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Carbohydrates
Monosaccharides ,Oligosaccharides And Polysaccharides
Proteins ,Structure Of Protein And Denaturation of Proteins
Vitamins And Nucleic Acids
DNA & RNA
Function of Nucleic Acids
Bio-molecules
Polymers Definition
Classification Of Polymers
Based On Molecular Force
Types Of Polymerization Reaction
Addition Polymerization Reaction Polymers
Condensation Polymerization Reaction Polymers
Co-polymerisation
Rubber Polymers
Biodegradable Polymers
Medicine And Drugs
Analgesics,Tranquilizers & Antiseptics
Disinfectants
Antimicrobial and its types
Antipyretics, Antihistamines & Antacids
Dyes And Its Characteristics
Creams, Perfumes, Deodorants, Ceramics etc.
Purification
Sublimation
Crystallization
Distillation and Differential Extraction
Chromatography ,Adsorption Chromatography And Partition Chromatography
Lassaigne’s Test
Detection Of Functional Group
Quantitative Analysis
Estimation Of Carbon And Hydrogen
Estimation of Nitrogen
Estimation Of Halogens
Estimation Of Oxygen
Emperical And Molecular Formula
Nitro Compound
Method of Preparation of Nitro alkanes
Method Of Preparation Of Nitrobenzene
Physical And Chemical Properties Of Nitro Compounds
Ring Substitution Reaction In Nitroarenes
Amines
General Method Of Preparation Of Amines
Physical And Chemical Properties Of Amines
Important Reaction Of Aniline
Alcohol Introduction
Methods of preparation of Alcohol
Physical Properties
Cleavage of OH bond
Cleavage of C-O bond
Reaction involving alcohol molecule as a whole
Oxidation
Test of Alcohol
Introduction Of Phenol
Physical Properties Phenol
Acidic nature of phenol
Effect of substituent on acidic strength of phenol
Electrophilic substitution reaction in phenol
Rimer-Tiemann Reaction
Ethers Introduction
Ethers General method of preparation
Ethers Physical Properties
Reaction due to ethereal oxygen
Formation of oxonium salts
Formation of coordination complex
Cleavage Of C-O bonds
Reaction due to alkyl group
Electrophilic substitution reaction
Aldehyde and Ketones Introduction
Strucutre of aldehyde and Ketone
Aldehyde and Ketones Physical Properties
Addition of Hydrogen and HCN
Addition of Grignard’s Reagent
Addition of Ammonia and Ammonia Derivatives
Oxidation Reaction
Clemmensen’s Reduction
Wolff-kishner Reduction
Aldol Condensation
Carboxylic Acids Introduction
Structure of Carboxylic acid
Carboxylic Acids Physical Properties
Carboxylic Acids Chemical Properties
Acidic nature of Carboxylic acids
Lassaign’s Test
Detection of Nitrogen
Detection of Sulphur
Detection Of Halogens
Test For Hydroxyl Group
Test For Carbonyl(Aldehyde And Ketone)
Test For Carboxylic Acids
Test For Amino Group
Tetravalency of carbon
Shapes of simple molecules
Hybridization
Homologous Series
Isomerism
Stereo-isomerism
Optical Isomerism
Characteristics of Enantiomers
Diastereomers
Characteristics of Diastereoisomers
Nomenclature of Organic Compound
Naming of Alkanes
The naming of organic compounds with a functional group
Nomenclature of Alicyclic compound
Nomenclature of Bicyclo Compounds
Hydrocarbon and Classification of Hydrocarbon
General Preparation of Alkanes
Properties of Alkanes
Chemical Properties of Alkanes
Newman Projection and Sawhorse Projection
Alkenes and Physical Properties of Alkenes
Chemical Properties of Alkenes
Ozonolysis
Alkynes and Physical properties of Alkynes
Chemical Properties of Alkynes
Benzene
Physical Properties of Benzene
Chemical Properties of Benzene
Molecules are the smallest constituent of any substances. They have some form of shapes. Let's study the different shapes of the molecule.
The molecules which align themselves in a straight line with a bond angle of 180 degree due to mutual repulsion about the electrons present in the molecule are called linear molecules.
Examples: H2, O2, CO2, Cl2, etc.
The molecules which do not align themselves in a straight line and have a variable bond angle between the atoms due to variation of repulsion about the electrons present in the molecule are called non-linear molecules.
Example: NH3(bond angle 107 degrees), H2O ( bond angle 104.5 degrees), etc.
The nonlinear molecules include the triangular planar, pyramidal or bent shape of the molecule
The element that undergoes Tetravalency (E.g., Silicon, Carbon) can form tetrahedral shape when they are covalently bonded with atoms of the same element. In three dimensions, the angle between the central atom and other atoms is 109.5 degrees.
Example: CH4, CCl4, SiH4, etc.\
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