First-year university chemistry: what the modules cover and how to practise
University Chemistry: Year 1
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What first-year chemistry modules cover
| Course | What it covers |
|---|---|
| MIT 5.111 Principles of Chemical Science | Atomic and molecular electronic structure, thermodynamics, acid-base and redox equilibria, kinetics and catalysis. MIT calls it a freshman-level course |
| MIT 5.12 Organic Chemistry I | The structure and reactivity of organic molecules, substitution and elimination reactions, carbonyl chemistry, and an introduction to aromatic compounds |
In the US this is usually called general chemistry, with organic chemistry as a separate course; other universities may split the same material into separate physical, inorganic and organic modules. Check your module handbook for the exact syllabus and exam format.
The core topics
- Atomic structure: quantum numbers, atomic orbitals and electron configurations.
- Bonding: Lewis structures, VSEPR, hybridisation and molecular orbital theory.
- Thermodynamics: enthalpy, entropy and Gibbs free energy.
- Kinetics: rate laws, integrated rate equations, half-lives, activation energy and catalysis.
- Equilibria: equilibrium constants, acids and bases, buffers and solubility.
- Electrochemistry: standard potentials, cell potentials and the link to ΔG.
- Inorganic chemistry: coordination compounds and transition metals.
- Organic chemistry: stereochemistry, substitution, elimination and addition mechanisms, and spectroscopy.
Worked examples
Gibbs free energy
For N₂ + 3H₂ → 2NH₃, ΔH = −92 kJ mol⁻¹ and ΔS = −199 J K⁻¹ mol⁻¹. At 298 K:
The reaction is spontaneous at 298 K. It stops being spontaneous above about 92 ÷ 0.199 ≈ 462 K, where ΔG becomes positive (assuming ΔH and ΔS stay constant).
First-order kinetics
A first-order reaction has k = 0.0231 min⁻¹, so its half-life is t½ = ln 2 ÷ k ≈ 30 minutes, whatever the starting concentration.
Electrochemistry
In a zinc-copper cell, E°cell = E°(Cu²⁺/Cu) − E°(Zn²⁺/Zn) = 0.34 − (−0.76) = 1.10 V. With n = 2, ΔG° = −nFE° = −2 × 96,485 × 1.10 ≈ −212 kJ mol⁻¹.
Molecular orbital theory
In O₂, the valence electrons fill 8 bonding and 4 antibonding orbital places, so the bond order is (8 − 4) ÷ 2 = 2. Two of the antibonding electrons are unpaired, which is why O₂ is paramagnetic, something a simple Lewis structure cannot explain.
Use a rate equation in our Reaction Kinetics course, then press Mark to check your answer in the course:
Use rate = k[A] or k[A] squared to work out a rate or the rate constant.
Press Mark to have your answer marked in the Reaction Kinetics course.
Use the daily paper as practice
Uni-Sine publishes a free daily University Chemistry: Year 1 paper. It is a short timed practice paper: 8 questions worth 25 to 35 marks, with a suggested 40 to 55 minutes, marked when you finish. It is not your university's exam, so use it alongside your module's problem sheets and past papers.
- What it covers well: atomic orbitals and quantum numbers, molecular orbital theory, thermodynamics and Gibbs free energy, kinetics and mechanisms, electrochemistry, coordination chemistry, stereochemistry, organic reaction mechanisms and spectroscopy.
- What it does not cover: lab skills, and gives less space to acids and bases, solubility, gases and main group chemistry than many courses do.
Common mistakes in first-year chemistry
- Mixing kJ and J in ΔG = ΔH − TΔS. Convert ΔS to kJ K⁻¹ mol⁻¹ first.
- Assuming rate laws come from the equation. Orders are found by experiment.
- Multiplying E° by the coefficients. Standard potentials don't scale with the equation.
- Curly arrows going the wrong way. Arrows show electrons moving from a lone pair or bond.
Common questions
Is there a standard first-year chemistry exam?
What is general chemistry?
How is university chemistry different from school chemistry?
What should I revise before first-year chemistry?
How can I practise first-year chemistry?
Revision cards
Say the answer first, then flip the card to check it.
Where to go next
- Solve it
Enthalpy Calculator
Use Hess's law and bond enthalpies to find energy changes
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Reaction Kinetics
Rates, catalysts and collision theory: what makes reactions fast or slow
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University Chemistry: Year 1
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