AP Chemistry Unit 8.7: Protonation and pKa
Practice AP Chemistry Unit 8.7 questions on comparing pH with pKa to predict species, indicator behavior, and titration composition.
- Syllabus
- Effective Fall 2025
- Course
- AP Chemistry
Practice AP Chemistry Unit 8.7 questions on comparing pH with pKa to predict species, indicator behavior, and titration composition.
A student reacts 0.300 g of methyl salicylate (C8H8O3) with a stoichiometric amount of a strong base. This product is then acidified to produce salicylic acid crystals (HC7H5O3).
When the pH of the titration mixture is 4.00, is there a higher concentration of the weak acid, HC7H5O3, or its conjugate base, C7H5O3−, in the flask? Justify your answer.
For the correct answer and a valid justification, consistent with part (e):
Accept one of the following:
- The conjugate base, C7H5O3−. When pH=4, the titration is beyond the half-
equivalence point, where [HC7H5O3]=[C7H5O3−]. Thus, [C7H5O3−]must be
greater than [HC7H5O3].
- The conjugate base, C7H5O3−. Because the pH of the solution is greater than the
pKa of the acid, the majority of the molecules will be deprotonated.
1 point