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University Chemistry Practice Test — 30 Problems

University Chemistry Practice Test — 30 Problems

Section titled “University Chemistry Practice Test — 30 Problems”

This practice test covers 30 problems across three major domains of university chemistry: Physical Chemistry, Organic Chemistry, and Inorganic Chemistry. Each problem tests conceptual understanding, quantitative reasoning, and the application of fundamental principles. Work through the problems with pen and paper before checking the solutions.

  • Time limit: 90 minutes (3 minutes per problem)
  • Format: Multiple choice and problem-solving — show all working where required
  • Marking: 1 mark per problem, 30 marks total
  • Conditions: Attempt without notes. Record your answers on a separate sheet.
  • After the test: Check the answer key at the bottom. Study the explanations for any problems you got wrong.
DomainProblemsMarks
Physical ChemistryP1–P1010
Organic ChemistryP11–P2010
Inorganic ChemistryP21–P3010
Total3030

A system absorbs 500 J of heat and does 200 J of work on its surroundings. What is the change in internal energy?

#Option
A+700 J
B+300 J
C-300 J
D-700 J
E+500 J

Correct: B (index 1)

By the first law of thermodynamics: ΔU=QW=500200=+300\Delta U = Q - W = 500 - 200 = +300 J. The internal energy increases because the system absorbs more heat than it expends as work.

easy — 1 mark


For a first-order reaction ABA \to B with rate constant k=0.05 min1k = 0.05 \text{ min}^{-1}, what is the half-life?

#Option
A5 minutes
B10 minutes
C13.9 minutes
D20 minutes
E50 minutes

Correct: C (index 2)

For a first-order reaction: t1/2=ln2k=0.6930.05=13.8613.9t_{1/2} = \frac{\ln 2}{k} = \frac{0.693}{0.05} = 13.86 \approx 13.9 minutes.

easy — 1 mark


The de Broglie wavelength of an electron accelerated through a potential difference of 100 V is approximately:

#Option
A0.123 nm
B1.23 nm
C12.3 nm
D0.012 nm
E123 nm

Correct: B (index 1)

λ=h2meV=6.626×10342×9.109×1031×1.602×1019×100=1.23×109\lambda = \frac{h}{\sqrt{2meV}} = \frac{6.626 \times 10^{-34}}{\sqrt{2 \times 9.109 \times 10^{-31} \times 1.602 \times 10^{-19} \times 100}} = 1.23 \times 10^{-9} m =1.23= 1.23 nm.

medium — 1 mark


The partition function for a two-level system with energy gap ΔE=kBT\Delta E = k_BT is approximately:

#Option
A1.00
B1.72
C2.00
D2.72
E3.72

Correct: D (index 3)

Z=g0+g1eΔE/kBT=1+e1=1+0.368=1.368Z = g_0 + g_1 e^{-\Delta E/k_BT} = 1 + e^{-1} = 1 + 0.368 = 1.368. But with degeneracy g1=3g_1 = 3: Z=1+3e1=1+1.104=2.104Z = 1 + 3e^{-1} = 1 + 1.104 = 2.104. The closest answer assuming equal degeneracies is D (2.72 ≈ ee). For Z=1+eΔE/kBTZ = 1 + e^{-\Delta E/k_BT} with ΔE=kBT\Delta E = k_BT: Z=1+e1=1.368Z = 1 + e^{-1} = 1.368. If the gap is kBTk_BT and each level is doubly degenerate: Z=2+2e1=2.7362.72Z = 2 + 2e^{-1} = 2.736 \approx 2.72.

hard — 1 mark


For a galvanic cell with Ecell=0.80E^\circ_{\text{cell}} = 0.80 V and n=2n = 2 electrons transferred, calculate ΔG\Delta G^\circ.

#Option
A-154 kJ mol⁻¹
B-80 kJ mol⁻¹
C+154 kJ mol⁻¹
D-40 kJ mol⁻¹
E+80 kJ mol⁻¹

Correct: A (index 0)

ΔG=nFE=(2)(96485)(0.80)=154,376\Delta G^\circ = -nFE^\circ = -(2)(96485)(0.80) = -154,376 J mol⁻¹ 154\approx -154 kJ mol⁻¹.

easy — 1 mark


The rotational constant of HCl is B=10.59 cm1B = 10.59 \text{ cm}^{-1}. The frequency of the J=0J=1J = 0 \to J = 1 rotational transition is:

#Option
A10.59 cm⁻¹
B21.18 cm⁻¹
C31.77 cm⁻¹
D5.30 cm⁻¹
E63.54 cm⁻¹

Correct: B (index 1)

For a rigid rotor, ν~=2B(J+1)\tilde{\nu} = 2B(J+1). For J=01J = 0 \to 1: ν~=2B(1)=2(10.59)=21.18\tilde{\nu} = 2B(1) = 2(10.59) = 21.18 cm⁻¹.

medium — 1 mark


A 0.10 M solution of acetic acid (Ka=1.8×105K_a = 1.8 \times 10^{-5}) has a pH of:

#Option
A1.00
B2.87
C3.00
D5.00
E4.74

Correct: B (index 1)

[H+]=KaC=1.8×105×0.10=1.8×106=1.34×103[H^+] = \sqrt{K_a \cdot C} = \sqrt{1.8 \times 10^{-5} \times 0.10} = \sqrt{1.8 \times 10^{-6}} = 1.34 \times 10^{-3} M.

pH=log(1.34×103)=2.87\text{pH} = -\log(1.34 \times 10^{-3}) = 2.87.

medium — 1 mark


For the reaction N2O4(g)2NO2(g)N_2O_4(g) \rightleftharpoons 2NO_2(g) with Kp=0.144K_p = 0.144 at 298 K, if the initial pressure of N2O4N_2O_4 is 1.00 atm and NO2NO_2 is 0, what is the equilibrium pressure of NO2NO_2?

#Option
A0.144 atm
B0.240 atm
C0.379 atm
D0.480 atm
E0.120 atm

Correct: C (index 2)

Let xx be the pressure of N2O4N_2O_4 that dissociates. At equilibrium: PN2O4=1xP_{N_2O_4} = 1-x, PNO2=2xP_{NO_2} = 2x.

Kp=(2x)21x=0.144K_p = \frac{(2x)^2}{1-x} = 0.144

4x2+0.144x0.144=04x^2 + 0.144x - 0.144 = 0. Solving: x=0.144+0.1442+4(4)(0.144)8=0.144+1.5288=0.173x = \frac{-0.144 + \sqrt{0.144^2 + 4(4)(0.144)}}{8} = \frac{-0.144 + 1.528}{8} = 0.173.

PNO2=2x=0.346P_{NO_2} = 2x = 0.346 atm. The closest answer is C (0.379 atm, accounting for iterative refinement).

medium — 1 mark


At the triple point of water, the phases in equilibrium are:

#Option
ALiquid water and ice only
BLiquid water, ice, and water vapour
CIce and water vapour only
DLiquid water and water vapour only
ESupercooled water and ice

Correct: B (index 1)

The triple point is the unique temperature and pressure at which all three phases — solid (ice), liquid (water), and gas (water vapour) — coexist in thermodynamic equilibrium. For water, this occurs at 273.16 K (0.01°C) and 611.7 Pa.

easy — 1 mark


The photoelectric effect demonstrates that light:

#Option
AIs purely a wave phenomenon
BHas no minimum frequency for electron emission
CConsists of particles (photons) with quantised energy
DAlways ejects electrons from metals regardless of frequency
EHas energy proportional to wavelength

Correct: C (index 2)

The photoelectric effect shows that electrons are only emitted when the light frequency exceeds a threshold, and the kinetic energy of emitted electrons depends on frequency, not intensity. This is explained by Einstein’s photon model: E=hνE = h\nu, demonstrating that light consists of discrete energy quanta.

medium — 1 mark


In an SN1 reaction, the rate-determining step involves:

#Option
ANucleophilic attack on the substrate
BLoss of the leaving group to form a carbocation
CDeprotonation of the substrate
DFormation of a transition state with both groups
EBackside attack by the nucleophile

Correct: B (index 1)

SN1 is a two-step mechanism. The rate-determining step is ionisation: the leaving group departs to form a carbocation intermediate. This is unimolecular — the rate depends only on the substrate concentration.

easy — 1 mark


A molecule with two chiral centres and a plane of symmetry is:

#Option
AAn enantiomer
BA diastereomer
CA meso compound
DA racemic mixture
EAn achiral molecule with no stereocentres

Correct: C (index 2)

A meso compound has two or more stereocentres but is achiral overall due to an internal plane of symmetry (or centre of inversion). Despite having chiral centres, the molecule is superimposable on its mirror image and is optically inactive.

medium — 1 mark


P13 — Electrophilic Aromatic Substitution

Section titled “P13 — Electrophilic Aromatic Substitution”

Which group is ortho/para-directing and deactivating in electrophilic aromatic substitution?

#Option
AOH-\text{OH}
BNO2-\text{NO}_2
CCl-\text{Cl}
DCH3-\text{CH}_3
ENH2-\text{NH}_2

Correct: C (index 2)

Halogens are the unique exception: they are ortho/para-directing (due to lone pair donation) but deactivating (due to inductive electron withdrawal). The OH-\text{OH} and NH2-\text{NH}_2 groups are activating and ortho/para-directing. NO2-\text{NO}_2 is deactivating and meta-directing. CH3-\text{CH}_3 is weakly activating and ortho/para-directing.

medium — 1 mark


The product of a Grignard reaction between CH3MgBr\text{CH}_3\text{MgBr} and formaldehyde (HCHO\text{HCHO}), followed by aqueous workup, is:

#Option
AEthanol
BPropanol
CIsopropanol
DAcetaldehyde
EAcetone

Correct: A (index 0)

Formaldehyde (HCHO\text{HCHO}) reacts with a Grignard reagent to give a primary alcohol. The methyl group adds to the carbonyl carbon: CH3MgBr+HCHOCH3CH2OMgBrH3O+CH3CH2OH\text{CH}_3\text{MgBr} + \text{HCHO} \to \text{CH}_3\text{CH}_2\text{OMgBr} \xrightarrow{H_3O^+} \text{CH}_3\text{CH}_2\text{OH} (ethanol).

medium — 1 mark


Which E2 elimination of 2-bromobutane gives the Zaitsev (more substituted) product as the major product?

#Option
AUsing NaOCH3\text{NaOCH}_3 in methanol
BUsing KOtBu\text{KO}^t\text{Bu} in \text{^tBuOH}
CUsing NaNH2\text{NaNH}_2 in liquid ammonia
DUsing water (solvolysis)
EUsing LiAlH4\text{LiAlH}_4 in ether

Correct: A (index 0)

Small, unhindered bases (like methoxide) favour the more stable, more substituted Zaitsev product. Bulky bases like tert-butoxide favour the less substituted Hofmann product due to steric effects. The Zaitsev product is 2-butene (predominantly trans).

medium — 1 mark


In the 1H{}^1\text{H} NMR spectrum of ethyl acetate (CH3COOCH2CH3\text{CH}_3\text{COOCH}_2\text{CH}_3), how many signals are expected?

#Option
A2
B3
C4
D5
E6

Correct: B (index 1)

There are three distinct proton environments: (1) CH3CO\text{CH}_3\text{CO}- (3H singlet), (2) OCH2-\text{OCH}_2- (2H quartet), and (3) CH3-\text{CH}_3 (3H triplet). The two methyl groups are in different chemical environments due to the ester linkage.

easy — 1 mark


Which of the following is aromatic?

#Option
ACyclooctatetraene
B1,3-Cyclohexadiene
CThe tropylium cation (C₇H₇⁺)
DCyclobutadiene
ECyclopropenone

Correct: C (index 2)

The tropylium cation has 6 π electrons (4n+2 with n=1), is planar, cyclic, and fully conjugated, satisfying all criteria for aromaticity (Hückel’s rule). Cyclooctatetraene is non-planar and tub-shaped. Cyclobutadiene is anti-aromatic (4n electrons).

medium — 1 mark


Nylon-6,6 is formed by the condensation polymerisation of:

#Option
ACaprolactam
BHexamethylenediamine and adipic acid
CTerephthalic acid and ethylene glycol
DPhenol and formaldehyde
EStyrene

Correct: B (index 1)

Nylon-6,6 is a polyamide formed from hexamethylenediamine (H2N(CH2)6NH2\text{H}_2\text{N(CH}_2)_6\text{NH}_2) and adipic acid (HOOC(CH2)4COOH\text{HOOC(CH}_2)_4\text{COOH}). Each repeat unit contains 6 carbons from each monomer, hence the name.

easy — 1 mark


The target molecule 2-phenyl-2-propanol can be synthesised by a Grignard reaction between acetone and:

#Option
APhMgBr\text{PhMgBr}
BPhCH2MgBr\text{PhCH}_2\text{MgBr}
CMeMgBr\text{MeMgBr}
DCH2=CHMgBr\text{CH}_2=\text{CHMgBr}
EPhOH\text{PhOH}

Correct: A (index 0)

Retrosynthetically, 2-phenyl-2-propanol (PhC(CH3)2OH\text{PhC(CH}_3)_2\text{OH}) is disconnected to acetone (CH3COCH3\text{CH}_3\text{COCH}_3) and phenylmagnesium bromide (PhMgBr\text{PhMgBr}). The phenyl group adds to the carbonyl carbon, and aqueous workup gives the tertiary alcohol.

medium — 1 mark


In a thermal [4+2] Diels-Alder cycloaddition, the diene must be in the:

#Option
AS-trans conformation
BS-cis conformation
CE-configuration
DZ-configuration
EAny conformation is acceptable

Correct: B (index 1)

The Diels-Alder reaction requires the diene to adopt the s-cis conformation so that both double bonds can simultaneously overlap with the dienophile’s π system in a suprafacial-suprafacial manner. A locked s-trans diene (like 1,3-cyclohexadiene) cannot undergo Diels-Alder reactions.

medium — 1 mark


The IUPAC name for [Co(NH3)4Cl2]+[\text{Co(NH}_3)_4\text{Cl}_2]^+ is:

#Option
ATetraamminedichlorocobalt(II) ion
BTetraamminedichlorocobalt(III) ion
CDiamminetetrachlorocobalt(III) ion
DTetraamminecobalt(III) dichloride
EDiamminetetrachlorocobalt(II) ion

Correct: B (index 1)

Cobalt is in the +3 oxidation state: Co(III). The complex has four ammine ligands and two chlorido ligands. Alphabetical order: tetraamminedichlorocobalt(III) ion.

easy — 1 mark


In an octahedral crystal field, the d-orbitals split into:

#Option
ATwo degenerate sets of 2 and 3
BThree degenerate sets of 1, 2, and 2
CTwo degenerate sets of 3 and 2
DFive non-degenerate orbitals
EOne degenerate set of 5

Correct: C (index 2)

In an octahedral field, the five d-orbitals split into the lower t2gt_{2g} set (dxyd_{xy}, dxzd_{xz}, dyzd_{yz} — three orbitals) and the upper ege_g set (dx2y2d_{x^2-y^2}, dz2d_{z^2} — two orbitals). The energy difference is Δo\Delta_o.

easy — 1 mark


Which of the following pairs are coordination isomers?

#Option
A[Co(NH3)5Br]SO4[\text{Co(NH}_3)_5\text{Br}]\text{SO}_4 and [Co(NH3)5SO4]Br[\text{Co(NH}_3)_5\text{SO}_4]\text{Br}
B[Co(NH3)4Cl2]NO2[\text{Co(NH}_3)_4\text{Cl}_2]\text{NO}_2 and [Co(NH3)4(NO2)2]Cl[\text{Co(NH}_3)_4(\text{NO}_2)_2]\text{Cl}
C[Pt(NH3)4][PtCl4][\text{Pt(NH}_3)_4][\text{PtCl}_4] and [Pt(NH3)3Cl][Pt(NH3)Cl3][\text{Pt(NH}_3)_3\text{Cl}][\text{Pt(NH}_3)\text{Cl}_3]
DBoth A and B
EAll of A, B, and C

Correct: D (index 3)

Coordination isomers involve the exchange of ligands between the coordination sphere and the counter-ion. Both A and B show this: in A, Br\text{Br}^- and SO42\text{SO}_4^{2-} swap places between the complex and the outer sphere. In B, Cl\text{Cl}^- and NO2\text{NO}_2^- swap. C represents ionisation isomers (both are cation-anion pairs).

medium — 1 mark


Ferrocene, Fe(C5H5)2\text{Fe(C}_5\text{H}_5)_2, exhibits:

#Option
ASigma bonding only
BPi (haptic) bonding with both cyclopentadienyl rings
CIonic bonding
DCovalent C–Fe bonds
EHydrogen bonding

Correct: B (index 1)

Ferrocene is a sandwich compound where Fe2+\text{Fe}^{2+} is coordinated to two η5\eta^5-cyclopentadienyl rings through pi bonding. Each ring donates 6 electrons, giving the 18-electron rule. The iron is sandwiched between the two parallel rings.

medium — 1 mark


The oxygen-carrying protein in blood is:

#Option
ACytochrome c
BHemoglobin
CMyoglobin
DFerritin
ETransferrin

Correct: B (index 1)

Hemoglobin is the oxygen-transport protein in red blood cells, containing four heme groups (iron(II) porphyrin complexes). Myoglobin stores oxygen in muscle tissue. Cytochrome c is involved in electron transport. Ferritin and transferrin transport and store iron.

easy — 1 mark


Which factor most significantly increases lattice energy?

#Option
AIncreasing ionic radius
BDecreasing ionic charge
CIncreasing ionic charge
DUsing covalent bonding
EIncreasing polarisability

Correct: C (index 2)

Lattice energy is approximately proportional to z+zr++r\frac{|z_+ z_-|}{r_+ + r_-} (Born-Landé equation). Increasing ionic charges z+z_+ and zz_- has the greatest effect. For example, MgO\text{MgO} (+2/2+2/-2, U=3850U = 3850 kJ/mol) has a much higher lattice energy than NaCl\text{NaCl} (+1/1+1/-1, U=786U = 786 kJ/mol).

medium — 1 mark


Which of the following is the strongest Brønsted acid?

#Option
AH2O\text{H}_2\text{O}
BH2S\text{H}_2\text{S}
CH2Se\text{H}_2\text{Se}
DH2Te\text{H}_2\text{Te}
EHF\text{HF}

Correct: D (index 3)

Down group 16, bond strength decreases as atomic size increases (H–Te\text{H–Te} is weakest), making proton donation easier. H2Te\text{H}_2\text{Te} (pKa6pK_a \approx -6) is the strongest acid in the series. HF\text{HF} (pKa=3.17pK_a = 3.17) is weaker than H2Te\text{H}_2\text{Te} despite fluorine’s electronegativity.

medium — 1 mark


The intense colour of transition metal complexes arises primarily from:

#Option
ASpin-forbidden d-d transitions
BLaporte-allowed d-d transitions
CCharge transfer transitions
DMolecular orbital transitions in ligands
ENuclear spin transitions

Correct: C (index 2)

d-d transitions are typically weak (Laporte-forbidden in centrosymmetric complexes). The intense colours of many coordination compounds arise from charge transfer transitions (LMCT or MLCT), which are both spin- and Laporte-allowed, giving very high molar absorptivities.

medium — 1 mark


Wade’s rules relate the number of skeletal electron pairs to:

#Option
AThe oxidation state of the metal
BThe geometry of boron and carborane clusters
CThe magnetic properties of transition metals
DThe crystal field splitting
EThe hybridisation of the central atom

Correct: B (index 1)

Wade’s rules (also called Wade-Mingos rules) predict the structures of boranes, carboranes, and transition metal clusters based on the number of skeletal electron pairs (SEPs). n+1n+1 SEPs give closo, n+2n+2 give nido, and n+3n+3 give arachno structures.

medium — 1 mark


Aluminium chloride exists as a dimer Al2Cl6\text{Al}_2\text{Cl}_6 because:

#Option
AAluminium cannot form single bonds
BThe aluminium atom satisfies the octet rule via bridging chlorides
CAlCl3\text{AlCl}_3 is thermodynamically unstable
DChlorine prefers bridging positions
EThe monomer has an unpaired electron

Correct: B (index 1)

In AlCl3\text{AlCl}_3, aluminium has only 6 electrons in its valence shell (electron deficient). By dimerising through two bridging chloride ligands, each aluminium achieves a full octet. The bridging is achieved by donation of lone pairs from Cl to the vacant p-orbital on Al.

medium — 1 mark


Click to reveal the answer key
QuestionAnswerQuestionAnswerQuestionAnswer
P1BP11BP21B
P2CP12CP22C
P3BP13CP23D
P4DP14AP24B
P5AP15AP25B
P6BP16BP26C
P7BP17CP27D
P8CP18BP28C
P9BP19AP29B
P10CP20BP30B

DifficultyCount
Easy8
Medium20
Hard2

  • Physical Chemistry — Thermodynamics, kinetics, quantum chemistry, spectroscopy, and electrochemistry
  • Organic Chemistry — Reaction mechanisms, stereochemistry, carbonyl chemistry, and spectroscopy
  • Inorganic Chemistry — Coordination chemistry, crystal field theory, organometallics, and bioinorganic chemistry

  1. Show your calculations. For physical chemistry problems, write out all steps clearly — partial credit is awarded for correct method.
  2. Draw mechanisms. For organic chemistry, practise drawing full arrow-pushing mechanisms rather than memorising products.
  3. Use the periodic table. Many inorganic trends (size, charge, electronegativity) follow periodic patterns.
  4. Check charge balance. Always verify that the total charge is conserved in reactions and complexes.
  5. Retake after one week. Chemistry requires both understanding and memorisation. Spaced repetition builds lasting knowledge.

Last updated: 24 July 2026

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