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11 Chemistry by Maktab

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  • 11 Chemistry by Maktab

11 Chemistry by Maktab

Curriculum

  • 11 Sections
  • 184 Lessons
  • 10 Weeks
Expand all sectionsCollapse all sections
  • 1.01 Basic Concepts
    13
    • 2.0
      Introduction
    • 2.1
      Molecules and Ions
    • 2.2
      Isotopes
    • 2.3
      Mass Spectrometry
    • 2.4
      Empirical Formula (1)
    • 2.5
      Empirical Formula (2)
    • 2.6
      Molecular Formula
    • 2.7
      Mole
    • 2.8
      Avogadro’s Number
    • 2.9
      Molar Volume
    • 2.10
      Stoichiometry
    • 2.11
      Limiting Reactant (1)
    • 2.12
      Limiting Reactant (2)
  • 1.02 Experimental Techniques in Chemistry
    6
    • 3.0
      Introduction
    • 3.1
      Filtration
    • 3.2
      Crystallization
    • 3.3
      Sublimation, Solvent Extraction
    • 3.4
      Chromatography
    • 3.5
      Lipids and Fatty Acids
  • 1.03 Gases
    12
    • 4.0
      Properties of Gases
    • 4.1
      Boyle’s Law
    • 4.2
      Charle’s Law
    • 4.3
      Gas Equation
    • 4.4
      Avogadro’s Law
    • 4.5
      Dalton’s Law
    • 4.6
      Graham’s Law
    • 4.7
      Kinetic Theory
    • 4.8
      Kinetic Interpretation of Temperature
    • 4.9
      Liquefaction
    • 4.10
      Ideal Gases
    • 4.11
      Plasma
  • 1.04 Liquids and Solids
    13
    • 5.0
      Introduction
    • 5.1
      Hydrogen Bonding
    • 5.2
      Evaporation
    • 5.3
      Boiling Point
    • 5.4
      Liquid Crystals
    • 5.5
      Solids
    • 5.6
      Crystal Lattice
    • 5.7
      Classification of Solids
    • 5.8
      Covalent Solids
    • 5.9
      Molecular Solids
    • 5.10
      Metallic Solids (1)
    • 5.11
      Metallic Solids (2)
    • 5.12
      Determination of Avogadro’s Number
  • 1.05 Atomic Structure
    25
    • 6.0
      Introduction
    • 6.1
      Discovery of Electron
    • 6.2
      Discovery of Proton
    • 6.3
      Discovery of Neutron
    • 6.4
      Determination of e/m of Electron
    • 6.5
      Millikan Oil Drop Method
    • 6.6
      Rutherford Atomic Model
    • 6.7
      Planck’s Quantum Theory
    • 6.8
      Bohr’s Atomic Model (1)
    • 6.9
      Bohr’s Atomic Model (2)
    • 6.10
      Spectrum
    • 6.11
      Hydrogen Spectrum
    • 6.12
      Problems in Bohr’s Atomic Model
    • 6.13
      X-Rays
    • 6.14
      Dual Nature of Matter
    • 6.15
      Experimental Verification of Dual Nature
    • 6.16
      Heisenberg’s Uncertainity Principle
    • 6.17
      Concept of Orbitals
    • 6.18
      Quantum Numbers
    • 6.19
      Principal Quantum Number
    • 6.20
      Azimuthal Quantum Number
    • 6.21
      Magnetic Quantum Number
    • 6.22
      Spin Quantum Number
    • 6.23
      Shapes of Orbitals
    • 6.24
      Electronic Distribution
  • 1.06 Chemical Bonding
    30
    • 7.0
      Introduction
    • 7.1
      Causes of Chemical Bonding
    • 7.2
      Energetics of Bond Formation
    • 7.3
      Atomic Sizes
    • 7.4
      Ionic Radii
    • 7.5
      Covalent Radii
    • 7.6
      Ionization Energy
    • 7.7
      Higher Ionization Energy
    • 7.8
      Electron Affinity
    • 7.9
      Electronegativity
    • 7.10
      Ionic Bond
    • 7.11
      Covalent Bond
    • 7.12
      Coordinate Covalent Bond
    • 7.13
      Limitations of Lewis Model
    • 7.14
      Valence-Shell Electron-Pair Repulsion Theory (1)
    • 7.15
      Valence-Shell Electron-Pair Repulsion Theory (2)
    • 7.16
      Valence Bond Theory
    • 7.17
      Atomic Orbital Hybridization
    • 7.18
      SP3 Hybridization
    • 7.19
      SP2 Hybridization
    • 7.20
      SP Hybridization
    • 7.21
      Molecular Orbital Theory
    • 7.22
      Energies of Molecular Orbitals
    • 7.23
      Molecular Orbital Structures
    • 7.24
      Bond Energy
    • 7.25
      Ionic Character and Bond Energy
    • 7.26
      Bond Length
    • 7.27
      Dipole Moment
    • 7.28
      Dipole Moment and Molecular Structure
    • 7.29
      Effect of Bonding
  • 1.07 Thermochemistry
    13
    • 8.0
      Introduction (1)
    • 8.1
      Introduction (2)
    • 8.2
      Spontaneous and Non-Spontaneous Reactions
    • 8.3
      System Surrounding and State Function
    • 8.4
      Internal Energy
    • 8.5
      First Law of Thermodynamics
    • 8.6
      Enthalpy
    • 8.7
      Different Enthalpies (1)
    • 8.8
      Different Enthalpies (2)
    • 8.9
      Glass Calorimeter
    • 8.10
      Bomb Calorimeter
    • 8.11
      Hess’s Law of Heat Summation
    • 8.12
      Born Haber Cycle
  • 1.08 Chemical Equilibrium
    23
    • 9.0
      Introduction
    • 9.1
      Reversible and Irreversible Reactions
    • 9.2
      Chemical Equilibrium
    • 9.3
      Law of Mass Action
    • 9.4
      Units of Equilibrium Constant
    • 9.5
      Equilibrium Constant of Some Chemical Reactions
    • 9.6
      Relation Between Equilibrium Constants
    • 9.7
      Applications of Equilibrium Constants (1)
    • 9.8
      Applications of Equilibrium Constants (2)
    • 9.9
      Le Chatlier’s Principle (1)
    • 9.10
      Le Chatlier’s Principle (2)
    • 9.11
      Le Chatlier’s Principle (3)
    • 9.12
      Industrial Applications of Chemical Equilibrium
    • 9.13
      Ionic Product of Water
    • 9.14
      Ionization Constant of Acids
    • 9.15
      Ionization Constant of Bases
    • 9.16
      Lowry-Bronsted Concept of Acids and Bases
    • 9.17
      Common Ion Effect
    • 9.18
      Buffer Solutions
    • 9.19
      pH of Buffer Solutions
    • 9.20
      Buffer Capacity
    • 9.21
      Solubility Product
    • 9.22
      Applications of Solubility Product
  • 1.09 Solutions
    16
    • 10.0
      Introduction
    • 10.1
      Concept of Solution
    • 10.2
      Molarity and Molality
    • 10.3
      Mole Fraction and PPM
    • 10.4
      Interconversion of Concentration Units
    • 10.5
      Types of Solution 1
    • 10.6
      Types of Solution 2
    • 10.7
      Raoult’s Law
    • 10.8
      Raoult’s Law with Volatile Components
    • 10.9
      Vapor Pressure of Ideal Solutions
    • 10.10
      Vapor Pressure of Non-Ideal Solutions
    • 10.11
      Solubility and Solubility Curve
    • 10.12
      Colligative Properties
    • 10.13
      Lowering of Vapor Pressure
    • 10.14
      Elevation of Boiling Point
    • 10.15
      Measurement of Boiling Point Elevation
  • 1.10 Electrochemistry
    14
    • 11.0
      Redox Reactions and Oxidation Number
    • 11.1
      Balancing of Redox Equations by Oxidation Number Method (1)
    • 11.2
      Balancing of Redox Equations by Oxidation Number Method (2)
    • 11.3
      Ion Electron Method in an Acidic Medium
    • 11.4
      Ion Electron Method in an Basic Medium
    • 11.5
      Fundamentals of Electrolytic Conduction
    • 11.6
      Electrolytic Cell
    • 11.7
      Electrolysis of Fused Salts and Aqueous Solutions
    • 11.8
      Electrolytic Processes of Industrial Importance
    • 11.9
      Galvanic vs Electrolyti Cell
    • 11.10
      Salt Bridge and Reversible Cell Functionality
    • 11.11
      Electrode Potential
    • 11.12
      Standard Hydrogen Electrode (SHE)
    • 11.13
      Measurement of Electrode Potential
  • 1.11 Reaction Kinetics
    19
    • 12.0
      Introduction to Reaction Kinetics
    • 12.1
      Rate of Reaction
    • 12.2
      Instantaneous and Average Rate
    • 12.3
      Specific Rate Constant
    • 12.4
      Order of Reaction
    • 12.5
      Rate Determining Step
    • 12.6
      Method if Initial Rates
    • 12.7
      Physical Methods for Rates of Reactions
    • 12.8
      Chemical Method for Rate of Reaction
    • 12.9
      Half Life Period
    • 12.10
      Determining Order Using Half Life Method
    • 12.11
      Activation Energy and Reaction Dynamics
    • 12.12
      Potential Energy Diagram for Reaction Mechanism
    • 12.13
      Effect of Nature and Concentration of Reactants on Reaction Rates
    • 12.14
      Effect of Surface Area and Light Reaction Rate
    • 12.15
      Effect of Temperature and Arrhenius Equation
    • 12.16
      More on Arrhenius Equation
    • 12.17
      Catalysis (1)
    • 12.18
      Catalysis (2)

Method if Initial Rates

This video lecture from Reaction Kinetics (F.Sc. first year Chemistry) covers the method of initial rates which helps to determine the order of reaction with respect to individual reactants which then helps to determine the rate law. In this method, one of the reactant’s concentration is altered while keeping the other one constant to know how it effects the rate. The method has been demonstrated using multiple examples. Find more e-learning material and educational video lectures in Urdu at maktab.pk. These videos are free to use for promotional and commercial purpose by keeping the credits to Maktab

Rate Determining Step
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Physical Methods for Rates of Reactions
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