Chemistry Chemistry homework
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Acid-BaseEquilibriaKeqApproximationHenderson-HasselbalchApplications1.pdf
WS22.pdf
Acid-BaseEquilibriaKeqApproximationHenderson-HasselbalchApplications1.pdf
Krystel Bergher
WS22.pdf
CHEM 205 Worksheet (WS2)
52 Points Total
Key Topics: Acid-Base Equilibria, Keq Approximation, Henderson-Hasselbalch Applications
1. (a) For each of the Bronsted-Lowery acid base reactions below, draw the conjugate acid and conjugate
base pairs most likely to form. (b) Circle the set of arrows that best describe the equilibrium for each
reaction. (3pts for each correct conjugate pair, 1pt for each correct set of arrows)
2. (a) Using the structures provided, draw an arrow-pushing mechanism for the acid base reaction below.
(3pts). (b) Estimate the equilibrium constant for this reaction (Keq). Show work which led to this value.
(3pts). (c) Draw a different acid (assuming the same base) that would reverse the equilibrium to favor the
other side. (2pts).
3. One form of Henderson-Hasselbalch Equation shown below (See also Chapter 19.4 and 26.3) can be
derived from the generic equation for an acid-dissociation reaction. It is useful for approximating the pH
of an aqueous buffer. The expression can also be arranged to solve for pKa or the ratio of [conjugate
base]:[acid] or [base]:[conjugate acid] depending on the functional group being ionized.
Consider the two different cases below. Decide if the compound shown is most likely acting as a base or
acid then draw the most likely ionized form of the compound as it would exist at pH 7. For each case
calculate the % ionization. For Case 2 only, using the appropriate form of the Henderson-Hasselbalch
expression, show your work which led to each % ionized answer. (2pts for each correct structure, 1pt
for each correct % ionization, 4pts for relevant work shown). Note, the % ionized value
approximated for each case should be some value < 100% and > 0%.
Note: You will need to use Table 1.8 in your text to find the relevant pKa. Round the pKa to the nearest
whole number.
Show work for how you solved for the % ionization for Case 2 below:
4. Suppose Compound B is the conjugate base of Compound A. Calculate the approximate concentration
of Compound A that must be present in a 0.042 M solution of Compound B to produce a pH of 4.96. The
Ka for Compound A is 1.8 x 10-5. Show your work. Round your final answer to the nearest hundredth
decimal place. (5pts)
5. Consider the structure below. Then using the empty boxes, answer parts (a)-(c).
(a) (1pts) Draw a constitutional isomer expected to have approximately the same pKa as the compound
above.
(b) (2pts) Draw a constitutional isomer that you expect to be less acidic than the compound above.
(c) (2pts) Draw a constitutional isomer that is roughly 1012 times more acidic than the compound above.
6. The relative acidity (or basicity) of compounds is influenced by factors including: periodic trends,
resonance, induction, and orbitals. For each case below there are two protons circled. Indicate which one
is most acidic and briefly explain the factor that is most responsible. If resonance is the determining factor,
draw relevant resonance structures to clearly illustrate. (1pt each correct answer, 2pt for each valid
explanation).
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