RI 2025 Acid-Base Equilibria Tut 15 - Answers to Self-check questions
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Text from the first pages-6- Suggested Answers to Self–Check Questions 1 (a) (i) A Brønsted–Lowry acid is a proton donor while a Brønsted–Lowry base is a proton acceptor. In this case, an acid–base reaction involves the transfer of a proton from the acid to the base. (ii) Acid 1 and base 1 constitute one conjugate acid–base pair. Acid 2 and base 2 constitute another conjugate acid–base pair. I. CH3COOH + H2SO4 ⇌ CH3COOH2+ + HSO4– base 1 acid 2 acid 1 base 2 II. CH3NH2(aq) + H2O(l) ⇌ CH3NH3+(aq) + OH–(aq) base 1 acid 2 acid 1 base 2 III. HNO2(aq) + CN–(aq) ⇌ HCN(aq) + NO2–(aq) acid 1 base 2 acid 2 base 1 (b) (i) A Lewis acid is an electron–pair acceptor while a Lewis base is an electron–pair donor. In this case, an acid–base reaction involves the formation of a dative covalent bond between the acid and the base. (ii) I. (CH3)3N(g) + BF3(g) ⇌ (CH3)3NBF3(s) base acid II. A l(OH)3(s) + OH–(aq) ⇌ [Al(OH)4]–(aq) acid base (c) (i) HBr(g) + H2O(l) → H3O+(aq) + Br–(aq) Brønsted–Lowry acid base Lewis acid base (ii) HIO + NH2– ⇌ NH3 + IO– Brønsted–Lowry acid base Lewis acid base (iii) Brønsted–Lowry base acid Lewis base acid 2 (a) 0.010 mol dm−3 H2SO4 (strong dibasic acid) H2SO4(aq) 2H+(aq) + SO42–(aq) [H+] = 2 0.010 = 0.0200 mol dm–3 pH = lg (0.0200) = 1.70 (b) 0.40 g dm −3 NaOH (strong base) NaOH(aq) Na+(aq) + OH–(aq) . ... . 304 0OH 0 0100 mol dm23 0 16 0 1 0 pOH = lg (0.0100) = 2.00 pH = 14 2.00 = 12.0 (c) 14.00 cm 3 of 0.10 mol dm−3 H2SO4 is added to 20.00 cm3 of 0.10 mol dm–3 NaOH (strong acid partially neutralised by strong base) 14.002 0.10 0.0028 mol1000 Hn 20.00 0.10 0.002 mol1000 OHn in resultant solution 0.0028 0.002 0.0008 mol Hn 3 0.0008H in resultant solution 100014.00 20.00 0.02353 mol dm pH of resultant solution = lg (0.02353) = 1.63 (d) 0.30 mol dm −3 CH3CH2COOH (weak acid) CH3CH2COOH(aq) ⇌ H+(aq) + CH3CH2COO–(aq) 𝐾 ൌ ሾ𝐻ାሿሾ𝐶𝐻ଷ𝐶𝐻ଶ𝐶𝑂𝑂– ሿ ሾ𝐶𝐻ଷ𝐶𝐻ଶ𝐶𝑂𝑂𝐻ሿ 4.89 5 310 10 1.288 10 mol dm apK aK Since CH3CH2COOH is a weak acid with a small Ka, [CH3CH2COOH]eqm [CH3CH2COOH]initial = 0.30 mol dm–3 5 32 33 H CH CH COOH 1.288 10 0.30 1.966 10 mol dm aK pH = –lg (1.966 x 10 –3) = 2.71
-7- (e) 2.00 mol dm −3 CH3CH2NH2 (weak base) CH3CH2NH2(aq) + H2O(l) ⇌ CH3CH2NH3+(aq) + OH– (aq) 𝐾 ൌ ሾ𝑂𝐻ିሿሾ𝐶𝐻ଷ𝐶𝐻ଶ𝑁𝐻ଷ ାሿ ሾ𝐶𝐻ଷ𝐶𝐻ଶ𝑁𝐻ଶሿ Since CH3CH2NH2 is a weak base with a small Kb, [CH3CH2NH2]eqm [CH3CH2NH2]initial = 2.00 mol dm–3 4 322 3 OH CH CH NH 5.1 10 2.00 0.03194 mol dm bK pOH = –lg (0.03194) = 1.496 pH = 14 – 1.496 = 12.5 (f) 0.015 mol dm−3 C6H5COOK+ (basic salt containing C6H5COO which is the conjugate base of the weak acid C6H5COOH) C6H5COO(aq) + H2O(l) ⇌ C6H5COOH(aq) + OH–(aq) 𝐾 ൌ ሾOHିሿሾC6H5COOHሿ ሾC6H5COOെሿ Since C6H5COO is a weak base with a small Kb, [C6H5COO]eqm [C6H5COO]initial = 0.015 mol dm–3 [OH−] = ඥ𝐾ሾ𝐶𝐻ହ𝐶𝑂𝑂ିሿ 14 65 5 63 1.0 10OH C H COO 0.015 6.5 10 1.519 10 mol dm w a K K pOH = –lg (1.519 x 10 –6) = 5.818 pH = 14 – 5.818 = 8.18 (g) 0.25 mol dm−3 methylammonium nitrate CH3NH3NO3 (acidic salt containing CH3NH3+ which is the conjugate acid of the weak base CH3NH2) CH3NH3+(aq) + H2O(l) ⇌ CH3NH2(aq) + H3O+(aq) 𝐾 ൌ ሾHଷOାሿሾCHଷNHଶሿ ሾCHଷNHଷ ାሿ Since CH 3NH3+ is a weak acid with a small Ka, [CH3NH3+]eqm [CH3NH3+]initial = 0.25 mol dm–3 33 3 33 14 4 63 HO C HN H CH NH 1.0 10 0.254.4 10 2.384 10 mol dm a w b K K K pH = –lg (2.384 x 10 –6) = 5.62 (h) A solution containing 0.50 mol dm–3 CH3CH2COOH and 0.35 mol dm–3 CH3CH2COO–K+ (buffer) CH 3CH2COOH(aq) ⇌ CH3CH2COO–(aq) + H+(aq) 32 32 5 CH CH COO lg CH CH COOH 0.35lg 1.3 10 lg 4.73 0.50 apH pK (i) A solution containing 0.060 mol dm –3 of NH3 and 0.080 mol dm–3 of NH4Cl (buffer) NH 3(aq) + H2O(l) ⇌ NH4+(aq) + OH–(aq) 4 3 5 NH lg NH 0.080lg 1.74 10 lg 0.060 bpOH pK 4. 884 pH = 14 – 4.884 = 9.12 3 (a) HX(aq) + H 2O(l) ⇌ H3O+(aq) + X–(aq) At equilibrium, [H 3O+] = [X–] = 10–3.25 = 5.623 x 10-4 mol dm–3 [HX] = 1.00 x 10 –3 – 5.623 x 10-4 = 4.377 x 10–4 mol dm–3 24 3 -4 -3 4 5.623 10HO X 7.23 × 10 mol dmHX 4.377 10 aK
-8- (b) CH3COO–Na+(aq) CH3COO–(aq) + Na+(aq) CH3COO–(aq) + H2O(l) ⇌ CH3COOH(aq) + OH–(aq) At equilibrium, [CH 3COOH] = [OH–] = 10–(14 – 8.37) = 2.344 x 10–6 mol dm–3 [CH3COO–] = 1.00 x 10–2 – 2.344 x 10–6 = 9.998 x 10–3 mol dm–3 26 3 -10 -3 3 3 2.344 10CH COOH OH 5.497 × 10 mol dm9.998 10CH COO bK pKb of CH3COO– = –lg (5.497 x 10–10) = 9.260 pKa of CH3COOH = 14 – 9.260 = 4.74 (c) (NH4)2SO4(aq) 2NH4+(aq) + SO42–(aq) NH 4+(aq) + H2O(l) ⇌ NH3(aq) + H3O+(aq) Initial [NH4+] = (2)(0.050) = 0.100 mol dm–3 At equilibrium, [NH 3] = [H3O+] = 10–5.12 = 7.586 x 10–6 mol dm–3 [NH 4+] = 0.100 – 7.586 x 10–6 = 0.100 mol dm–3 26 33 10 3 4 7.586 10NH H O 5.755 10 mol dm0.100NH aK pKa of NH4+ = –lg (5.755 x 10–10) = 9.240 pKb of NH3 = 14 – 9.240 = 4.76 4 (Ans: B) In the absence of water, HCl(g) remains as an undissociated simple molecule, and is not dissociated into H+ and Cl ions, thus it does not have acidic properties (options A, C and D are incorrect) and does not act as mobile charge carriers (option B is correct). 5 (Ans: D) Ka only changes with temperature. Since the temperature is constant, Ka remains constant as volume changes. 6 (Ans: D) Overall Equation: 2MnO4+ 5SO2 + 2H2O 2Mn2+ + 5SO42 + 4H+ Since H+ is produced, [H+] increases, causing pH to decrease gradually. 7 (Ans: B) At 25 oC, pH = – lg [H+] = – lg (10–7) = 7 and pKw = 14 At equilibrium, [H+] = [OH–] = 10-7 mol dm3 [H2O] = 1000/18 = 55.56 mol dm3 (See note below) Ka= ሾHሿሾOH-ሿ ሾH2Oሿ = ൫10-7൯ 2 55.56 =1.800×10-16 mol dm-3 pKa of H2O = –lg (1.800 x 10–16) = 15.7 Hence, pH < pKw < pKa Note: How to find [H2O]? Consider 1 dm3 of water, Assume density of water = 1 g cm–3 mass of 1 dm3 of H2O = 1000 g 2 1000 55.56 mol2 1.0 16.0 HOn [H2O] = 55.56 mol dm–3 8 (Ans: A) Pyruvic acid is a weak acid, hence upon titration with NaOH (strong base), at equivalence point, pH > 7 due to anion hydrolysis. CH3COCOO- CH3COCOOH + H2O + OH-
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