pH calculation
- Response of a Buffer to Strong Base — Neutralisation of weak-acid component and capacity limits
- Dilution of Buffers — Nearly constant ratio pH versus declining capacity
- Mixing Two Buffer Solutions — Conjugate-pair mole balances and equilibrium re-establishment
- Polyprotic Buffer Regions — Selecting a relevant conjugate pair near a stepwise pKa
- Phosphate Buffer Design — H₂PO₄⁻/HPO₄²⁻ ratio and realistic assumptions
- Carbonate Buffer Design — Bicarbonate-carbonate balance and gas exchange cautions
- Buffers and Biological pH — Open-system bicarbonate and phosphate roles
- Buffer Failure and Extremes — Exhaustion, very unequal ratios and strong-acid excess
- Buffer Design Integrated Problems — Target pH, volume, composition and capacity together
- Hydrolysis of Salts in Advanced Problems — Conjugate acid-base behavior and competing equilibria
- Weak-Acid Strong-Base Titration Curves — Initial, half-equivalence and equivalence-region calculations
- Weak-Base Strong-Acid Titration Curves — Protonation stages and acidic equivalence region
- Indicator Choice and Titration Error — Transition range versus steep pH region
- Solubility Product as an Equilibrium Constant — Ksp expressions from dissolution stoichiometry
- Molar Solubility from Ksp — Stoichiometric exponents for AB and AB₂ salts
- Ion Product and Precipitation Direction — Comparing Qsp with Ksp before and after mixing
- Common-Ion Suppression of Solubility — Mass-action shift and controlled approximation
- Dissolution by Acid-Base Consumption — Protonation of basic anions and conditional solubility
- Complexation and Apparent Solubility — Free-metal reduction by ligand binding
- Conditional Solubility Products — Activities, pH and complexation behind measured solubility
- Onset of Precipitation — Threshold ion concentration from Ksp and a counter-ion level
- Selective Precipitation of Two Cations — Comparing onset thresholds and separation windows
- Fraction Remaining During Selective Precipitation — Residual dissolved ion when the second solid begins
- Selective Sulfide Precipitation — pH-dependent sulfide availability and metal-sulfide Ksp
- Selective Hydroxide Precipitation — Metal-hydroxide thresholds controlled by pH
- Amphoteric Hydroxides and Re-Dissolution — Precipitation then complex formation in excess base
- Precipitation After Mixing Solutions — Dilution, ion product and material-balance checks
- Advanced Ionic Equilibrium Integrated Problems — Coupled acid-base, buffer and solubility reasoning
- Advanced Ionic Equilibrium Review — Evidence-led choice of balances, constants and approximations