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PCAT (Pharmacy College Admission Test) Chemical Processes Syllabus

The Chemical Processes syllabus for PCAT (Pharmacy College Admission Test) in full: 5 chapters, 17 topics and 51 sub-topics, every one listed below, plus 51 Chemical Processes flashcards with answers.

5Chapters
17Topics
51Sub-topics
51Flashcards

Chemical Processes syllabus: all 5 chapters

Expand any chapter to see its topics and sub-topics.

  1. General Chemistry: Atomic and Molecular Structure

    3 topics
    • Atomic Theory and Electron Configuration
      • Quantum numbers and orbitals
      • Electron configuration and exceptions
      • Periodic trends
    • Chemical Bonding
      • Ionic, covalent, and metallic bonds
      • Lewis structures and formal charge
      • VSEPR theory and molecular geometry
      • Hybridization and polarity
    • Intermolecular Forces
      • Hydrogen bonding and dipole interactions
      • London dispersion forces
      • Effects on physical properties
  2. General Chemistry: Reactions and Stoichiometry

    3 topics
    • Chemical Reactions and Balancing
      • Reaction types and predicting products
      • Oxidation-reduction reactions
      • Net ionic equations
    • Stoichiometry
      • Mole concept and molar mass
      • Limiting reactants and percent yield
      • Empirical and molecular formulas
    • Gases and Solutions
      • Ideal gas law and gas laws
      • Concentration units and molarity
      • Colligative properties
  3. General Chemistry: Thermodynamics, Kinetics, and Equilibrium

    4 topics
    • Thermochemistry
      • Enthalpy, entropy, and Gibbs free energy
      • Hess's law and calorimetry
    • Chemical Kinetics
      • Reaction rates and rate laws
      • Activation energy and catalysts
      • Reaction mechanisms
    • Chemical Equilibrium
      • Equilibrium constants and reaction quotient
      • Le Chatelier's principle
    • Acids, Bases, and Electrochemistry
      • pH, pKa, and buffer systems
      • Titrations and indicators
      • Galvanic and electrolytic cells
  4. Organic Chemistry: Structure and Reactivity

    4 topics
    • Bonding and Functional Groups
      • Hybridization in organic molecules
      • Identifying functional groups
      • IUPAC nomenclature
    • Stereochemistry
      • Chirality and enantiomers
      • R/S and E/Z designations
      • Conformational analysis
    • Reaction Mechanisms
      • Nucleophilic substitution (SN1/SN2)
      • Elimination reactions (E1/E2)
      • Addition reactions of alkenes and alkynes
    • Functional Group Chemistry
      • Alcohols, ethers, and epoxides
      • Aldehydes, ketones, and carbonyl chemistry
      • Carboxylic acids and derivatives
      • Aromatic substitution reactions
  5. Basic Biochemistry

    3 topics
    • Biomolecules
      • Amino acids and protein structure
      • Carbohydrates and their classification
      • Lipids and membrane components
      • Nucleotides and nucleic acids
    • Enzymes and Catalysis
      • Enzyme mechanisms and active sites
      • Inhibition and Michaelis-Menten kinetics
    • Metabolic Pathways
      • Carbohydrate metabolism overview
      • Lipid and protein metabolism
      • Energy currency and ATP yield

PCAT (Pharmacy College Admission Test) Chemical Processes flashcards — 51 questions with answers

  1. What four quantum numbers describe an electron, and what does each specify?

    $n$ (principal) = energy level/shell; $l$ (azimuthal) = subshell shape ($s,p,d,f$); $m_l$ (magnetic) = orbital orientation, ranging $-l$ to $+l$; $m_s$ (spin) = $+\tfrac{1}{2}$ or $-\tfrac{1}{2}$.

  2. State the Aufbau principle, Pauli exclusion principle, and Hund's rule.

    Aufbau: fill lowest-energy orbitals first. Pauli: no two electrons share all four quantum numbers (max 2 per orbital, opposite spins). Hund's: fill degenerate orbitals singly with parallel spins before pairing.

  3. Write the ground-state electron configuration of iron ($\ce{Fe}$, $Z=26$).

    $1s^{2}\,2s^{2}\,2p^{6}\,3s^{2}\,3p^{6}\,4s^{2}\,3d^{6}$, or $[\ce{Ar}]\,4s^{2}\,3d^{6}$.

  4. How do atomic radius, ionization energy, and electronegativity trend across a period (left to right)?

    Atomic radius decreases; ionization energy increases; electronegativity increases (due to increasing effective nuclear charge).

  5. Distinguish ionic, covalent, and metallic bonding.

    Ionic: electron transfer between metal and nonmetal forming cations/anions held by electrostatic attraction. Covalent: shared electron pairs between nonmetals. Metallic: cations in a delocalized 'sea' of electrons.

  6. What is the difference between a polar covalent and nonpolar covalent bond?

    Polar covalent: unequal electron sharing due to an electronegativity difference (roughly $0.4$–$1.7$), creating partial charges. Nonpolar covalent: nearly equal sharing (difference $<0.4$).

  7. In VSEPR theory, what are the molecular geometries for 2, 3, and 4 electron domains (no lone pairs)?

    2 domains: linear ($180^{\circ}$); 3 domains: trigonal planar ($120^{\circ}$); 4 domains: tetrahedral ($109.5^{\circ}$).

  8. What hybridization corresponds to linear, trigonal planar, and tetrahedral geometries?

    Linear: $sp$; trigonal planar: $sp^{2}$; tetrahedral: $sp^{3}$.

  9. List the three main types of intermolecular forces from weakest to strongest.

    London dispersion forces (weakest) $<$ dipole-dipole forces $<$ hydrogen bonding (strongest of the three).

  10. What conditions are required for hydrogen bonding?

    An H atom covalently bonded to a highly electronegative atom (N, O, or F) interacting with a lone pair on another N, O, or F atom.

  11. How do intermolecular forces affect boiling point and vapor pressure?

    Stronger intermolecular forces raise boiling point (more energy to separate molecules) and lower vapor pressure (fewer molecules escape to gas phase).

  12. Identify the five major types of chemical reactions.

    Synthesis (combination), decomposition, single displacement, double displacement (metathesis), and combustion.

  13. Balance the combustion of propane: $\ce{C3H8 + O2 -> CO2 + H2O}$.

    $\ce{C3H8 + 5O2 -> 3CO2 + 4H2O}$.

  14. What is conserved in a balanced chemical equation, and what principle requires it?

    The number of atoms of each element (and total mass and charge) is conserved, required by the law of conservation of mass.

  15. Define a mole and state Avogadro's number.

    A mole is the amount of substance containing $6.022\times10^{23}$ particles (Avogadro's number, $N_A$).

  16. How do you find the limiting reagent in a reaction?

    Convert each reactant to moles of product using stoichiometric ratios; the reactant yielding the least product is the limiting reagent.

  17. Define percent yield and give its formula.

    Percent yield measures reaction efficiency: $$\%\text{ yield} = \frac{\text{actual yield}}{\text{theoretical yield}}\times100\%.$$

  18. State the ideal gas law and identify each variable.

    $$PV = nRT$$ where $P$ = pressure, $V$ = volume, $n$ = moles, $R$ = gas constant ($0.0821\,\text{L·atm·mol}^{-1}\text{K}^{-1}$), $T$ = absolute temperature (K).

  19. State Boyle's, Charles's, and Gay-Lussac's gas laws.

    Boyle's: $P_1V_1 = P_2V_2$ (constant $T$). Charles's: $\frac{V_1}{T_1}=\frac{V_2}{T_2}$ (constant $P$). Gay-Lussac's: $\frac{P_1}{T_1}=\frac{P_2}{T_2}$ (constant $V$).

  20. State Dalton's law of partial pressures.

    The total pressure of a gas mixture equals the sum of the partial pressures of its components: $P_{\text{total}} = P_1 + P_2 + \cdots + P_n$.

Show the other 31 Chemical Processes flashcards
  1. Define molarity and molality with their formulas.

    Molarity $M = \frac{\text{moles solute}}{\text{liters solution}}$; molality $m = \frac{\text{moles solute}}{\text{kg solvent}}$.

  2. List the four colligative properties of solutions.

    Vapor pressure lowering, boiling point elevation, freezing point depression, and osmotic pressure — all depend on the number of solute particles, not their identity.

  3. Give the formulas for boiling point elevation and freezing point depression.

    $\Delta T_b = i K_b m$ and $\Delta T_f = i K_f m$, where $i$ is the van't Hoff factor and $m$ is molality.

  4. State the first law of thermodynamics and the enthalpy sign conventions.

    $\Delta U = q + w$ (energy is conserved). For enthalpy: exothermic $\Delta H < 0$ (releases heat); endothermic $\Delta H > 0$ (absorbs heat).

  5. State Hess's law.

    The total enthalpy change of a reaction is the sum of the enthalpy changes of its steps, independent of pathway: $\Delta H_{\text{rxn}} = \sum \Delta H_{\text{steps}}$.

  6. Write the Gibbs free energy equation and the spontaneity criterion.

    $$\Delta G = \Delta H - T\Delta S$$ A reaction is spontaneous when $\Delta G < 0$, at equilibrium when $\Delta G = 0$, nonspontaneous when $\Delta G > 0$.

  7. How is heat calculated from specific heat capacity?

    $$q = mc\Delta T$$ where $m$ = mass, $c$ = specific heat capacity, and $\Delta T$ = temperature change.

  8. Write the general rate law and define reaction order.

    $\text{rate} = k[\ce{A}]^{m}[\ce{B}]^{n}$; the order in each reactant is its exponent, and the overall order is $m+n$. Orders are determined experimentally.

  9. How does a catalyst affect a reaction?

    A catalyst lowers the activation energy ($E_a$), speeding both forward and reverse rates, without being consumed or changing $\Delta G$, $\Delta H$, or equilibrium position.

  10. Give the half-life expression for a first-order reaction.

    $$t_{1/2} = \frac{0.693}{k}$$ It is independent of initial concentration for first-order reactions.

  11. State the Arrhenius equation and what it relates.

    $$k = A e^{-E_a/RT}$$ It relates the rate constant $k$ to activation energy $E_a$ and temperature $T$; higher $T$ or lower $E_a$ increases $k$.

  12. State Le Chatelier's principle.

    When a system at equilibrium is disturbed (change in concentration, pressure, or temperature), it shifts to counteract the disturbance and restore equilibrium.

  13. Write the equilibrium constant expression for $\ce{aA + bB <=> cC + dD}$.

    $$K_{eq} = \frac{[\ce{C}]^{c}[\ce{D}]^{d}}{[\ce{A}]^{a}[\ce{B}]^{b}}$$ Pure solids and liquids are omitted.

  14. How does the reaction quotient $Q$ predict the direction of an equilibrium shift?

    If $Q < K$, reaction shifts forward (toward products); if $Q > K$, shifts reverse (toward reactants); if $Q = K$, at equilibrium.

  15. Define Arrhenius, Brønsted-Lowry, and Lewis acids.

    Arrhenius acid: produces $\ce{H+}$ in water. Brønsted-Lowry acid: proton ($\ce{H+}$) donor. Lewis acid: electron-pair acceptor.

  16. Give the definitions of pH and pOH, and their relationship at $25^{\circ}\text{C}$.

    $\text{pH} = -\log[\ce{H+}]$, $\text{pOH} = -\log[\ce{OH-}]$, and $\text{pH} + \text{pOH} = 14$.

  17. Write the Henderson-Hasselbalch equation for a buffer.

    $$\text{pH} = \text{p}K_a + \log\frac{[\text{A}^{-}]}{[\text{HA}]}$$ used to find buffer pH from the conjugate base/acid ratio.

  18. In electrochemistry, what occurs at the anode and cathode, and where is oxidation?

    Oxidation (loss of electrons) occurs at the anode; reduction (gain of electrons) at the cathode. Mnemonic: 'An Ox, Red Cat.'

  19. How is standard cell potential calculated, and what sign indicates a galvanic cell?

    $E^{\circ}_{\text{cell}} = E^{\circ}_{\text{cathode}} - E^{\circ}_{\text{anode}}$. A positive $E^{\circ}_{\text{cell}}$ (with $\Delta G < 0$) indicates a spontaneous galvanic cell.

  20. Identify the functional groups: $\ce{-OH}$, $\ce{-COOH}$, $\ce{-CHO}$, and $\ce{-NH2}$.

    $\ce{-OH}$ = hydroxyl (alcohol); $\ce{-COOH}$ = carboxyl (carboxylic acid); $\ce{-CHO}$ = carbonyl as aldehyde; $\ce{-NH2}$ = amino (amine).

  21. Define structural isomers, enantiomers, and diastereomers.

    Structural isomers: same formula, different connectivity. Enantiomers: nonsuperimposable mirror images. Diastereomers: stereoisomers that are not mirror images.

  22. What is a chiral center, and how do R/S configurations get assigned?

    A chiral center is a carbon bonded to four different groups. Assign R/S by ranking substituents (CIP priority); with lowest priority pointing away, clockwise $1\to2\to3$ = R, counterclockwise = S.

  23. Compare $\text{S}_\text{N}1$ and $\text{S}_\text{N}2$ reaction mechanisms.

    $\text{S}_\text{N}1$: two steps via carbocation, first-order, favors tertiary substrates and polar protic solvents, racemization. $\text{S}_\text{N}2$: one step, second-order, favors primary substrates and strong nucleophiles, inversion of configuration.

  24. Compare E1 and E2 elimination mechanisms.

    E1: two steps via carbocation, first-order, weak base, favors tertiary substrates. E2: concerted, second-order, strong base, requires anti-periplanar geometry; both form alkenes following Zaitsev's rule.

  25. What products form when a carboxylic acid reacts with an alcohol (Fischer esterification)?

    An ester and water: $\ce{RCOOH + R'OH <=> RCOOR' + H2O}$ (acid-catalyzed, reversible).

  26. Name the four major classes of biomolecules and their monomers.

    Carbohydrates (monosaccharides), proteins (amino acids), lipids (fatty acids + glycerol; not true polymers), and nucleic acids (nucleotides).

  27. What bond links amino acids, and what reaction forms it?

    A peptide bond (an amide linkage) forms between the carboxyl of one amino acid and the amino group of another via a dehydration (condensation) reaction.

  28. Describe the four levels of protein structure.

    Primary: amino acid sequence. Secondary: local folding ($\alpha$-helices, $\beta$-sheets) via H-bonds. Tertiary: overall 3D shape. Quaternary: assembly of multiple polypeptide subunits.

  29. How do enzymes catalyze reactions, and what is the active site?

    Enzymes lower activation energy by binding substrate at the active site (induced-fit model), stabilizing the transition state without altering reaction equilibrium or $\Delta G$.

  30. Compare competitive and noncompetitive enzyme inhibition in terms of $V_{max}$ and $K_m$.

    Competitive: binds active site; $K_m$ increases, $V_{max}$ unchanged (overcome by more substrate). Noncompetitive: binds allosteric site; $V_{max}$ decreases, $K_m$ unchanged.

  31. Summarize glycolysis: starting molecule, products, and net ATP yield.

    Glycolysis converts one glucose ($\ce{C6H12O6}$) into 2 pyruvate, with a net gain of 2 ATP and 2 NADH; it occurs in the cytoplasm and is anaerobic.

PCAT (Pharmacy College Admission Test) Chemical Processes FAQ

What is in the PCAT (Pharmacy College Admission Test) Chemical Processes syllabus?

PCAT (Pharmacy College Admission Test) Chemical Processes is split into 5 chapters: General Chemistry: Atomic and Molecular Structure, General Chemistry: Reactions and Stoichiometry, General Chemistry: Thermodynamics, Kinetics, and Equilibrium, Organic Chemistry: Structure and Reactivity and Basic Biochemistry. Together they contain 17 topics and 51 sub-topics.

How many chapters are in PCAT (Pharmacy College Admission Test) Chemical Processes?

5 chapters, containing 17 topics and 51 sub-topics. The largest chapter is General Chemistry: Thermodynamics, Kinetics, and Equilibrium, with 4 topics.

Are there flashcards for PCAT (Pharmacy College Admission Test) Chemical Processes?

Yes — a 51-card Chemical Processes deck, printed in full in the flashcards section of this page and available in the Examius app with spaced repetition. The free plan covers one exam of your choice, including its flashcards; Examius Pro, a one-time purchase, unlocks every other exam and deck.