Use Le Châtelier’s principle to explain how the common ion effect affects the pH of a solution.
Expert Solution & Answer
Interpretation Introduction
Interpretation:
By using Le Chatelier’s principle, the changes of pH of a weak acid solution due to common ion effect has to be explained.
Concept introduction:
Le Chatelier's principle states that if a system in equilibrium gets disturbed due to modification of concentration, temperature, volume, and pressure, then it reset to counteract the effect of disturbance.
When the concentration of one of the ions of a chemical solution got higher, it reacts with counter charged ions and precipitated out as salt till the ion product equals solubility product is called common ion effect.
Incomplete dissociation of an acid in aqueous solution is called weak acid.
The pH of weak acid (acetic acid) increases due to addition of acetate ions from sodium acetate which suppress ionization of acetic acid leads to decrease in percent ionization of acetic acid. The equilibrium shifts towards left because of more acetate ion (common ion).
Explanation of Solution
To explain: The changes of pH of a weak acid solution due to common ion effect.
The equilibrium reaction of acetic acid and sodium acetate are as follows,
In an aqueous solution, dissolve acetic acid (weak acid) thoroughly which dissociates as acetate ions and hydronium ions. Then add sodium acetate (strong electrolyte) and it dissociates completely to form sodium ions and acetate ions. The common ion produced from both acetic acid and sodium acetate is acetate ion. By following the principle of Le Chatelier Principle, the acetate ions from sodium acetate combine with hydronium ions and the equilibrium shifts towards left which reduce the ionization of acetic acid.Thus lowers the percent dissociation of acetic acid and due to decrease in hydrogen ion concentration the pH of the solution will increase.
Conclusion
The change of pH of a weak acid solution due to common ion effect was explained by Le Chatelier's principle.
Want to see more full solutions like this?
Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Draw the Fischer projection of D-fructose.
Click and drag to start drawing a
structure.
Skip Part
Check
AP
14
tv
SC
F1
F2
80
F3
a
F4
!
2
#
3
CF
F5
75
Ax
MacBook Air
894
$
5olo
%
Λ
6 >
W
F6
K
F7
&
Consider this step in a radical reaction:
Y
What type of step is this? Check all that apply.
Draw the products of the step on the right-hand side of the drawing area
below. If more than one set of products is possible, draw any set.
Also, draw the mechanism arrows on the left-hand side of the drawing
area to show how this happens.
ionization
propagation
initialization
passivation
none of the above
22.16 The following groups are ortho-para directors.
(a)
-C=CH₂
H
(d)
-Br
(b)
-NH2
(c)
-OCHS
Draw a contributing structure for the resonance-stabilized cation formed during elec-
trophilic aromatic substitution that shows the role of each group in stabilizing the
intermediate by further delocalizing its positive charge.
22.17 Predict the major product or products from treatment of each compound with
Cl₁/FeCl₂-
OH
(b)
NO2
CHO
22.18 How do you account for the fact that phenyl acetate is less reactive toward electro-
philic aromatic substitution than anisole?
Phenyl acetate
Anisole
CH
(d)
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.