Henderson-Hasselbalch Practice Problems: 12 Fully Worked Examples
These Henderson-Hasselbalch practice problems walk through every question type you’ll encounter in general chemistry, biochemistry, and MCAT-style exams — from basic pH calculations to buffer design, temperature correction, and titration. Each of the 12 Henderson-Hasselbalch example problems below shows every algebraic step so you can check your own work or learn the method from scratch. If you just need quick numeric answers, our companion Buffer pH Calculator solves any Henderson-Hasselbalch equation practice problem instantly.
Henderson-Hasselbalch Quick Reference
Before diving into the Henderson-Hasselbalch practice problems below, it helps to have all five common forms of the Henderson-Hasselbalch equation in one place. Every hasselbalch equation example on this page uses one of these five forms.
Henderson-Hasselbalch Practice Problems — 12 Worked Examples
Click “Show Solution” on any Henderson-Hasselbalch practice problem below to reveal the full step-by-step working. These Henderson-Hasselbalch example problems progress from basic pH calculations to comprehensive, exam-level buffer design questions.
Problem 1 — Basic pH from ConcentrationsBasic
Problem: A buffer contains 0.20 M acetic acid (pKa = 4.756) and 0.30 M sodium acetate. Find the pH using the Henderson-Hasselbalch equation.
Problem 2 — Find Concentrations from pHBasic
Problem: You need an acetate buffer at pH 5.0 (pKa = 4.756) with total concentration 0.5 M. Find [CH₃COOH] and [CH₃COO⁻] using the Henderson-Hasselbalch equation.
Problem 3 — Find pKa from pH and ConcentrationsBasic
Problem: A buffer at pH 7.2 contains 0.40 M H₂PO₄⁻ and 0.60 M HPO₄²⁻. Find pKa using the Henderson-Hasselbalch equation.
Problem 4 — Weak Base BufferIntermediate
Problem: An ammonia buffer (pKa of NH₄⁺ = 9.25) contains 0.15 M NH₃ and 0.05 M NH₄Cl. Find the pH using the Henderson-Hasselbalch equation.
Note: even though NH₃ is a weak base, the Henderson-Hasselbalch equation still applies using the pKa of its conjugate acid, NH₄⁺, with NH₃ playing the role of [A⁻] (base) and NH₄⁺ playing the role of [HA] (acid).
Problem 5 — Buffer Outside Effective RangeIntermediate
Problem: Calculate the pH of a buffer with pKa = 4.756, [A⁻] = 0.001 M, [HA] = 1.0 M using the Henderson-Hasselbalch equation.
The ratio [A⁻]/[HA] = 0.001 is far outside the effective buffering range of 0.1 to 10 (i.e., pH within ±1 of pKa). This is not an effective buffer — the Henderson-Hasselbalch equation still produces a numeric answer, but the solution will have almost no actual buffering capacity against added acid or base.
Problem 6 — Find Volume of NaOH to AddIntermediate
Problem: 500 mL of 0.1 M acetate buffer is at pH 4.756. How many mL of 1 M NaOH must be added to shift it to pH 5.0? (pKa = 4.756)
Problem 7 — Tris Buffer with Temperature CorrectionAdvanced
Problem: A Tris buffer is made at 25°C to pH 8.0 (pKa = 8.072 at 25°C). What is the pH at 37°C, given pKa changes by −0.031 per °C?
This is why Tris buffers are notorious in biochemistry labs — a Henderson-Hasselbalch calculation done at room temperature can be off by nearly half a pH unit once the buffer is used at body temperature, because Tris’s pKa is unusually temperature-sensitive compared to phosphate or acetate buffers.
Problem 8 — Buffer CapacityAdvanced
Problem: Calculate the maximum buffer capacity of a 0.2 M phosphate buffer.
This means the buffer can neutralize about 0.115 mol of strong acid per liter before the pH shifts by a full unit — but only when the buffer is at pH = pKa. Away from pKa, buffer capacity drops off, which connects directly to the effective range discussed in Problem 5.
Problem 9 — Multi-Step Buffer DesignAdvanced
Problem: Design a phosphate buffer at pH 7.4 with total [phosphate] = 50 mM in 1 L, using NaH₂PO₄ (MW = 120.0 g/mol) and Na₂HPO₄ (MW = 142.0 g/mol). pKa = 7.198.
This is a real laboratory buffer preparation calculation — the Henderson-Hasselbalch equation gives the molar ratio, and multiplying by molecular weight converts it into a practical recipe you can actually weigh out on a balance.
Problem 10 — MCAT-Style Conceptual QuestionConceptual
Problem: If [A⁻] in a buffer is increased while [HA] is held constant, does the pH increase, decrease, or stay the same?
This type of reasoning-only Henderson-Hasselbalch practice problem is common on the MCAT — you’re expected to predict the direction of a pH shift without plugging in any numbers at all, just from understanding the structure of the equation.
Problem 11 — Citrate BufferAdvanced
Problem: A citrate buffer has pKa₂ = 4.761. At pH 4.5, [H₂Cit⁻] = 0.08 M. Find [HCit²⁻] using the Henderson-Hasselbalch equation.
Citrate is a triprotic acid with three separate pKa values — always confirm you’re using the correct pKa (here, pKa₂) that corresponds to the specific conjugate acid/base pair given in the problem.
Problem 12 — Henderson-Hasselbalch Applied to a TitrationExam-Level
Problem: 20 mL of 0.1 M acetic acid (pKa = 4.756) is titrated with 0.1 M NaOH. Find the pH after adding 8 mL of NaOH.
Key insight: notice that the total volume (28 mL) never actually appears in the calculation, because it cancels out identically in both the numerator and denominator of the ratio. This is a detail many students miss — in titration problems, you can use moles directly instead of converting to concentrations, since the Henderson-Hasselbalch equation only needs the ratio, not the absolute concentrations.
Common Mistakes in Henderson-Hasselbalch Problems
Frequently Asked Questions
What is the Henderson-Hasselbalch equation?
The Henderson-Hasselbalch equation is pH = pKa + log([A⁻]/[HA]), used to calculate the pH of a buffer solution from the pKa of a weak acid and the ratio of its conjugate base to undissociated acid concentrations.
What does pKa represent in the Henderson-Hasselbalch equation?
pKa is the negative log of the acid dissociation constant Ka. It equals the pH at which [HA] = [A⁻], and it marks the center of a buffer’s most effective pH range.
How do you solve Henderson-Hasselbalch practice problems?
Identify the pKa, identify (or calculate) the concentrations or moles of conjugate base and weak acid, compute the ratio [A⁻]/[HA], take its log, and add it to pKa. To solve in reverse for concentrations, rearrange to isolate the ratio using 10^(pH − pKa) first.
When can you not use the Henderson-Hasselbalch equation?
It becomes unreliable when the [A⁻]/[HA] ratio falls far outside 0.1 to 10 (more than one pH unit from pKa), for strong acids or bases, or in very dilute solutions where the acid’s own dissociation becomes significant relative to the buffer components.