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Derive an equation similar to the HendersonHasselbalch equation relating the pOH of a buffer to the \(\mathrm{p} K_{b}\) of its base component.

Short Answer

Expert verified
The derived equation relating pOH to the \(pK_b\) of a weak base in a buffer solution is: \[ pOH = \log{\left( \frac{[B]}{[HB^+]} \right)} + pK_b \] This equation can be used to determine the pOH of a buffer system given the concentration of the base and its conjugate acid, and the \(pK_b\) of the base component.

Step by step solution

01

Write down the generic reaction with a weak base and water.

For a buffer solution composed of a weak base, B, and its conjugate acid, HB+, the following equilibrium reaction takes place when the base is mixed with water: \( B + H_2O \leftrightarrows HB^+ + OH^- \) Here, B is the weak base, \(H_2O\) is water, \(HB^+\) is the conjugate acid of B, and \(OH^-\) is hydroxide ion.
02

Write down the expression for the base ionization constant.

The base ionization constant, \(K_b\), can be defined as follows. \[ K_b = \frac{[HB^+][OH^-]}{[B]} \] This equation represents the equilibrium between the base (B), the conjugate acid (HB+), and the hydroxide (OH-) ions.
03

Define pOH and pKb.

The pOH is a measure of the acidity of a solution and is calculated as the negative logarithm of the hydroxide ion concentration. \[ pOH = -\log{[OH^-]} \] Similarly, \(pK_b\) is a measure of the basicity of a substance and is calculated as the negative logarithm of the base ionization constant. \[ pK_b = -\log{K_b} \]
04

Rewrite the expression for the base ionization constant in terms of pOH and pKb.

We can rewrite the expression for the base ionization constant from Step 2 as follows. \[ 10^{pOH} = \frac{[HB^+]}{[B]} \cdot \frac{1}{K_b} \] Take the negative logarithm of both sides of the equation. \[ -\log{10^{pOH}} = -\log{\left( \frac{[HB^+]}{[B]} \cdot \frac{1}{K_b} \right)} \] Using the properties of logarithms, we can simplify the equation to: \[ pOH = \log{\left( \frac{[B]}{[HB^+]} \right)} + \log{K_b} \] But, since \(pK_b = -\log{K_b}\), we can substitute it into the equation.
05

Derive the final equation relating pOH and pKb.

Replacing the appropriate terms in the equation, we get the final equation relating pOH and \(pK_b\): \[ pOH = \log{\left( \frac{[B]}{[HB^+]} \right)} + pK_b \] This equation can be used to determine the pOH of a buffer system given the concentration of the base and its conjugate acid, and the \(pK_b\) of the base component.

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Most popular questions from this chapter

A buffer contains a weak acid, \(\mathrm{HX}\), and its conjugate base. The weak acid has a \(\mathrm{pK}_{a}\) of \(4.5\), and the buffer solution has a \(\mathrm{pH}\) of \(4.3\). Without doing a calculation, predict whether \([\mathrm{HX}]=\left[\mathrm{X}^{-}\right],[\mathrm{HX}]>\left[\mathrm{X}^{-}\right]\), or \([\mathrm{HX}]<\left[\mathrm{X}^{-}\right]\) Explain. [Section 17.2]

Describe the solubility of \(\mathrm{CaCO}_{3}\) in each of the following solutions compared to its solubility in water: (a) in \(0.10 \mathrm{M} \mathrm{NaCl}\) solution; \((\mathrm{b})\) in \(0.10 \mathrm{M} \mathrm{Ca}\left(\mathrm{NO}_{3}\right)_{2}\) solution; (c) \(0.10 \mathrm{M} \mathrm{Na}_{2} \mathrm{CO}_{3}\); (d) \(0.10 \mathrm{M}\) HCl solution. (Answer same, less soluble, or more soluble.)

What is the \(\mathrm{pH}\) at \(25^{\circ} \mathrm{C}\) of water saturated with \(\mathrm{CO}_{2}\) at a partial pressure of \(1.10 \mathrm{~atm}\) ? The Henry's law constant for \(\mathrm{CO}_{2}\) at \(25^{\circ} \mathrm{C}\) is \(3.1 \times 10^{-2} \mathrm{~mol} / \mathrm{L}-\mathrm{atm}\). The \(\mathrm{CO}_{2}\) is an acidic oxide, reacting with \(\mathrm{H}_{2} \mathrm{O}\) to form \(\mathrm{H}_{2} \mathrm{CO}_{3}\).

A hypothetical weak acid, HA, was combined with \(\mathrm{NaOH}\) in the following proportions: \(0.20 \mathrm{~mol}\) of \(\mathrm{HA}\), \(0.080 \mathrm{~mol}\) of \(\mathrm{NaOH}\). The mixture was diluted to a total volume of \(1.0 \mathrm{~L}\), and the pH measured. (a) If \(\mathrm{pH}=4.80\), what is the \(\mathrm{p} K_{a}\) of the acid? (b) How many additional moles of \(\mathrm{NaOH}\) should be added to the solution to increase the \(\mathrm{pH}\) to \(5.00 ?\)

Two buffers are prepared by adding an equal number of moles of formic acid (HCOOH) and sodium formate (HCOONa) to enough water to make \(1.00\) L of solution. Buffer A is prepared using \(1.00 \mathrm{~mol}\) each of formic acid and sodium formate. Buffer \(B\) is prepared by using \(0.010\) mol of each. (a) Calculate the pH of each buffer, and explain why they are equal. (b) Which buffer will have the greater buffer capacity? Explain. (c) Calculate the change in \(\mathrm{pH}\) for each buffer upon the addition of \(1.0 \mathrm{~mL}\) of \(1.00 M \mathrm{HCl}\). (d) Calculate the change in \(\mathrm{pH}\) for each buffer upon the addition of \(10 \mathrm{~mL}\) of \(1.00 \mathrm{M} \mathrm{HCl}\). (e) Discuss your answers for parts (c) and (d) in light of your response to part (b).

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