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Calculate the \(\mathrm{pH}\) of a \(0.200 \mathrm{M}\) solution of \(\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NHF}\). Hint: \(\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NHF}\) is a salt composed of \(\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+}\) and \(\mathrm{F}^{-}\) ions. The prin- cipal equilibrium in this solution is the best acid reacting with the best base; the reaction for the principal equilibrium is \(\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+}(a q)+\mathrm{F}^{-}(a q) \rightleftharpoons\) \(\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{~N}(a q)+\mathrm{HF}(a q) \quad K=8.2 \times 10^{-3}\)

Short Answer

Expert verified
The pH of the 0.200 M C鈧匟鈧匩HF solution is approximately 6.06.

Step by step solution

01

Write the Equation for the Principal Equilibrium Reaction

Since the salt contains C鈧匟鈧匩H鈦 and F鈦 ions, and we are given that the principal equilibrium is C鈧匟鈧匩H鈦(aq) + F鈦(aq) 鈬 C鈧匟鈧匩(aq) + HF(aq), we will use this reaction to analyze the species involved.
02

Determine Initial Concentrations of Reactants and Products

Given a 0.200 M solution of C鈧匟鈧匩HF, the initial concentrations of C鈧匟鈧匩H鈦 and F鈦 ions are: \[ [\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+}]_{0} = [\mathrm{F}^{-}]_{0} = 0.200 \, \mathrm{M} \] Since the reaction has not yet taken place, the initial concentrations of C鈧匟鈧匩 and HF are both zero.
03

Write the Equilibrium Expression and Define the Change in Concentration

Using the given equilibrium constant K, we can write an equilibrium expression for the reaction: \[ K = \frac{ [\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{N}][\mathrm{HF}]}{ [\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+}][\mathrm{F}^{-}] } \] During the course of the reaction, the change in concentration of C鈧匟鈧匩H鈦 and F鈦 is equal. So, we can denote it as minus-x, which means the decrease in their concentrations. The change in concentration of C鈧匟鈧匩 and HF is equal as well, and it can be denoted as plus-x, which means the increase in their concentrations.
04

Plug Initial and Change Concentrations into K Expression and Solve for x

Now, we substitute the initial concentrations and the change in concentrations into the K expression: \[ K = \frac{ (0.200 + x)(x)}{ (0.200 - x)^2 } \] Given K = 8.2 脳 10鈦宦, we can solve for x: \[ 8.2 \times 10^{-3} = \frac{x(0.200 + x)}{(0.200 - x)^2} \] This quadratic equation can be solved to find the value of x. After an approximation, we get x 鈮 0.00134.
05

Calculate the H鈦 Concentration and the pH of the Solution

As we found the change in concentrations, we can calculate the [HF] concentration in the solution: \[ [\mathrm{HF}] = [\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{N}] = x \approx 0.00134 \, \mathrm{M} \] Since HF is a weak acid, we can use its expression for K鈧 to find the H鈦 concentration in the solution: \[ K_\mathrm{a} = 6.6 \times 10^{-4} = \frac{ [\mathrm{H}^{+}][\mathrm{F}^{-}]}{ [\mathrm{HF}] } = \frac{ [\mathrm{H}^{+}]}{ 0.00134 } \] Solving for H鈦 concentration, we get: \[ [\mathrm{H}^{+}] \approx 8.8 \times 10^{-7} \, \mathrm{M} \] Now, we can calculate the pH using the formula: \[ \mathrm{pH} = -\log_{10} [\mathrm{H}^{+}] \] Hence, the pH of the solution is: \[ \mathrm{pH} \approx -\log_{10} (8.8 \times 10^{-7}) \approx 6.06 \] So, the pH of the 0.200 M C鈧匟鈧匩HF solution is approximately 6.06.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Equilibrium Expression
Understanding the equilibrium expression is key in analyzing reactions that don't go to completion. In any chemical reaction, the equilibrium expression helps us understand the balance between the reactants and products at equilibrium. For a general reaction:
  • Reactants are on the left side of the arrow.
  • Products are on the right side.
The equilibrium expression, often denoted by the equilibrium constant \( K \), is written as a ratio of the concentrations of products to reactants, each raised to the power of their coefficients in the balanced equation.
In our exercise, the equilibrium expression for the reaction \( \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+}(a q) + \mathrm{F}^{-}(a q) \rightleftharpoons \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{N}(a q) + \mathrm{HF}(a q) \) is given by:\[ K = \frac{ [\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{N}][\mathrm{HF}]}{ [\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+}][\mathrm{F}^{-}] }\]This equation allows us to predict the concentrations of species involved when the reaction reaches equilibrium. The equilibrium constant \( K \) provides a measure of how far the reaction will proceed and is crucial in calculating any changes in concentration during the reaction.
Acid-Base Reaction
An acid-base reaction involves the transfer of protons \((\mathrm{H}^+)\) between a pair of substances. Generally, the substance donating a proton is the acid, while the one accepting it is the base. In our scenario, we deal with a reaction involving the cation \( \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+} \) acting as a weak acid and the anion \( \mathrm{F}^{-} \) acting as a base.
The principle reaction for these ions, given as \( \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+} + \mathrm{F}^{-} \rightleftharpoons \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{~N} + \mathrm{HF} \), highlights a fundamental acid-base interaction:
  • \( \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{NH}^{+} \) donates a proton becoming \( \mathrm{C}_{5} \mathrm{H}_{5} \mathrm{N} \).
  • \( \mathrm{F}^{-} \) accepts a proton becoming \( \mathrm{HF} \).
These reactions help us understand the process of neutralization between acids and bases, where a weak acid and a weak base are involved. The position of equilibrium indicates which side of the reaction is favored. Thus, in calculating the pH, understanding the acid-base reaction allows us to determine the strength and extent each species will contribute to the overall acidity of the solution.
Weak Acid Dissociation Constant
The dissociation constant \( K_a \) is an essential concept when working with weak acids. It quantifies the degree to which a weak acid (like HF in this exercise) dissociates into its ions in a solution. The smaller the \( K_a \) value, the weaker the acid.
For the equilibrium involving HF:\[ \mathrm{HF} \rightleftharpoons \mathrm{H}^{+} + \mathrm{F}^{-}\]The expression for the dissociation constant \( K_a \) is given by:\[ K_a = \frac{ [\mathrm{H}^{+}][\mathrm{F}^{-}] }{ [\mathrm{HF}] }\]The pH of a solution can be calculated using \( K_a \) by determining the concentration of \( \mathrm{H}^+ \) ions in the equilibrium state. Since HF is not a strong acid, only a small fraction of HF molecules dissociate to release \( \mathrm{H}^+ \).When calculating the \( \mathrm{pH} \), knowing the extent of dissociation鈥攁 critical factor鈥攊s achieved through \( K_a \). This calculation influences how we understand the solution's acidity, shown when solving for \( \mathrm{H}^+ \) concentration, and ultimately helps determine the pH using \( \mathrm{pH} = -\log_{10} [\mathrm{H}^+] \). With this knowledge, we can appreciate how weak acids contribute to system's pH. Such insights show why certain substances behave the way they do in solutions, particularly concerning their acidic or basic nature.

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Most popular questions from this chapter

A typical sample of vinegar has a pH of \(3.0\). Assuming that vinegar is only an aqueous solution of acetic acid \(\left(K_{\mathrm{a}}=1.8 \times 10^{-5}\right)\), calculate the concentration of acetic acid in vinegar.

What mass of \(\mathrm{NaOH}(s)\) must be added to \(1.0 \mathrm{~L}\) of \(0.050 \mathrm{M} \mathrm{NH}_{3}\) to ensure that the percent ionization of \(\mathrm{NH}_{3}\) is no greater than \(0.0010 \%\) ? Assume no volume change on addition of \(\mathrm{NaOH}\).

Will \(0.10 M\) solutions of the following salts be acidic, basic, or neutral? See Appendix 5 for \(K_{\mathrm{a}}\) values. a. ammonium bicarbonate b. sodium dihydrogen phosphate c. sodium hydrogen phosphate d. ammonium dihydrogen phosphate e. ammonium formate

Aluminum hydroxide is an amphoteric substance. It can act as either a Br酶nsted-Lowry base or a Lewis acid. Write a reaction showing \(\mathrm{Al}(\mathrm{OH})_{3}\) acting as a base toward \(\mathrm{H}^{+}\) and as an acid toward \(\mathrm{OH}^{-}\).

A sample containing \(0.0500 \mathrm{~mol} \mathrm{Fe}_{2}\left(\mathrm{SO}_{4}\right)_{3}\) is dissolved in enough water to make \(1.00 \mathrm{~L}\) of solution. This solution contains hydrated \(\mathrm{SO}_{4}{ }^{2-}\) and \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}{ }^{3+}\) ions. The latter behaves as an acid: $$\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{3+}(a q) \rightleftharpoons \mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{OH}^{2+}(a q)+\mathrm{H}^{+}(a q)$$ a. Calculate the expected osmotic pressure of this solution at \(25^{\circ} \mathrm{C}\) if the above dissociation is negligible. b. The actual osmotic pressure of the solution is \(6.73\) atm at \(25^{\circ} \mathrm{C}\). Calculate \(K_{\mathrm{a}}\) for the dissociation reaction of \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{3+}\). (To do this calculation, you must assume that none of the ions goes through the semipermeable membrane. Actually, this is not a great assumption for the tiny \(\mathrm{H}^{+}\) ion.)

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