CH 4.1
Chapter 4: Molecular View of Reactions in Aqueous Solutions Part I
Chapter Objectives and Learning Goals
Describe solutions qualitatively and quantitatively.
Distinguish electrolytes from non-electrolytes.
Write balanced molecular, ionic, and net ionic equations.
Identify acids and bases, including their names and formulas.
Use metathesis reactions to plan chemical syntheses.
Define and use molarity in calculations.
Understand titrations and chemical analysis.
Importance of Water
Common Compound: Abundant on Earth.
Solvent Properties: Dissolves many substances, vital for life.
Biological Relevance: Approximately 60% of the human body.
Role as a Solvent: Dissolves ionic compounds and facilitates acid-base reactions.
Reactions in Solution
Physical Contact: Reactants must physically contact (gas or liquid phases).
Definition of a Solution: A homogeneous mixture where components mix freely.
Definitions
Solvent
The medium that dissolves solutes, present in the largest amount.
Aqueous Solution: Water is the solvent.
Solute
Substance dissolved in a solvent.
Examples: Gas (\text{CO}_2 in soda), Liquid (Ethylene glycol), Solid (Sugar).
Concentration of Solutions
Characterization: Solute-to-solvent ratio, defined in grams per gram.
Percent Concentration: \text{g solute} \times \frac{100}{\text{g solution}}
Relative Concentration
Dilute Solution: Small solute-to-solvent ratio.
Concentrated Solution: Large solute-to-solvent ratio.
Terms are relative.
Concentration and Solubility
Solubility: Amount of solute (g) to create a saturated solution at a specific temperature: \text{Solubility} = \frac{\text{g solute}}{100 \text{ g solvent}}
Temperature Dependence: Solubility varies with temperature.
Saturated Solution: Maximum solute dissolved at a given temperature.
Unsaturated Solution: Less than maximum capacity; more can dissolve.
Common Substance Solubility Example
Sodium chloride (NaCl): 35.7 g/100g water at 0 °C; 39.1 g/100g water at 100 °C.
Supersaturated Solutions
Definition: Contains more solute than saturation at a given temperature.
Formation and Stability: Formed by cooling saturated solutions; unstable, crystallize upon adding a seed crystal (precipitate formation).
Precipitates
Definition of a Precipitate
Solid formed in solutions when a product has low solubility.
Insoluble Product: Separates from the solution.
Precipitation Reactions
Example Reaction: \text{Pb(NO}3\text{)}2(aq) + 2 \text{KI}(aq) \rightarrow \text{PbI}2(s) + 2 \text{KNO}3(aq)
Electrolytes in Aqueous Solution
Definition of Electrolytes: Ionic compounds that conduct electricity when dissolved in water.
Ionic Compounds in Water
Dissociation Process: Water molecules surround and remove ions from the lattice (e.g., NaCl into \text{Na}^{+} and \text{Cl}^{-}). Polyatomic ions stay intact.
Molecular Compounds in Water
Dissolution Behavior: Molecules dissolve but do not dissociate into ions.
Electrical Conductivity
Types of Electrolytes
Strong Electrolyte: Completely dissociates in water (e.g., NaCl, \text{HClO}_4).
Weak Electrolyte: Partially dissociates (small percentage ionize) (e.g., \text{CH}3\text{COOH}, \text{NH}3).
Non-Electrolyte: Does not conduct electricity (intact molecular structure) (e.g., sugar, alcohols).
Dissociation Reactions
Process Description: Ionic compounds dissolve to form hydrated ions, indicated by (aq).
Example Dissociation Reaction Formula: \text{KBr}(s) \rightarrow \text{K}^{+}(aq) + \text{Br}^{-}(aq)
Equations of Ionic Reactions
Types of Equations
Molecular Equation: Substances listed with complete formulas.
Ionic Equation: All soluble substances broken into ions.
Net Ionic Equation: Only species undergoing chemical change.
Example of Reaction Equations between Pb(\text{NO}3)2 and KI
Molecular Equation: \text{Pb(NO}3\text{)}2(aq) + 2 \text{KI}(aq) \rightarrow \text{PbI}2(s) + 2 \text{KNO}3(aq)
Ionic Equation: \text{Pb}^{2+}(aq) + 2 \text{NO}3^{-}(aq) + 2 \text{K}^{+}(aq) + 2 \text{I}^{-}(aq) \rightarrow \text{PbI}2(s) + 2 \text{K}^{+}(aq) + 2 \text{NO}_3^{-}(aq)
Net Ionic Equation: \text{Pb}^{2+}(aq) + 2 \text{I}^{-}(aq) \rightarrow \text{PbI}_2(s)
Spectator Ions
Definition: Ions that do not participate in the chemical reaction.
Criteria for Balancing Ionic and Net Ionic Equations
Material Balance: Same number of each atom on both sides.
Electrical Balance: Net electrical charge equal on both sides.
Acids and Bases
Common Laboratory Reagents: Acids (tart/sour taste like vinegar) and bases (bitter taste, slippery feel like ammonia). Safety Note: Never taste, feel, or smell chemicals.
Definitions of Acids and Bases
Arrhenius Acid
Definition: Produces hydronium ions (\text{H}_3\text{O}^{+}) in water.
Example: \text{HC}2\text{H}3\text{O}2(aq) + \text{H}2\text{O} \rightarrow \text{H}3\text{O}^{+}(aq) + \text{C}2\text{H}3\text{O}2^{-}(aq)
Arrhenius Base
Definition: Produces hydroxide ions (\text{OH}^{-}).
Example: \text{NaOH}(s) \rightarrow \text{Na}^{+}(aq) + \text{OH}^{-}(aq)
Strong Acids
Characteristics: Fully dissociate in water (e.g., \text{HClO}4 , HCl, \text{H}2\text{SO}_4).
Strong Bases
Characteristics: Completely dissociate in water (e.g., Group 1A & 2A metal hydroxides like LiOH, NaOH).
Weak Acids and Bases
Weak Acids: < 100% ionization (e.g., \text{CH}_3\text{COOH}).
Weak Bases: Molecular bases that don't dissociate efficiently (e.g., \text{NH}_3).
Dynamic Equilibrium
Definition: Opposing reactions at the same rate, constant concentrations.
Example: \text{HC}2\text{H}3\text{O}2(aq) \rightleftharpoons \text{H}3\text{O}^{+}(aq) + \text{C}2\text{H}3\text{O}_2^{-}(aq)
General Ionization Equations
Strong Acids: \text{HX}(aq) + \text{H}2\text{O} \rightarrow \text{H}3\text{O}^+(aq) + X^-(aq)
Strong Bases: \text{M(OH)}_n(s) \rightarrow \text{M}^{n+}(aq) + n \text{OH}^-(aq)
Weak Acids: \text{HA}(aq) + \text{H}2\text{O} \rightleftharpoons \text{H}3\text{O}^+(aq) + \text{A}^-(aq)
Weak Bases: \text{B}(aq) + \text{H}_2\text{O} \rightleftharpoons \text{HB}^+(aq) + \text{OH}^-(aq)
Summary of Electrolytes
Strong Electrolytes: Completely ionize, predominantly products.
Weak Electrolytes: Partially ionize, significant reverse reactions (more reactants).
Polyprotic Acids
Characteristics
Monoprotic Acids: Furnish one \text{H}^{+} (e.g., \text{HNO}_3).
Diprotic Acids: Furnish two \text{H}^{+} (e.g., \text{H}2\text{SO}3).
Triprotic Acids: Furnish three \text{H}^{+} (e.g., \text{H}3\text{PO}4).
Stepwise Ionization Example for \text{H}3\text{PO}4
\text{H}3\text{PO}4(aq) + \text{H}2\text{O} \rightarrow \text{H}3\text{O}^{+}(aq) + \text{H}2\text{PO}4^{-}(aq)
\text{H}2\text{PO}4^{-}(aq) + \text{H}2\text{O} \rightleftharpoons \text{H}3\text{O}^{+}(aq) + \text{HPO}_4^{2-}(aq)
\text{HPO}4^{2-}(aq) + \text{H}2\text{O} \rightleftharpoons \text{H}3\text{O}^{+}(aq) + \text{PO}4^{3-}(aq)
Acidic and Basic Anhydrides
Acidic Anhydrides: Nonmetal oxides reacting with water to form acids (e.g., \text{SO}3 + \text{H}2\text{O} \rightarrow \text{H}2\text{SO}4).
Basic Anhydrides: Metal oxides reacting with water to form bases (e.g., \text{CaO} + \text{H}2\text{O} \rightarrow \text{Ca(OH)}2).
Nomenclature of Acids and Bases
Naming Acids
Binary Acids: Hydrogen and a nonmetal (e.g., HCl [g] \rightarrow hydrochloric acid [aq]).
Oxoacids: Hydrogen, oxygen, and another non-metal, named based on parent oxoanion.
Naming Bases
Metal Hydroxides: Named by the metal (e.g., \text{Ca(OH)}_2 \rightarrow \text{calcium hydroxide}).
Molecular Bases: Named like organic molecules (e.g., \text{NH}_3 is ammonia).