| Physical Properties  | Chemical Properties  | 
|---|---|---|
Meaning  | Physical properties are those properties that can be observed or measured without changing the substances' identity; that is, there is no change in the substance's chemical structure. It does not undergo any chemical reaction that results in a structural transformation, and no new substance is formed.  | The chemical properties are those properties of the substance that one can only measure by changing the substance’s chemical structure. During the experiments, it is observed that a new substance is formed, which differs entirely from the starting material.  | 
Examples  | Color, melting and boiling point, density, solubility, refractive index measurements.  | Flammability, reactivity, oxidation state, acidity/basicity, heat of combustion.  | 
Uses  | Identifying or describing a substance.  | To predict how substance may behave in a chemical reaction environment.  | 
Experiments Type  | Simple experiments, such as heating and dissolving, etc.  | It involves a chemical reaction, such as burning or reacting with an acid, etc.  | 
Difference Between Physical and Chemical Properties
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What is Organic Chemistry?
- Introduction
 - Elements of a Chemical Reaction
 - Components of a Chemical Reaction
 
Atom
- Size of an atom- The world belongs to the tiniest!
 - Power of Protons
 - Mass Number
 - Average Atomic Mass
 - Molecule and Molecular Mass
 - The Electrons- An Atom’s Reactive Component
 - Atomic Orbitals- s, p, d, f
 - Filing of Atomic Orbitals and Writing Electronic Configuration
 - Valence and Core Electrons- How to Determine
 
Bonding In Atoms
- Octet Rule - Introduction and Bonding
 - Limitations of Octet Rule
 - Ionic Bond- Introduction and Formation
 - Formation of Ionic Compound
 - Requirements for Ionic Bonding
 - Appearance and Nature of Ionic Compounds
 - Physical Properties of Ionic Solids- Conductance, Solubility, Melting Point, and Boiling Point
 - Covalent Bond - How it Forms
 - Covalent Bond - Why it Forms?
 - Covalent Bond - Bond Pair (Single, Double, Triple) and Lone Pair
 - Number of Covalent Bonds- Valency
 - Types of Covalent Bonds- Polar and Nonpolar
 - Metallic Bond - Introduction and Nature
 - Significance of Metallic Bonding
 - Impact of Metallic Bonding on the Physical Properties
 - Applications of Metallic Bonding
 - Difference Between Metallic and Ionic Bond
 
Covalent Bond
- Theories on Covalent Bond Formation
 - Valence Bond Theory- Introduction and Covalent Bond Formation
 - Valence Bond Theory- Types of Orbital Overlap Forming Covalent Bonds
 - Applications, Limitations, and Extensions of Valence Bond Theory
 - Hybridization- Introduction and Types
 - sp3 Hybridization of Carbon, Nitrogen, and Oxygen
 - sp2 Hybridization of Carbon, Carbocation, Nitrogen, and Oxygen
 - sp Hybridization of Carbon and Nitrogen
 - Shortcut to Determine Hybridization
 - The shape of sp hybrid orbital - Why is the lobe unequal?
 - VSEPR Theory- Introduction
 - Difference between Electron Pair Geometry and Molecular Structure
 - Finding Electron Pair Geometry and Related Shape
 - Predicting Electron-Pair Geometry and Molecular Structure Guideline
 - Predicting Electron pair geometry and Molecular structure - Examples
 - Finding Electron-Pair Geometry and Shape in Multicentre Molecules
 - Drawbacks of VSEPR Theory
 - Electron Wave Property, LCAO and MOT - Introduction
 - Linear Combination of Atomic Orbitals - Formation of Sigma and Pie bonds using MO Approach
 - The Energetics of Bonding and Antibonding Molecular orbitals
 - Conditions for the Valid Linear Combination of Atomic Orbitals
 - Features of LCAO Theory
 - Finding the Electronic Configuration of Molecules using MO and Predicting Comparative Stability using Bond Order
 - Setting up the MO diagram for homonuclear diatomic molecules – Second Period Elements
 - Setting up the Molecular Orbital Diagram for Heteronuclear Diatomic Molecules
 - The Non-bonding Molecular Orbitals
 - Weakness of the Molecular Orbital Theory
 - Covalent bond Characteristics - Bond Length
 - Factors affecting Bond Length
 - How does Electron delocalization (Resonance) affect the Bond length?
 - Covalent bond Characteristics- Bond Angle
 - Factors affecting Bond Angle
 - Covalent bond Characteristics - Bond Order
 - How Bond Order Corresponds to the Bond Strength and Bond Length
 - Solved Examples of Bond Order Calculations
 - Covalent Bond Rotation
 - Covalent Bond Breakage
 - Covalent Bond Properties -Physical State, Melting and Boiling Points, Electrical Conductivity, Solubility, Isomerism, Non-ionic Reactions Rate, Crystal structure
 
Electronic Displacement in a Covalent Bond
- Electronegativity- Introduction
 - Factors Affecting Electronegativity- Atomic number, Atomic size, Shielding effect
 - Factors Affecting Electronegativity-s-orbitals, Oxidation state, Group electronegativity
 - Application of Electronegativity in Organic Chemistry
 - Physical Properties Affected by Electronegativity
 - Inductive effect - Introduction, Types, Classification, and Representation
 - Factors Affecting Inductive Effect- Electronegativity
 - Factors Affecting Inductive Effect- Bonding Order and Charge
 - Factors Affecting Inductive Effect- Bonding Position
 - Application of Inductive Effect- Acidity Enhancement and Stabilization of the counter ion due to -I effect
 - Application of Inductive Effect-Basicity enhancement and stabilization of the counter ion due to +I effect
 - Application of Inductive Effect-Stability of the Transition States
 - Application of Inductive Effect-Elevated Physical Properties of Polar Compounds
 - Is the Inductive Effect the same as Electronegativity?
 - Resonance - Introduction and Electron Delocalization
 - Partial Double Bond Character and Resonance Hybrid
 - Resonance Energy
 - Significance of Planarity and Conjugation in Resonance
 - p-orbital Electron Delocalization in Resonance
 - Sigma Electron Delocalization (Hyperconjugation)
 - Significance of Hyperconjugation
 - Resonance Effect and Types
 - Structure Drawing Rules of Resonance (Includes Summary)
 - Application of Resonance
 - Introduction to Covalent Bond Polarity and Dipole Moment
 - Molecular Dipole Moment
 - Lone Pair in Molecular Dipole Moment
 - Applications of Dipole Moment
 - Formal Charges - Introduction and Basics
 - How to Calculate Formal Charges (With Solved Examples)
 - Difference between Formal charges and Oxidation State
 
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Common Types of Reactions
- Classification of common reactions based on mechanisms
 - Addition Reactions
 - Elimination Reactions (E1, E2, E1cb)
 - Substitutions (SN1, SN2, SNAr, Electrophilic, Nucleophilic)
 - Decomposition
 - Rearrangement
 - Oxidation-Reduction
 
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Drawing Organic Structures
- Introduction
 - Empirical Formula
 - How to Calculate Empirical Formula from percentage composition and atomic masses
 - Related Numerical Problems - Finding Empirical Formula (Solved)
 - Molecular Formula
 - Numerical Problems related to finding molecular formula (Solved)
 - How to calculate molecular formula from empirical formula and molecular masses
 - Hill Nomenclature - The Empirical and Molecular Formula Writing Rules
 - E/Z Nomenclature - Structure Writing Rules for Substituted Alkenes
 - Kekulé
 - Condensed
 - Skeletal or Bond line
 - Polygon formula
 - Lewis Structures- What are Lewis structures and How to Draw
 - Rules to Draw Lewis structures- With Solved Examples
 - Lewis structures- Solved Examples, Neutral molecules, Anions, and Cations
 - Limitation of Lewis structures
 - 3D structure representation- Dash and Wedge line
 - Molecular models for organic structure representation- Stick model, Ball-stick, and Space-filling
 - Newman Projection- Introduction and Importance
 - How to Draw Newman Projections from Bond-Line Formula (5 step-by-step solved examples on alkane, substituted alkane, alkene, ketone, and cycloalkane)
 - Drawing Newman Projections to the Bond line Formula (solved examples)
 - Sawhorse Projection
 
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Functional Groups in Organic Chemistry
- What are functional groups?
 - Chemical and Physical Properties affected by the Functional Groups
 - Identifying Functional Groups by name and structure
 - Functional Group Categorization- Exclusively Carbon-containing Functional Groups
 - Functional Group Categorization- Functional Groups with Carbon-Heteroatom Single Bond
 - Functional Group Categorization- Functional Groups with Carbon-Heteroatom Multiple Bonds
 - Rules for IUPAC nomenclature of Polyfunctional Compounds
 - Examples of polyfunctional compounds named according to the priority order
 - Examples of reactions wherein the functional group undergoes transformations
 
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Structural Isomerism
- Introduction
 - Chain Isomerism
 - Position Isomerism
 - Functional Isomerism
 - Tautomerism
 - Metamerism
 - Ring-Chain Isomerism
 
Intermolecular Forces
- Ion-Dipole Interactions-Introduction and Occurrence
 - Factors Affecting the Ion-Dipole Strength
 - Importance of Ion-Dipole Interactions
 - Ion-Induced Dipole - Introduction, Strength and Occurrence
 - Factors Affecting the Strength of Ion-Induced Dipole Interactions
 - Ion-Induced Dipole Interactions in Polar Molecules
 - Vander Waals Forces -Introduction
 - Examples of Vander Waals' forces
 - Vander Waals Debye (Polar-Nonpolar) Interactions
 - Factors affecting the Strength of Debye Forces
 - Vander Waals Keesom Force - Introduction, Occurrence and Strength
 - Vander Waals London Force - Introduction, Occurrence, And Importance
 - Factors Affecting the Strength of London Dispersion Forces- Atomic size and Shape
 - Introduction, Occurrence and Donor, Acceptors of Hydrogen Bond
 - Hydrogen bond Strength, Significance and Types
 - Factors Affecting Hydrogen Bond Strength
 - Impact of Hydrogen bonding on Physical Properties- Melting and boiling point, Solubility, and State
 - Calculation of the Number of Hydrogen Bonds and Hydrogen bond Detection
 
Physical Properties
- Physical Properties- Introduction, Role of Intermolecular Forces
 - Physical State Change-Melting Point
 - Role of Symmetry, Role of Carbon numbers, Role of Geometry
 - Physical State Change-Boiling Point
 - Intermolecular Forces and their Effect on the Boiling Point, Role of Molecular Weight (Size), Molecular Shape, Polarity
 - Boiling Point of Special Compounds- Amino acids, Carbohydrates, Fluoro compounds
 - Solubility in Water
 - Density
 - Preliminary Qualitative Analysis of some Organic Compounds | Intensive Physical Property Measurements
 
Fundamentals of Organic Reactions
- Types of Arrows Used in Chemistry
 - Curved Arrows in Organic Chemistry- with Examples
 - Electrophiles - Introduction, Identification and Reaction
 - Formation and Classification of Electrophiles- Neutral and Charged
 - Difference between Electrophiles and Lewis Acids
 - Nucleophiles - Identification and Role in a Reaction
 - Types of Nucleophiles- Lone Pair
 - Types of Nucleophiles- Pie Bond
 - Types of Nucleophiles- Sigma Bond
 - Periodic Trend and Order in Nucleophilicity
 - Introduction to Reactions Involving Nucleophiles
 - Nucleophile Reactions- Aliphatic Displacement type - SN1, SN2
 - Nucleophile Reactions- Acyl Displacement type
 - Nucleophile reactions- Aromatic Displacement type- Electrophilic, Nucleophilic
 - Addition Reactions- Electrophilic, Nucleophilic, and Acyl
 - Ambident Nucleophiles- Introduction and Formation
 - Ambident Nucleophile - Nature of the Substrate
 - Ambident Nucleophile- Influence of the Positive Counter Ions
 - Ambident Nucleophile- Effect of Solvent
 - Lone Pair - Introduction and Formation
 - Physical Properties Affected by the Lone Pair- Shape and Bond Angle
 - Physical Properties Affected by the Lone Pair- Hydrogen Bonding
 - Physical Properties Affected by the Lone Pair- Polarity and Dipole Moment
 - Chemical property affected by the Lone pair- Nucleophilicity
 - Leaving Group - Introduction and Nature
 - Good and Bad Leaving Group
 - Factors Determining Stability of the Leaving Groups- Electronegativity, Size, Resonance Stability
 - Using pKa as a Measure of Leaving Group Ability
 - Leaving Groups in Displacement Reactions
 - Leaving Groups in Elimination Reactions
 
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Reactive Intermediates
- Carbocation - Introduction, Nature, and Types
 - Formation of Carbocation
 - Stability of Carbocations- Inductive, Resonance, and Hyperconjugation
 - Other Structural Features Increasing Carbocation Stability
 - Structural Feature Decreasing Carbocation Stability
 - Fate of the Carbocation
 - General Carbocation Formation Reactions
 - Carbanion - Introduction, Nature, and Types
 - Formation of Carbanions
 - Carbanion Stabilization
 - Ease of Formation of Carbanion -Acidic proton
 - Fate of the Carbanion
 - Free Radical - Introduction and Types of Carbon-Centred Radicals
 - Structure of Carbon-Centred Free Radical
 - Formation of Radicals
 - Stability of the Carbon-Centred Radicals
 - Other Structural Feature Increasing Free Radical Stability
 - Comparing Free Radical Stability using Dissociation energies (D-H)
 - Fate of Free Radicals
 - Common Reactions Involving Carbon-Free Radicals
 
Stereoisomerism - Conformation and Configurational Isomerism
- Conformations in Organic Chemistry - An Introduction
 - How are Conformational Isomers Depicted
 - Open Chain and Closed Chain Conformations
 - Nomenclature related to sp3-sp3 and sp3-sp2 bond rotations
 - Conformational Analysis
 - Factors affecting the stability of conformers - Stabilizing Interactions |Hyperconjugation
 - Factors affecting the stability of conformers - Stabilizing Interactions | Intramolecular Hydrogen Bonding
 - Factors affecting the stability of conformers - Stabilizing Interactions | Dipole Minimizations
 - Factors affecting the stability of conformers - Destabilizing Interactions | Steric strain
 - Factors affecting the stability of conformers - Destabilizing Interactions | Torsional strain
 - Factors affecting the stability of conformers - Destabilizing Interactions | Angle strain
 - Importance of Conformational Analysis
 - Conformation in Compounds with Lone Pairs
 - Role of Solvents in Conformations
 - An Example of Conformation Dependent Reaction and Product Selectivity
 - Geometrical Isomerism - Introduction
 - Impact of cis-trans isomerism on physical properties
 - Impact of cis-trans isomerism on chemical reactions
 - Scope of Geometrical Isomerism in Biological Systems and Industrial Applications
 - E/Z Nomenclature in Substituted Alkenes