This course will cover the chemistry’s syllabus of IIT-JAM, M.Sc Entrance and all other UG level competitive-cum-academic examination.
Owing to the same syllabus, this course will also cover KVS, HTET, CTET, RTET and PGT lecturer screening also.
Curriculum
- 45 Sections
- 526 Lessons
- 25 Weeks
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- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 1: CHAPTER 1: Mathematical Concepts14
- 1.0Definition and Types of Units
- 1.1Unit Conversion
- 1.2Significant Figures and Their Importance
- 1.3Equations
- 1.4Functions
- 1.5Logarithm and Antilogarithm
- 1.6Limit and Continuity of a Function
- 1.7Deafferentation and Integration
- 1.8Stationary Points: Finding Maxima and Minima in a Function
- 1.9Ordinary Differential Equations
- 1.10Vectors and Matrices
- 1.11Determinant of a Matrix and Its Significance
- 1.12Elementary Statistics
- 1.13Probability Theory
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 1: CHAPTER 2: Atomic Structure23
- 2.0Early Atomic Models
- 2.1Need for Quantum Mechanics
- 2.2Blackbody Radiation
- 2.3Photoelectric Effect
- 2.4Heat Capacity of Monoatomic Solids
- 2.5Bohr Model of Atom
- 2.6Hydrogen Spectrum
- 2.7Sommerfeld Atomic Model
- 2.8Wave-Particle Duality of Radiation
- 2.9Wave-Particle Duality of Matter
- 2.10Heisenberg Uncertainty Principle
- 2.11Postulates of Quantum Mechanics
- 2.12Operators in Quantum Mechanics
- 2.13Max-Born Interpretation of a Wave Function
- 2.14Normalized and Orthogonal Wavefunctions
- 2.15Particle in a One-Dimensional Box
- 2.16Particle in a Three-Dimensional Box
- 2.17Wave Mechanical Model of Hydrogen Atom
- 2.18Pauli Exclusion Principle
- 2.19Aufbau Principle
- 2.20Slater’s Rules
- 2.21Electronic States of Atoms: Term Symbols
- 2.22Hund’s Rules
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 1: CHAPTER 3: Chemical Bonding7
- 3.0Lewis Model of Covalent Bonding
- 3.1Born-Oppenheimer Approximation in Quantum Mechanics
- 3.2Valence Bond Theory for Diatomic Molecules
- 3.3Valence Bond Theory for Polyatomic Molecules
- 3.4Molecular Orbital Theory for Diatomic Molecules
- 3.5Molecular Orbitals (MO) Diagrams of Diatomic Molecules
- 3.6Molecular Orbital Theory of Polyatomic Molecules
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 1: CHAPTER 4: Gaseous State15
- 4.0Definition and Characteristic Features of Gaseous State of Matter
- 4.1Gas Laws
- 4.2Kinetic Theory of Gases
- 4.3Maxwell Distribution of Velocities
- 4.4Collision Diameter and Collision Cross Section
- 4.5Collision Number and Collision Frequency
- 4.6Mean Free Path
- 4.7Viscosity of Gases
- 4.8Principle of Equipartition of Energy
- 4.9Ideal and Real Gases
- 4.10Deviation of Real gases from ideal Behavior
- 4.11Van Der Waal’s Gas Equation
- 4.12Critical State: Critical Phenomena and Critical Constants
- 4.13Reduced Equation of State and the Law of Corresponding States
- 4.14Liquification of Gases
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 1: CHAPTER 5: Liquid State9
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 2: CHAPTER 1: Solid State21
- 6.0Introduction to Solids
- 6.1External Symmetry in Crystals
- 6.2Laws of Crystallography and Their Significance
- 6.3Internal Symmetry of Crystals
- 6.4Close Packing Spheres
- 6.5Number of Particles in a Cubic Unit Cell
- 6.6Formule of Mass, Volume, and Density of a Unit Cell
- 6.7Atomic Radius in a Simple, Face-Centered, and Body-Centered Cubic Unit Cell
- 6.8Voids in Cubic Crystal Systems
- 6.9Radius Ratio Rule
- 6.10Packing Efficiency in Simple, Face Centered, and Body-Centered Cubic Lattice
- 6.11Distance and Angle Between to Crystal Planes
- 6.12Isomorphism and Polymorphism in Crystallography
- 6.13Defects in Crystals
- 6.14Band Theory of Solids and Its Application to Conductors, Insulators and Semiconductors
- 6.15X-Ray Diffraction by Crystals: Bragg’s Law
- 6.16Powder X-Ray Diffraction Technique
- 6.17X-Ray Diffraction Pattern of a Cubic Lattices
- 6.18Crystal Structure of Some Binary Compounds
- 6.19Born-Haber Cycle: Experimental Lattice Energy of Ionic Crystals
- 6.20Born-Landé Equation and Its Significance
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 2: CHAPTER 2: Thermodynamics23
- 7.0Introduction to Thermodynamics
- 7.1Zeroth Law of Thermodynamics
- 7.2First law of Thermodynamics
- 7.3Heat Capacity of Gases, Liquids and Solids
- 7.4Joule’s Law
- 7.5Joule Thomson Effect
- 7.6Isothermal and Adiabatic Expansion of an Ideal Gas
- 7.7Second Law of Thermodynamics and Its Significance
- 7.8Entropy Concept and Its Significance
- 7.9Internal Energy and Enthalpy
- 7.10Free Energy and Its Types
- 7.11Spontaneity of a Process in Terms of Entropy, Enthalpy, Internal Energy, Gibbs Free Energy and Helmholtz Free Energy
- 7.12Maxwell Relations
- 7.13Thermodynamic Equations of State
- 7.14Partial Molar Quantities
- 7.15Gibbes-Duhem Equation
- 7.16Gibbs-Helmholtz Equation
- 7.17Thermodynamic Relations from Ideal Gas Law
- 7.18Third Law of Thermodynamics
- 7.19Thermodynamics of Chemical Relations (Thermochemistry)
- 7.20Hess’s Law and Its Significance
- 7.21Heat of the Reaction at Constant Volume and Constant Pressure
- 7.22Kirchhoff’s Equations
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 2: CHAPTER 3: Chemical Kinetics19
- 8.0Introduction to Chemical Kinetics
- 8.1Rate of Reaction
- 8.2Rate Law for Elementary and Complex Reactions
- 8.3Differential Rate Law for Zero, First, Second, and Third Order Reactions
- 8.4Integrated Rate Laws or Rate Equations and Their Significance
- 8.5Experimental Methods of Evaluating Order of the Reaction
- 8.6Temperature Dependence of Reaction Rates (Arrhenius Equation)
- 8.7Pre-Equilibrium and Steady-State Approximations in Reaction Mechanism
- 8.8Simultaneous Reactions: Kinetics of Opposing, Parallel, and Consecutive Reactions
- 8.9Chain Reactions: Definition, Mechanism, Kinetics, Examples and Chain Length
- 8.10Collision Theory of Bimolecular and Unimolecular Reactions
- 8.11Theory Of Absolute Reaction Rates (Transition State Theory)
- 8.12Definition and Types of Catalysis
- 8.13Turnover Number and Turnover Frequency of a Catalyst
- 8.14Enzyme Catalysis (Michaelis-Menten Mechanism)
- 8.15Double Reciprocal Plot (Lineweaver–Burk Equation)
- 8.16Eadie-Hofstee Plot and Its Significance
- 8.17Photochemical Reactions
- 8.18Luminescence: Kinetics of Fluorescence and Phosphoresces
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 2: CHAPTER 4: Electrochemistry27
- 9.0Introduction to Electrochemistry
- 9.1Definition and Types of Electric Current
- 9.2Electrical Resistance and Conductance
- 9.3Electrolytic Conductance and its Measurement
- 9.4Factors Affecting Electrolytic Conductance
- 9.5Transference or Transport Number of an Ion
- 9.6Kohlrausch’s Law and its Applications
- 9.7Conductometric Titrations and Their Significance
- 9.8Arrhenius Theory of Electrolytic Dissociation
- 9.9Ostwald Dilution Law and Its Limitations
- 9.10Debey-Huckel-Onsager theory of Strong Electrolytes
- 9.11Debye-Huckel Limiting Law
- 9.12Galvanic Cell or Voltic Cell
- 9.13Electrolytic Cell
- 9.14Comparison Between Galvanic and Electrolytic Cells
- 9.15Relationship Between Electrical Energy and Chemical Energy
- 9.16Calculation Of Thermodynamic Quantities of Cell Reactions (∆ G, ∆H, ∆S)
- 9.17Electrode Potential and Its Measurement
- 9.18Electrochemical Series: Definition and Applications
- 9.19Nernst Equation
- 9.20Potentiometric Titrations: Definition, Types and Applications
- 9.21Concentration Cells
- 9.22Kinetic Salt Effect
- 9.23Definition and Types of Electrode Polarization
- 9.24Electrolysis and Its Mechanism
- 9.25Overvoltage and Its Applications
- 9.26Faraday’s Laws of Electrolysis
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 2: CHAPTER 5: Polymers7
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 3: CHAPTER 1: Chemical Equilibria11
- 11.0Introduction to Chemical Equilibria
- 11.1Law of Chemical Equilibria
- 11.2Definition, Types and Characteristic Features of Equilibrium Constants
- 11.3Relationship Between Kp, Kc, Ka, and Kx
- 11.4Equilibrium Constant for Different Reactions and Its Correlation with Degree of Dissociation
- 11.5Applications of Equilibrium Constant
- 11.6Chemical Equilibrium in Terms of Free Energy Change
- 11.7Relationship Between Standard Free Energy and Equilibrium Constant
- 11.8Le Chatelier’s Principle
- 11.9Van’t Hoff Equation of Reaction Isotherm
- 11.10Van’t Hoff Equation of Reaction Isochore
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 3: CHAPTER 2: Phase Equilibria7
- 12.0Introduction to Phase Equilibrium
- 12.1Phase, Component and Degree of Freedom
- 12.2Thermodynamic Criteria for Phase Equilibrium
- 12.3Clausius-Clapeyron Equation: Definition, Derivation and Applications
- 12.4Gibbs Phase Rule and Its Derivation
- 12.5Phase Equilibria of One Component Systems
- 12.6Phase Equilibria of Two Component Systems
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 3: CHAPTER 3: Surface Chemistry11
- 13.0Definition and Types of Adsorption
- 13.1Factors Affecting Adsorption
- 13.2Energetics of Adsorption
- 13.3Adsorption Isotherms: Definition and Types
- 13.4Freundlich Adsorption Isotherm Equation
- 13.5Langmuir Adsorption Isotherm Equation
- 13.6BET Adsorption Isotherm Equation: Surface Area of Adsorbents
- 13.7Adsorption Isobars
- 13.8Adsorption Isostere
- 13.9Gibbs Adsorption Equation
- 13.10Surface Films on Liquids
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 3: CHAPTER 4: Colloidal State11
- 14.0Introduction to Colloidal State of Matter
- 14.1Classification of Different Colloids
- 14.2Methods of Preparation of Lyophilic and Lyophobic Colloids
- 14.3Techniques for colloid Purification
- 14.4Physical, Colligative, Mechanical, optical and Electrical Properties of Colloids
- 14.5Stability of Sols
- 14.6Coagulation
- 14.7Hardy Schulze Rule and Coagulation Value
- 14.8Colloid Protection in Terms of Gold Number
- 14.9Emulsions and Gels
- 14.10Main Applications of Colloids
- PRINCIPLES OF PHYSICAL CHEMISTRY - VOLUME 3: CHAPTER 5: Molecular Spectroscopy21
- 15.0Introduction to Spectroscopy
- 15.1Electromagnetic Radiation
- 15.2Regions of the Electromagnetic Spectrum
- 15.3Instrumentation and Working of a Typical Spectrophotometer
- 15.4Signal-to-Noise Ratio of a Spectrophotometer
- 15.5Width of the Spectral Line
- 15.6Intensity of the Spectral Line
- 15.7Beer-Lambert Law
- 15.8Resolving Power of a Spectrophotometer
- 15.9Degrees of Freedom of Motion
- 15.10Types of Molecular Energies and Born-Oppenheimer Approximation
- 15.11Introduction to Rotational Spectra
- 15.12Pure Rotational (Microwave) Spectra of Diatomic Molecules
- 15.13Pure Rotational Raman Spectra of Diatomic Molecules
- 15.14Introduction to Vibrational Spectroscopy
- 15.15Vibrational Spectra of Diatomic Molecules
- 15.16Vibrational Raman Spectra of Diatomic Molecules
- 15.17Vibrational Rotational Spectra of Diatomic Molecules
- 15.18Vibrational Rotational Raman Spectra of Diatomic Molecules
- 15.19Electronic Spectroscopy of Molecules: Franck-Condon Principle
- 15.20Electronic Spectroscopy of Diatomic Molecules
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 1: CHAPTER 1: Periodic Properties of Elements7
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 1: CHAPTER 2: Coordination Complexes: Definition, Nomenclature and Initial Understanding5
- 17.1Definition, Origin and Important Terminology in Coordination Complexes
- 17.2Types of Metal Centre and Ligands in Coordination Complex
- 17.3Composition, Charge, Oxidation State, Coordination Number and Geometry of Coordination Complexes
- 17.4Correlation between Coordination Number and Possible Stereochemistry of Coordination Complexes
- 17.5Nomenclature of Coordination Complexes
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 1: CHAPTER 3: Theories of Coordination Complexes7
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 1: CHAPTER 4: Isomerism in Coordination Complexes7
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 1: CHAPTER 5: Stability of Coordination Complexes5
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 2: CHAPTER 1: Reaction Mechanism of Coordination Complexes6
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 2: CHAPTER 2: Electronic Spectra of Coordination Complexes5
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 2: CHAPTER 3: Magnetic Properties of Coordination Complexes8
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 2: CHAPTER 4: f-Block Elements6
- 24.0Introduction of Inner f-Block Elements
- 24.1Electronic Configuration of f-Block Elements
- 24.2Physical and Chemical Properties of Lanthanides and Actinides
- 24.3UV-Visible Spectra of Lanthanides and Actinides Complexes
- 24.4Magnetic Moment of Lanthanides and Actinides Complexes
- 24.5Extraction of f-Block Elements
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 2: CHAPTER 5: Chemistry of s- and p-Block Elements3
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 3: CHAPTER 1: Chemistry of Organometallic Compounds20
- 26.0Introduction to Organometallic Compounds
- 26.118 Electron Rule in Organometallic Chemistry
- 26.2Metal Carbonyls
- 26.3Infrared Stretching Frequency of Metal Carbonyl Complexes
- 26.4Metal Nitrosyls
- 26.5Anionic Carbonyl Complexes
- 26.6Metal Carbonyl Hydrides
- 26.7Metal Nitrile and Isonitrile Complexes
- 26.8Metal Complexes of Phosphine and Its Derivatives
- 26.9Metal-Alkene Complexes
- 26.10Metal Complexes of Alkyl, Carbene, Carbine, and Carbido Ligands
- 26.11Sandwich Complexes
- 26.12Isolobal Analogy
- 26.13Unique Types of Reactions in Organometallic Chemistry
- 26.14Alkene Hydrogenation
- 26.15Hydroformylation
- 26.16Methanol Carbonylation
- 26.17Oxidation of Olefins
- 26.18Water Gas Shift Reaction
- 26.19Olefin Polymerization with Ziegler-Natta Catalyst
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 3: CHAPTER 2: Bioinorganic Compounds9
- 27.0Introduction to Bioinorganic Chemistry
- 27.1Essential and Non-Essential Elements for Life
- 27.2Role of Metal Ions in Biological Systems and Medicine
- 27.3Metalloporphyrins: Definition, Structure, Bonding and Typical Examples
- 27.4Structure and Function of Hemoglobin and Myoglobin
- 27.5Carbonic Anhydrase: Definition, Structure and Function
- 27.6Photosystems: Definition, Types and Mechanism
- 27.7Transport of Na+ and K+ Ions: Sodium-Potassium Pump
- 27.8Biological and Abiological Nitrogen Fixation
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 3: CHAPTER 3: Acid-Base Chemistry6
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 3: CHAPTER 4: Cluster Compounds5
- PRINCIPLES OF INORGANIC CHEMISTRY - VOLUME 3: CHAPTER 5: Nuclear Chemistry14
- 30.0Introduction to Nuclear Chemistry
- 30.1Atomic Nucleus
- 30.2Proton-Electron and Proton-Neutron Hypothesis of the Atomic Nucleus
- 30.3Structural Models of Atomic Nucleus
- 30.4Packing Fraction of a Nucleus
- 30.5Mass Defect and Binding Energy of a Nucleus
- 30.6Emission of α, β and γ-Particles and its Effect on N/P Ratio
- 30.7Radioactive Disintegration
- 30.8Nuclear Reactions and Their Q-Value
- 30.9Nuclear Transmutation
- 30.10Nuclear Fission and Chain Reaction
- 30.11Nuclear Fusion and its Significance
- 30.12Nuclear Cross Section
- 30.13Radioactive Tracer and Neutron Activation
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 1: CHAPTER 1: Overview, History and Nomenclature of Organic Compounds5
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 1: CHAPTER 2: Fundamental Concepts of Organic Chemistry22
- 32.0Catenation of Carbon
- 32.1Bond Length, Bond Energy and Bond Angles in Carbon Compounds
- 32.2Definition and Characteristics Homologous Series
- 32.3Formal Charge and Oxidation Number
- 32.4Delocalization of Chemical Bond
- 32.5Conjugation: Definition, Types and Significance
- 32.6Bonds Weaker Than Covalent Interaction
- 32.7Inductive Effect: Definition, Types, Mechanism, Characteristics, and Application
- 32.8Electromeric Effect: Definition, Mechanism and Applications
- 32.9Field Effect: Definition, Mechanism and Significance
- 32.10Definition and Conditions for Resonance
- 32.11Resonance Energy and Its Experimental Determination
- 32.12Mesomeric Effect and Its Applications
- 32.13Hyperconjugation and Its Significance
- 32.14Tautomerism in Organic Compounds
- 32.15Comparison (Similarities and Differences) Between Tautomerism and Mesomerism
- 32.16Aromaticity: Definition, Types and Huckel Rule
- 32.17Aromatic, Antiaromatic and Non-Aromatic Compounds
- 32.18Homoaromaticity: Definition, Types and Typical Examples
- 32.19Annulenes
- 32.20Frontier Molecular Orbital and their Symmetry
- 32.21Principle of Conservation of Orbital Symmetry
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 1: CHAPTER 3: Reaction Intermediates8
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 1: CHAPTER 4: Mechanism of Organic Reactions: Structure and Reactivity11
- 34.0Definition of Reaction Mechanism
- 34.1Arrow Notation in Organic Reactions
- 34.2Reagents and Substrate in Organic Chemistry
- 34.3Types of Reagents: Electrophiles and Nucleophiles
- 34.4Types of Organic Reaction Mechanism
- 34.5Classification of Organic Reactions
- 34.6Energy Considerations of Reactions in Organic Chemistry
- 34.7Thermodynamic vs Kinetic Control of a Chemical Reaction
- 34.8Hammond Postulate
- 34.9Methods of Determination Mechanisms of Organic Reaction
- 34.10Definition and Types of Isotope Effects
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 1: CHAPTER 5: Stereochemistry of Organic Compounds29
- 35.1Isomerism in Organic Chemistry
- 35.2Elements of Symmetry
- 35.3Optical Activity or Chirality
- 35.4Types of Chiral Molecules
- 35.5Enantiomers
- 35.6Identical Isomers: an Oxymoron
- 35.7Diastereomers
- 35.8Three-Dimensional Representation of Organic Molecules
- 35.9Interconversion of Different Representation of Organic Molecules
- 35.10Definition and Types of Stereogenic Centre
- 35.11Enantiomers and Diastereomers in Organic Compounds with Two Dissimilar Chiral Centres
- 35.12Meso Compounds: Optical Isomerism in Organic Compounds Containing Two Similar Chiral Centers
- 35.13Racemic Mixtures (External Compensation)
- 35.14Stereomerism in Organic Compounds with Two or More Chiral Centre
- 35.15Prochirality and Prochiral Molecules
- 35.16Topicity: Definition, Types and Examples
- 35.17Relative Configuration: D-L Nomenclature of Organic Compounds
- 35.18Absolute Configuration: R-S Nomenclature for in Compounds with and without Chiral Center
- 35.19Enantiomeric Excess: Definition, Formula and Formula
- 35.20Racemization
- 35.21Resolution of Racemic Mixtures
- 35.22Bayer’s Strain Theory: Postulates, Applications and Limitations
- 35.23Conformation of Acyclic Systems
- 35.24Isomerism in Cycloalkanes
- 35.25Isomers of Decalins
- 35.26E-Z Nomenclature of Geometrical Isomers
- 35.27Geometrical Isomerism in Oximes
- 35.28Methods of Determining Geometrical Isomers
- 35.29Definition and Types of Stereoselectivity
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 2: CHAPTER 1: Substitution Reactions28
- 36.0Definition and Types of Substitution Reactions
- 36.1SN1 or Unimolecular Nucleophilic Substitution Reactions
- 36.2SN1′or Unimolecular Nucleophilic Substitution Prime Reactions
- 36.3SN2 or Bimolecular Nucleophilic Substitution Reactions
- 36.4SN2′ or Bimolecular Nucleophilic Substitution Prime Reactions
- 36.5SN1-SN2 Mixed Reactions
- 36.6SNi or Internal Nucleophilic Substitution Reactions
- 36.7SNi′ or Internal Nucleophilic Substitution Prime Reactions
- 36.8Nucleophilic Substitution by Single-Electron Transfer (SET)
- 36.9Neighbouring Group Participation in Nucleophilic Substitution Reactions
- 36.10Factors Affecting Aliphatic Nucleophilic Substitution
- 36.11Regioselectivity of Aliphatic Nucleophilic Substitution from Ambident Nucleophiles
- 36.12Aliphatic Nucleophilic Substitution at Trigonal Carbon
- 36.13ArSN1 or Aromatic Unimolecular Nucleophilic Substitution Reactions
- 36.14ArSN2 or Aromatic Bimolecular Nucleophilic Substitution Reactions
- 36.15Aryne Mechanism of Nucleophilic Substitution
- 36.16SRN1 or Unimolecular Nucleophilic Radical Substitution
- 36.17Factors Affecting Aromatic Nucleophilic Substitution
- 36.18Williamson Ether Synthesis
- 36.19Electrophilic Aromatic Substitution (Arenium Ion Mechanism)
- 36.20Friedel-Crafts Alkylation and Acylation Reactions
- 36.21SE1 or Substitution Electrophilic Unimolecular Reactions
- 36.22SE2 Substitution Electrophilic Bimolecular Reactions
- 36.23SEi Internal Electrophilic Substitution Reactions
- 36.24Gattermann-Koch Reaction
- 36.25Reimer-Tiemann Reaction
- 36.26Free Radical Substitution
- 36.27Hunsdiecker-Borodin Reaction
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 2: CHAPTER 2: Addition Reactions22
- 37.0Definition and Types of Addition Reactions
- 37.1Nucleophilic Addition to Carbon-Carbon Double Bond
- 37.2Michael Addition Reaction
- 37.3Nucleophilic Addition to Carbon-Heteroatom Multiple Bond
- 37.4Addition of Grignard Reagents, Organolithium and Organocopper Reagents to Carbonyl Compounds
- 37.5Wittig Reaction
- 37.6Aldol Condensation
- 37.7Claisen Condensation
- 37.8Hydrolysis and Ammonolysis of Esters
- 37.9Amide Hydrolysis
- 37.10Darzens Reaction
- 37.11Electrophilic Addition to Carbon-Carbon Multiple Bond
- 37.12Markovnikov Rule
- 37.13Halogenation and Hydrohalogenation of Alkenes
- 37.14Addition to Cyclopropane Ring
- 37.15Oxymercuration
- 37.16Electrophilic Addition to Carbon-Hetero Atom Multiple Bond
- 37.17Sharpless Asymmetric Epoxidation
- 37.18Free Radical Addition to Alkenes
- 37.19Cycloaddition Reactions
- 37.20Diels-Alder Reaction
- 37.21Simmons–Smith Reaction
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 2: CHAPTER 3: Rearrangement Reactions15
- 38.0Introduction to Rearrangement Reactions
- 38.1Electrocyclic Reactions
- 38.2Sigmatropic Rearrangements
- 38.3Cope Rearrangement
- 38.4Claisen Rearrangement
- 38.5Olefin Metathesis
- 38.61,2-Rearrangements
- 38.7Benzilic Acid Rearrangement
- 38.8Pinacol-Pinacolone Reaction
- 38.9Wolf Rearrangement
- 38.10Hofmann Rearrangement
- 38.11Curtius Rearrangement
- 38.12Lossen Rearrangement
- 38.13Favorskii Rearrangement
- 38.14Beckmann Rearrangement
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 2: CHAPTER 4: Elimination Reactions11
- 39.0Introduction to Elimination Reactions
- 39.1E1 or Unimolecular Elimination Reactions
- 39.2E2 or Bimolecular Elimination Reactions
- 39.3E1CB Unimolecular Conjugate Base Elimination Reactions
- 39.4Ei Elimination Internal Reactions
- 39.5Regiochemistry of the Double Bond in Elimination Reactions
- 39.6Stereochemistry of the Double Bond in Eliminations Reactions
- 39.7Competition of Elimination with Substitution
- 39.8E1 vs E2 vs E1CB Reactions
- 39.9Hofmann Elimination Reaction
- 39.10Cope Elimination Reaction
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 2: CHAPTER 5: Organic Redox Reactions0
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 3: CHAPTER 1: Electronic or UV-Visible Spectroscopy of Organic Compounds10
- 41.0Introduction to UV-Visible Absorption Spectroscopy of Organic Compounds
- 41.1Types of Electronic Transitions in Organic Molecules
- 41.2UV-Visible Spectrophotometer
- 41.3Presentation and Analysis of UV-Visible Spectra
- 41.4Chromophores and Auxochromes
- 41.5Change in the Position (Red and Blue Shifts) and Intensity (Hyperchromic and Hypochromic Effects) of Absorption Bands
- 41.6Effect Of Solvent on Electronic Transitions in Organic Compounds
- 41.7Effect of Conjugation on UV-Visible Absorption Bands
- 41.8Woodward Fieser Rules for Conjugated Dienes and Enones
- 41.9Applications of UV-Visible Spectra of Organic Compounds
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 3: CHAPTER 2: Infra-Red (IR) Spectra of Organic Compounds10
- 42.0Fundamental Concepts of Vibrational-Infrared Spectra of Organic Molecules
- 42.1Types of Molecular Vibrations
- 42.2Calculation of Vibrational Frequencies or Wavenumbers: Hook’s Law
- 42.3Position and Intensity of IR Absorption Bands
- 42.4Factors Affecting Vibrational Frequency in Organic Compounds
- 42.5Measurement of an IR Spectrum
- 42.6Parts of IR Spectrum: Finger Print and Functional Group Region
- 42.7Ring Size Effect in IR Spectroscopy
- 42.8Characteristic Absorption of Various Functional Groups
- 42.9Applications of IR Spectra of Organic Compounds
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 3: CHAPTER 3: Nuclear Magnetic Resonance or NMR Spectroscopy of Organic Compounds16
- 43.0Brief Introduction to NMR Spectroscopy
- 43.1Magnetic Properties of Nuclei
- 43.2Nuclear Spin States
- 43.3Principle of Nuclear Magnetic Resonance
- 43.4PMR Spectrum – Origin of NMR Signal
- 43.5NMR Spectrophotometer: Instrumentation and Working
- 43.6Shielding And Deshielding Effect: Number and Position of NMR Signal
- 43.7Chemical Shift in NMR Spectroscopy
- 43.8Peak Area and Proton Counting (Intensity Ratio of NMR Signals)
- 43.9Spin-Spin Coupling (Splitting of NMR Signal)
- 43.10Relaxation in NMR (Spin-Spin and Spin Lattice)
- 43.11Chemical Exchange and Its Effect on NMR Spectrum
- 43.12Typical Chemical Shifts and Coupling Constant Values in H1 NMR
- 43.13Solvent’s Peaks PMR Spectroscopy
- 43.14Structure Elucidation of Some Typical Organic Compounds Using NMR Data
- 43.15Applications of NMR Spectroscopy
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 3: CHAPTER 4: Amino Acids, Peptides and Nucleic acids0
- PRINCIPLES OF ORGANIC CHEMISTRY - VOLUME 3: CHAPTER 5: Carbohydrate Chemistry0
Hello sir, it’s a great website. Congratulations. Although I am not a chemistry student however i will circulate it to my friends.
Do you know of any economics institute like yours? Pls let me know.
ok Astha… I will let you know for sure
Sir ye videos k side me lock ka sticker show ho rha hai or videos nhi chl rii hai
please login again
Good work
Hlo sir I m pooja msc 1st year books provided
Hello sir my name is kiran book provided