A Complete Guide to Pharmaceutical Organic Chemistry II | Discount Coupon for Udemy Course

Scope:This subject deals with general methods of preparation and reactions of some organic compounds. Reactivity of organic compounds are also studied here. The syllabus emphasizes on mechanisms and orientation of reactions. Chemistry of fats and oils are also included in the syllabus.Objectives:Upon completion of the course the student shall be able to:- write the structure, name and the type of isomerism of the organic compound- write the reaction, name the reaction and orientation of reactions- account for reactivity/stability of compounds,- prepare organic compoundsCourse content:Unit IBenzene and its derivativesA. Analytical, synthetic and other evidences in the derivation of structure of benzene, Orbital picture, resonance in benzene, aromatic characters, Huckel’s ruleB. Reactions of benzene – nitration, sulphonation, halogenation- reactivity, Friedelcrafts alkylation- reactivity, limitations, Friedelcrafts acylation.C. Substituents, effect of substituents on reactivity and orientation of mono substituted benzene compounds towards electrophilic substitution reactionD. Structure and uses of DDT, Saccharin, BHC and ChloramineUnit IIPhenols – Acidity of phenols, effect of substituents on acidity, qualitative tests, Structure and uses of phenol, cresols, resorcinol, naphtholsAromatic Amines - of amines, effect of substituents on basicity, and synthetic uses of aryl diazonium saltsAromatic Acids –Acidity, effect of substituents on acidity and important reactions of benzoic acid.Unit IIIFats and Oilsa. Fatty acids – reactions. b. Hydrolysis, Hydrogenation, Saponification and Rancidity of oils, Drying oils. c. Analytical constants – Acid value, Saponification value, Ester value, Iodine value, Acetyl value, Reichert Meissl (RM) value – significance and principle involved in their determination.Unit IVPolynuclear hydrocarbons:a. Synthesis, reactionsb. Structure and medicinal uses of Naphthalene, Phenanthrene, Anthracene, Diphenylmethane, Triphenylmethane and their derivativesUnit VCyclo alkanesStabilities – Baeyer’s strain theory, limitation of Baeyer’s strain theory,Coulson and Moffitt’s modification, Sachse Mohr’s theory (Theory of strainless rings), reactions of cyclopropane and cyclobutane onlyWho this course is for:Any Undergraduate / Postgraduate / Researcher / chemistry studentAny Undergraduate / Postgraduate / Researcher / pharmacy student

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