Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Derive an equation analogous to the Henderson-Hasselbalch equation but relating \(\mathrm{pOH}\) and \(\mathrm{p} K_{\mathrm{b}}\) of a buffered solution composed of a weak base and its conjugate acid, such as \(\mathrm{NH}_{3}\) and \(\mathrm{NH}_{4}^{+}\).

Short Answer

Expert verified
The final equation analogous to the Henderson-Hasselbalch equation, relating pOH and pKb for a buffered solution composed of a weak base and its conjugate acid, such as NH3 and NH4+, is: \[ \mathrm{pOH} = \mathrm{p}K_{\mathrm{b}} + \log \frac{[\mathrm{BH}^{+}]}{[\mathrm{B}]} \]

Step by step solution

01

Recall Henderson-Hasselbalch Equation

The Henderson-Hasselbalch equation is used to describe the pH of a buffer solution composed of a weak acid and its conjugate base, and can be written as: \[ \mathrm{pH} = \mathrm{p}K_{\mathrm{a}} + \log \frac{[\mathrm{A}^{-}]}{[\mathrm{HA}]} \] Where pH is the pH of the solution, pKa is the negative logarithm of the acid dissociation constant, [A-] is the concentration of the conjugate base, and [HA] is the concentration of the weak acid.
02

Write the Expression for Kb

Now, let's write the expression for the equilibrium constant Kb for the dissociation of a weak base, B, and its conjugate acid, BH+: \[ \mathrm{B} + \mathrm{H}_{2}\mathrm{O} \rightleftharpoons \mathrm{BH}^{+} + \mathrm{OH}^{} \] The equilibrium constant, Kb, for this reaction can be written as: \[ K_{\mathrm{b}} = \frac{[\mathrm{BH}^{+}][\mathrm{OH}^{-}]}{[\mathrm{B}]} \]
03

Find pOH and pKb

In order to create an equation analogous to the Henderson-Hasselbalch equation, we have to relate the pOH and pKb to this equilibrium constant. To do so, we first find pOH and pKb: pOH = -log[OH-] pKb = -log(Kb)
04

Substitution and Manipulation of Equations

Now, let's rearrange the equation of Kb so that it is in terms of [OH-]: \[ [\mathrm{OH}^{-}] = \frac{\mathrm{K}_{\mathrm{b}}[\mathrm{B}]}{[\mathrm{BH}^{+}]} \] Then, calculate the logarithm of the equation above: \[ -\log [\mathrm{OH}^{-}] = -\log \frac{\mathrm{K}_{\mathrm{b}}[\mathrm{B}]}{[\mathrm{BH}^{+}]} \] Since pOH = -log[OH-] and pKb = -log(Kb), we can make a substitution: \[ \mathrm{pOH} = \mathrm{p}K_{\mathrm{b}} + \log \frac{[\mathrm{BH}^{+}]}{[\mathrm{B}]} \]
05

Final Equation

The final equation analogous to the Henderson-Hasselbalch equation, but relating pOH and pKb for a buffered solution composed of a weak base and its conjugate acid, such as NH3 and NH4+, is: \[ \mathrm{pOH} = \mathrm{p}K_{\mathrm{b}} + \log \frac{[\mathrm{BH}^{+}]}{[\mathrm{B}]} \]

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Sketch a \(\mathrm{pH}\) curve for the titration of a weak acid (HA) with a strong base \((\mathrm{NaOH})\). List the major species and explain how you would go about calculating the \(\mathrm{pH}\) of the solution at various points, including the halfway point and the equivalence point.

One method for determining the purity of aspirin \(\left(\mathrm{C}_{9} \mathrm{H}_{8} \mathrm{O}_{4}\right)\) is to hydrolyze it with NaOH solution and then to titrate the remaining \(\mathrm{NaOH}\). The reaction of aspirin with \(\mathrm{NaOH}\) is as follows: \(\mathrm{C}_{?} \mathrm{H}_{3} \mathrm{O}_{4}(s)+2 \mathrm{OH}^{-}(a q)\) Aspirin $$ \begin{array}{c} \text { Bail } \mathrm{C}_{7} \mathrm{H}_{5} \mathrm{O}_{3}^{-}(a q)+\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{O}_{2}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}(l) \\ \text { Salicylate ion Acetate ion } \end{array} $$ A sample of aspirin with a mass of \(1.427 \mathrm{~g}\) was boiled in \(50.00 \mathrm{~mL}\) of \(0.500 M \mathrm{NaOH}\). After the solution was cooled, it took \(31.92 \mathrm{~mL}\) of \(0.289 \mathrm{M} \mathrm{HCl}\) to titrate the excess \(\mathrm{NaOH}\). Calculate the purity of the aspirin. What indicator should be used for this titration? Why?

A few drops of each of the indicators shown in the accompanying table were placed in separate portions of a \(1.0 \mathrm{M}\) solution of a weak acid, \(\mathrm{HX}\). The results are shown in the last column of the table. What is the approximate \(\mathrm{pH}\) of the solution containing HX? Calculate the approximate value of \(K_{\alpha}\) for \(\mathrm{HX}\). \begin{tabular}{|lclcc|} \hline Indicator & Color of Hin & Color of \(\mathrm{In}^{-}\) & \(\mathrm{p} \boldsymbol{K}_{\mathrm{a}}\) of Hin & Color of \(1.0 \mathrm{M} \mathrm{HX}\) \\\ \hline Bromphenol blue & Yellow & Blue & \(4.0\) & Blue \\ Bromcresol purple & Yellow & Purple & \(6.0\) & Yellow \\ Bromcresol green & Yellow & Blue & \(4.8\) & Green \\ Alizarin & Yellow & Red & \(6.5\) & Yellow \\ \hline \end{tabular}

A \(10.00-g\) sample of the ionic compound \(\mathrm{NaA}\), where \(\mathrm{A}^{-}\) is the anion of a weak acid, was dissolved in enough water to make \(100.0 \mathrm{~mL}\) of solution and was then titrated with \(0.100 \mathrm{M} \mathrm{HCl}\). After \(500.0 \mathrm{~mL}\) HCl was added, the \(\mathrm{pH}\) was \(5.00\). The experimenter found that \(1.00 \mathrm{~L}\) of \(0.100 \mathrm{M} \mathrm{HCl}\) was required to reach the stoichiometric point of the titration. a. What is the molar mass of NaA? b. Calculate the \(\mathrm{pH}\) of the solution at the stoichiometric point of the titration.

A friend asks the following: "Consider a buffered solution made up of the weak acid HA and its salt NaA. If a strong base like \(\mathrm{NaOH}\) is added, the HA reacts with the \(\mathrm{OH}^{-}\) to form \(\mathrm{A}^{-}\). Thus the amount of acid (HA) is decreased, and the amount of base \(\left(\mathrm{A}^{-}\right)\) is increased. Analogously, adding \(\mathrm{HCl}\) to the buffered solution forms more of the acid (HA) by reacting with the base \(\left(\mathrm{A}^{-}\right) .\) Thus how can we claim that a buffered solution resists changes in the \(\mathrm{pH}\) of the solution?' How would you explain buffering to this friend?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free