Lesson 12: Common Ion Effect

Lesson 109/175 | Study Time: 30 Min
Course: Chemistry XI
Lesson 12: Common Ion Effect

Learning Outcomes:



i. Comprehend the concept of the common ion effect, a phenomenon that reduces the solubility of slightly soluble ionic compounds in the presence of a common ion.



ii. Explain the mechanism behind the common ion effect and its relationship to Le Chatelier's principle.



iii. Utilize the common ion effect to predict the extent of precipitation and the solubility of ionic compounds.



iv. Explore the practical applications of the common ion effect in qualitative analysis and the separation of ions.



 



Introduction:



In the intricate world of aqueous solutions, the common ion effect plays a significant role in influencing the solubility of ionic compounds. This phenomenon, characterized by the reduced solubility of a slightly soluble ionic compound when a common ion is added to the solution, reveals a delicate balance between opposing forces. This lesson delves into the fascinating realm of the common ion effect, unraveling its mechanism and exploring its practical applications in the field of chemistry.



i. The Common Ion Effect: A Shift towards the Solid State



The common ion effect arises from the influence of a common ion, an ion that is present in both the salt and the solution, on the equilibrium of the dissolution reaction. When a common ion is added to a solution containing a slightly soluble ionic compound, the equilibrium shifts towards the left, favoring the formation of the solid precipitate. This reduction in solubility is attributed to the increased competition between the common ions for solvation by water molecules.



ii. Le Chatelier's Principle in Action: Restoring Equilibrium



The common ion effect can be explained in the context of Le Chatelier's principle, which states that when a system at equilibrium is subjected to a stress, the system will respond in a way that partially counteracts the stress. In this case, the addition of a common ion represents a stress on the dissolution equilibrium, and the system responds by shifting towards the left, reducing the concentration of dissolved ions and minimizing the effect of the added common ion.



 



iii. Applications of the Common Ion Effect: From Qualitative Analysis to Separation of Ions



The common ion effect finds application in various fields of chemistry, including:



Qualitative Analysis: In qualitative analysis, the common ion effect is used to separate and identify ions based on their relative solubilities. By adding a common ion to a solution containing a mixture of ions, one can selectively precipitate certain ions while leaving others in solution.



Separation of Ions: The common ion effect is employed in various separation techniques, such as fractional precipitation and ion exchange chromatography. These techniques utilize the differences in solubility of compounds in the presence of a common ion to separate and purify ions from solutions.



Buffer Solutions: The common ion effect is crucial for the preparation and understanding of buffer solutions. Buffers are solutions that resist significant changes in pH when small amounts of acid or base are added. The presence of a common ion in a buffer helps maintain a relatively constant pH by minimizing the effect of added protons or hydroxide ions.



 



The common ion effect stands as a fundamental concept in aqueous chemistry, providing a deeper understanding of the solubility of ionic compounds and their behavior in the presence of common ions. By comprehending this phenomenon, scientists can design efficient separation processes, formulate effective buffer solutions, and harness the power of chemistry for various applications.



 

Ahmed Hassan

Ahmed Hassan

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Class Sessions

1- Lesson 01: Mole and Avogadro's Number 2- Lesson 02: Mole Calculations 3- Lesson 03: Percentage Composition 4- Lesson 04: Excess and Limiting Reagents 5- Lesson 05: Theoretical Yield and Actual Yield as Percentage 6- Lesson 01: Discharge Tube Experiments 7- Lesson 02: Application of Bohr's Model 8- Lesson 03: Derivation of Radius, Energy, Frequency, Wave Length, Wave Number 9- Lesson 04: Spectrum of Hydrogen Atom 10- Lesson 05: Defects of Bohr's Theory 11- Lesson 06: Planck's Quantum Theory 12- Lesson 07: Postulates With Derivation of E =hcν 13- 14- 15- 16- 17- Lesson 08: X-Rays Production, Properties, and Uses 18- Lesson 09: X-rays and Atomic Number 19- Lesson 10: Moseley's Experiment 20- Lesson 11: Moseley's Law 21- Lesson 12: Quantum Numbers and Orbitals 22- Lesson 13: Principle Quantum Number 23- Lesson 14: Azimuthal Quantum Number 24- Lesson 15: Magnetic Quantum Number 25- Lesson 16: Spin Quantum Number 26- Lesson 17: Shapes of s, p, and d Orbitals 27- Lesson 18: Electronic Configuration 28- Lesson 19: Aufbau Principle 29- Lesson 20: Pauli's Exclusion Principle 30- Lesson 21: Hund's Rule 31- Lesson 22: Bonus Lesson: Electron Configurations of Elements 32- Lesson 01: Shapes of Molecules 33- Lesson 02: Resonance 34- Lesson 03: Theories of Covalent Bonding 35- Lesson 04: Bond Characteristics 36- Lesson 05: Bond Energy 37- Lesson 06: Bond Length 38- Lesson 07: Ionic Character 39- Lesson 08: Dipole Moment 40- Lesson 09: Effect of Bonding on Physical and Chemical Properties 41- Lesson 10: Solubility of Ionic and Covalent Compounds 42- Lesson 11: Reactions of Ionic and Covalent Compounds 43- Lesson 12: Directional and Non-Directional Nature of Ionic and Covalent Bonds 44- Lesson 01: Kinetic Molecular Theory of Gases 45- Lesson 02: Postulates of Kinetic Molecular Theory 46- Lesson 03: Pressure and Its Units 47- Lesson 04: Absolute Temperature Scale on the Basis of Charles Law 48- Lesson 05: Brief Recall of Boyle’s and Charles’ Law 49- Lesson 06: Graphical Explanation of Absolute Zero 50- Lesson 07: Avogadro’s Law 51- Lesson 08: Ideal Gas Equation Derivation 52- Lesson 09: Gas Constant and Its Units 53- Lesson 10: Deviation From Ideal Gas Behavior 54- Lesson 11: Graphical Explanation of Deviations 55- Lesson 12: Causes for Deviation 56- Lesson 13: Van der Waals Equation 57- Lesson 14: Volume Correction 58- Lesson 15: Pressure Correction 59- Lesson 16: Dalton’s Law of Partial Pressure 60- Lesson 17: Graham’s Law of Diffusion and Effusion 61- Lesson 18: Liquefaction of Gases 62- Lesson 19: Joule-Thomson Effect 63- Lesson 20: Linde’s Method of Liquefaction of Gases 64- Lesson 21: Fourth State of Matter: Plasma 65- Lesson 01: Kinetic Molecular Interpretation of Liquids 66- Lesson 02: Simple Properties of Liquids 67- Lesson 03: Intermolecular Forces (Vander Waals Forces) 68- Lesson 04: Dipole-Dipole Interaction 69- Lesson 05: Hydrogen Bonding 70- Lesson 06: London Forces 71- Lesson 07: Energetics of Phase Changes 72- Lesson 08: Molar Heat of Fusion, Molar Heat of Vaporization, Molar Heat of Sublimation 73- Lesson 09: Energy Changes and Intermolecular Attractions 74- Lesson 10: Change of State and Dynamic Equilibrium 75- Lesson 11: Liquid Crystals, Brief Description and their Uses from Daily Life 76- Lesson 01: Kinetic Molecular Interpretation of Solids 77- Lesson 02: Simple Properties of Solids Describing Vibration of Molecules, Intermolecular Forces, Kinetic Energy 78- Lesson 03: Types of Solids; Amorphous, Crystalline 79- Lesson 04: Properties of Crystalline Solids 80- Lesson 05: Melting Point 81- Lesson 06: Cleavage Plane 82- Lesson 07: Habit of Crystal 83- Lesson 08: Crystal Growth 84- Lesson 09: Anisotropy 85- Lesson 10: Isomorphism 86- Lesson 11: Polymorphism 87- Lesson 12: Allotropy 88- Lesson 13: Transition Temperature 89- Lesson 14: Crystal Lattice 90- Lesson 15: Unit Cell 91- Lesson 16: NaCl Crystal 92- Lesson 17: Lattice Energy 93- Lesson 18: Types of Crystalline Solids 94- Lesson 19: Ionic Solids 95- Lesson 20: Covalent Solids 96- Lesson 21: Metallic Solids 97- Lesson 22: Molecular Solids 98- Lesson 01: Reversible Reactions and Dynamic Equilibrium 99- Lesson 02: Concept and Explanation 100- Lesson 03: Law of Mass Action and Expression for Equilibrium Constant 101- Lesson 04: Relationship between Kc, Kp, Kx, Kn 102- Lesson 05: Importance of K and Reaction Quotient 103- Lesson 06: Factors Affecting Equilibrium ( Le-Chatelier’s Principle ) 104- Lesson 07: Effect of Change in Concentration 105- Lesson 08: Effect of Change in Pressure or Volume 106- Lesson 09: Effect of Change in Temperature 107- Lesson 10: Industrial Application of Le-Chatelier’s Principle (Haber’s Process) 108- Lesson 11: Solubility Product and Precipitation Reactions 109- Lesson 12: Common Ion Effect 110- Lesson 01: Acidic, Basic and Amphoteric Substances 111- Lesson 02: Bronsted-Lowry Definitions of Acids and Bases 112- Lesson 03: Proton Donors and Acceptors 113- Lesson 04: Relative Strength of Acids and Bases 114- Lesson 05: Conjugate Acid-Base Pairs 115- Lesson 06: Expressing the Strength of Acids and Bases 116- Lesson 07: Ionization Equation of Water 117- Lesson 08: pH, pOH and pKw 118- Lesson 09: Acid Ionization Constant, Ka and pKa 119- Lesson 10: Leveling Effect 120- Lesson 11: Base Ionization Constant, Kb and pKb 121- Lesson 12: Relationship of Ka and Kb 122- Lesson 13: Lewis Definitions of Acids and Bases 123- Lesson 14: Buffer Solutions and their Applications 124- Lesson 15: Salt Hydrolysis 125- Lesson 01: Chemical Kinetics 126- Lesson 02: Rates of Reactions 127- Lesson 03: Rate Law or Rate Expression 128- Lesson 04: Elementary and Overall Rate Constant and Units 129- Lesson 05: Order of Reaction and its Determination 130- Lesson 06: Factors Affecting Rate of Reaction 131- Lesson 07: Collision Theory, Transition State and Activation Energy 132- Lesson 08: Catalysis 133- Lesson 09: Characteristics of Catalysts 134- Lesson 10: Homogeneous Catalysis 135- Lesson 11: Heterogeneous Catalysis 136- Lesson 12: Enzyme Catalysis 137- Lesson 01: General Properties of Solutions 138- Lesson 02: Solution, Suspension and Colloids 139- Lesson 03: Hydrophilic and Hydrophobic Molecules 140- Lesson 04: The Nature of Solutions in the Liquid Phase 141- Lesson 05: The Effect of Temperature and Pressure on Solubility 142- Lesson 06: Concentration Units 143- Lesson 07: Percent, Molarity, Molality, Mole Fraction 144- Lesson 08: Parts per million, billion, and trillion 145- Lesson 09: Raoult's Law 146- Lesson 10: Non-Volatile Non-Electrolyte Solutes in Volatile Solvents 147- Lesson 12: Colligative Properties of Dilute Solutions 148- Lesson 11: When Both Components are Volatile 149- Lesson 13: Vapor Pressure Lowering 150- Lesson 14: Boiling Point Elevation and Freezing Point Depression 151- Lesson 15: Molar Mass Determination by Vapor Pressure Lowering, Boiling 152- Lesson 16: Point Elevation and Freezing Point Depression 153- Lesson 17: Osmotic Pressure and Reverse Osmosis 154- Lesson 18: Colloids 155- Lesson 19: Properties of Colloids 156- Lesson 20: Types of Colloids 157- Lesson 01: Energy in Chemical Reactions 158- Lesson 02: Thermodynamics 159- Lesson 03: Internal Energy 160- Lesson 04: First Law of Thermodynamics 161- Lesson 05: Standard State and Standard Enthalpy Changes 162- Lesson 06: Heat Capacity 163- Lesson 07: Calorimeter 164- Lesson 08: Hess's Law: Enthalpy Change Calculations 165- Lesson 09: Born-Haber Cycle 166- Lesson 01: Oxidation-Reduction Concepts 167- Lesson 02: Oxidation and Reduction 168- Lesson 03: Oxidation Numbers 169- Lesson 04: Recognizing Oxidation Reduction Reactions 170- Lesson 05: Balancing Oxidation Reduction Equations by Oxidation Number Method 171- Lesson 06: Balancing Oxidation Reduction Equations by the Half Reaction Method 172- Lesson 07: Chemistry of Some Important Oxidizing and Reducing Agents 173- Lesson 08: Electrode, Electrode Potential and Electrochemical Series 174- Lesson 09: Types of Electrochemical Cells 175- Lesson 10: Electrolytic Cells