Central Library

          Bio-Organic Chemistry
Proximity & Orientation Effects
Molecular Adaptation
Bio-Synthesis Reactions
Calixarenes
Crown Ethers
Cyclodextrins
Enzymes (Basic Concepts)
Enzymes (Nomenclature & Classification)
Enzyme Models (Molecular/Chiral Recognition)
Enzyme Models (Host-Guest Chemistry)
Enzyme Models (Artificial Enzymes)
Enzyme Regulation
Enzyme Inhibitors
Enzyme Kinetics
Mechanism of Enzyme Action (Acid/Base Catalysis)
Mechanism of Enzyme Action (Chymotrypsin)
Mechanism of Enzyme Action (Basic Concepts)
Mechanism of Enzyme Action (Lysozyme)
Mechanism of Enzyme Action (Carboxypeptidase A)
Mechanism of Enzyme Action (Hydrolysis of RNA)
Enzyme Catalyzed Reactions (Basic Concepts)
Enzyme Catalyzed Reactions (Addition & Elimination Reactions)
Enzyme Catalyzed Reactions (Condensation Reactions)
Enzyme Catalyzed Reactions (Isomerization Reactions)
Enzyme Catalyzed Reactions (Carboxylation / Decarboxylation Reactions)
Co-enzyme Chemistry (Coenzyme A)
Co-enzyme Chemistry (Thiamine Pyrophosphate)
Co-enzyme Chemistry Pyridoxal Phosphate)
Co-enzyme Chemistry (NAD/NADP)
Co-enzyme Chemistry (FAD / FAM)

          Photochemistry & Pericyclic Reactions
1,3 Dipolar Reactions 
4+2 Cycloaddition Reactions (Diels-Alder Reaction)
Basic Principles of photochemistry
β-Cleavage reactions
Cis-trans Isomerization (Photochemistry of Alkenes)
Cycloaddition Reactions [2+2]
Di-π-Methane Rearrangement
Electrocyclic reactions
Group transfer reactions (Pericyclic Reactions)
Norrish Type I Reactions
Norrish Type II Reactions
Organic Photochemistry (Tutorial I)
Paterno Buchi Reaction
Photochemistry of Arenes (Photo Isomerization Reactions
Photochemistry of Arenes (Photo Cycloaddition Reactions)
Photochemistry of Arenes (Photo substitution Reactions)
Photoreduction of Carbonyl Compounds
Sigmatropic Rearrangement

            Organic Reaction Mechanism
Aeromatic Nucleophilic Substitution (S_N^Ar)
Aliphatic Electrophilic Substitution
Aliphatic Nucleophilic Substitution (SET Mechanism)
Aliphatic Nucleophilic Substitution (S_N¹)
Aliphatic Nucleophilic Substitution (S_N²)
Aliphatic Nucleophilic Substitution (TUTORIAL I)
Aromatic Nucleophilic Substitution (Benzyine)
Aromatic Nucleophilic Substitution (Reaction)
Aromatic Nucleophilic Substitution (Unimolecular)
Aromaticity (Huckle Rules/Graig’s Rules)
Birch Reduction
Carbanions
Carbenes
Carbocation Rearrangements I (Wagner Meerwein Rearrangement)
Carbocation Rearrangements II (Pinacol Rearrangement)
Carbocations
Delocalized Chemical Bonding (Conjugation)
Delocalized Chemical Bonding (Resonance)
Diazonium Coupling (Electrophilic Aromatic Substitution)
Effect of Structure on Reactivity
Effect of Structure on Reactivity (Quantitative Treatment)
Electrophilic Aromatic Substitution
Electrophilic Aromatic Substitution (Orientation and Reactivity)
Electrophilic Aromatic Substitution (Quantitative Treatment)
Elimination Reactions
Free Radical Reactions
Free Radicals
Friedel-Craft Acylation
Friedel-Craft Alkylation
Gattermann Reaction
General Organic Chemistry (Tutorial I/Endo/Exo)
Halogenation (AES)
Houben-Hoesch Reaction
Methods of Determining Reaction Mechanism – I
Methods of Determining Reaction Mechanism – II
Neighbouring Group Participation
N-Heterocyclic Carbenes
Nitration and Sulphonation (AES)
Nitrenes
ORM (Hammond Postulate)
ORM (Potential Energy Diagram, Intermediates and Transition States)
ORM (Thermodynamic & Kinetic Control)
Reaction Intermediates (Tutorial I)
Reaction Intermediates (Tutorial II)
Reactions of Carbanions
Reactions of Carbenes
Smile Rearrangement
Sommelet-Hauser Rearrangement
Syn-Elimination Pyrolytic Elimination
Vilsmeier Reaction
Von-Richter Reaction

             Organic Reaction Mechanism-Multiple Choice Questions
MCQ-01 Organic Reaction Mechanism
MCQ-02 Organic Reaction Mechanism
MCQ-03 Organic Reaction Mechanism
MCQ-04 Organic Reaction Mechanism
MCQ-05 Organic Reaction Mechanism
MCQ-06 Organic Reaction Mechanism

           Organometallic Reagents
Dialyl lithium Regemts (GILMAN’S Reagent)
Organolithium Regents
Organopalladium Reagents
Organosilicon Reagents
Organotitanium (TiCl4)
Organotitanium Reagents (Titanium tetra-isopropoxide)
Organotitanium Reagents (Titanocene Dichloride)

            NAMED REACTIONS/ORGANIC REARRANGEMENTS
Arndt-Eistert Synthesis (Wolff Rearrangement)
Asymmetric Aldol Condensation
Asymmetric Baylish Hillman Reaction
Baeyer-Villiger Oxidation
Baylish Hillman Reaction
Beckmann Fragmentation
Beckmann Rearrangement
Benzil-Benzilic acid Rearrangement
Benzoin Condensation
Bischler–Napieralski Reaction
Brook Rearrangement
Buchwald-Hartwig Amination Reaction
Chugaev Reaction
Claisen Rearrangement
Cope Rearrangement
Curtius Rearrangement
Dienone-Phenol Rearrangement
Favorskii Rearrangement
Fritsch Buttenberg Wiechell Rearrangement
Hajos Parrish Reaction
Haller Baurer Reaction
Haloform Reaction
Hantzsch Dihydropyridine Synthesis
Heck Reaction
Hiyama Coupling Reaction
Hofmann–Löffler–Freytag Reaction
Hofmann Rearrangement
Kumada Reaction
Lossen Rearrangement
Neber Rearrangement
Negishi Coupling Reaction
Pyrrole Dihydropyridine Synthesis
Robinson Annulation
Schmidt Rearrangement
Shapiro Reaction
Songogashira Coupling
Stetter Reaction
Still Carbonylative Cross Coupling Reaction
Stille  Kelly Coupling
Stille Coupling Reaction Suzuki Coupling
Takai Olegination Reaction
Tebbe Olefination
Tempo Oxidation
Thorpe Zielger Reaction
Tsuji Trost Reaction
             Reduction Reactions
Catalytic Hydrogenation
Clemmensen Reduction
Dissolving Metal Reduction
Enzyme Catalyzed Reduction
LiAlH₄ Reduction
Meerwein Ponndorf Verley (MPV) Reduction
Metal Hydride Reduction (Alkoxy Aluminate Reagents)
Metal Hydride Reduction (DIBAL-H)
Metal Hydride Reduction (RED-Al)
NaBH₄ Reduction
Wolff-Kishner Reduction

           Oxidation Reactions
Oxidation Reactions (Manganese Reagents)
Oxidation Reactions (Osmium Reagents)
Oxidation Reactions (Selenium Dioxide Oxidation)
Oxidation Reactions (Peracid Oxidation)
Oxidation Reactions (Ozonolysis)
Oxidation Reactions (Chromium Reagents)
Oxidation Reactions (Lead Tetraacetate)
Oxidation Reactions (Silver Reagents)
Oxidation Reactions (Molecular Oxygen)