* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download suman_organic
Enantioselective synthesis wikipedia , lookup
Aromaticity wikipedia , lookup
Woodward–Hoffmann rules wikipedia , lookup
Ring-closing metathesis wikipedia , lookup
Marcus theory wikipedia , lookup
Hydroformylation wikipedia , lookup
Elias James Corey wikipedia , lookup
Ene reaction wikipedia , lookup
Asymmetric induction wikipedia , lookup
Aldol reaction wikipedia , lookup
Aza-Cope rearrangement wikipedia , lookup
George S. Hammond wikipedia , lookup
Wolff–Kishner reduction wikipedia , lookup
Tiffeneau–Demjanov rearrangement wikipedia , lookup
Aromatization wikipedia , lookup
Hofmann–Löffler reaction wikipedia , lookup
Baylis–Hillman reaction wikipedia , lookup
Petasis reaction wikipedia , lookup
Nucleophilic acyl substitution wikipedia , lookup
Wolff rearrangement wikipedia , lookup
Vinylcyclopropane rearrangement wikipedia , lookup
What to study in organic chemistry? General organic chemistry(Ref:Peter Sykes) Electrophiles & Nucleophiles: Which type of systems act as E+ or Nu-? Same system act as E+ or Nu- depending on which system it reacts. Acidity and Basicity: General idea of order of acidity and basicity. Bronsted & Lewis theory. Effect of back-bonding , aromaticity, SIR,etc. Funda is conjugate acid or conjugate base as the case may be if stable then that base or acid is strong. Solvent and its role in reaction mechanism. Inductive effect, Hyperconjugation, Resonance. Aromaticity. Tautomerism (keto-enol) Keto-Enol Ratio – Various factors like relief of angle strain. Solvent & Temp. Effect on Keto-Enol Ratio H-Bonding: Some cases for which gemdiol is stable. Nu- of ions in protic and aprotic solvent. Effect of H-Bond on acidity,basicity,B.P. Order,H-Bonding during tautomerism. Organic Intermdiates Carbanion:--(a)Grignard’s Reagent 1. Preparartion 2. As a Base & Nucleophile. 3. Abnormal behaviour of Grignard. 4. Iodoform reaction. 5. WITTIG Reaction(Vinyl Ether Hydrolysis). 6. Decarboxylation. 7. Heating Effect of other compounds. 8. Dry distillation 9. Perkin Reaction `(b) Free Radical 1. 2. 3. Sources of free radical Wurtz & Kolbey Electrolytic Method. Halogenation of Alkane ©Carbene Reactions: 1. Riemer Teimann 2. carbylamine 3. Arndt Eistert 4. Hoffmann,Schmidt,Curtius Aromatic Chemistry 1. 2. 3. 4. Ref: I.L.Finar (Problems and solution chp 20 to 30) Electrophilic Aromatic Substitution(Nitration,Halogenation,Friedel Craft Alkylation,Freidel Craft Acylation,Kolbey Schmidt Reaction,sulphonation) Diazo Coupling Cannizarro(V.V.I.) Benzoin Condensation,Benzil-Benzilic Acid Rearrangement 5. Phenol Chemistry:-- Preparation:-- Imp.(Cumene Process,Diazo Method) Claisen Rearrangement. Sulphonation of Phenol Dienone Phenol Rearrangement Identification Of Phenol Ortho Para Ratio Other imp. Name reactions: aldol Cannizaro beckmann knovelgen condensation hell-volhard zelinsky reformatsky Practical Organic Chemistry Lassaigne Test Test For functional group(Amines, Amides, Substituted Amides, Nitro, Cyanide, Isocyanide,Imine, Nitroso) Separation of mixtures Preparation and reactions of : 1.Aldehyde & ketone 2.Carboxylic acids 3.Hydrocarbons 4.Amines 5.Alcohols Try to identify the link between chapters . That can be achieved by knowing method of interconversion. Conversion should be properly done with the sole purpose of getting maximum yield of product. In Roadmap problems clue of the solution should be identified.it is generally advisable in such problems to start from the end. Practising will bring about the knowledge of reagents to be used.Understanding mechanism& electron movement will lead to know intermediates in a reaction(v.v.I.)