Calculate the pH of 100.00 mL 0.182 M NaAc
Use this premium sodium acetate calculator to determine the pH of a 100.00 mL, 0.182 M NaAc solution with step-by-step chemistry. The tool applies weak base hydrolysis for acetate, estimates hydroxide concentration, and visualizes the result on a pH scale chart.
Sodium acetate is a salt of a weak acid and strong base. Acetate hydrolyzes in water:
CH3COO– + H2O ⇌ CH3COOH + OH–
Kb = Kw / Ka, then for a weak base solution:
[OH–] ≈ √(Kb × C)
pOH = -log[OH–], and pH = 14.00 – pOH
Expert guide: how to calculate the pH of 100.00 mL 0.182 M NaAc
If you need to calculate the pH of 100.00 mL 0.182 M NaAc, the key idea is that sodium acetate is not a neutral salt. It is the sodium salt of acetic acid, a weak acid. Because the acetate ion is the conjugate base of acetic acid, it reacts with water to produce hydroxide ions, making the solution basic. That means the pH will be greater than 7 at standard laboratory temperature.
Chemically, NaAc is commonly written for sodium acetate, although you may also see CH3COONa or NaC2H3O2. Once it dissolves, sodium ions act as spectator ions for this calculation, while acetate ions participate in hydrolysis. The calculation therefore focuses on the acetate concentration and the acid dissociation constant of acetic acid.
Why sodium acetate gives a basic pH
Sodium acetate dissociates essentially completely in water:
CH3COONa → Na+ + CH3COO–
The sodium ion comes from the strong base sodium hydroxide and does not significantly affect pH. The acetate ion, however, is the conjugate base of acetic acid, so it can remove a proton from water:
CH3COO– + H2O ⇌ CH3COOH + OH–
Since hydroxide ions are produced, the solution becomes basic. This is why the pH of sodium acetate is above 7, even though there is no strong base added directly.
Step-by-step calculation for 100.00 mL of 0.182 M NaAc
-
Identify the concentration of acetate. Because sodium acetate dissociates completely, the initial acetate concentration is the same as the sodium acetate concentration:
[CH3COO–] = 0.182 M -
Use the acid dissociation constant for acetic acid. A common value at 25 degrees C is:
Ka = 1.8 × 10-5 -
Convert Ka to Kb for acetate.
Kb = Kw / Ka = 1.0 × 10-14 / 1.8 × 10-5
Kb ≈ 5.56 × 10-10 -
Apply the weak base approximation. For a weak base with initial concentration C:
[OH–] ≈ √(KbC)
[OH–] ≈ √((5.56 × 10-10)(0.182))
[OH–] ≈ √(1.01192 × 10-10)
[OH–] ≈ 1.006 × 10-5 M -
Calculate pOH.
pOH = -log(1.006 × 10-5) ≈ 4.997 -
Calculate pH.
pH = 14.000 – 4.997 ≈ 9.003
Therefore, the pH of 100.00 mL 0.182 M NaAc is approximately 9.00 at 25 degrees C when Ka for acetic acid is taken as 1.8 × 10-5.
Does the 100.00 mL volume affect the pH?
In this specific problem, the listed volume is important for finding the total number of moles, but it does not change the pH as long as the concentration remains 0.182 M. That is because pH depends on concentration, not on the absolute amount, for a simple homogeneous solution like this one.
You can still calculate the moles to better understand the system:
moles NaAc = M × V = 0.182 mol/L × 0.10000 L = 0.01820 mol
This tells you that the sample contains 0.01820 mol of sodium acetate, and therefore initially 0.01820 mol of acetate ion. But because the concentration is already given, the pH computation remains based on 0.182 M, not the volume alone.
ICE table interpretation
Many chemistry students prefer to confirm the weak base setup using an ICE table. For acetate hydrolysis:
- Initial: [CH3COO–] = 0.182, [CH3COOH] = 0, [OH–] ≈ 0
- Change: -x, +x, +x
- Equilibrium: 0.182 – x, x, x
Then:
Kb = x2 / (0.182 – x)
Since Kb is very small, x is much smaller than 0.182, so 0.182 – x ≈ 0.182. This leads to:
x ≈ √(Kb × 0.182)
Here x represents [OH–] at equilibrium. The approximation is valid because the percent ionization is tiny, on the order of a few thousandths of a percent.
| Quantity | Value | Meaning |
|---|---|---|
| Sodium acetate concentration | 0.182 M | Initial acetate concentration in solution |
| Volume | 100.00 mL = 0.10000 L | Used to calculate total moles present |
| Moles of NaAc | 0.01820 mol | Total dissolved sodium acetate |
| Ka of acetic acid | 1.8 × 10-5 | Standard literature value near room temperature |
| Kb of acetate | 5.56 × 10-10 | Hydrolysis constant of acetate in water |
| [OH–] | 1.006 × 10-5 M | Hydroxide formed by base hydrolysis |
| pOH | 4.997 | Negative log of hydroxide concentration |
| pH | 9.003 | Final solution pH at 25 degrees C |
How accurate is the square root shortcut?
The shortcut [OH–] ≈ √(KbC) is widely used because it is both fast and reliable when the weak base dissociates only slightly. In this sodium acetate case, it works very well because Kb is much smaller than the initial concentration. If you solved the full quadratic equation, the result would be extremely close to the approximation.
This is a useful lesson in analytical chemistry and general chemistry: not every equilibrium problem needs a full exact numerical solution. Once you recognize a weak conjugate base in moderate concentration, the hydrolysis approximation becomes the standard approach.
Comparison with other sodium acetate concentrations
The pH of sodium acetate rises gradually as concentration increases, but not dramatically, because pH depends on the logarithm of hydroxide concentration. The table below shows approximate pH values using the same Ka assumption and 25 degrees C conditions.
| NaAc Concentration (M) | Approximate [OH–] (M) | Approximate pOH | Approximate pH |
|---|---|---|---|
| 0.010 | 2.36 × 10-6 | 5.627 | 8.373 |
| 0.050 | 5.27 × 10-6 | 5.278 | 8.722 |
| 0.100 | 7.45 × 10-6 | 5.128 | 8.872 |
| 0.182 | 1.01 × 10-5 | 4.997 | 9.003 |
| 0.500 | 1.67 × 10-5 | 4.778 | 9.222 |
| 1.000 | 2.36 × 10-5 | 4.627 | 9.373 |
Common mistakes students make
- Assuming sodium acetate is neutral because it is a salt.
- Using Ka directly instead of converting to Kb.
- Forgetting that acetate is the conjugate base of a weak acid.
- Confusing moles with molarity when volume is given.
- Using the Henderson-Hasselbalch equation without a buffer pair being present initially.
- Entering 100.00 mL directly as liters when calculating moles.
When would you use Henderson-Hasselbalch instead?
Henderson-Hasselbalch is primarily used for buffer systems where both a weak acid and its conjugate base are present in appreciable amounts. A pure sodium acetate solution is not, by itself, a full acetic acid acetate buffer unless acetic acid is also present. For a pure salt of a weak acid, the hydrolysis approach is conceptually cleaner and usually expected in coursework.
Laboratory relevance of sodium acetate pH
Sodium acetate is widely used in biochemical buffers, crystallization procedures, DNA precipitation workflows, and acid-base equilibrium demonstrations. In many practical systems, sodium acetate is combined with acetic acid to produce acetate buffers spanning the pH range near the pKa of acetic acid, around 4.76. On its own, however, sodium acetate gives a mildly basic solution. A 0.182 M solution with pH near 9.00 is consistent with the conjugate base behavior expected from equilibrium theory.
Authoritative references for equilibrium constants and acid-base concepts
For verified educational and reference material, consult:
- Chemistry LibreTexts for weak acid and conjugate base equilibrium explanations.
- U.S. Environmental Protection Agency for pH fundamentals and aqueous chemistry context.
- NIST Chemistry WebBook for compound data and scientific reference support.
- Princeton University Chemistry for academic chemistry resources and instructional context.
Final answer summary
To calculate the pH of 100.00 mL 0.182 M NaAc, first recognize that sodium acetate is the salt of a weak acid and strong base. The acetate ion undergoes hydrolysis, so the solution is basic. Using Ka = 1.8 × 10-5 for acetic acid, you find Kb = 5.56 × 10-10. Then applying the weak base approximation gives [OH–] ≈ 1.006 × 10-5 M, pOH ≈ 4.997, and pH ≈ 9.003.
In short, the pH is approximately 9.00. The 100.00 mL figure helps determine that the sample contains 0.01820 mol of sodium acetate, but the pH itself is governed by the concentration and equilibrium constant rather than volume alone.