PPT - M6 Focus1 Acid Base Properties
HSC Chemistry Module 6: Equilibrium and Acid Reactions
Focus 1: Properties of Acids and Bases
Inquiry Question: What is an acid and what is a base?
6.1.1: IUPAC Nomenclature and Properties of Acids and Bases
IUPAC: International Union of Pure and Applied Chemistry; responsible for naming compounds.
Nomenclature: Rules for naming compounds in science, differing for:
Inorganic compounds (not containing carbon)
Organic compounds (containing carbon)
Polymers
Types of Acids and Bases:
Inorganic Bases: oxides and hydroxides of metals, ammonia.
Organic Bases: typically contain nitrogen (e.g., DNA base pairs).
Inorganic Acids: derived from inorganic compounds (e.g., hydrochloric acid, sulfuric acid).
Organic Acids: derived from organic compounds, often with carboxylic acid groups (-COOH).
6.1.2: Indicators for Acids and Bases
Indicators: Substances (vegetable and synthetic dyes) that change colour based on solution acidity.
Original Method: Based on the effect of substances on vegetable dyes (e.g., litmus).
Investigation Task: Demonstrate characteristics of acids and bases using indicators (reference: Chemistry in Focus, page 122).
6.1.3: Acid Reactions
Types of Reactions:
Neutralisation (Acid & Base) Reactions:
General Equation: ACID + BASE → SALT + WATER
Example: Hydrochloric Acid + Sodium Hydroxide → Sodium Chloride + Water
HCl + NaOH → NaCl + H2O
Reaction with Carbonates:
General Equation: ACID + CARBONATE → SALT + CARBON DIOXIDE + WATER
Example: Sulfuric Acid + Magnesium Carbonate → Magnesium Sulfate + Carbon Dioxide + Water
Dilute Acid & Metal Reactions:
General Equation: DILUTE ACID + METAL → SALT + HYDROGEN GAS
Example: Nitric Acid + Sodium → Sodium Nitrate + Hydrogen Gas
HNO3 + Na → NaNO3 + H2
6.1.4: Applications of Neutralisation
Skill Development:
Provide examples from everyday life and industrial processes.
Example Requirements:
Identify chemicals involved.
Write a balanced chemical equation.
Describe purpose and context of use.
Justify why this application is beneficial.
6.1.5: Enthalpy of Neutralisation
Definition:
Measure of total energy in a substance or group when reactants bond-breaking occurs.
Change in Enthalpy (ΔH):
Formula: ΔH = enthalpy of products - enthalpy of reactants
Measured in kJ mol-1
Positive ΔH: energy absorption (endothermic)
Negative ΔH: energy release (exothermic)
Standard Conditions:
25°C (298K), 100kPa
Enthalpy changes during neutralisation: Generally negative, indicating exothermic nature.
6.1.6: Historical Definitions of Acids and Bases
Antoine Lavoisier (1776):
Proposed that acids contained oxygen.
Limitations:
Did not explain lack of acidity in metal oxides or common acids like HCl.
Humphry Davy (1815):
Suggested acids contained hydrogen.
Limitations:
Classified NH3 as acidic, which is not correct.
Svante Arrhenius (1884):
Defined acids as H+ producers, bases as OH- producers in solutions.
Limitations:
Did not account for solvent effects on strength; failed to explain ammonia's behavior.
Bronsted-Lowry Theory (1923):
Acids as proton donors, bases as proton acceptors.
Limitations:
Relied on solvent presence; could not explain acid-base reactions without a solvent.
Gilbert Lewis (1923):
Defined acids as electron pair acceptors and bases as electron pair donors.
Advancement:
Broader definition not limited to protons or solvents (e.g., BF3 reacting with NH3).
Limitations:
Did not explain strength differences or provide clarity on reactions of common acids like HCl.