Thermodynamics is a branch of physical chemistry focused on the relationships between heat, work, temperature, and energy.
Essential for understanding how energy transfers and transforms in chemical processes.
Explains phenomena like phase changes and reaction spontaneity.
Studying thermodynamics enhances the appreciation of energy conservation and chemical reaction directionality.
First Law of Thermodynamics
States that energy cannot be created or destroyed, only transformed.
Second Law of Thermodynamics
Introduces entropy, suggesting that natural processes lead to greater disorder over time.
Predictive Role
Thermodynamics helps predict whether a chemical reaction will occur spontaneously.
Thermodynamic Cycles
Example: Carnot cycle, critical for understanding the efficiency of heat engines and energy conversion.
Real-World Applications
Important for areas such as calorimetry, refrigeration, and engines, affecting varied industries.
A thermodynamic system is defined as a matter or radiation body separate from its surroundings.
Characterized by mass/volume, composition, energy, temperature, and pressure.
Types of Systems based on energy and matter exchange:
Closed, open, and isolated systems.
State Variables (thermodynamic variables):
Pressure, volume, temperature, internal energy, enthalpy, entropy.
Heat energy in chemical reactions is measured using calorimetry.
Change in internal energy results in heat and work.
Endothermic vs Exothermic Reactions:
Endothermic: Energy absorbed (ΔH > 0).
Exothermic: Energy released.
Characteristics:
Absorb energy, requiring input energy.
Products have higher energy content than reactants.
Factors Affecting Reactions:
Increasing temperature or using a catalyst can help reach activation energy.
Le Châtelier’s Principle:
System at equilibrium adjusts to counteract changes (e.g., adding heat shifts equilibrium right).
Characteristics:
Release energy, increasing environmental temperature.
Applications:
Drive chemical processes like combustion.
Examples:
Dissolution of ionic compounds in water is often exothermic.
Common in industrial processes such as fuel combustion.
Definition: Change in enthalpy when one mole of a compound forms from its elements under standard conditions.
Standard Enthalpy of Formation: Zero for elements in their stable form.
Calculation: Values crucial for determining heat during reactions, especially combustion.
Negative Values: Indicate energy release when forming compounds.
Significance: Helps evaluate energy changes in combustion reactions.
Definition: Energy required to break one mole of a specific bond type.
Strength Correlation: Stronger bonds have higher bond enthalpies.
Energy Changes:
Breaking bonds: endothermic.
Forming bonds: exothermic.
Estimation Formula: ΔH = Σ(bond enthalpies of broken bonds) - Σ(bond enthalpies of formed bonds).
Principle: Total enthalpy change is the same regardless of reaction pathway.
Calculation Utility: Allows enthalpy changes for complex reactions to be calculated.
State Function: Dependence only on initial and final states.
Definition: Thermodynamic potential measuring maximum reversible work from a closed system at constant temperature and pressure.
Formula: ΔG = ΔH - TΔS
ΔH: Enthalpy change, ΔS: Entropy change.
Spontaneity Indicator:
ΔG < 0: spontaneous processes.
ΔG = 0: equilibrium.
Impact of Temperature: Influences spontaneity based on changes in entropy/enthalpy.
Phase Stability: Helps in understanding conditions for different phases to coexist, relevant for phase diagrams.
Combustion of Fuels: Releases energy for transport (e.g., petrol).
Digestion: Releases energy from food through chemical processes.
Battery Usage: Conversion of stored chemical energy to electricity.
Power Generation: Utilizes exothermic reactions for electricity.
Chemical Industry: Relies on energy-changing reactions for production and synthesis.