CAIE A-Level Chemistry A2 25.1 Acids and Bases Questions
Practise acid-base equilibrium work, from conjugate-pair identification to pH, buffer and Ksp calculations with units.
- Syllabus
- 2028–2030
- Course
- Chemistry 9701
- Level
- A2
Practise acid-base equilibrium work, from conjugate-pair identification to pH, buffer and Ksp calculations with units.
Hypophosphorous acid is an inorganic acid.
The conjugate base of hypophosphorous acid is H2PO2−.
Give the formula of hypophosphorous acid.
H3PO2
Define conjugate acid-base pair.
two species that differ by one proton / H+
Give the formulas of the conjugate acid and the conjugate base of the hydrogen phosphate ion, HPO42−.
H2PO4− AND PO4 3−
The Ka of propanoic acid, CH3CH2COOH, is 1.35×10−5moldm−3 at 298 K.
Solution C is a solution of CH3CH2COOH with a pH of 3.60 at 298 K.
Calculate the concentration of CH3CH2COOH in solution C.
[2]
M1: [H+]=2.51×10−4
M2: [CH3CH2COOH]=4.67×10−3
Calculate the concentration of hydroxide ions in solution C.
3.98×10−11
Calculate the concentration of a solution of hydrochloric acid with the same pH as solution C.
[HCl]=2.51×10−4
Table 3.1 shows three possible values of the Ka of dimethylpropanoic acid, (CH3)3CCOOH.
Place a tick in Table 3.1 to show the correct value. Explain your answer.
Table 3.1
explanation
M1: top box ticked AND weaker acid
M2: alkyl group is electron donating
M3: O-H bond strengthened / anion is destabilised
Solution D is made by mixing 100 cm3 of 0.100 moldm−3CH3CH2COOH and 100 cm3 of 0.100 moldm−3NaCl.
The pH of solution D is measured as small amounts of H2SO4(aq) are added to it, and when small amounts of NaOH(aq) are added to it.
Solution D only acts as a buffer solution when one of these solutions is added to it.
Complete the sentence and write an equation for the reaction that occurs.
Solution D acts as a buffer when is added to it.
equation
NaOH AND CH3CH2COOH+OH−→CH3CH2COO−+H2O
Complete the sentence and explain why solution D does not act as a buffer when the other solution is added.
Solution D does not act as a buffer when is added to it.
explanation
H2SO4 AND conjugate base of CH3CH2COOH is not present
Manganese(II) hydroxide, Mn(OH)2, is only slightly soluble in water.
The solubility of Mn(OH)2 in water is 3.28×10−3gdm−3 at 298 K .
Calculate the concentration of a saturated solution of Mn(OH)2 at 298 K.
3.69×10−5
Write an expression for the Ksp of Mn(OH)2. Give the units of Ksp.
units =
M1: Ksp=[Mn2+][OH−]2
M2: units =mol3dm−9
Use your answers to (d)(i) and (d)(ii) to calculate the value of Ksp of Mn(OH)2 at 298 K.
2.0×10−13
A student uses thin-layer chromatography (TLC) to analyse a mixture containing different metal cations. The student repeats the experiment using different solvents.
Fig. 6.1 shows the chromatogram obtained by the student using water as a solvent.
Fig. 6.1
In a third experiment, the pH of the mixture of metal ions is kept constant using a buffer solution.
The student prepares the buffer solution by mixing 20.0 cm3 of 0.150moldm−3KOH(aq) and 50.0 cm3 of 0.100 moldm−3C8H5O4 K(aq).
C8H5O4 K is a weak carboxylic acid that has pKa=5.40.
Fig. 6.2
Complete the equation for the reaction of C8H5O4 K(aq) with KOH(aq).
C8H5O4 K+
C8H5O4 K+KOH→C8H4O4 K2+H2O OR C8H5O4 K+OH−→C8H4O4 K−+H2O
Calculate the pH of the buffer solution. Show all your working.
M1 initially: moles of KOH=0.150×20.0÷1000=3.0×10−3
AND moles of acid HA =0.100×50.0÷1000=5.0×10−3
M2 at equilibrium: moles of salt KA =3.0×10−3 ecf
AND moles of acid HA=5.0×10−3 - moles of NaOH =2.0×10−3 ecf
M3 Ka=10−5.40=3.98×10−63.98×10−6=[H+][3.0×10−3]÷[2.0×10−3][H+]=2.65×10−6 eff
M4 pH=−log(2.65×10−6)=5.58/5.6 ecf on a calculated and identified [H+]
ALLOW alternative approach using Henderson-Hasselbalch equation for M3 and M4
A student uses thin-layer chromatography (TLC) to analyse a mixture containing different metal cations. The student repeats the experiment using different solvents.
Fig. 6.1 shows the chromatogram obtained by the student using water as a solvent.
Fig. 6.1
In a third experiment, the pH of the mixture of metal ions is kept constant using a buffer solution.
The student prepares the buffer solution by mixing 20.0 cm3 of 0.150moldm−3KOH(aq) and 50.0 cm3 of 0.100 moldm−3C8H5O4 K(aq).
C8H5O4 K is a weak carboxylic acid that has pKa=5.40.
Fig. 6.2
Calculate the pH of the buffer solution. Show all your working.
M1 initially: moles of KOH=0.150×20.0÷1000=3.0×10−3
AND moles of acid HA =0.100×50.0÷1000=5.0×10−3
M2 at equilibrium: moles of salt KA =3.0×10−3 ecf
AND moles of acid HA=5.0×10−3 - moles of NaOH =2.0×10−3 ecf
M3 Ka=10−5.40=3.98×10−63.98×10−6=[H+][3.0×10−3]÷[2.0×10−3][H+]=2.65×10−6 eff
M4 pH=−log(2.65×10−6)=5.58/5.6 ecf on a calculated and identified [H+]
ALLOW alternative approach using Henderson-Hasselbalch equation for M3 and M4
Manganese(II) hydroxide, Mn(OH)2, is only slightly soluble in water.
The solubility of Mn(OH)2 in water is 3.28×10−3gdm−3 at 298 K .
Write an expression for the Ksp of Mn(OH)2. Give the units of Ksp.
units =
M1: Ksp=[Mn2+][OH−]2
M2: units =mol3dm−9
Iodine is found naturally in compounds in many different oxidation states.
An orange precipitate of HgI2 forms when Hg2+ ions are added to KI(aq). The solubility of HgI2 at 25∘C is 1.00×10−7gdm−3.
Calculate the solubility product, Ksp, of HgI2. Include units in your answer.
[Mr:HgI2,454.4]
value of Ksp=
units =
Calcium iodate (V),Ca(IO3)2, is sparingly soluble in water.
The concentration of its saturated solution is 5.6×10−3 moldm−3 at 298 K .
When a few cm3 of concentrated Ca(NO3)2(aq) is added to a saturated solution of Ca(IO3)2 a white precipitate forms.
Identify the white precipitate and give an explanation for this observation.
M1 Ca(IO3)2 AND as solubility of Ca(IO3)2 decreases
M2 due to common ion effect