-
-
-
-
Molarity
Preparing a solution
Dilution
Solubility rules
Complete & Net Ionic Equations
Colligative properties
-
Heat Flow
Energy diagrams
Thermochemical equations
Heating/ Cooling curves
Specific Heat Capacity
Calorimetry
Hess's Law
Enthalpies of formation
Bond enthalpies
-
Collision Theory
Rate Comparisons
Integrated Rate Law
Differential Rate Law
-
Equilibrium
Equilibrium Expression
ICE Tables
Calculating K
K vs Q
Le Chatelier's Principle
-
Definitions
Conjugate Acids & Base Pairs
Autoionization of water
pH Scale
Strong Acids/ Bases
Ka and Kb
Buffer
Titrations
Indicators
pH salts
-
Entropy
Gibb's Free Energy
G and Temperature
-
Oxidation numbers
Half Reactions
Balancing Redox reactions
Voltaic cells
Cell potential (standard conditions)
Cell potential (non-standard)
Electrolysis
Quantitative Electrochemistry
Enthalpies of Formation
Related Examples and Practice Problems
Additional Worked Out Examples/ Practice
Identifying classification types: Differentiation between elements, compounds or mixtures and homogeneous and heterogenous mixtures
Separation techniques: Selected and explaining limitation of appropriate separation
Relating Properties to Composition: Predicting classification based on descriptive properties
and more …
Topic Summary & Highlights
and Help Videos
Core Concept
Enthalpy of Formation ($\Delta H_f^\circ$) is the enthalpy change when 1 mole of a compound is formed from its elements in their standard states under standard conditions (298 K and 1 atm). Standard enthalpies of formation are essential for calculating the enthalpy changes of reactions.
Key Concepts
Standard Enthalpy of Formation ($\Delta H_f^\circ$):
The enthalpy change when 1 mole of a compound is formed from its elements in their most stable forms at 1 atm pressure and 298 K.
Symbol: $\Delta H_f^\circ$ (the degree symbol $\circ$∘ denotes standard conditions).
Measured in kilojoules per mole (kJ/mol).
Standard State:
Elements are in their most stable physical forms at 1 atm and 298 K (e.g., $\text{O}_2$ for oxygen, $\text{N}_2$ for nitrogen, and graphite for carbon).
Enthalpy of Formation of Elements:
The standard enthalpy of formation of any pure element in its standard state is zero.
Example: $\Delta H_f^\circ$ for $\text{O}_2\text{(g)}$ and $\text{N}_2\text{(g)}$ is zero.
Applications:
Enthalpies of formation are used to calculate the enthalpy change for chemical reactions.
Hess’s Law and standard enthalpies of formation can be combined to find $\Delta H_{\text{reaction}}^\circ$.
Calculating Enthalpy of a Reaction Using Enthalpies of Formation
The enthalpy change of a reaction can be calculated using the enthalpies of formation of the reactants and products:
$\Delta H_{\text{reaction}}^\circ = \sum \Delta H_f^\circ(\text{products}) - \sum \Delta H_f^\circ(\text{reactants})$
Identify the Products and Reactants:
Write the balanced chemical equation for the reaction.
Find the Enthalpies of Formation:
Look up the $\Delta H_f^\circ$ values for each reactant and product in a table.
Multiply by Coefficients:
Multiply each $\Delta H_f^\circ$ value by its coefficient in the balanced equation.
Subtract the Sum of Reactants from Products:
Sum the enthalpies of formation for the products and reactants separately, then subtract the total for the reactants from the total for the products.
Tips for Using Enthalpies of Formation
Use Standard Enthalpies: Always use $\Delta H_f^\circ$ values from standard tables to ensure accuracy.
Check Physical States: Ensure each substance’s physical state (solid, liquid, gas) matches its enthalpy of formation, as $\Delta H_f^\circ$ values vary by state.
Remember Elements Have $Delta H_f^\circ = 0$: Pure elements in their standard states have a formation enthalpy of zero.
Multiply by Stoichiometric Coefficients: Don’t forget to multiply each $\Delta H_f^\circ$∘ by its coefficient from the balanced chemical equation.