Acid-Base Titrations

Emily Wilson
10 min read
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Study Guide Overview
This study guide covers acid-base titrations, including the purpose of titrations, the equivalence point, and calculations using nMaVa = mMbVb. It explains titration curves for strong acid-strong base and weak acid/base titrations, highlighting the significance of buffers, half-equivalence points, and pH calculations. It also covers practical aspects like reading a burette and provides example problems and practice questions.
#Acid-Base Titrations: Your Ultimate Guide π§ͺ
Hey there, future AP Chem master! Let's tackle acid-base titrations together. It might seem like a beast, but we'll break it down step-by-step. Think of this as your go-to guide for the night before the exam. Let's get started!
#What's a Titration Anyway?
Titration is a lab technique used to find the unknown concentration of a solution (the analyte or titrand). We do this by adding a solution of known concentration (the titrant) using a burette. The key is to add the titrant until we reach the equivalence point.
The equivalence point is when the moles of titrant added equals the moles of analyte in the solution. This is where the magic happens! πͺ
#The Magic Equation
At the equivalence point, we use the equation: nMaVa = mMbVb
- n and m are the stoichiometric coefficients from the balanced equation.
- Ma and Mb are the molarities of the acid and base.
- Va and Vb are the volumes of the acid and base at the equivalence point.
Remember to always balance your equations first! Stoichiometry is key!
#Titration Setup
Here's a visual of a typical acid-base titration setup:
- Analyte: The solution with the unknown concentration.
- Titrant: The solution with the known concentration, added from the burette.
- Equivalence Point: The point where the reaction is complete.
#Titration Curves: The pH Story π
As we add titrant, the pH of the solution changes. Plotting this change creates a titration curve.
#Strong Acid - Strong Base Titration
Let's look at the titration of 1M NaOH into 25 mL of 1M HCl:
#Pre-Titration
Before adding any NaOH, we have only HCl. The pH is calculated as: pH = -log[H+] = -log(1) = 0. #### Pre-Equivalence Point
As we add NaOH, the reaction is: H+ + OH- β H2O
- We still have excess H+, so the solution is still acidic.
- The pH slowly increases as we neutralize the H+.
#Equivalence Point
At the equivalence point, moles of HCl = moles of NaOH. For our example, this occurs at 25 mL of NaOH added.
- We have only water and salt (NaCl) at this point.
- The pH is 7 for strong acid-strong base titrations.
#Post-Equivalence Point
After the equivalence point, we have excess OH-, so the solution becomes basic, and the pH increases.
#Full Titration Curve
Hereβs the full curve for a strong acid-strong base titration:
#Titrations with Weak Acids and Bases π§ͺ
Most acids and bases are weak, so let's look at those titrations. The process is similar, but with a few key differences.
#Buffers are Here!
Before the equivalence point, you'll have both the weak acid and its conjugate base (or weak base and its conjugate acid). This means we have a buffer! π‘
- The solution is less responsive to pH changes.
- We have a half-equivalence point at half the volume of the equivalence point where pH=pKa or pOH=pKb.
#Equivalence Point pH
Unlike strong acid-strong base titrations, the pH at the equivalence point is not 7. It will be:
- Acidic for a weak base titrated with a strong acid.
- Basic for a weak acid titrated with a strong base.
This is because, at the equivalence point, you form a conjugate base or acid that affects the pH.
#Titration Curves for Weak Acids/Bases
Here are some examples:
Practice identifying the half-equivalence and equivalence points on these curves. This is a common AP question!
Remember: Halfway to the equivalence point = Halfway to the buffer zone!
#Reading a Burette π
Accurately reading a burette is crucial for titrations. Always read from the bottom of the meniscus at eye level.
#Example Problems π
Let's work through some examples to solidify our understanding.
#Finding Molarity at Equivalence Point
Problem: Find the concentration of HF when titrating with NaOH. The equivalence point occurs when 20mL of 0.1M NaOH is added to 10mL of HF.
Solution:
Using MaVa = MbVb:
Ma(10mL) = (0.1M)(20mL)
Ma = (0.1)(20)/10 = 0.2M
Therefore, the concentration of HF is 0.2M.
#Weak Acid/Strong Base Titration
Problem: Find the pH of the solution formed from the titration of 25mL of 0.1M CH3COOH with 10mL 0.1M KOH (Ka = 1.8 * 10^-5).
Solution:
- Reaction: CH3COOH + OH- <=> CH3COO- + H2O
- Initial mmols:
- CH3COOH: 25mL * 0.1M = 2.5 mmol
- OH-: 10mL * 0.1M = 1.0 mmol
- Stoichiometry:
- After reaction: 1.5 mmol CH3COOH, 1.0 mmol CH3COO-
- Henderson-Hasselbalch:
- pH = pKa + log([CH3COO-]/[CH3COOH])
- pH = -log(1.8 * 10^-5) + log(1.0/1.5) = 4.74 + log(1/1.5) = 4.56
#Weak Base/Strong Acid Titration
Problem: Find the pH of the solution formed from the titration of 30mL of 0.5M NH3 with 10mL 0.1M HCl (Kb = 1.8 * 10^-5).
Solution:
- Reaction: NH3 + H+ <=> NH4+
- Initial mmols:
- NH3: 30mL * 0.5M = 15 mmol
- H+: 10mL * 0.1M = 1 mmol
- Stoichiometry:
- After reaction: 14 mmol NH3, 1 mmol NH4+
- Henderson-Hasselbalch (for bases):
- pOH = pKb + log([NH4+]/[NH3])
- pOH = -log(1.8 * 10^-5) + log(1/14) = 4.74 + log(1/14) = 3.59
- pH:
- pH = 14 - pOH = 14 - 3.59 = 10.41
Don't forget to use pOH when dealing with bases and then subtract from 14 to get the pH!
#Final Exam Focus π―
- Key Concepts: Equivalence point, half-equivalence point, buffer region, titration curves (shape and interpretation), Henderson-Hasselbalch equation.
- High-Value Topics: Titrations of weak acids/bases, calculating pH at different points in the titration, understanding the impact of conjugate acids/bases.
- Common Question Types:
- MCQs: Identifying equivalence points, choosing indicators, calculating pH.
- FRQs: Drawing and interpreting titration curves, performing stoichiometry calculations, using Henderson-Hasselbalch.
Titration curves are a high-value topic. Make sure you can interpret and draw them.
#Last-Minute Tips
- Time Management: Quickly identify the type of titration and the key points to calculate.
- Common Pitfalls: Forgetting to use pOH for bases, not considering the stoichiometry of the reaction, misreading the burette.
- Strategies:
- Always write out the balanced equation and net ionic equation.
- Use the Henderson-Hasselbalch equation when buffers are present.
- Double-check your calculations and units.
Practice, practice, practice! The more you work through problems, the more comfortable you'll become.
#Practice Questions
Practice Question
Multiple Choice Questions
-
A 25.0 mL sample of a 0.200 M solution of a monoprotic weak acid is titrated with a 0.100 M NaOH solution. The equivalence point is reached after adding 50.0 mL of the NaOH solution. What is the approximate pH of the solution at the half-equivalence point? (A) 1.0 (B) 2.0 (C) 5.0 (D) 7.0
-
Which of the following is the best indicator to use for the titration of a weak acid with a strong base? (A) Methyl orange (pH range: 3.1-4.4) (B) Bromothymol blue (pH range: 6.0-7.6) (C) Phenolphthalein (pH range: 8.3-10.0) (D) Alizarin yellow (pH range: 10.1-12.0)
-
A titration is performed using a 0.10 M solution of NaOH to determine the concentration of an unknown solution of HCl. The following data was collected:
Trial Initial Burette Reading (mL) Final Burette Reading (mL) 1 0.00 24.50 2 0.20 24.65 3 0.10 24.70 What is the average volume of NaOH used in the titration? (A) 24.50 mL (B) 24.58 mL (C) 24.62 mL (D) 24.70 mL
Free Response Question
A 20.0 mL sample of 0.100 M solution of a weak acid, HA, is titrated with a 0.100 M solution of NaOH. The Ka of the weak acid is 1.0 x 10^-5. (a) Write the net ionic equation for the reaction that occurs during the titration.
(b) Calculate the initial pH of the 0.100 M HA solution before any NaOH is added.
(c) Calculate the pH of the solution after 10.0 mL of the 0.100 M NaOH has been added.
(d) Calculate the volume of NaOH required to reach the equivalence point.
(e) Calculate the pH at the equivalence point.
(Scoring Breakdown)
(a) 1 point for the correct net ionic equation: HA + OH- -> A- + H2O
(b) 2 points for the correct calculation of initial pH:
* Set up the ICE table for HA <=> H+ + A-
* Ka = [H+][A-]/[HA] = x^2/(0.100-x) β x^2/0.100 = 1.0 x 10^-5
* x = [H+] = 0.001 M
* pH = -log(0.001) = 3.0
(c) 3 points for the correct calculation of pH at the half-equivalence point:
* Calculate moles of HA and OH-: moles HA = 0.020 L * 0.100 M = 0.002 mol; moles OH- = 0.010 L * 0.100 M = 0.001 mol
* Use the Henderson-Hasselbalch equation: pH = pKa + log([A-]/[HA]) = pKa + log(0.001/0.001) = pKa
* pKa = -log(1.0 x 10^-5) = 5.0, so pH = 5.0
(d) 1 point for the correct volume of NaOH at the equivalence point:
* Using MaVa = MbVb: (0.100 M)(20.0 mL) = (0.100 M)Vb
* Vb = 20.0 mL
(e) 3 points for the correct calculation of pH at the equivalence point:
* At equivalence point, all HA is converted to A-. Moles of A- = 0.002 mol, total volume = 40 mL = 0.040 L
* [A-] = 0.002 mol/0.040 L = 0.050 M
* A- + H2O <=> HA + OH- Kb = Kw/Ka = 1.0 x 10^-14 / 1.0 x 10^-5 = 1.0 x 10^-9
* Kb = [HA][OH-]/[A-] = x^2/0.050 = 1.0 x 10^-9
* x = [OH-] = 7.07 x 10^-6 M; pOH = 5.15; pH = 14 - 5.15 = 8.85
You've got this! Remember, understanding the concepts is key. Good luck on your exam! π
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