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PART ONE “Systemic Approach in Organic Chemistry” Hassan A. Albar 1, Ali A. Khalaf and Ameen F. Fahmy 3 King Abdulaziz University, Chem. Dept., Saudi Arabia 1 Asuit University, Chem. Dept., Egypt 2 Ain Sahms University, Egypt 3
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Economy ScienceArts Earth
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Biology Economy Analysis Physics Chemistry Basic Science Mathematics
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Chemistry Analytical CHEMISTRY Inorganic Chemistry Physical Chemistry Organic Chemistry FSC
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Stereochemistry Spectroscopy Chemical Kinetics Thermodynamics Synthesis Analysis Chemistry
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Synthesis Heterocyclic chemistry Spectrochemistry Organic Chemistry Bioorganic Chemistry Natural Products Industrial Chemistry Physical organic Chemistry
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Unknown Organic Compound NMR IR UV EA MS
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Structure of Compounds Quantitative Analysis Qualitative Analysis Hydrogen deficient Index NMR UV IR Elemental Analysis Simplest Formula Molecular Formula Mass Spectroscopy X-Ray
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Physical organic Chemistry Kinetic Ste reo ch em istr y Sp ect ros co py Steric Effect Salt Effect Solvent Effect Isotope effect Trapping intermediate Acid Base Catalytic Effect Electronic Effect E#E# S#S# Femtosecond Chemistry Tunneling Microscope Atomic Force Microscopy
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Salt Effect Electronic Effects Catalytic Effects Solvent Effect Isotope Effect Trapping intermediate Spectral studies Stereoscopy T.S theory S # Kinetic Study Mechanism of Organic Reaction Femtosecond Chemistry
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Primary Metabolism Secondary Metabolism Carbohydrates Enzymes LipidsProteins Vitamins Hormones Metals Natural Products DNR & RNA Alkaloids SteroidsTerpenoids Glycosides …..etc Femtosecond Chemistry
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Natural Products Economic Agriculture Environment Industry Analysis Biology Science Organic Chemistry Medicinal Biochemistry Biosynthesis Pharmacotherapy Pharmacology Medicinal Science Genetics ….etc Microbiology Histopathology Physiology Pathology FSC
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Hydrocarbons 1,3-Dienes , -Unsaturated Carbonyl 1,3-Dicarbonyl Compounds Synthesis OO O
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CH 3 CH 2 CH 2 Cl CH 3 CH = CH 2 CH 3 C C-H CH 4 CH 3 Cl CH 3 OH CH 3 COOH CH 3 COCH 3 Hydrocarbons Alkylhalides Alkenes Alcohols & Amines Carboxylic acids Acylhalides Esters Amides Anhydrides
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O O O CH 3 – C - CH 2 – C - CH 3 O CH 3 – CH - CH 2 – C - CH 3 HO CH 2 = C - CH 3 N CH 3 COOR + + N + N
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