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PHARMACEUTICAL ORGANIC CHEMISTRY - II



Aromatic Hydrocarbons (Benzene and Derivatives) 
Structure of Benzene, stability of Benzene ( Heats of hydrogenation), Aromatic character –Huckel’s (4n + 2 electron) rule. Nomenclature of Benzene derivatives. Electrophilic substitution reactions (Halogenation, Nitration, Sulphonation, Friedel- Crafts alkylation and acylation), Effect of substituent on Reactivity and orientation of monosubstiuted Benzenes. Nucleophilic substitution in Halobenzenes. Acidity and Reactions of Phenols. 
Polynuclear Hydrocarbons: Napthalene and Anthracene: Structure, relative stability and aromaticity, Electrophilic substitution reactions - orientation, reduction and oxidation. 

Stereo Chemistry 
Stereoisomerism, conformational isomerism, Cis-trans (E & Z) isomerism, sequence rules for E & Z configurations. Enantiomerism and optical activity: 
Plane of symmetry, asymmetry or chirality, plane polarized light, Relative (D & L) configurations, Absolute (R & S) configurations, sequence rules, Diastereomers, Meso structures, racemic modifications, concept of stereospecificity. 

Heterocyclic Compounds Containing One Hetero Atom 
Introduction, classification and nomenclature of Heterocyclic compounds, Ring structure, methods of preparation and characteristic reactions of pyrrole, furan, thiophene, Pyridine, Indole, Quinoline, Isoquinoline and Acridine. Structure and specific uses of two medicinally important compounds representing each of the heterocyclic systems. 

Heterocyclic Compounds Containing Two Hetero Atoms 
Structure and preparation of Pyrazole, Imidazole, Benzimidazole, Oxazole, Isoxozole, thiazole, diazine, pyrimidius, pyrazine and phenothiazine. 
Nomenclature and Ring Structure and specific uses of two medicinally important compounds representing each of the above heterocyclic systems; Benzofuran, Benzopyran, dioxane, cinnoline, phenazine, oxazine, triazine, triazole, tetrazole, phenam and cepham. 

Synthetic Reagents and Reactions 
Specific synthetic Applications (at least two) of the following reagents: 
Lithium Aluminium Hydride (LAH), Lead Tetra Acetate (LTA), N-Bromosucinimide (NBS), Selenium oxide, sodium periodate, perchloric acid, 
Mechanism of the following reactions: Fries migration, Beckmann Re-arrangement, Birch reduction, Hoffman's hypobromite reaction, oppenneur oxidation. MPV reduction, ArndtEistert synthesis. 

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