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CHEM 104/ CHEM104 Module 2 Exam (Latest 2026/2027 Update) | Complete Exam Questions with Verified Answers and Detailed Rationales | Acid-Base Chemistry, Equilibrium, pH, Buffers, Titrations | A+ Graded

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INSTANT PDF DOWNLOAD – This is the comprehensive Module 2 Exam study guide for CHEM 104 General Chemistry II with Lab at Portage Learning (Latest 2026/2027 Update), featuring verified exam questions with correct answers and detailed rationales. Covers acid-base chemistry (identifying acids/bases/salts, Brønsted-Lowry theory, strong vs weak acids, Ka), equilibrium reactions and Le Chatelier’s principle, buffer solutions and pH calculations, and titration calculations. Aligned with Portage Learning CHEM 104 curriculum. CHEM 104 Module 2 Exam Portage Acid Base Chemistry Bronsted Lowry Acid Proton Donor Bronsted Lowry Base Proton Acceptor Strong Acid Weak Acid Ka Le Chatelier Principle Equilibrium Shift Equilibrium Constant Kc Keq Buffer Solution Henderson Hasselbalch Titration Calculations Ka Acid Dissociation Constant pH pOH Calculations General Chemistry II Module 2 Portage Learning CHEM 104 A+ Grade Chemistry Study Guide

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2 MAXE · 401 MEHC

University of Wisconsin–Madison
College of Letters & Science — Department of Chemistry
NUMEN LUMEN
EST. 1848
NUMEN LUMEN · GOD, OUR LIGHT




CHEM 104 EXAM 2
E Q U I L I B R I U M · AC I D S & B A S E S · B U F F E RS · T I T RAT I O N S · S O LU B I L I TY

INSTITUTION University of Wisconsin–Madison COURSE CODE CHEM 104
PROGRAM Bachelor of Science — General ACADEMIC YEAR
Chemistry Sequence
EXAM TITLE CHEM 104 EXAM 2 TOTAL QUESTIONS 131 Questions
COURSE TITLE General Chemistry II FORMAT Multiple Choice — Select the
Single Best Answer


EXAMINATION INSTRUCTIONS
▸ Select the single best answer for each question.
▸ Equilibrium constants, Le Chatelier's principle, acid-base theories, buffer systems, titration curves, and
solubility equilibria are core testable content.
▸ ICE table calculations, pH/pKa relationships, and Ksp problems are emphasized.
▸ Correct answers and clinical/academic rationales appear below each question for review.
▸ All content reflects CHEM 104 General Chemistry II — Exam 2 learning objectives.

, SECTION I — EQUILIBRIUM, ACIDS & BASES, BUFFERS,
Questions 1 – 131
TITRATIONS, SOLUBILITY

1. According to the Arrhenius definition, an acid is a substance that does what in aqueous
solution?
A. Increases the concentration of hydroxide ions
B. Increases the concentration of hydronium ions/protons
C. Donates a lone pair of electrons
D. Decreases the concentration of all ions
CORRECT ANSWER B — Increases the concentration of hydronium ions/protons
RATIONALE An Arrhenius acid is a substance that increases the concentration of hydronium
ions (H₃O⁺) or protons (H⁺) in aqueous solution. This is the oldest and most
restrictive acid definition. An Arrhenius base (A) increases OH⁻ concentration. A
Lewis base (C) donates an electron pair. Option D is incorrect — acids increase,
not decrease, ion concentration.

2. A student compares two weak acids: Acid A has a pKa of 3.2, and Acid B has a pKa of 9.5.
Which statement correctly relates pKa to acid strength?
A. Higher pKa means stronger acid; Acid B is stronger
B. Higher pKa means weaker acid; Acid A is stronger
C. pKa is unrelated to acid strength
D. Both acids have equal strength because both are weak acids
CORRECT ANSWER B — Higher pKa means weaker acid; Acid A is stronger
RATIONALE pKa = −log(Ka). The higher the pKa, the smaller the Ka, and the weaker the acid.
Acid A (pKa 3.2) is stronger than Acid B (pKa 9.5) because it has a lower pKa and
therefore a larger Ka. This inverse logarithmic relationship is fundamental to
comparing acid strengths. A strong acid like HCl has a very low (even negative)
pKa.

,3. The equilibrium constant for the dissolution of a sparingly soluble ionic compound is
called:
A. Ka — acid dissociation constant
B. Kb — base dissociation constant
C. Ksp — solubility product constant
D. Kw — ion product constant for water
CORRECT ANSWER C — Ksp — solubility product constant
RATIONALE Ksp is the solubility product constant — the equilibrium constant for the
dissolution of a sparingly soluble ionic solid into its constituent ions in aqueous
solution. For example, AgCl(s) ⇌ Ag⁺(aq) + Cl⁻(aq), Ksp = [Ag⁺][Cl⁻]. Ka (A) is for
acid dissociation. Kb (B) is for base dissociation. Kw (D) is the ion product
constant of water (1.0×10⁻¹⁴ at 25°C).


4. For the reaction A ⇌ B, the forward equilibrium constant is K = 4.0. What is the equilibrium
constant for the reverse reaction B ⇌ A?
A. 4.0
B. −4.0
C. 0.25
D. 16.0
CORRECT ANSWER C — 0.25
RATIONALE The equilibrium constant for a reverse reaction is the reciprocal of the forward
equilibrium constant: K_reverse = 1/K_forward. K = 4.0, so K_reverse = 1/4.0 =
0.25. This relationship holds because the products of the forward reaction
become the reactants of the reverse reaction, inverting the equilibrium
expression.

, 5. Which of the following is NOT one of the seven common strong acids?
A. HCl — hydrochloric acid
B. HNO₃ — nitric acid
C. HF — hydrofluoric acid
D. H₂SO₄ — sulfuric acid
CORRECT ANSWER C — HF — hydrofluoric acid
RATIONALE The seven strong acids are HCl, HBr, HI, HClO₃, HClO₄, HNO₃, and H₂SO₄. HF
(hydrofluoric acid) is notably a weak acid despite being a halogen acid — it only
partially ionizes in water due to the strong H–F bond. This is a common
misconception. All other options listed (HCl, HNO₃, H₂SO₄) are strong acids that
dissociate completely.


6. Le Chatelier's principle states that when stress is applied to a system at equilibrium, the
system will shift to relieve that stress. Which of the following are examples of such
stressors?
A. Concentration, temperature, pressure, and presence of a catalyst
B. Only concentration changes
C. Only temperature changes
D. Only pressure changes for gas reactions
CORRECT ANSWER A — Concentration, temperature, pressure, and presence of a catalyst
RATIONALE Stressors that can disturb a system at equilibrium include changes in
concentration (adding or removing reactants/products), temperature (exothermic
vs endothermic shifts), pressure (for gaseous systems with unequal moles of gas),
and the presence of a catalyst. Note: a catalyst speeds up the rate of reaching
equilibrium but does NOT shift the equilibrium position — it affects kinetics, not
thermodynamics.

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