Acids, Bases and Salts

99 questions

Question 1Question

Match each of the following chemical compounds to its characteristic behavior when exposed to moist atmospheric air.

Click a left item, then click its matching right item

Items

Na2CO310H2O\text{Na}_2\text{CO}_3\cdot 10\text{H}_2\text{O}
CaCl2\text{CaCl}_2
CaO\text{CaO}

Matches

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Answer

Na2CO310H2O\text{Na}_2\text{CO}_3\cdot 10\text{H}_2\text{O} matches with losing water of crystallization to form a powdery residue (efflorescence); CaCl2\text{CaCl}_2 matches with absorbing moisture to form a solution (deliquescence); CaO\text{CaO} matches with absorbing moisture without dissolving (hygroscopy).
Each compound exhibits a specific behavior upon exposure to air: hydrated sodium carbonate loses water of crystallization (efflorescence), calcium chloride absorbs moisture and dissolves (deliquescence), and calcium oxide absorbs moisture without dissolving (hygroscopy).

Step-by-Step Solution

1
Identify the atmospheric phenomenon characteristic of hydrated sodium carbonate (Na2CO310H2O\text{Na}_2\text{CO}_3\cdot 10\text{H}_2\text{O}).
It undergoes efflorescence, losing water molecules to the surrounding dry air.
Hydrated salts with higher vapor pressure than the atmospheric water vapor pressure tend to lose hydration water.
2
Identify the atmospheric behavior of anhydrous calcium chloride (CaCl2\text{CaCl}_2).
It undergoes deliquescence, absorbing atmospheric moisture until it completely dissolves in the absorbed water.
Deliquescent compounds have an extremely high affinity for water and lower saturated solution vapor pressure than ambient air.
3
Identify the behavior of quicklime (CaO\text{CaO}).
It undergoes hygroscopy, absorbing atmospheric moisture without dissolving into a liquid solution.
Hygroscopic substances absorb moisture into their structure without forming a liquid solution.

Key Concept

Differentiation between efflorescence, deliquescence, and hygroscopy.
Question 2Question

An aqueous solution at 25C25^\circ\text{C} has a hydroxide ion concentration ([OH][OH^-]) of 1.0×1011 mol dm31.0 \times 10^{-11}\text{ mol dm}^{-3}. What is the pH of this solution?

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Answer: 3.03.0

Answer

The pH of the solution is 3.03.0.
Taking the negative logarithm of the hydroxide ion concentration gives a pOH value of 11.011.0. Subtracting this from 14.014.0 yields a pH of 3.03.0, accurately indicating an acidic solution.

Step-by-Step Solution

1
Calculate the pOH from the hydroxide ion concentration
pOH=log10(1.0×1011)=11.0\text{pOH} = -\log_{10}(1.0 \times 10^{-11}) = 11.0
pOH is defined as the negative logarithm to base 10 of the hydroxide ion concentration.
2
Calculate the pH using the water ionic product relationship at 25C25^\circ\text{C}
pH=14.0pOH=14.011.0=3.0\text{pH} = 14.0 - \text{pOH} = 14.0 - 11.0 = 3.0
The sum of pH and pOH in aqueous solutions at 25C25^\circ\text{C} is equal to 14.0.

Key Concept

Relationship between [OH][OH^-], pOH, and pH in aqueous solutions
Estimated Time:45s
Question 3Question

Which of the following salts dissolves in water to form an alkaline solution that turns red litmus paper blue?

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Answer: Sodium trioxocarbonate(IV)

Answer

Sodium trioxocarbonate(IV) forms an alkaline solution in water due to anion hydrolysis.
Sodium trioxocarbonate(IV) dissolves in water to form sodium ions and trioxocarbonate(IV) ions. Because trioxocarbonate(IV) is the conjugate base of a weak acid, it reacts with water to release hydroxide ions (OHOH^-), creating an alkaline solution that turns red litmus paper blue.

Step-by-Step Solution

1
Identify the parent acid and base for the salt.
Sodium trioxocarbonate(IV) (Na2CO3Na_2CO_3) is formed from sodium hydroxide (NaOHNaOH, a strong base) and carbonic acid (H2CO3H_2CO_3, a weak acid).
The hydrolysis behavior of a salt is determined by the relative strengths of its parent acid and base.
2
Analyze the ion hydrolysis reaction.
The carbonate anion (CO32CO_3^{2-}) reacts with water according to: CO32+H2OHCO3+OHCO_3^{2-} + H_2O \rightleftharpoons HCO_3^- + OH^-.
Anions derived from weak acids act as conjugate bases and hydrolyze in water to generate hydroxide ions (OHOH^-).
3
Determine the solution acidity/alkalinity and indicator response.
The production of excess OHOH^- ions makes the solution basic (pH>7pH > 7), causing red litmus paper to turn blue.
Alkaline solutions contain a higher concentration of hydroxide ions than hydrogen ions, turning red litmus blue.

Key Concept

Salt Hydrolysis
Estimated Time:45s
Question 4Question

What is the pH of an aqueous solution prepared by dissolving 0.49 g0.49\text{ g} of tetraoxosulfate(VI) acid (H2SO4\text{H}_2\text{SO}_4) in distilled water to make 500 cm3500\text{ cm}^3 of solution? [Molar mass of H2SO4=98 g mol1\text{H}_2\text{SO}_4 = 98\text{ g mol}^{-1}, log102=0.301\log_{10} 2 = 0.301]

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Answer: 1.701.70

Answer

The pH of the solution is 1.701.70.
Dissolving 0.49 g0.49\text{ g} of H2SO4\text{H}_2\text{SO}_4 (molar mass 98 g mol198\text{ g mol}^{-1}) in 0.5 dm30.5\text{ dm}^3 yields a 0.01 mol dm30.01\text{ mol dm}^{-3} solution. Because tetraoxosulfate(VI) acid fully ionizes into 2H+2\text{H}^+ and SO42\text{SO}_4^{2-}, the hydrogen ion concentration [H+][\text{H}^+] is 0.02 mol dm30.02\text{ mol dm}^{-3}. Taking the negative logarithm base 10 gives pH=log10(0.02)=1.70\text{pH} = -\log_{10}(0.02) = 1.70.

Step-by-Step Solution

1
Calculate the amount of H2SO4\text{H}_2\text{SO}_4 in moles
Moles of H2SO4=0.49 g98 g mol1=0.005 mol\text{Moles of } \text{H}_2\text{SO}_4 = \frac{0.49\text{ g}}{98\text{ g mol}^{-1}} = 0.005\text{ mol}
Converting mass of solute to moles using molar mass.
2
Determine the molar concentration of the acid solution
Volume=500 cm3=0.5 dm3\text{Volume} = 500\text{ cm}^3 = 0.5\text{ dm}^3; Molarity=0.005 mol0.5 dm3=0.01 mol dm3\text{Molarity} = \frac{0.005\text{ mol}}{0.5\text{ dm}^3} = 0.01\text{ mol dm}^{-3}
Molarity is defined as moles of solute per cubic decimetre of solution.
3
Calculate the hydrogen ion concentration [H+][\text{H}^+]
[H+]=2×0.01 mol dm3=0.02 mol dm3=2.0×102 mol dm3[\text{H}^+] = 2 \times 0.01\text{ mol dm}^{-3} = 0.02\text{ mol dm}^{-3} = 2.0 \times 10^{-2}\text{ mol dm}^{-3}
H2SO4\text{H}_2\text{SO}_4 is a strong dibasic acid that ionizes completely to produce two H+\text{H}^+ ions per molecule.
4
Calculate the pH of the solution
pH=log10[H+]=log10(2.0×102)=2log102=20.301=1.6991.70\text{pH} = -\log_{10}[\text{H}^+] = -\log_{10}(2.0 \times 10^{-2}) = 2 - \log_{10} 2 = 2 - 0.301 = 1.699 \approx 1.70
Applying the logarithmic definition of pH.

Key Concept

pH Calculation of Dibasic Strong Acids
Question 5Question

A 6.95 g6.95\text{ g} sample of hydrated iron(II) tetraoxosulfate(VI), FeSO4xH2O\text{FeSO}_4 \cdot x\text{H}_2\text{O}, is dissolved in dilute tetraoxosulfate(VI) acid and made up to 250 cm3250\text{ cm}^3 in a volumetric flask. A 25.0 cm325.0\text{ cm}^3 portion of this solution requires 25.0 cm325.0\text{ cm}^3 of 0.020 mol dm30.020\text{ mol dm}^{-3} acidified potassium tetraoxomanganate(VII), KMnO4\text{KMnO}_4, for complete titration. Given the relative atomic masses Fe=56\text{Fe} = 56, S=32\text{S} = 32, O=16\text{O} = 16, and H=1\text{H} = 1, what is the integer value of xx, the number of molecules of water of crystallization per formula unit?

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Answer: 7

Answer

The integer value of x is 7.
By using the titration volume and concentration of acidified potassium tetraoxomanganate(VII), the amount of iron(II) ions in the sample is calculated. Knowing the total mole amount of anhydrous iron(II) tetraoxosulfate(VI) allows determination of the mass of the anhydrous salt component (3.80 g). Subtracting this from the initial hydrated sample mass (6.95 g) gives the mass of water of crystallization (3.15 g). Dividing the moles of water (0.175 mol) by the moles of anhydrous salt (0.025 mol) yields exactly 7 water molecules of crystallization per formula unit.

Step-by-Step Solution

1
Calculate the moles of KMnO4\text{KMnO}_4 consumed in the titration
n(KMnO4)=0.020 mol dm3×0.0250 dm3=0.00050 moln(\text{KMnO}_4) = 0.020 \text{ mol dm}^{-3} \times 0.0250 \text{ dm}^3 = 0.00050 \text{ mol}
Concentration and volume of titrant are provided.
2
Determine moles of Fe2+\text{Fe}^{2+} present in the 25.0 cm325.0\text{ cm}^3 aliquot using the redox reaction stoichiometry
n(Fe2+)25cm3=5×0.00050 mol=0.0025 moln(\text{Fe}^{2+})_{25\text{cm}^3} = 5 \times 0.00050 \text{ mol} = 0.0025 \text{ mol}
The mole ratio of MnO4\text{MnO}_4^- to Fe2+\text{Fe}^{2+} in acidic redox titration is 1:51:5 according to MnO4+5Fe2++8H+Mn2++5Fe3++4H2O\text{MnO}_4^- + 5\text{Fe}^{2+} + 8\text{H}^+ \rightarrow \text{Mn}^{2+} + 5\text{Fe}^{3+} + 4\text{H}_2\text{O}.
3
Calculate the total moles of FeSO4\text{FeSO}_4 in the original 250 cm3250\text{ cm}^3 volumetric flask
n(FeSO4)total=0.0025 mol×(250 cm325.0 cm3)=0.025 moln(\text{FeSO}_4)_{\text{total}} = 0.0025 \text{ mol} \times \left(\frac{250\text{ cm}^3}{25.0\text{ cm}^3}\right) = 0.025 \text{ mol}
The aliquot represents one-tenth of the total solution volume.
4
Calculate the mass of anhydrous FeSO4\text{FeSO}_4 in the sample
Molar mass of FeSO4=56+32+(4×16)=152 g mol1\text{FeSO}_4 = 56 + 32 + (4 \times 16) = 152 \text{ g mol}^{-1}. Mass =0.025 mol×152 g mol1=3.80 g= 0.025 \text{ mol} \times 152 \text{ g mol}^{-1} = 3.80 \text{ g}.
Converting moles of anhydrous salt to mass using molar mass.
5
Determine the mass and moles of water of crystallization
Mass of H2O=6.95 g3.80 g=3.15 g\text{H}_2\text{O} = 6.95 \text{ g} - 3.80 \text{ g} = 3.15 \text{ g}. Moles of H2O=3.15 g18 g mol1=0.175 mol\text{H}_2\text{O} = \frac{3.15 \text{ g}}{18 \text{ g mol}^{-1}} = 0.175 \text{ mol}.
Subtracting anhydrous mass from initial mass gives water of crystallization mass, converted to moles using molar mass of H2O=18 g mol1\text{H}_2\text{O} = 18 \text{ g mol}^{-1}.
6
Compute the hydration coefficient x=n(H2O)n(FeSO4)x = \frac{n(\text{H}_2\text{O})}{n(\text{FeSO}_4)}
x=0.175 mol0.025 mol=7x = \frac{0.175 \text{ mol}}{0.025 \text{ mol}} = 7
The coefficient xx represents the mole ratio of water of crystallization to anhydrous salt.

Key Concept

Quantitative determination of water of crystallization in hydrated salts via redox volumetric analysis
Question 6Question

A 0.04 mol dm30.04\text{ mol dm}^{-3} aqueous solution of a weak monobasic acid, HA\text{HA}, is 2.0%2.0\% ionized at 25C25^\circ\text{C}. If distilled water is added to this solution until its total volume is quadrupled, what is the degree of ionization of the acid in the diluted solution?

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Answer: 4.0%4.0\%

Answer

The degree of ionization of the acid in the diluted solution is 4.0%4.0\%.
By Ostwald's dilution law for weak monobasic acids, Ka=α2CK_a = \alpha^2 C, which rearranges to α=KaC\alpha = \sqrt{\frac{K_a}{C}}. Since KaK_a is constant at a fixed temperature, the degree of ionization α\alpha is inversely proportional to the square root of the concentration (α1C\alpha \propto \frac{1}{\sqrt{C}}). Quadrupling the volume decreases the concentration by a factor of 4 (C2=C14C_2 = \frac{C_1}{4}), which increases the degree of ionization by a factor of 4=2\sqrt{4} = 2. Therefore, the new degree of ionization is 2.0%×2=4.0%2.0\% \times 2 = 4.0\%.

Step-by-Step Solution

1
Calculate the acid dissociation constant (KaK_a) using the initial concentration and degree of ionization.
Initial concentration C1=0.04 mol dm3C_1 = 0.04\text{ mol dm}^{-3}, initial degree of ionization α1=2.0%=0.02\alpha_1 = 2.0\% = 0.02. Using Kaα12C1K_a \approx \alpha_1^2 C_1, we get Ka=(0.02)2×0.04=4.0×104×0.04=1.6×105 mol dm3K_a = (0.02)^2 \times 0.04 = 4.0 \times 10^{-4} \times 0.04 = 1.6 \times 10^{-5}\text{ mol dm}^{-3}.
The value of KaK_a depends only on temperature and remains constant upon dilution.
2
Determine the new concentration (C2C_2) after quadrupling the solution volume.
C2=C14=0.04 mol dm34=0.01 mol dm3C_2 = \frac{C_1}{4} = \frac{0.04\text{ mol dm}^{-3}}{4} = 0.01\text{ mol dm}^{-3}.
Diluting a solution to 4 times its original volume reduces its molar concentration by a factor of 4.
3
Calculate the new degree of ionization (α2\alpha_2) in the diluted solution.
\alpha_2 = \sqrt{\frac{K_a}{C_2}} = \sqrt{\frac{1.6 \times 10^{-5}}{0.01}} = \sqrt{1.6 \times 10^{-3}} = \sqrt{16 \times 10^{-4}} = 4.0 \times 10^{-2} = 0.04 = 4.0\%$.
Applying Ostwald's dilution law to find the updated degree of dissociation at the lower concentration.

Key Concept

Ostwald's Dilution Law and the relationship between dilution, concentration, and degree of ionization of weak electrolytes.
Estimated Time:2m 30s
Question 7Question

Which of the following gases is evolved when dilute hydrochloric acid (HClHCl) reacts with calcium trioxocarbonate(IV) (CaCO3CaCO_3)?

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Answer: Carbon(IV) oxide (CO2CO_2)

Answer

Carbon(IV) oxide (CO2CO_2)
A characteristic chemical property of acids is that they react with trioxocarbonate(IV) salts (such as CaCO3CaCO_3) to produce a salt, water, and carbon(IV) oxide gas (CO2CO_2).

Step-by-Step Solution

1
Identify the reactants and the class of reaction
Dilute hydrochloric acid (HClHCl) reacts with calcium trioxocarbonate(IV) (CaCO3CaCO_3), which is an acid-carbonate reaction.
Acids characteristically react with trioxocarbonates to form salt, water, and carbon dioxide.
2
Write the balanced chemical equation
2HCl(aq)+CaCO3(s)CaCl2(aq)+H2O(l)+CO2(g)2HCl(aq) + CaCO_3(s) \rightarrow CaCl_2(aq) + H_2O(l) + CO_2(g)
The equation shows that carbon(IV) oxide gas (CO2CO_2) is liberated during the chemical process.

Key Concept

Action of acids on trioxocarbonate(IV) salts
Estimated Time:45s
Question 8Question

A weak monobasic acid has a concentration of 0.20 mol dm30.20\text{ mol dm}^{-3} in aqueous solution. At equilibrium, the hydrogen ion concentration, [H+][H^+], is measured to be 1.0×103 mol dm31.0 \times 10^{-3}\text{ mol dm}^{-3}. What is the percentage degree of ionization of the acid in this solution?

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Answer: 0.5

Answer

The percentage degree of ionization of the weak acid is 0.5%.
The percentage degree of ionization measures the fraction of acid molecules that ionize in water, expressed as a percentage. By substituting [H+]=1.0×103 mol dm3[H^+] = 1.0 \times 10^{-3}\text{ mol dm}^{-3} and initial concentration C=0.20 mol dm3C = 0.20\text{ mol dm}^{-3} into Percentage ionization=([H+]C)×100%\text{Percentage ionization} = \left(\frac{[H^+]}{C}\right) \times 100\%, we obtain (0.0010.20)×100%=0.5%\left(\frac{0.001}{0.20}\right) \times 100\% = 0.5\%.

Step-by-Step Solution

1
Identify the relationship between degree of ionization (\alpha), hydrogen ion concentration ([H+][H^+]), and initial acid concentration (CC).
α=[H+]C\alpha = \frac{[H^+]}{C}
For a weak monobasic acid ionizing according to HAH++AHA \rightleftharpoons H^+ + A^-, the concentration of ionized hydrogen ions equals αC\alpha C.
2
Calculate the fractional degree of ionization (\alpha).
\alpha = \frac{1.0 \times 10^{-3}\text{ mol dm}^{-3}}{0.20\text{ mol dm}^{-3}} = 0.005
Dividing the equilibrium hydrogen ion concentration by the initial acid concentration gives the fraction of acid molecules that ionized.
3
Convert the fractional degree of ionization into a percentage.
\text{Percentage ionization} = 0.005 \times 100\% = 0.5\%
Multiplying the decimal fraction by 100 converts the degree of ionization into percentage form.

Key Concept

Degree of Ionization of Weak Acids
Estimated Time:1m 30s
Question 9Question

When potassium ethanoate, CH3COOKCH_3COOK, is dissolved in distilled water, the resulting solution has a pH greater than 7. Which ion is responsible for this alkalinity by undergoing hydrolysis?

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Answer: The ethanoate ion, CH3COOCH_3COO^-

Answer

The ethanoate ion, CH3COOCH_3COO^-
The ethanoate ion (CH3COOCH_3COO^-) is the conjugate base of the weak acid ethanoic acid (CH3COOHCH_3COOH). When potassium ethanoate dissolves in water, CH3COOCH_3COO^- hydrolyzes by accepting a proton from water to form CH3COOHCH_3COOH and releasing OHOH^- ions into the solution: CH3COO(aq)+H2O(l)CH3COOH(aq)+OH(aq)CH_3COO^-(aq) + H_2O(l) \rightleftharpoons CH_3COOH(aq) + OH^-(aq). The accumulation of free hydroxide ions makes the solution alkaline (pH>7pH > 7).

Step-by-Step Solution

1
Identify the ions formed when potassium ethanoate dissolves in water.
Potassium ethanoate dissociates completely into potassium ions (K+K^+) and ethanoate ions (CH3COOCH_3COO^-).
Soluble ionic salts completely dissociate into their constituent cations and anions in aqueous solution.
2
Determine which ion reacts with water (hydrolyzes).
Potassium (K+K^+) is derived from a strong base (KOHKOH) and does not hydrolyze. Ethanoate (CH3COOCH_3COO^-) is derived from a weak acid (CH3COOHCH_3COOH) and reacts with water.
Anions derived from weak acids act as weak conjugate bases and undergo anion hydrolysis.
3
Write the hydrolysis equation to identify the species giving rise to alkalinity.
CH3COO(aq)+H2O(l)CH3COOH(aq)+OH(aq)CH_3COO^-(aq) + H_2O(l) \rightleftharpoons CH_3COOH(aq) + OH^-(aq)
Hydrolysis of ethanoate generates free OHOH^- ions, making the solution basic (pH>7pH > 7).

Key Concept

Anion hydrolysis of salts formed from a weak acid and a strong base
Question 10Question

Complete the statement regarding the choice of indicator and the expected endpoint color change when titrating aqueous ammonia with hydrochloric acid.

Fill in the blanks below

When titrating aqueous ammonia against hydrochloric acid, the appropriate indicator is , which changes from yellow in alkaline solution to at the equivalence point.
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Answer

The appropriate indicator is methyl orange, which changes from yellow to red (or pink) at the equivalence point.
In a titration between a strong acid (HCl\text{HCl}) and a weak base (NH3\text{NH}_3), ammonium chloride (NH4Cl\text{NH}_4\text{Cl}) is formed. The hydrolysis of NH4+\text{NH}_4^+ ions makes the solution acidic at the equivalence point (pH<7\text{pH} < 7). Methyl orange is the correct indicator because its transition range (pH 3.14.4\text{pH } 3.1 - 4.4) coincides with this acidic equivalence point, turning red (or pink) when the endpoint is reached.

Step-by-Step Solution

1
Analyze the nature of the reactants
Hydrochloric acid (HCl\text{HCl}) is a strong acid, and aqueous ammonia (NH3(aq)\text{NH}_3(aq)) is a weak base.
The relative strengths of the acid and base determine the pH at the equivalence point.
2
Determine the pH range at the equivalence point
The salt formed (NH4Cl\text{NH}_4\text{Cl}) undergoes hydrolysis, producing an acidic solution with an equivalence point at pH<7\text{pH} < 7 (typically between pH 3\text{pH } 3 and 66).
Salt hydrolysis of a strong acid and weak base yields ammonium ions (NH4+\text{NH}_4^+) which hydrolyze to produce H3O+\text{H}_3\text{O}^+ ions.
3
Select the suitable indicator and recall its color change
Methyl orange functions in the pH\text{pH} range of 3.14.43.1 - 4.4, changing from yellow in basic solution to red (or pink) at the acidic endpoint.
An indicator must undergo a distinct color transition within the steep pH\text{pH} region of the titration curve near the equivalence point.

Key Concept

Indicator Selection and Endpoint Determination in Volumetric Analysis
Estimated Time:1m 0s
Question 11Question

What is the pH of an aqueous solution containing 0.365 g dm30.365\text{ g dm}^{-3} of hydrochloric acid (HCl\text{HCl})? [Molar mass of HCl=36.5 g mol1\text{HCl} = 36.5\text{ g mol}^{-1}]

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Answer: 2.02.0

Answer

The pH of the solution is 2.0.
The solution has a molar concentration of 0.01 mol dm30.01\text{ mol dm}^{-3} (0.365 g dm3/36.5 g mol10.365\text{ g dm}^{-3} / 36.5\text{ g mol}^{-1}). Taking the negative base-10 logarithm of 1.0×102 mol dm31.0 \times 10^{-2}\text{ mol dm}^{-3} yields a pH of 2.0.

Step-by-Step Solution

1
Convert mass concentration to molar concentration (molarity)
[HCl]=0.365 g dm336.5 g mol1=0.01 mol dm3=1.0×102 mol dm3[\text{HCl}] = \frac{0.365\text{ g dm}^{-3}}{36.5\text{ g mol}^{-1}} = 0.01\text{ mol dm}^{-3} = 1.0 \times 10^{-2}\text{ mol dm}^{-3}
pH calculations require concentration in units of mol dm3\text{mol dm}^{-3}.
2
Determine the hydrogen ion concentration [H+][\text{H}^+]
[H+]=1.0×102 mol dm3[\text{H}^+] = 1.0 \times 10^{-2}\text{ mol dm}^{-3}
Hydrochloric acid is a strong monoprotic acid that fully dissociates in water.
3
Calculate the pH using the pH formula
pH=log10[H+]=log10(1.0×102)=2.0\text{pH} = -\log_{10}[\text{H}^+] = -\log_{10}(1.0 \times 10^{-2}) = 2.0
pH is defined as the negative logarithm to base 10 of the hydrogen ion concentration.

Key Concept

Calculating pH from mass concentration of a strong acid
Estimated Time:1m 0s
Question 12Question

Fill in the blank to complete the statement regarding the Brønsted-Lowry theory of acids and bases.

Fill in the blanks below

According to the Brønsted-Lowry theory, an acid is defined as a species that acts as a proton .
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Answer

According to the Brønsted-Lowry theory, an acid is defined as a species that acts as a proton donor.
In the Brønsted-Lowry concept, acids are species capable of donating a hydrogen ion (proton, H+H^+) to another chemical species. Therefore, the term 'donor' correctly completes the definition.

Step-by-Step Solution

1
Recall the fundamental definitions of the Brønsted-Lowry acid-base theory.
The Brønsted-Lowry theory defines an acid as a proton (H+H^+) donor and a base as a proton (H+H^+) acceptor.
Acid-base behavior under this theory is governed by the transfer of protons between chemical species.

Key Concept

Brønsted-Lowry Acid Definition
Question 13Question

At 60C60^\circ\text{C}, the solubility of a trioxonitrate(V) salt YY (molar mass =160 g mol1= 160\text{ g mol}^{-1}) is 1.25 mol dm31.25\text{ mol dm}^{-3}. When the solution is cooled to 20C20^\circ\text{C}, its solubility decreases to 0.25 mol dm30.25\text{ mol dm}^{-3}. What mass of salt YY will crystallize out when 300 g300\text{ g} of a saturated solution of YY at 60C60^\circ\text{C} is cooled to 20C20^\circ\text{C}? (Assume the density of water is 1.0 g cm31.0\text{ g cm}^{-3}).

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Answer: 40.0 g40.0\text{ g}

Answer

The mass of salt YY that crystallizes out upon cooling is 40.0 g40.0\text{ g}.
Converting concentrations to mass per 1000 g1000\text{ g} of water gives 200 g200\text{ g} at 60C60^\circ\text{C} and 40 g40\text{ g} at 20C20^\circ\text{C}. A 300 g300\text{ g} sample of saturated solution at 60C60^\circ\text{C} contains 50 g50\text{ g} of solute dissolved in 250 g250\text{ g} of solvent (water). Upon cooling to 20C20^\circ\text{C}, 250 g250\text{ g} of water can only hold 10 g10\text{ g} of solute. Thus, 50 g10 g=40.0 g50\text{ g} - 10\text{ g} = 40.0\text{ g} crystallizes out.

Step-by-Step Solution

1
Convert solubility at 60C60^\circ\text{C} from mol dm3\text{mol dm}^{-3} to g dm3\text{g dm}^{-3}
Solubility at 60C=1.25 mol dm3×160 g mol1=200 g dm3\text{Solubility at } 60^\circ\text{C} = 1.25\text{ mol dm}^{-3} \times 160\text{ g mol}^{-1} = 200\text{ g dm}^{-3}
Solubility calculations involving mass of solution require mass concentration (g dm3\text{g dm}^{-3}).
2
Determine mass of water in 300 g300\text{ g} of saturated solution at 60C60^\circ\text{C}
Mass of solution per dm3=1000 g (water)+200 g (salt)=1200 g\text{Mass of solution per dm}^3 = 1000\text{ g (water)} + 200\text{ g (salt)} = 1200\text{ g}. Therefore, mass of water in 300 g solution=1000 g1200 g×300 g=250 g\text{mass of water in } 300\text{ g solution} = \frac{1000\text{ g}}{1200\text{ g}} \times 300\text{ g} = 250\text{ g}.
Solubility expresses mass of solute per fixed mass of solvent (1000 g1000\text{ g} water).
3
Convert solubility at 20C20^\circ\text{C} to g dm3\text{g dm}^{-3} and find mass of salt remaining dissolved in 250 g250\text{ g} water
Solubility at 20C=0.25 mol dm3×160 g mol1=40 g dm3\text{Solubility at } 20^\circ\text{C} = 0.25\text{ mol dm}^{-3} \times 160\text{ g mol}^{-1} = 40\text{ g dm}^{-3}. In 250 g250\text{ g} of water, dissolved salt =40 g×250 g1000 g=10 g= 40\text{ g} \times \frac{250\text{ g}}{1000\text{ g}} = 10\text{ g}.
Determining how much solute stays dissolved at the lower temperature.
4
Calculate the mass of salt precipitated
Original salt in solution=200 g×250 g1000 g=50 g\text{Original salt in solution} = 200\text{ g} \times \frac{250\text{ g}}{1000\text{ g}} = 50\text{ g}. Mass precipitated=50 g10 g=40.0 g\text{Mass precipitated} = 50\text{ g} - 10\text{ g} = 40.0\text{ g}.
Mass precipitated is the difference between initial dissolved mass and remaining dissolved mass.

Key Concept

Mass of salt precipitated upon cooling saturated solutions
Estimated Time:2m 30s
Question 14Question

Which of the following terms describes the phenomenon where a solid substance absorbs moisture from the atmosphere and dissolves in it to form a solution?

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Answer: Deliquescence

Answer

Deliquescence is the phenomenon where a solid absorbs water vapor from the atmosphere until it dissolves in that water to form a saturated solution.
Deliquescence is the spontaneous absorption of atmospheric moisture by a solid until it liquefies into a solution. Typical examples of deliquescent compounds include calcium chloride (CaCl2CaCl_2), iron(III) chloride (FeCl3FeCl_3), and sodium hydroxide (NaOHNaOH).

Step-by-Step Solution

1
Identify the characteristic atmospheric behavior described in the prompt.
The process involves absorbing moisture from the air to the extent of forming a liquid solution.
This specific property defines deliquescence (e.g., as observed with anhydrous calcium chloride, CaCl2CaCl_2, or sodium hydroxide, NaOHNaOH pellets).

Key Concept

Distinction between deliquescence, hygroscopy, and efflorescence
Question 15Question

A 25.0 cm325.0\text{ cm}^3 portion of a 6.30 g dm36.30\text{ g dm}^{-3} solution of an impure hydrated diprotic weak acid, H2X2H2O\text{H}_2\text{X}\cdot 2\text{H}_2\text{O}, requires 20.0 cm320.0\text{ cm}^3 of 0.10 mol dm30.10\text{ mol dm}^{-3} sodium hydroxide (NaOH\text{NaOH}) solution for complete neutralization. What is the percentage purity of the acid sample, and which indicator is most suitable for this titration?
[Molar mass of H2X2H2O=126 g mol1\text{H}_2\text{X}\cdot 2\text{H}_2\text{O} = 126\text{ g mol}^{-1}]

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Answer: 80.0%80.0\%, using phenolphthalein

Answer

80.0%, using phenolphthalein
The neutralization reaction requires two moles of sodium hydroxide for every mole of diprotic acid. Using CAVACBVB=12\frac{C_A V_A}{C_B V_B} = \frac{1}{2}, the concentration of pure acid is 0.040 mol dm30.040\text{ mol dm}^{-3}. Multiplying by the molar mass (126 g mol1126\text{ g mol}^{-1}) gives 5.04 g dm35.04\text{ g dm}^{-3} of pure acid. Dividing by the sample mass concentration (6.30 g dm36.30\text{ g dm}^{-3}) and multiplying by 100%100\% yields 80.0%80.0\%. Because the titration involves a weak acid and a strong base, the solution at the end point is alkaline, which requires phenolphthalein as the indicator.

Step-by-Step Solution

1
Write the balanced chemical equation to determine the mole ratio.
H2X2H2O+2NaOHNa2X+4H2O\text{H}_2\text{X}\cdot 2\text{H}_2\text{O} + 2\text{NaOH} \rightarrow \text{Na}_2\text{X} + 4\text{H}_2\text{O}, giving mole ratio nAnB=12\frac{n_A}{n_B} = \frac{1}{2}.
Diprotic acid yields two hydrogen ions per molecule, requiring two moles of sodium hydroxide for neutralization.
2
Calculate the molar concentration of the pure acid in solution using the titration formula.
CA×25.00.10×20.0=12    CA=0.10×20.025.0×2=0.040 mol dm3\frac{C_A \times 25.0}{0.10 \times 20.0} = \frac{1}{2} \implies C_A = \frac{0.10 \times 20.0}{25.0 \times 2} = 0.040\text{ mol dm}^{-3}.
Relating acid and base concentrations via volumes and stoichiometric coefficients.
3
Convert the molar concentration of pure acid to mass concentration.
\text{Mass concentration} = 0.040\text{ mol dm}^{-3} \times 126\text{ g mol}^{-1} = 5.04\text{ g dm}^{-3}.
Mass concentration equals molar concentration multiplied by molar mass.
4
Calculate the percentage purity of the acid sample.
\text{Percentage purity} = \left(\frac{5.04\text{ g dm}^{-3}}{6.30\text{ g dm}^{-3}}\right) \times 100\% = 80.0\%.
Percentage purity is the ratio of pure mass concentration to total sample mass concentration.
5
Select the correct indicator for the titration.
Phenolphthalein is selected.
Titrating a weak acid against a strong base produces a basic salt solution at equivalence (pH > 7), making phenolphthalein (pH range 8.3–10.0) the suitable indicator.

Key Concept

Volumetric Stoichiometry and Indicator Selection in Acid-Base Titrations
Question 16Question

Match each chemical substance with its characteristic atmospheric behavior or hydration property when exposed to ambient laboratory air or heat:

Click a left item, then click its matching right item

Items

Na2CO310H2O\text{Na}_2\text{CO}_3 \cdot 10\text{H}_2\text{O} (Washing soda crystals)
Anhydrous CaCl2\text{CaCl}_2 (Calcium chloride pellets)
Concentrated H2SO4\text{H}_2\text{SO}_4 (Sulfuric acid)
CuSO45H2O\text{CuSO}_4 \cdot 5\text{H}_2\text{O} (Blue vitriol)

Matches

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Answer

Washing soda crystals undergo efflorescence; anhydrous calcium chloride undergoes deliquescence; concentrated sulfuric acid is hygroscopic; copper(II) sulfate pentahydrate loses its water of crystallization upon heating.
Washing soda crystals (Na2CO310H2O\text{Na}_2\text{CO}_3 \cdot 10\text{H}_2\text{O}) undergo efflorescence when exposed to dry air. Anhydrous calcium chloride (CaCl2\text{CaCl}_2) absorbs moisture until it forms a solution, which is deliquescence. Concentrated sulfuric acid (H2SO4\text{H}_2\text{SO}_4) absorbs moisture without dissolving a solid matrix, illustrating hygroscopic behavior. Copper(II) sulfate pentahydrate (CuSO45H2O\text{CuSO}_4 \cdot 5\text{H}_2\text{O}) loses its water of crystallization thermally to yield a white anhydrous salt.

Step-by-Step Solution

1
Analyze the behavior of Na2CO310H2O\text{Na}_2\text{CO}_3 \cdot 10\text{H}_2\text{O}.
It loses 9 molecules of water of crystallization to dry air, forming a powdery monohydrate Na2CO3H2O\text{Na}_2\text{CO}_3 \cdot \text{H}_2\text{O} (efflorescence).
Efflorescence occurs when the vapor pressure of the hydrated salt is greater than the partial pressure of water vapor in the atmosphere.
2
Analyze anhydrous CaCl2\text{CaCl}_2.
It absorbs moisture from air and eventually dissolves in the absorbed water to form a saturated solution (deliquescence).
Deliquescence occurs when a solid compound's saturated solution has a lower vapor pressure than the atmospheric water vapor pressure.
3
Analyze concentrated H2SO4\text{H}_2\text{SO}_4.
It absorbs moisture from the atmosphere without changing state to form a new dissolved phase, acting as a liquid hygroscopic substance.
Hygroscopic substances absorb water vapor from the surrounding environment without dissolving into a liquid solution from a solid state.
4
Analyze CuSO45H2O\text{CuSO}_4 \cdot 5\text{H}_2\text{O}.
Heating drives off the 5 water molecules of crystallization, converting blue crystalline pentahydrate to white anhydrous copper(II) sulfate.
Water of crystallization is chemically bound in the crystal lattice and can be expelled thermally, altering optical/crystalline properties.

Key Concept

Water of Crystallization, Deliquescence, Efflorescence, and Hygroscopy
Question 17Question

Two weak monobasic acids, HX\text{HX} (Ka=1.0×105 mol dm3K_a = 1.0 \times 10^{-5}\text{ mol dm}^{-3}) and HY\text{HY} (Ka=4.0×105 mol dm3K_a = 4.0 \times 10^{-5}\text{ mol dm}^{-3}), are prepared as aqueous solutions. Solution X contains 0.40 mol dm30.40\text{ mol dm}^{-3} of HX\text{HX}, whereas Solution Y contains 0.10 mol dm30.10\text{ mol dm}^{-3} of HY\text{HY}. Based on Ostwald's dilution law and the principles of acid ionization, which of the following statements correctly compares the two solutions?

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Answer: Both solutions have the same hydrogen ion concentration of 2.0×103 mol dm32.0 \times 10^{-3}\text{ mol dm}^{-3}, but HY\text{HY} has a four-fold greater degree of ionization than HX\text{HX}.

Answer

Both solutions have the exact same hydrogen ion concentration of 2.0×103 mol dm32.0 \times 10^{-3}\text{ mol dm}^{-3}, but HY\text{HY} has a four-fold greater degree of ionization than HX\text{HX}.
Evaluating [H+]=KaC[H^+] = \sqrt{K_a \cdot C} for both solutions gives [H+]X=1.0×105×0.40=2.0×103 mol dm3[H^+]_X = \sqrt{1.0 \times 10^{-5} \times 0.40} = 2.0 \times 10^{-3}\text{ mol dm}^{-3} and [H+]Y=4.0×105×0.10=2.0×103 mol dm3[H^+]_Y = \sqrt{4.0 \times 10^{-5} \times 0.10} = 2.0 \times 10^{-3}\text{ mol dm}^{-3}, showing both solutions have identical hydrogen ion concentrations. Calculating the degree of ionization α=Ka/C\alpha = \sqrt{K_a / C} yields αX=0.005\alpha_X = 0.005 (0.5%0.5\%) and αY=0.020\alpha_Y = 0.020 (2.0%2.0\%), demonstrating that HY\text{HY} is four times more ionized than HX\text{HX} in these conditions.

Step-by-Step Solution

1
Calculate [H+][H^+] for Solution X
[H+]X=Ka,X×CX=(1.0×105)×0.40=4.0×106=2.0×103 mol dm3[H^+]_X = \sqrt{K_{a,X} \times C_X} = \sqrt{(1.0 \times 10^{-5}) \times 0.40} = \sqrt{4.0 \times 10^{-6}} = 2.0 \times 10^{-3}\text{ mol dm}^{-3}
For a weak monobasic acid, [H+]=KaC[H^+] = \sqrt{K_a \cdot C} derived from Ostwald's dilution law.
2
Calculate [H+][H^+] for Solution Y
[H+]Y=Ka,Y×CY=(4.0×105)×0.10=4.0×106=2.0×103 mol dm3[H^+]_Y = \sqrt{K_{a,Y} \times C_Y} = \sqrt{(4.0 \times 10^{-5}) \times 0.10} = \sqrt{4.0 \times 10^{-6}} = 2.0 \times 10^{-3}\text{ mol dm}^{-3}
Applying the weak acid ionization expression to Solution Y.
3
Calculate the degree of ionization (\alpha) for both acids
αX=Ka,XCX=1.0×1050.40=5.0×103=0.5%\alpha_X = \sqrt{\frac{K_{a,X}}{C_X}} = \sqrt{\frac{1.0 \times 10^{-5}}{0.40}} = 5.0 \times 10^{-3} = 0.5\%; αY=Ka,YCY=4.0×1050.10=2.0×102=2.0%\alpha_Y = \sqrt{\frac{K_{a,Y}}{C_Y}} = \sqrt{\frac{4.0 \times 10^{-5}}{0.10}} = 2.0 \times 10^{-2} = 2.0\%
The degree of ionization is given by α=KaC\alpha = \sqrt{\frac{K_a}{C}}.
4
Compare the calculated parameters
[H+]X=[H+]Y=2.0×103 mol dm3[H^+]_X = [H^+]_Y = 2.0 \times 10^{-3}\text{ mol dm}^{-3} and αYαX=2.0%0.5%=4\frac{\alpha_Y}{\alpha_X} = \frac{2.0\%}{0.5\%} = 4
Comparing [H+][H^+] and the ratio of degrees of ionization.

Key Concept

Relative Strength and Ionization of Acids and Bases
Estimated Time:2m 0s
Question 18Question

A saturated solution contains 12.0 g12.0\text{ g} of sodium hydroxide (NaOH\text{NaOH}) dissolved in 500 cm3500\text{ cm}^3 of solution at 25C25^\circ\text{C}. What is the solubility of sodium hydroxide in mol dm3\text{mol dm}^{-3} at this temperature?
[Molar mass of NaOH=40.0 g mol1\text{NaOH} = 40.0\text{ g mol}^{-1}]

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Answer: 0.60 mol dm30.60\text{ mol dm}^{-3}

Answer

0.60 mol dm30.60\text{ mol dm}^{-3}
To find the solubility in mol dm3\text{mol dm}^{-3}, first determine the number of moles of NaOH\text{NaOH} by dividing the mass (12.0 g12.0\text{ g}) by the molar mass (40.0 g mol140.0\text{ g mol}^{-1}), yielding 0.30 mol0.30\text{ mol}. Next, convert the volume to cubic decimeters (500 cm3=0.50 dm3500\text{ cm}^3 = 0.50\text{ dm}^3). Finally, divide the amount in moles by the volume in dm3\text{dm}^3 to get 0.60 mol dm30.60\text{ mol dm}^{-3}.

Step-by-Step Solution

1
Calculate the amount of NaOH\text{NaOH} in moles
Moles=12.0 g40.0 g mol1=0.30 mol\text{Moles} = \frac{12.0\text{ g}}{40.0\text{ g mol}^{-1}} = 0.30\text{ mol}
Solubility in mol dm3\text{mol dm}^{-3} requires expressing the amount of solute in moles.
2
Convert the solution volume from cm3\text{cm}^3 to dm3\text{dm}^3
Volume=500 cm31000 cm3 dm3=0.50 dm3\text{Volume} = \frac{500\text{ cm}^3}{1000\text{ cm}^3\text{ dm}^{-3}} = 0.50\text{ dm}^3
Standard concentration units require volume expressed in cubic decimeters.
3
Divide the number of moles by the volume in dm3\text{dm}^3
Solubility=0.30 mol0.50 dm3=0.60 mol dm3\text{Solubility} = \frac{0.30\text{ mol}}{0.50\text{ dm}^3} = 0.60\text{ mol dm}^{-3}
Solubility is the maximum amount of solute in moles that dissolves per dm3\text{dm}^3 of solution at a given temperature.

Key Concept

Solubility calculation in mol/dm³
Question 19Question

A standard solution is prepared by dissolving 1.575 g1.575\text{ g} of hydrated ethanedioic acid (H2C2O4xH2O\text{H}_2\text{C}_2\text{O}_4 \cdot x\text{H}_2\text{O}) in distilled water to make 250.0 cm3250.0\text{ cm}^3 of solution. A 25.0 cm325.0\text{ cm}^3 sample of this acid solution requires 25.0 cm325.0\text{ cm}^3 of a 0.100 mol dm30.100\text{ mol dm}^{-3} sodium hydroxide (NaOH\text{NaOH}) solution for complete neutralization. What is the integer value of xx in the formula of the hydrated acid? [Relative atomic masses: H=1\text{H} = 1, C=12\text{C} = 12, O=16\text{O} = 16]

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Answer: 2

Answer

The integer value of xx is 2.
The value of xx is calculated as 22. Based on the reaction stoichiometry, 25.0 cm325.0\text{ cm}^3 of 0.100 mol dm30.100\text{ mol dm}^{-3} NaOH\text{NaOH} contains 0.0025 mol0.0025\text{ mol} of base, which neutralizes 0.00125 mol0.00125\text{ mol} of the diprotic acid in the 25.0 cm325.0\text{ cm}^3 sample. The entire 250.0 cm3250.0\text{ cm}^3 solution therefore contains 0.0125 mol0.0125\text{ mol} of acid. Dividing the mass (1.575 g1.575\text{ g}) by 0.0125 mol0.0125\text{ mol} gives a molar mass of 126 g mol1126\text{ g mol}^{-1} for H2C2O4xH2O\text{H}_2\text{C}_2\text{O}_4 \cdot x\text{H}_2\text{O}. Subtracting the molar mass of anhydrous H2C2O4\text{H}_2\text{C}_2\text{O}_4 (90 g mol190\text{ g mol}^{-1}) gives 36 g mol136\text{ g mol}^{-1} for water, which corresponds to x=36/18=2x = 36 / 18 = 2.

Step-by-Step Solution

1
Determine the mole ratio from the balanced chemical neutralization equation.
H2C2O4xH2O+2NaOHNa2C2O4+(x+2)H2O\text{H}_2\text{C}_2\text{O}_4 \cdot x\text{H}_2\text{O} + 2\text{NaOH} \rightarrow \text{Na}_2\text{C}_2\text{O}_4 + (x+2)\text{H}_2\text{O}. The stoichiometric ratio of acid to base is 1:21 : 2.
Ethanedioic acid is a diprotic acid requiring two moles of hydroxide ions for complete neutralization per mole of acid.
2
Calculate the amount in moles of sodium hydroxide solution used in the titration.
Moles of NaOH=0.100 mol dm3×25.01000 dm3=0.0025 mol\text{Moles of NaOH} = 0.100\text{ mol dm}^{-3} \times \frac{25.0}{1000}\text{ dm}^3 = 0.0025\text{ mol}.
Number of moles is equal to molar concentration multiplied by volume in cubic decimeters.
3
Calculate the total moles of hydrated acid present in the 250.0 cm3250.0\text{ cm}^3 volumetric flask.
Moles in 25.0 cm3 aliquot=0.00252=0.00125 mol\text{Moles in } 25.0\text{ cm}^3 \text{ aliquot} = \frac{0.0025}{2} = 0.00125\text{ mol}. Total moles in 250.0 cm3=0.00125×250.025.0=0.0125 mol250.0\text{ cm}^3 = 0.00125 \times \frac{250.0}{25.0} = 0.0125\text{ mol}.
Using the stoichiometric ratio (na/nb=1/2n_a/n_b = 1/2) and scaling up from the 25.0 cm325.0\text{ cm}^3 aliquot to the full 250.0 cm3250.0\text{ cm}^3 solution volume.
4
Compute the molar mass of the hydrated acid and solve for xx.
Molar mass=1.575 g0.0125 mol=126 g mol1\text{Molar mass} = \frac{1.575\text{ g}}{0.0125\text{ mol}} = 126\text{ g mol}^{-1}. Molar mass of anhydrous H2C2O4=2(1)+2(12)+4(16)=90 g mol1\text{H}_2\text{C}_2\text{O}_4 = 2(1) + 2(12) + 4(16) = 90\text{ g mol}^{-1}. Mass of xH2O=12690=36 g mol1x\text{H}_2\text{O} = 126 - 90 = 36\text{ g mol}^{-1}. Thus, x=3618=2x = \frac{36}{18} = 2.
Subtracting the molar mass of the anhydrous acid from the total molar mass gives the mass of the water of crystallization, which is divided by the molar mass of water (18 g mol118\text{ g mol}^{-1}) to find xx.

Key Concept

Volumetric Analysis and Water of Crystallization Determination
Question 20Question

Complete the statement below regarding the volumetric analysis of a mixture containing sodium carbonate and sodium hydrogen carbonate using double indicators.

Fill in the blanks below

During the titration of a mixture of sodium carbonate and sodium hydrogen carbonate against standard hydrochloric acid, the first equivalence point marking the half-neutralization of sodium carbonate to sodium hydrogen carbonate is indicated by , which turns from pink to at a pH range of approximately 8.3 to 10.0.
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Answer

The first equivalence point is detected using phenolphthalein indicator, which transitions from pink to colorless (or colourless).
Phenolphthalein is the correct indicator for the first equivalence point because its transition interval (pH 8.3–10.0) matches the pH of the sodium hydrogen carbonate solution formed when all carbonate ions are neutralized. Its color changes from pink in alkaline medium to colorless at the endpoint.

Step-by-Step Solution

1
Identify the chemical reaction occurring at the first equivalence point of the carbonate-bicarbonate titration.
At the first endpoint, all CO32\text{CO}_3^{2-} ions are protonated to form HCO3\text{HCO}_3^- according to CO32+H+HCO3\text{CO}_3^{2-} + \text{H}^+ \rightarrow \text{HCO}_3^-. The pH at this stage is weakly alkaline (around pH 8.3).
Sodium hydrogen carbonate is an amphiprotic salt that forms a solution with a pH near 8.3, requiring an indicator with a pH transition range in the alkaline region.
2
Determine the appropriate indicator and its observed color change at this pH transition.
Phenolphthalein has a pH transition range of 8.3–10.0. In basic solution containing carbonate ions, it displays a pink color, and turns colorless once all carbonate ions are converted to hydrogen carbonate ions.
Methyl orange changes color at pH 3.1–4.4, which corresponds to the second equivalence point where hydrogen carbonate is completely converted to carbon dioxide and water.

Key Concept

Double Indicator Titration of Carbonate and Hydrogen Carbonate Mixtures
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