Objectives
Objectives — Study Notes
NCERT-aligned · 9 notes · 3 shown free
Objectives
ExplanationObjectives
This introductory section outlines the key learning goals for the chapter on Solutions. After studying this unit, students will be able to describe the formation of various types of solutions, express solution concentrations in multiple units, and understand fundamental laws governing gas solubility such as Henry's law and Raoult's law. They will learn to distinguish between ideal and non-ideal solutions and explain deviations from Raoult's law. The chapter also covers colligative properties of solutions—properties that depend on the number of solute particles rather than their identity—and how these relate to molar masses of solutes. Finally, students will explore abnormal colligative properties exhibited by some solutes due to association or dissociation phenomena.
- Describe formation of different types of solutions
- Express concentration of solutions in various units
- State and explain Henry's law and Raoult's law
- Distinguish between ideal and non-ideal solutions
- Explain deviations from Raoult's law
- Describe colligative properties and relate them to molar masses
- 📌 Solution: homogeneous mixture of two or more components
- 📌 Henry's law: solubility of gas proportional to its partial pressure
- 📌 Raoult's law: vapour pressure proportional to mole fraction
1.1 Types of Solutions
Explanation1.1 Types of Solutions
Solutions are homogeneous mixtures where the composition and properties are uniform throughout. The component present in the largest quantity is called the solvent and determines the physical state of the solution, while other components are called solutes. This section focuses on binary solutions (two components), which can be gases, liquids, or solids. The types of solutions are classified based on the physical states of solute and solvent. Gaseous solutions include mixtures like oxygen and nitrogen gases. Liquid solutions include gases dissolved in liquids (oxygen in water), liquids dissolved in liquids (ethanol in water), and solids dissolved in liquids (glucose in water). Solid solutions include gases dissolved in solids (hydrogen in palladium), liquids dissolved in solids (amalgam of mercury with sodium), and solids dissolved in solids (copper in gold). The nature of the components and their physical states define the type of solution formed.
- Solutions are homogeneous mixtures with uniform composition
- Solvent is the major component determining physical state
- Solutes are components other than solvent
- Binary solutions consist of two components
- Types include gaseous, liquid, and solid solutions
- Examples: oxygen-nitrogen gas mixture, ethanol in water, copper in gold
- 📌 Solvent: component present in largest quantity
- 📌 Solute: other components dissolved in solvent
- 📌 Binary solution: solution of two components
1.2 Expressing Concentration of Solutions
Explanation1.2 Expressing Concentration of Solutions
This section explains various quantitative methods to express the concentration of solutions, essential for clarity and precision in chemical calculations. Concentration can be described qualitatively as dilute or concentrated but quantitative measur
Practice Questions — Objectives
Includes NCERT exercise questions with answers
Q1.1.1 Calculate the mass percentage of benzene $(\mathrm{C_6H_6})$ and carbon tetrachloride $(\mathrm{CCl_4})$ if $22\,\mathrm{g}$ of benzene is dissolved in $122\,\mathrm{g}$ of carbon tetrachloride.
Answer:
Mass percentage of benzene = (Mass of benzene / Total mass of solution) × 100 = (22 / (22 + 122)) × 100 = (22 / 144) × 100 = 15.28% Mass percentage of carbon tetrachloride = (Mass of CCl4 / Total mass of solution) × 100 = (122 / 144) × 100 = 84.72%
Explanation:
Mass percentage is calculated by dividing the mass of the component by the total mass of the solution and multiplying by 100.
Q2.1.2 Calculate the mole fraction of benzene in solution containing $30\%$ by mass in carbon tetrachloride.
Answer:
Assuming 100 g solution: Mass of benzene = 30 g Mass of CCl4 = 70 g Molar mass of benzene (C6H6) = 78 g/mol Molar mass of CCl4 = 154 g/mol Moles of benzene = 30 / 78 = 0.3846 mol Moles of CCl4 = 70 / 154 = 0.4545 mol Mole fraction of benzene = moles of benzene / (moles of benzene + moles of CCl4) = 0.3846 / (0.3846 + 0.4545) = 0.458
Explanation:
Mole fraction is calculated by dividing the moles of the component by the total moles of all components in the solution.
Q3.1.3 Calculate the molarity of each of the following solutions: (a) $30\,\mathrm{g}$ of $\mathrm{Co(NO_3)_2 \cdot 6H_2O}$ in $4.3\,\mathrm{L}$ of solution (b) $30\,\mathrm{mL}$ of $0.5\,\mathrm{M}\,\mathrm{H_2SO_4}$ diluted to $500\,\mathrm{mL}$.
Answer:
(a) Molar mass of $\mathrm{Co(NO_3)_2 \cdot 6H_2O}$ = Co (58.93) + 2 × (14.01 + 3 × 16.00) + 6 × (2 × 1.008 + 16.00) = 58.93 + 2 × 62.01 + 6 × 18.016 = 58.93 + 124.02 + 108.096 = 291.046 g/mol Moles of solute = 30 / 291.046 = 0.103 mol Volume of solution = 4.3 L Molarity = moles / volume = 0.103 / 4.3 = 0.024 M (b) Initial moles of $\mathrm{H_2SO_4}$ = Molarity × Volume (in L) = 0.5 × 0.030 = 0.015 mol Final volume = 500 mL = 0.5 L Molarity after dilution = moles / final volume = 0.015 / 0.5 = 0.03 M
Explanation:
Molarity is calculated by dividing moles of solute by volume of solution in liters. For dilution, moles remain constant; volume changes.
Q4.1.4 Calculate the mass of urea $(\mathrm{NH_2CONH_2})$ required in making $2.5\,\mathrm{kg}$ of 0.25 molal aqueous solution.
Answer:
Molality (m) = moles of solute / mass of solvent (kg) Given: m = 0.25 mol/kg, mass of solvent = 2.5 kg Moles of urea = molality × mass of solvent = 0.25 × 2.5 = 0.625 mol Molar mass of urea = 12.01 × 1 + 1.008 × 4 + 14.01 × 2 + 16.00 × 1 = 60.06 g/mol Mass of urea = moles × molar mass = 0.625 × 60.06 = 37.54 g
Explanation:
Molality is moles of solute per kg of solvent. Calculate moles from molality and solvent mass, then convert to mass using molar mass.
Q5.1.5 Calculate (a) molality (b) molarity and (c) mole fraction of KI if the density of $20\%$ (mass/mass) aqueous KI is $1.202\,\mathrm{g}\,\mathrm{mL}^{-1}$.
Answer:
Assuming 100 g solution: Mass of KI = 20 g Mass of water = 80 g = 0.080 kg Density = 1.202 g/mL Volume of solution = mass / density = 100 / 1.202 = 83.19 mL = 0.08319 L Molar mass of KI = 39.10 + 126.90 = 166.00 g/mol (a) Molality = moles of solute / mass of solvent (kg) = (20 / 166) / 0.080 = 0.1205 / 0.080 = 1.506 mol/kg (b) Molarity = moles of solute / volume of solution (L) = (20 / 166) / 0.08319 = 0.1205 / 0.08319 = 1.449 M (c) Moles of KI = 20 / 166 = 0.1205 mol Moles of water = 80 / 18 = 4.444 mol Mole fraction of KI = moles KI / (moles KI + moles water) = 0.1205 / (0.1205 + 4.444) = 0.0264
Explanation:
Calculate moles of KI and water, then use definitions of molality, molarity, and mole fraction with given density and mass percentages.
Q6.H₂S, a toxic gas with rotten egg like smell, is used for the qualitative analysis. If the solubility of H₂S in water at STP is 0.195 m, calculate Henry's law constant.
Answer:
Given: Solubility of H₂S in water at STP = 0.195 mol/kg (molality) At STP, pressure P = 1 atm = 1.013 × 10^5 Pa Henry's law states: C = k_H × P where C = concentration (mol/L), k_H = Henry's law constant (mol/(L·Pa)), P = partial pressure Since solubility is given in molality (mol/kg), approximate molality ≈ molarity (mol/L) assuming density ~1 kg/L for dilute solution. Therefore, C = 0.195 mol/L Rearranging Henry's law constant: k_H = C / P = 0.195 mol/L / 1.013 × 10^5 Pa = 1.924 × 10^{-6} mol/(L·Pa) Hence, Henry's law constant for H₂S in water at STP is approximately 1.92 × 10^{-6} mol/(L·Pa).
Explanation:
Step 1: Identify given data - solubility (0.195 mol/kg), pressure (1 atm = 1.013 × 10^5 Pa). Step 2: Assume molality ≈ molarity for dilute solution. Step 3: Use Henry's law C = k_H × P. Step 4: Rearrange to find k_H = C / P. Step 5: Substitute values and calculate k_H. Step 6: Final answer: k_H ≈ 1.92 × 10^{-6} mol/(L·Pa).
Q7.Henry's law constant for CO₂ in water is 1.67×10⁸ Pa at 298 K. Calculate the quantity of CO₂ in 500 mL of soda water when packed under 2.5 atm CO₂ pressure at 298 K.
Answer:
Given: Henry's law constant, k_H = 1.67 × 10^8 Pa Pressure, P = 2.5 atm = 2.5 × 1.013 × 10^5 Pa = 2.5325 × 10^5 Pa Volume of soda water = 500 mL = 0.5 L Henry's law relates pressure and concentration: P = k_H × C Rearranged: C = P / k_H = (2.5325 × 10^5 Pa) / (1.67 × 10^8 Pa) = 1.517 × 10^{-3} mol/L Quantity of CO₂ in 0.5 L: n = C × V = 1.517 × 10^{-3} mol/L × 0.5 L = 7.585 × 10^{-4} mol Molar mass of CO₂ = 44 g/mol Mass of CO₂ = n × molar mass = 7.585 × 10^{-4} mol × 44 g/mol = 0.0334 g Therefore, the quantity of CO₂ dissolved in 500 mL soda water is approximately 0.0334 g.
Explanation:
Step 1: Convert pressure to Pascals. Step 2: Use Henry's law P = k_H × C to find concentration. Step 3: Calculate moles of CO₂ in given volume. Step 4: Convert moles to mass using molar mass. Step 5: Final answer: 0.0334 g CO₂ in 500 mL soda water.
Q8.Vapour pressure of pure water at 298 K is 23.8 mmHg. 50 g of urea (NH2CONH2) is dissolved in 850 g of water. Calculate the vapour pressure of water for this solution and its relative lowering.
Answer:
Given: Vapour pressure of pure water, p₁⁰ = 23.8 mmHg Mass of urea, w₂ = 50 g Mass of water, w₁ = 850 g Molar mass of urea, M₂ = 60 g/mol Molar mass of water, M₁ = 18 g/mol Step 1: Calculate moles of solute (urea) and solvent (water): n₂ = w₂ / M₂ = 50 / 60 = 0.8333 mol n₁ = w₁ / M₁ = 850 / 18 ≈ 47.22 mol Step 2: Calculate mole fraction of water: x₁ = n₁ / (n₁ + n₂) = 47.22 / (47.22 + 0.8333) ≈ 47.22 / 48.05 ≈ 0.9827 Step 3: Calculate vapour pressure of water in solution: p₁ = x₁ × p₁⁰ = 0.9827 × 23.8 = 23.39 mmHg Step 4: Calculate relative lowering of vapour pressure: Relative lowering = (p₁⁰ - p₁) / p₁⁰ = (23.8 - 23.39) / 23.8 = 0.41 / 23.8 ≈ 0.0172 or 1.72% Answer: Vapour pressure of water in solution = 23.39 mmHg Relative lowering of vapour pressure = 0.0172 (1.72%)
Explanation:
The vapour pressure lowering is calculated using Raoult's law. First, moles of solute and solvent are calculated. Then mole fraction of solvent is found. Vapour pressure of solvent in solution is product of mole fraction and vapour pressure of pure solvent. Relative lowering is the fractional decrease in vapour pressure.
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Chemistry · Class 12