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5: Le Chatelier's Principle (Experiment)

  • Page ID
    127026
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    Objectives

    • To perturb chemical reactions at equilibrium and observe how they respond.
    • To explain these observations using Le Chatelier’s Principle.
    • To relate Le Chatelier’s Principle to the concept of coupled reactions.

    All chemical reactions eventually reach a state in which the rate of the reaction in the forward direction is equal to the rate of the reaction in the reverse direction. When a reaction reaches this state, it is said to be at chemical equilibrium. The concentrations of reactants and products at equilibrium are constant as a function of time. Thus, for a homogeneous aqueous system of the form

    \[a \text{A} (aq) + b\text{B} (aq) \ce{<=>}c\text{C} (aq) + d\text{D} (aq) \label{1}\]

    we can express the equilibrium-constant expression for this reaction as,

    \[K_{c}= \frac{[\text{C}]^{c}[\text{D}]^{d}}{[\text{A}]^{a}[\text{B}]^{b}} \label{2}\]

    where the values of \([\text{A}]\), \([\text{B}]\), \([\text{C}]\), and \([\text{D}]\) correspond to the equilibrium concentrations (or equilibrium positions) of all the aqueous chemical components, and \(a\), \(b\), \(c\), and \(d\) are their respective stoichiometric coefficients. Note that for a heterogeneous system including pure solids or liquids of the form

    \[a \text{A} (aq) + b\text{B} (s) \ce{<=>}c\text{C} (aq) + d\text{D} (l) \label{3}\]

    the pure liquids and solids do not appear in the equilibrium-constant expression:

    \[K_{c}= \frac{[\text{C}]^{c}}{[\text{A}]^{a}} \label{4}\]

    It has been observed that when a reaction at equilibrium is perturbed by applying a stress, the reaction will respond by shifting its equilibrium position so as to counteract the effect of the perturbation/stress. In other words, the concentrations of the reactants and products will shift so that the relationship described by Equation \ref{2} is again satisfied. This idea was first proposed by Henri-Louis Le Chatelier and has since been referred to as “Le Chatelier’s Principle.”

    Note that when a reaction makes more products as a response to the perturbation, we call it a right-shift. When a reaction makes more reactants in response to the perturbation, we call it a left-shift. We often designate these respective shifts by drawing right and left arrows below the chemical equation.

    For chemical reactions at equilibrium in aqueous solutions, the most common types of perturbations include changing the concentration of one of the aqueous solutes, changing the concentrations of all aqueous solutes by changing the total solution volume, or changing the temperature. The general responses of an aqueous system to these particular perturbations are tabulated below.

    Perturbation Effect on Equilibrium Position Effect on \(K_{c}\)
    Increase in concentration of a single reactant, or, decrease in concentration of a single product. Shift to the right None
    Decrease in concentration of a single reactant, or, increase in concentration of a single product. Shift to the left None
    Decrease in all aqueous concentrations due to an increase in solution volume resulting from the addition of solvent Shift towards the side with more solute particles None
    Increase in all aqueous concentrations due to a decrease in solution volume resulting from the removal of solvent (evaporation) Shift towards the side with fewer solute particles None
    Increase temperature of an exothermic reaction Shift to the left Decrease
    Decrease temperature of an exothermic reaction Shift to the right Increase
    Increase temperature of an endothermic reaction Shift to the right Increase
    Decrease temperature of an endothermic reaction Shift to the left Decrease
    Addition of an inert substance, catalyst, pure liquid, or pure solid None None

    Notice that only a temperature change can affect the value of \(K_{c}\); in all other cases, the value of \(K_{c}\) remains constant.

    In this experiment, you will perturb reactions that have attained equilibrium. You will then observe how each reaction responds to that perturbation in order to restore equilibrium. In your report, you describe these changes in terms of Le Chatelier’s Principle.

    Part A – Acid-Base Equilibrium

    Here you will use coupled equilibria to change the equilibrium position of an acid-base reaction. In order to understand how coupled equilibria work consider the reactions described by the chemical equations below:

    \[ \text{A} (aq) \ce{<=>}\text{B} (aq) \label{5}\]

    \[\text{B} (aq) + \text{C} (aq) \ce{<=>} \text{D} (aq) \label{6}\]

    Notice that the species \(\text{B} (aq)\) is common to both reactions. The presence of this common species couples these two reactions.

    We can perturb the equilibrium position of Reaction \ref{6} by the addition of some \(\text{C} (aq)\).The addition of \(\text{C} (aq)\) will cause the equilibrium position of Reaction \ref{6} to shift right in accordance with Le Chatelier’s Principle. This right shift in the equilibrium position of Reaction \ref{6} will also result a corresponding decrease in the concentration of \(\text{B} (aq)\). Because \(\text{B} (aq)\) is also present in Reaction \ref{5}, the decrease in the concentration of \(\text{B} (aq)\) will in turn result in a right shift in the equilibrium position of Reaction \ref{5}. Thus, the addition of \(\text{C} (aq)\) to Reaction \ref{6} actually results in a right shift in the equilibrium position of Reaction \ref{5} because the equilibria are coupled.

    In Part A we will observe the effect of various solutes on an acid-base indicator (a weak acid) at equilibrium. The equilibrium system can be written in the general form

    \[\ce{ HA (aq) <=> H^{+} (aq) + A^{-} (aq)} \label{7}\]

    The equilibrium-constant expression for this reaction is

    \[K_{a}= \frac{[\ce{H^{+}}][\ce{A^{-}}]}{[\ce{HA}]} \label{8}\]

    where we denote the equilibrium constant, \(K\), with a subscript \(a\) for acid. In this experiment, \(\ce{HA}\) and \(\ce{A^{-}}\) are the acidic and basic forms of the indicator bromothymol blue. Since the two forms are different colors, you will be able to determine which form is predominant in the equilibrium mixture. In other words, you will be able to determine whether the equilibrium position lies to the left (more reactants and less products) or whether the equilibrium lies to the right (more products and less reactants).

    Your goal will be to find a reagent that will shift the position of this equilibrium to the opposite side, and then another reagent that will shift it back towards its original position. Instead of directly adding \(\ce{HA}\) or \(\ce{A^{-}}\) to the system, you will affect these shifts by adding \(\ce{H^{+}}\) or \(\ce{OH^{-}}\). Note that in order to determine the effect of \(\ce{OH^{-}}\) we must consider a second chemical reaction that shares a common species with the Reaction \ref{7}. The second reaction is the autoionization of water, which can be described by the equation

    \[\ce{ H2O (l) <=> H^{+} (aq) + OH^{-} (aq)} \label{9}\]

    The equilibrium constant for this reaction is denoted by \(K_{w}\), where the subscript \(w\) stands for water, and the associated equilibrium constant expression is

    \[K_{w}= [\ce{H^{+}}][\ce{OH^{-}}] \label{10}\]

    Because Reactions \ref{7} and \ref{9} share a common chemical species (\(\ce{H^{+}}\)), you can use the concept of coupled equilibria to shift the equilibrium position of Reaction \ref{7} by increasing or decreasing the concentration of \(\ce{OH^{-} (aq)}\).

    Part B – Solubility Equilibrium

    Here you will test the effects of changing temperature and volume on the solubility of a slightly soluble salt at equilibrium. Some examples of slightly soluble salts are \(\ce{AgCl}\), \(\ce{Cu(OH)2}\), \(\ce{PbCl2}\), and \(\ce{Fe2S3}\) and are general referred to as being “insoluble in water.” However, a very small amount of each of these substances dissolves in aqueous solutions, but the amount is so small that we often classify each of these compounds as “insoluble.”

    This type of equilibrium is often called a solubility equilibrium because it is written in the direction of the dissolution of the solid, as shown in the following example:

    \[ \text{A}_{\text{x}} \text{B}_{\text{y}} (s) \ce{<=>} x\text{A}^{+} (aq) + y\text{B}^{-} (aq) \label{11}\]

    The equilibrium-constant expression for Reaction \ref{11} is

    \[K_{sp}= [\text{A}^{+}]^{x}[\text{B}^{-}]^{y} \label{12}\]

    where we denote the equilibrium constant, \(K\), with a subscript \(sp\) for solubility product.

    Now let’s consider the process of precipitation. In a typical precipitation reaction two aqueous salt solutions are mixed together resulting in the production of an insoluble salt. Notice that this process corresponds to a left shift of Reaction \ref{11}, and so Equation \ref{12} can also be used to examine the conditions required for the precipitation of a solid to occur. We can denote the product \([\text{A}^{+}]^{x}[\text{B}^{-}]^{y}\) under arbitrary conditions (not necessarily at equilibrium) as,

    \[Q_{sp}= [\text{A}^{+}]^{x} [\text{B}^{-}]^{y} \label{13}\]

    where \(Q_{sp}\) is called the solubility product reaction quotient. Note that, upon mixing two solutions, one containing \(\text{A}^{+}\) and the other containing \(\text{B}^{-}\), if \(Q_{sp}<K_{sp}\) the system is not at equilibrium, but since no solid \(\text{A}_{\text{x}} \text{B}_{\text{y}}\) is present the reaction cannot shift to the right and therefore no reaction will be observed. In contrast, if \(Q_{sp}>K_{sp}\) the solution contains an excess of aqueous species, and Reaction \ref{11} will shift left, forming the solid precipitate \(\text{A}_{\text{x}} \text{B}_{\text{y}}\) until the system reaches a state of equilibrium where \(Q_{sp}=K_{sp}\) . Thus, we can use the values of \(Q_{sp}\) and \(K_{sp}\) to predict the conditions under which a precipitation reaction will occur.

    In Part B we will study the solubility equilibrium of \(\ce{PbCl2 (s)}\). We will observe the effect on this solubility equilibrium of changes in solution volume (quantity of solvent) and temperature. We will express these changes in terms of the respective values of \(Q_{sp}\) and \(K_{sp}\).

    Part C – Complex Ion Equilibrium

    Certain metal ions, most often transition metals, exist in solution as complex ions in combination with other ions or molecules, called ligands. Common ligands include \(\ce{H2O}\), \(\ce{NH3}\), \(\ce{Cl^{–}}\), and \(\ce{OH^{–}}\). Many of these complex ions exhibit vibrant colors in solution. For example, the \(\ce{Co(H2O)6^{2+} (aq)}\) complex ion is pink and the \(\ce{CoCl4^{2-} (aq)}\) complex ion is blue.

    In Part C you will study the following complex ion formation reaction:

    \[\ce{Co(H2O)6^{2+} (aq) + 4Cl^{-} (aq) <=> CoCl4^{2-} (aq) + 6H2O (l)} \label{14}\]

    The equilibrium-constant expression for Reaction \ref{14} is

    \[K_{f}= \frac{[\ce{CoCl4^{2-}}]}{[\ce{Co(H2O)6^{2+}}][\ce{Cl^{-}}]^{4}} \label{15}\]

    where we denote the equilibrium constant, \(K\), with a subscript \(f\) for complex ion formation.

    Your goal in Part C is to observe how Reaction \ref{14} shifts from its equilibrium position as the result of various perturbations.

    Part D – Dissolving Insoluble Solids

    In Part D you will use coupled equilibria to affect the solubility equilibrium of \(\ce{Zn(OH)2 (s)}\). The solubility equilibrium can be described by the equation

    \[\ce{Zn(OH)2 (s) <=> Zn^{2+} (aq) + 2OH^{-} (aq)}\quad\quad K_{sp} = 5 \times 10^{-17} M^{3} \label{16}\]

    Notice that \(K_{sp} << 1\) for this reaction, demonstrating that \(\ce{Zn(OH)2 (s)}\) is only very slightly soluble in aqueous solution.

    Now consider the reactions described by the following chemical equations, each of which shares a common species with the Reaction \ref{16}:

    \[\ce{H2O (l) <=> H^{+} (aq) + OH^{-} (aq)}\quad\quad\quad\quad\quad\quad\quad K_{w} = 1 \times 10^{-14} M^{2} \label{17}\]

    \[\ce{Zn^{2+} (aq) + 4 OH^{-} (aq) <=> Zn(OH)4^{2-} (aq)}\quad\quad K_{f} = 3 \times 10^{15} M^{-4} \label{18}\]

    \[\ce{Zn^{2+} (aq) + 4 NH3 (aq) <=> Zn(NH3)4^{2+} (aq)}\quad\quad K_{f} = 1 \times 10^{9} M^{-4} \label{19}\]

    Because Reactions \ref{17}, \ref{18}, and \ref{19} each share a common species with Reaction \ref{16} they can be coupled together. In Part D of this experiment, you will observe the effect of coupling each of these equilibria on the solubility of \(\ce{Zn(OH)2 (s)}\).

    Procedure

    Equipment

    From lab/locker: Six large test tubes, test tube rack, stirring rod, scoopula, small 10-mL graduated cylinder, large 100-mL graduated cylinder, 400-mL beaker, hot plate

    From hallway: Ice Machine

    Chemicals

    Bromothymol blue, a 6 M strong acid, a 6 M strong base, 0.3 M \(\ce{Pb(NO3)2 }\) (aq), 0.3 M \(\ce{HCl}\) (aq), \(\ce{CoCl2*6H2O}\) (s), 12 M \(\ce{HCl}\) (aq), 0.1 M \(\ce{Zn(NO3)2}\) (aq), 0.1 M \(\ce{Mg(NO3)2}\) (aq), 6 M \(\ce{NaOH}\) (aq), 6 M \(\ce{HCl}\) (aq), 6 M \(\ce{NH3}\) (aq) (often labeled as \(\ce{NH4OH}\)), and deionized water

    Safety And Waste Disposal

    • 12-M \(\ce{HCl}\), is extremely caustic and great care must be taken to avoid contact with eyes or skin. The bottle should be kept in a plastic tray and not removed from the fume hood. Should any of this solution enter your eyes rinse immediately in the emergency eyewash. Should any of this solution come in contact with your skin rinse with copious amounts of water and apply saturated sodium bicarbonate to the affected area from the stock bottle located on the sink.
    • The solutions you will use in Part B contain lead. Be certain that all of these lead-containing solutions are disposed of in the proper waste container and rinse your hands following this procedure.
    • Many of the chemicals used in this lab are hazardous to the environment. All waste must be disposed of in the hazardous-waste container in the fume hood. Rinse all glassware directly into the waste container twice using a small squirt bottle to be certain all hazardous waste ends up in the waste container.

    General Procedural Notes

    The amounts of reagents used in this experiment are approximate only. If you are unsure how to estimate a milliliter, then measure out about one milliliter of water using your graduated cylinder, transfer this amount to a large test tube, and then use this approximate volume as a reference throughout the experiment.

    All glassware needs to be rinsed at least once with deionized water. It is not necessary to dry glassware since all reagent volumes are approximate and all solutions are aqueous.

    Part A: Acid-Base Equilibrium

    Here you will find a reagent that will shift the acid-base equilibrium given by Reaction \ref{7} in one direction and then a second reagent that will cause the equilibrium position to shift back in the opposite direction.

    Reagents needed for this part are: deionized water, bromothymol blue solution, a 6 M strong acid, and a 6 M strong base.

    1. Add approximately 5 mL of deionized water to a large test tube. Add 3 drops of the bromothymol blue indicator solution. Report the color of your solution on your datasheet.
    2. Your solution from Step 1 currently contains one form of bromothymol blue (see background). Now predict which of the two 6 M reagents you obtained, the strong acid or the strong base, will cause a color change in your solution by making the bromothymol blue indicator shift to its other form. Add the 6 M reagent of your choice drop-by-drop and if your solution changes color, write the color of the solution and formula of the reagent on your datasheet. If the addition of your reagent does not result in a color change, try other reagents until you are successful.
    3. Since equilibrium systems are reversible, it is possible to shift a reaction left or right repeatedly by changing the conditions. Now find another 6 M reagent that will cause your solution from Step 2 to revert back to its original color. Add the 6 M reagent of your choice drop-by-drop and if your solution changes color, write the formula of the reagent on the datasheet. If the addition of your second reagent does not result in a color change, try other reagents until you are successful.

    Part B: Solubility Equilibrium

    You will test the effects of changing the solution volume and temperature on the solubility equilibrium of lead (II) chloride.

    Reagents needed are: 0.3 M \(\ce{Pb(NO3)2}\) (aq), 0.3 M \(\ce{HCl}\) (aq), and deionized water.

    1. Set up a hot-water bath by filling a 400-mL beaker about half-full with tap water and heating the water using a hot plate while you work on the following steps. The hot-water bath will be used in Step 6 (and also in Part C).
    2. Measure 5.0 mL of the 0.3 M \(\ce{Pb(NO3)2}\) solution into a large test tube using a 10-mL graduated cylinder.
    3. Thoroughly rinse the graduated cylinder with deionized water, then measure 5.0 mL of the 0.3 M \(\ce{HCl}\) solution using the 10-mL graduated cylinder.
    4. Add about 1 mL of the 0.3 M \(\ce{HCl}\) solution to the \(\ce{Pb(NO3)2}\) solution in the large test tube. Stir the mixture gently using your stirring-rod and record your observations on your data sheet.
    5. Continue to add the 0.3 M \(\ce{HCl}\) solution to the \(\ce{Pb(NO3)2}\) solution in the large test tube in roughly 1 mL increments until you just begin to see white \(\ce{PbCl2}\) solid appear in your test tube. To confirm that the solid is present, let the test tube sit on the bench for about 3 minutes, allowing all solid to settle to the bottom where it is easier to see. On your data sheet record, the total volume of 0.3 M \(\ce{HCl}\) needed to produce the solid.
    6. Put the test tube containing the solid into your hot-water bath from Step 1. Stir the contents of the test tube gently for a few seconds using the glass stirring-rod and record your observations on your datasheet. Continue heating and stirring until a change is observed.
    7. Make a cold-water bath by filling a 400-mL beaker half full with tap water and ice. Cool the test tube down by placing it into this cold-water bath. Observe what happens and record your observations. Save this cold-water bath for use in Part C.
    8. Dispose of the remainder of the 0.3 M \(\ce{HCl}\) solution in your 10-mL graduated cylinder by pouring it into the appropriate waste container and then rinse the cylinder using deionized water. Next measure 5.0 mL of deionized water using this graduated cylinder.
    9. Add about 1 mL of deionized water to the large test tube containing the \(\ce{PbCl2}\) solid. Stir the mixture and observe what happens. Continue to add the deionized water in 1 mL increments until the white \(\ce{PbCl2}\) solid just dissolves (or disappears). On your datasheet, record the volume of water needed to dissolve the solid.
    10. Pour the contents of the large test tube into your large graduated cylinder and measure the total volume of the solution. Record this volume on your datasheet.
    11. Dispose of all solutions used in Part B in the proper waste container. Rinse all glassware twice using a wash bottle of deionized water to ensure that all of the lead solution has been removed and transferred to the waste container. Save the hot- and cold-water baths for Part C.

    Part C: Complex Ion Equilibrium

    Here you will test the effects of changing the volume and temperature on the complex ion equilibrium between Co(H2O)62+ (aq) and CoCl42- (aq) as in Reaction \ref{14}.

    Reagents needed for this part are: \(\ce{CoCl2*6H2O}\) (s), 12 M \(\ce{HCl}\) (aq) (do not remove from fume hood), and deionized water.

    1. Reheat your hot-water bath from part B to a near boil. The hot-water bath will be used in Step 4.
    2. Put a few small crystals (an amount that fits at the tip of the scoopula) of \(\ce{CoCl2*6H2O}\) (s) in a large test tube. Working in the fume hood, carefully add 2 mL of 12 M \(\ce{HCl}\) (aq) (this acid is extremely caustic; see cautions in the safety section of this experiment). Add a 1/2 inch magnetic stir bar and stir to dissolve the crystals. Record the color of this solution.
    3. Using a 10-mL graduated cylinder, add deionized water to the solution in your test tube in approximately 2 mL increments, stirring after each addition, until no further color change occurs. Record the new color.
    4. Place the test tube into the hot-water bath from Step 1 and record any color change.
    5. Cool the solution down in the cold-water bath and record any color change.

    Part D: Dissolving Insoluble Solids

    Here you will further examine how one reaction can affect the behavior of another reaction when the reactions share one or more common chemical species.

    Reagents needed for are: 0.1 M \(\ce{Zn(NO3)2}\) (aq), 0.1 M \(\ce{Mg(NO3)2}\) (aq), 6 M \(\ce{NaOH}\) (aq), 6 M \(\ce{HCl}\) (aq), and 6 M \(\ce{NH3}\) (aq) (often labeled as \(\ce{NH4OH}\)).

    1. Label three large test tubes A, B, and C. Add about 2 mL of 0.1 M \(\ce{Zn(NO3)2}\) solution to each test tube. Add one drop of 6 M \(\ce{NaOH}\) solution to each test tube. Stir each solution and record your observations.
    2. Into test tube A, add at least 20 drops of 6 M \(\ce{HCl}\) (aq) drop-by-drop while stirring. Record all observations.
    3. Into test tube B, add at least 20 drops of 6 M \(\ce{NaOH}\) (aq) drop-by-drop while stirring. Record all observations.
    4. Into test tube C, add at least 20 drops of 6 M \(\ce{NH3}\) (aq) drop-by-drop while stirring. Record all observations.
    5. Label three additional large test tubes D, E, and F. Add about 2 mL of 0.1 M \(\ce{Mg(NO3)2}\) solution to each test tube. Add one drop of 6 M \(\ce{NaOH}\) solution to each test tube. Stir each solution and record your observations.
    6. Into test tube D, add at least 20 drops of 6 M \(\ce{HCl}\) (aq) drop-by-drop while stirring. Record all observations.
    7. Into test tube E, add at least 20 drops of 6 M \(\ce{NaOH}\) (aq) drop-by-drop while stirring. Record all observations.
    8. Into test tube F, add at least 20 drops of 6 M \(\ce{NH3}\) (aq) drop-by-drop while stirring. Record all observations.

    This page titled 5: Le Chatelier's Principle (Experiment) is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by Santa Monica College.