Instructor: Mohan Sir (CMS Sir)
Platform: Physics Wallah
Thermochemistry
Study of heat changes that occur during chemical reactions and changes of state.
Importance in understanding energy transfers in physical and chemical processes.
Enthalpy of Formation
Defines the heat change when one mole of a compound is formed from its elements in their standard states.
Essential for calculating reaction enthalpies using Hess's Law.
Enthalpy of Neutralization
Specific enthalpy change when one equivalent of an acid reacts with one equivalent of a base to form water and a salt.
Usually negative for strong acids and bases indicating exothermic nature.
Enthalpy of Combustion
Measures the heat released when a compound undergoes complete combustion in oxygen.
Important for energy content calculations in fuels.
ΔH > 0 and ΔS < 0 - Non-spontaneous at all temperatures.
ΔH < 0 and ΔS > 0 - Always spontaneous (exothermic processes).
ΔH < 0 and ΔS < 0 - Spontaneous at low temperatures (exothermic but with a decrease in disorder).
ΔH > 0 and ΔS > 0 - Spontaneous at high temperatures (endothermic processes with an increase in disorder).
Example Calculation: Given: ΔH = 200 J/mol, ΔS = 40 J/K·mol To find Minimum Temperature (T) for spontaneity:
ΔG = ΔH - TΔS For spontaneity, ΔG must be less than 0.
Choices for Minimum Temperature:
(a) 20K
(b) 4K
(c) 5K
(d) 12K
A general reaction can be represented as:
aA + bB ⇌ cC + dD
ΔH: Total enthalpy change during the reaction can be either positive (endothermic) or negative (exothermic).
Exothermic Reactions
Heat is released to the surroundings, indicated by ΔH < 0.
Examples: Combustion (e.g., burning of hydrocarbons), Neutralization reactions.
Endothermic Reactions
Heat is absorbed from the surroundings, indicated by ΔH > 0.
Examples include photosynthesis and certain dissolution processes.
Reaction Conditions:
Most reactions are conducted under constant temperature and pressure or volume.
Under constant T and P, we have.
Enthalpy of Reaction (ΔH) is a key indicator of heat exchange during chemical processes.
The enthalpy change for reactions can vary significantly depending on the physical state of the reactants and products:
Example: H₂(g) + O₂(g) → H₂O(l)
The physical state (gas vs liquid) influences ΔH values due to the intermolecular forces involved.
Notation and Enthalpy Changes:
Different representations can indicate ΔH changes based on various states and conditions of reactants.
Kirchoff's Equation: Shows relationship between temperature changes and enthalpic changes in reactions.
Defined as the enthalpy change for a reaction when all reactants and products are in their standard states (1 bar pressure for gases and specific concentrations for solutions).
Enthalpy of Formation:
Significant for determining stability and reactivity as it measures energy change when forming one mole of a compound from its elements.
Reference states for elements are defined specifically for thermodynamic calculations.
The calculation method of enthalpy changes using standard values:
Formula: ΔH = {(ΣΔH products) - (ΣΔH reactants)}
Includes practical examples to calculate enthalpy changes in specific reactions, example:
N₂(g) + 3H₂(g) → 2NH₃(g)
An example of calculating the overall heat of formation:
Reaction: F₂O(g) + H₂O(g) → O₂(g) + 2HF(g)
Demonstrates the heat required defined by the heat values of reactants.
Calculation example for determining the heat for forming a specific mass of a compound:
Example: 1.28 kg of CaC₂ requiring 2240 kcal, including reactant values for CaO, CaC₂, and CO.
Defining the enthalpy change associated with neutralizing a defined amount of acid and base, typically one equivalent:
The example discusses diverse strong acid/base reactions leading to salt and water.
Reaction Example: HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
Standard values of enthalpy change for the reaction are noted for strong acids and bases evaluated.
DPP-08 homework assigned to reinforce topics covered in this lecture.
Closure and acknowledgment of participants for engaging in the lecture, encouraging further exploration of thermodynamic principles.