Table of Content (Organic Chemistry)
Basic Organic Chemistry:-
Day 1: Introduction To Organic Chemistry, Acyclic or open chain compounds, Modern Definition of Organic Chemistry, Reasons for Large Number of Organic Compounds, Condensed and Bond-line Structural Formulas, Classification of Organic Compounds, Alicyclic or Closed Chain or Ring Compounds, Heterocyclic, Aromatic compounds, Benzenoid aromatic compounds, Homologous Series,
Day 2: Nomenclature, Root ward, Primary suffix, Secondary Suffix, Primary Prefix, Secondary prefix, Nomenclature Rules – Saturated and Branched Chain, Unsaturated and Functional Groups,
Day 3: Cyclic Compounds, Aromatic Compounds are Cyclic,
Day 4: Isomerism, Structural Isomerism, Chain Isomerism, Functional Isomerism, Positional Isomers, Metamers, Tautomerism,
Day 5: Stereo Isomerism, Wedge and Dash, Fisher Projection, Sawhorse projections, Newman Projections, Conformers of Butane C4H10, Cyclo Hexane, Geometrical Isomerism.
Day 6: Optical Isomerism, Discovery of Optical Isomerism, Measuring Optical Activity, Number of Optical Isomers of an Compound, Importance of Optical Compounds
In Biochemistry, Nomenclature of Geometric Isomers (E and Z) in Case More Than Two Different Groups are Present and Optical Isomers (R and S), Isotopes, Double and Triple Bonds, Double bonds: E/Z, Chiral Carbons:- R/S, Assigning Stereocentres Using Fischer Projections,
Day 7: Purification and Elemental Analysis Methods of Purification of Organic Compounds, Sublimation, Crystallisation, Distillation, Fractional Distillation, Distillation Under Reduced Pressure, Steam Distillation, Differential Extraction, Chromatography, Qualitative Analysis of Organic Compounds, Detection of Carbon and Hydrogen, Detection of other Elements, Test for Nitrogen, Quantitative Analysis, Carbon and Hydrogen,
Day 8: Nitrogen, Halogens Carius Method, Sulphur, Phosphorus, Oxygen, Empirical Formula and Molecular Formula, Determination of Molecular Mass, Duma’s Method, Chemical Method,
Day 9: Illustration.
Day 1: Reaction Mechanism, Introduction, Carbocations, Carbanions, Nucleophiles and Electrophiles, Electron Displacement in Substance, Strength of Various Atom and Groups, Resonance.
Day 2: Conditions For Resonance, Resonance Effect or Mesomeric Effect, Hyperconjugation, Electromeric Effect (E-Effect), Classification of Reactions, Strength of Acid (in General org. chemistry),
Day 3: Reaction Mechanism of Different Types, Electrophilic Addition Reactions, Addition of HX to Alkene, Markownikoff’s Rule, Nucleophilic Addition Reaction, Stereochemistry of Addition Nucleophillic, Anti-Markownikoff’s Rule (Kharash Peroxide Effect), Chain-Initiating Step, Chain-Propagation Step, Chain-terminating Step, Free Radical Addition Reaction.( Is Shown Only By Hbr), Substitution Reactions,
Day 4: Free Radical Reactions in Cyclic Compounds, Stereochemistry of Radical Substitution Reaction, Electrophilic Substitution Reaction (SE), Substitution Electrophillic and Addition Electrophillic, Nucleophilic Substitution Reactions, SN1 Reaction, SN2 Reaction,
Day 5: Elimination Reactions, E1 (Elimination) Reaction, E1-CB (Elimination) Reaction, E2 (Elimination) Reaction,
Day 6: Illustration.