For volumes of HCl greater than the equivalence point, the pH is determined by the concentration of excess HCl. Again, we start by calculating the volume of NaOH needed to reach the equivalence point; thus. Before we begin the titration the pH is that for a solution of 0. Because acetic acid is a weak acid, we calculate the pH using the method outlined in Chapter 6. Any solution that contains comparable amounts of a weak acid, HA, and its conjugate weak base, A — , is a buffer. As we learned in Chapter 6 , we can calculate the pH of a buffer using the Henderson—Hasselbalch equation.
Before the equivalence point the concentration of unreacted acetic acid is. At the equivalence point the moles of acetic acid initially present and the moles of NaOH added are identical. Because their reaction effectively proceeds to completion, the predominate ion in solution is CH 3 COO — , which is a weak base.
Next, we calculate the pH of the weak base as shown earlier in Chapter 6. After the equivalence point, the titrant is in excess and the titration mixture is a dilute solution of NaOH. We can calculate the pH using the same strategy as in the titration of a strong acid with a strong base. You can use this same approach to calculate the titration curve for the titration of a weak base with a strong acid, except the initial pH is determined by the weak base, the pH at the equivalence point by its conjugate weak acid, and the pH after the equivalence point by excess strong acid.
Before adding HCl the pH is that for a solution of 0. After the equivalence point, the pH is determined by the excess HCl. We can extend this approach for calculating a weak acid—strong base titration curve to reactions that involve multiprotic acids or bases, and mixtures of acids or bases.
As the complexity of the titration increases, however, the necessary calculations become more time consuming. Not surprisingly, a variety of algebraic and spreadsheet approaches are available to aid in constructing titration curves. The following papers provide information on algebraic approaches to calculating titration curves: a Willis, C.
The following papers provide information on the use of spreadsheets to generate titration curves: a Currie, J. In this section we demonstrate a simple method for sketching an acid—base titration curve. Our goal is to sketch the titration curve quickly, using as few calculations as possible. This is the same example that we used to develop the calculations for a weak acid—strong base titration curve.
You can review the results of that calculation in Table 9. To indicate the equivalence point volume, we draw a vertical line that intersects the x -axis at Figure 9. The actual values are 9. The third step is to add two points after the equivalence point. The pH after the equivalence point is fixed by the concentration of excess titrant, NaOH. Calculating the pH of a strong base is straightforward, as we saw earlier.
Finally, we complete our sketch by drawing a smooth curve that connects the three straight-line segments Figure 9. A comparison of our sketch to the exact titration curve Figure 9. Sketch a titration curve for the titration of The figure below shows a sketch of the titration curve.
The black dots and curve are the approximate sketch of the titration curve. The points in red are the calculations from Exercise 9.
As shown in the following example, we can adapt this approach to any acid—base titration, including those where exact calculations are more challenging, including the titration of polyprotic weak acids and bases, and the titration of mixtures of weak acids or weak bases. Sketch titration curves for the following two systems: a the titration of For both titrations, assume that the titrant is 0. After the second equivalence point the pH reflects the concentration of excess NaOH.
Again, there are two equivalence points; however, in this case the equivalence points are not equally spaced because the concentration of HA is greater than that for HB.
Because HA is the stronger of the two weak acids it reacts first; thus, the pH before the first equivalence point is controlled by a buffer of HA and A —.
After the second equivalence point excess NaOH determines the pH. Sketch the titration curve for The fact that p K a2 falls within the buffer range of p K a1 presents a challenge that you will need to consider. The titration curve has two equivalence points, one at In sketching the curve, we plot two points before the first equivalence point using the p K a1 of 3 for H 2 A.
This is, of course, absurd; as we add NaOH the pH cannot decrease. The results is a reasonable approximation of the exact titration curve.
The difference between these two terms is important and deserves repeating. An equivalence point, which occurs when we react stoichiometrically equal amounts of the analyte and the titrant, is a theoretical not an experimental value. Earlier we learned how to calculate the pH at the equivalence point for the titration of a strong acid with a strong base, and for the titration of a weak acid with a strong base.
We also learned how to sketch a titration curve with only a minimum of calculations. Can we also locate the equivalence point without performing any calculations. The answer, as you might guess, often is yes! The red arrows in Figure 9. An inflection point actually precedes its corresponding equivalence point by a small amount, with the error approaching 0.
Acta , 29 , —]. The principal limitation of an inflection point is that it must be present and easy to identify. For some titrations the inflection point is missing or difficult to find. An inflection point is visible, even if barely so, for acid dissociation constants larger than 10 —9 , but is missing when K a is 10 — An inflection point also may be missing or difficult to see if the analyte is a multiprotic weak acid or weak base with successive dissociation constants that are similar in magnitude.
During the titration the following two reactions occur. Malonic acid, on the other hand, has acid dissociation constants that differ by a factor of approximately The same holds true for mixtures of weak acids or mixtures of weak bases. To detect separate inflection points when titrating a mixture of weak acids, their p K a values must differ by at least a factor of One interesting group of weak acids and weak bases are organic dyes. Because an organic dye has at least one highly colored conjugate acid—base species, its titration results in a change in both its pH and its color.
Unfortunately, we rarely know the exact pH at the equivalence point. As shown in Figure 9. The properties of several common acid—base indicators are listed in Table 9. The explanation is simple. For some indicators only the weak acid or the weak base is colored. For other indicators both the weak acid and the weak base are colored, but one form is easier to see. For example, in Figure 9. Bromothymol blue, on the other hand, is an inappropriate indicator because its change in color begins well before the initial sharp rise in pH, and, as a result, spans a relatively large range of volumes.
The early change in color increases the probability of obtaining an inaccurate result, and the range of possible end point volumes increases the probability of obtaining imprecise results. Suggest a suitable indicator for the titration of You constructed a titration curve for this titration in Exercise 9. The pH at the equivalence point is 5. Of the indicators in Table 9. The result is a plot of the entire titration curve, which we can use to locate the end point with a minimal error.
A pH electrode is the obvious sensor for monitoring an acid—base titration and the result is a potentiometric titration curve. For example, Figure 9. This is also the least accurate method, particularly if the titration curve has a shallow slope at the equivalence point.
See Chapter 11 for more details about pH electrodes. Another method for locating the end point is to plot the first derivative of the titration curve, which gives its slope at each point along the x -axis. Examine Figure 9. Because the slope reaches its maximum value at the inflection point, the first derivative shows a spike at the equivalence point Figure 9.
The second derivative of a titration curve can be more useful than the first derivative because the equivalence point intersects the volume axis. Using the first two points, the first derivative is. For the second and third points, the first derivative is 0. Using the two points from our calculation of the first derivative, the second derivative is. Note that calculating the first derivative comes at the expense of losing one piece of information three points become two points , and calculating the second derivative comes at the expense of losing two pieces of information.
Derivative methods are particularly useful when titrating a sample that contains more than one analyte. If we rely on indicators to locate the end points, then we usually must complete separate titrations for each analyte so that we can see the change in color for each end point.
If we record the titration curve, however, then a single titration is sufficient. The precision with which we can locate the end point also makes derivative methods attractive for an analyte that has a poorly defined normal titration curve. Derivative methods work well only if we record sufficient data during the rapid increase in pH near the equivalence point. This usually is not a problem if we use an automatic titrator, such as the one seen earlier in Figure 9.
Because the pH changes so rapidly near the equivalence point—a change of several pH units over a span of several drops of titrant is not unusual—a manual titration does not provide enough data for a useful derivative titration curve. A manual titration does contain an abundance of data during the more gently rising portions of the titration curve before and after the equivalence point.
Substituting these equations into the K a expression and rearranging leaves us with. This method of data analysis, which converts a portion of a titration curve into a straight-line, is a Gran plot. Values of K a determined by this method may have a substantial error if the effect of activity is ignored.
See Chapter 6. The reaction between an acid and a base is exothermic. Heat generated by the reaction is absorbed by the titrand, which increases its temperature.
This part of a thermometric titration curve is called the titration branch. The temperature continues to rise with each addition of titrant until we reach the equivalence point. Ideally, the equivalence point is a distinct intersection of the titration branch and the excess titrant branch. The latter problem is minimized by using a titrant that is 10— times more concentrated than the analyte, although this results in a very small end point volume and a larger relative error.
If necessary, the end point is found by extrapolation. Although not a common method for monitoring an acid—base titration, a thermometric titration has one distinct advantage over the direct or indirect monitoring of pH.
As discussed earlier, the use of an indicator or the monitoring of pH is limited by the magnitude of the relevant equilibrium constants. Thus far we have assumed that the titrant and the titrand are aqueous solutions. You should recognize that K w is just specific form of K s when the solvent is water.
The most important limitation imposed by K s is the change in pH during a titration. Before the equivalence point, the pH is determined by the untitrated strong acid. However, the pH after adding Here, too, the solvent plays an important role. The strength of an acid or a base is a relative measure of how easy it is to transfer a proton from the acid to the solvent or from the solvent to the base.
If we place acetic acid in a solvent that is a stronger base than water, such as ammonia, then the reaction. All other things being equal, the strength of a weak acid increases if we place it in a solvent that is more basic than water, and the strength of a weak base increases if we place it in a solvent that is more acidic than water.
In some cases, however, the opposite effect is observed. For example, the p K b for NH 3 is 4. In contradiction to our expectations, NH 3 is a weaker base in the more acidic solvent. You should be aware, however, that a titration that is not feasible in water may be feasible in a different solvent. The best way to appreciate the theoretical and the practical details discussed in this section is to carefully examine a typical acid—base titrimetric method. Although each method is unique, the following description of the determination of protein in bread provides an instructive example of a typical procedure.
The description here is based on Method The amount of unreacted HCl is determined by a back titration using a standard strong base titrant. Because different cereal proteins contain similar amounts of nitrogen—on average there are 5. Transfer a 2. Ideally you would want these points to coincide. This is known as "salt hydrolysis".
For more details you can look up "theory of indicators". Simon Moore. Oct 28, They are similar but not identical Explanation: Equivalence point is the point where equal number of moles of acid and the number of moles of base that have been mixed together are equal. End point is the point at which the indicator being used in such a reaction changes colour.
Related questions How do you do acid base titration calculations? How do you use titration calculations to find pH? What is a redox titration and what is it used for? One of the most common titration, an acid—base titration determines the concentration of an acid or base by exactly neutralizing the acid or base with an acid or base of known concentration. You place the acid in the buret and the base in the flask, or vice versa.
The buret solution is dripped into the flask until neutralization is reached, as shown by a pH indicator. At this point, the titration is complete. Claire is a writer and editor with 18 years' experience. She writes about science and health for a range of digital publications, including Reader's Digest, HealthCentral, Vice and Zocdoc. TL;DR Too Long; Didn't Read The completion of a titration is the end point, detected by some type of physical change produced by the solution, such as a color change.
Related Articles Definition of Automated Titration. How to Find an Equivalence Point Titration. Precipitation Titration Techniques. The Advantages of Potentiometric Titration. What Does Titration Mean? Reasons for Error in a Chemistry Experiment.
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