Chapter 19 - Ionic Equilibria in Aqueous Systems
The sodium ion is a spectator ion since it does not interact with water (as shown in the image attached). According to Le Châtelier's principle, adding CH3COO ion shifts the equilibrium position to the left; consequently, [H3O+] drops, decreasing the degree of acid dissociation:
CH3COOH(aq) + H2O(l) ⥫⥬ H3O+(aq) + CH3COO− (aq; added)
When we add acetic acid to a sodium acetate solution instead of water, we obtain the same effect.
The previously existent acetate ion prevents the acid from dissociating as much as it does in water, keeping the [H3O+] lower (and pH higher). The result is less acid dissociation in either situation.
The ion acetate is known as the common ion because it is present in both acetic acid and sodium acetate solutions.
When a particular ion is introduced to an equilibrium mixture that already includes that ion, the point of equilibrium changes away from producing it.
The image attached above indicates that when the concentration of acetate ion (provided by dissolving sodium acetate) increases, the percent dissociation (and the [H3O+]) of an acetic acid solution drops.
As a result, the common ion, A, prevents the dissociation of HA, as it reduces the acidity of the solution (higher pH).
As a result, the buffer components absorb virtually all of the additional H3O+ or OH. To restate, as long as the quantity of additional H3O+ or OH is modest in comparison to the quantities of the buffer components, converting one component into the other results in a minor change in the buffer-component concentration ratio and, as a result, a tiny change in [H3O+] and pH.
The pH variations in Sample Problem 19.1 are generally quite modest. It is worth noting that the latter two sections of the issue have a stoichiometry component.
When H3O+ or OH is introduced to a buffered solution, the pH changes significantly less than in an unbuffered solution.
A buffer is made up of a weak acid and a conjugate base (or a weak base and a conjugate acid). To be effective, the component quantities must be substantially larger than the quantity of H3O+ or OH that has been added.
The pH is determined by the buffer-component concentration ratio; the ratio and the pH are related.
The Henderson-Hasselbalch equation connects them. When H3O+ or OH is introduced to a buffer, one component interacts to produce the other, resulting in the formation of the buffer. [H3O+] (and pH) barely minimally alter.
A concentrated (high capacity) buffer has lower pH fluctuations than a dilute buffer. When H3O+ or OH is introduced to a buffer, one component interacts to create the other, resulting in just a small change in [H3O+] (and pH). A concentrated (high capacity) buffer has lower pH fluctuations than a dilute buffer.
The buffer has the greatest capacity when the pH of the buffer equals the pKa of the acid component.
A buffer's effective pH range is pKa 1 pH unit. To make a buffer, select a conjugate acid-base pair and determine the component ratio. Calculate the buffer concentration and adjust the final solution to the desired pH.
The pH of a strong acid–strong base titration begins low, steadily increases, and suddenly rockets up towards the equivalence point (pH = 7).
In a weak acid–strong base titration, the pH begins higher and gradually rises in the buffer zone (at the midway, pH = pKa), and then rapidly rises towards the equivalence point (pH > 7).
A weak base–strong acid titration curve has the inverse form of a weak acid–strong acid titration curve. The pH decreases to the equivalence point (pH 7) in the strong base scenario.
A weak acid with a distinct colored conjugate base form is an acid-base (pH) indicator and changes hue during the course of roughly two pH units. Polyprotic acids contain two or more acidic protons, each with its own ion.
Polyprotic acids are composed of two or more acidic protons, each with its own Ka value. Because the Kas varies by many orders of magnitude, each proton is titrated individually.
Amino acids exist in charged forms that are determined by the pH of the solution. The total charge of a protein, which can impact its function.
The sodium ion is a spectator ion since it does not interact with water (as shown in the image attached). According to Le Châtelier's principle, adding CH3COO ion shifts the equilibrium position to the left; consequently, [H3O+] drops, decreasing the degree of acid dissociation:
CH3COOH(aq) + H2O(l) ⥫⥬ H3O+(aq) + CH3COO− (aq; added)
When we add acetic acid to a sodium acetate solution instead of water, we obtain the same effect.
The previously existent acetate ion prevents the acid from dissociating as much as it does in water, keeping the [H3O+] lower (and pH higher). The result is less acid dissociation in either situation.
The ion acetate is known as the common ion because it is present in both acetic acid and sodium acetate solutions.
When a particular ion is introduced to an equilibrium mixture that already includes that ion, the point of equilibrium changes away from producing it.
The image attached above indicates that when the concentration of acetate ion (provided by dissolving sodium acetate) increases, the percent dissociation (and the [H3O+]) of an acetic acid solution drops.
As a result, the common ion, A, prevents the dissociation of HA, as it reduces the acidity of the solution (higher pH).
As a result, the buffer components absorb virtually all of the additional H3O+ or OH. To restate, as long as the quantity of additional H3O+ or OH is modest in comparison to the quantities of the buffer components, converting one component into the other results in a minor change in the buffer-component concentration ratio and, as a result, a tiny change in [H3O+] and pH.
The pH variations in Sample Problem 19.1 are generally quite modest. It is worth noting that the latter two sections of the issue have a stoichiometry component.
When H3O+ or OH is introduced to a buffered solution, the pH changes significantly less than in an unbuffered solution.
A buffer is made up of a weak acid and a conjugate base (or a weak base and a conjugate acid). To be effective, the component quantities must be substantially larger than the quantity of H3O+ or OH that has been added.
The pH is determined by the buffer-component concentration ratio; the ratio and the pH are related.
The Henderson-Hasselbalch equation connects them. When H3O+ or OH is introduced to a buffer, one component interacts to produce the other, resulting in the formation of the buffer. [H3O+] (and pH) barely minimally alter.
A concentrated (high capacity) buffer has lower pH fluctuations than a dilute buffer. When H3O+ or OH is introduced to a buffer, one component interacts to create the other, resulting in just a small change in [H3O+] (and pH). A concentrated (high capacity) buffer has lower pH fluctuations than a dilute buffer.
The buffer has the greatest capacity when the pH of the buffer equals the pKa of the acid component.
A buffer's effective pH range is pKa 1 pH unit. To make a buffer, select a conjugate acid-base pair and determine the component ratio. Calculate the buffer concentration and adjust the final solution to the desired pH.
The pH of a strong acid–strong base titration begins low, steadily increases, and suddenly rockets up towards the equivalence point (pH = 7).
In a weak acid–strong base titration, the pH begins higher and gradually rises in the buffer zone (at the midway, pH = pKa), and then rapidly rises towards the equivalence point (pH > 7).
A weak base–strong acid titration curve has the inverse form of a weak acid–strong acid titration curve. The pH decreases to the equivalence point (pH 7) in the strong base scenario.
A weak acid with a distinct colored conjugate base form is an acid-base (pH) indicator and changes hue during the course of roughly two pH units. Polyprotic acids contain two or more acidic protons, each with its own ion.
Polyprotic acids are composed of two or more acidic protons, each with its own Ka value. Because the Kas varies by many orders of magnitude, each proton is titrated individually.
Amino acids exist in charged forms that are determined by the pH of the solution. The total charge of a protein, which can impact its function.