M.Sc/Graduate and
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B.Sc.& M.Sc. Organic Notes:
B.Sc.& M.Sc. Organic Notes:
1. Aromatic - Aromaticity, Homoaromaticity, Antiaromatic – Annulenes,
Aromaticity in charged rings, Benzene – Kekulé, Hückel 4n+2 Rule, Fused
ring systems, Azulene, Acenaphthylene, Aromaticity of heterocycles,
Electrophilic aromatic substitutions, arenium ion mechanism, The SE1 mechanism, Electrophilic aromatic substitutions, Reactivity of heteroaromatic compounds,
Electrophilicsubstitutions,Electrophilic aromatic substitutions of metallated aromatics –
Electrophilic substitutions involving hydrogen-lithium exchange, Electrophilic substitutions of Aryl-Grignard (Aryl-Lithium)
reagents, Nucleophilic aromatic substitution – The addition-elimination mechanism (Meisenheimer complexes),
Nucleophilicsubstitution of diazonium salts, The
elimination-addition mechanism (benzyne intermediate), Spectroscopy of Aromatic Compounds – (a)DOWNLOAD (b) DOWNLOAD (c) DOWNLOAD (d) DOWNLOAD
2. Stereochemistry - Enantiomers and Chirality, 3-D Representations of Enantiomers,
Properties of Chiral Molecules- Optical Activity, Chiral centers and chiral
molecules, Conformations and chirality, assigning absolute configuration,
Representations of R and S Structures, R/S nomenclature system, Assigning
absolute configuration in cyclic molecule, Assigning absolute configuration in
fischer formula, Translating 3-D formulas into fischer formula, Diastereomers
and meso form, summary of relationship between molecules with 2 or more chiral
centre, shortcut for assigning absolute configuration on paper, Cahn-Ingold-Prelog
Sequence Rules, D and L Notation, Configurations of D-Aldose, Configurations of
Ketose, Reactions of Monosaccharides – (a) DOWNLOAD (b) DOWNLOAD (c)DOWNLOAD (d) DOWNLOAD (e) DOWNLOAD (f) DOWNLOAD
3. Conformational analysis – introduction
of terms – conformers, configuration, dihedral angle, torsional strain –
Conformational analysis of ethane and n-butane including energy diagrams –
conformers of cyclo hexane (chair, boat and skew boat forms) – axial and equatorial.
Bonds-ring flipping showing axial equatorial inter conversions – conformers of
mono and id substituted cyclohexanes – 1:2 and 1:3 interactions , Conformations
of Other Cycloalkanes,
strain, anomeric effect,Naming Polycyclic
Ring Systems, Stereochemistry of Polycyclic Ring Systems – (a) DOWNLOAD (b)DOWNLOAD
4. Asymmetric synthesis - Stereoselective synthesis –
Chemoselectivity, Regioselectivity, Stereoselectivity – (a)DOWNLOAD (b) DOWNLOAD (c) DOWNLOAD (d) DOWNLOAD
5. Carbonyl group chemistry - Reactivity
of carbonyl group – alphasubstitution of enol, Acidity of a-Hydrogen atoms, Aldehyde and Ketone – Addition Reaction of the carbonyl group,Mechanisms of Aldol,
Perkin, Knoevenagal reactions and benzoin condensation – Claisen, Wiffig,
Cannizaro, Reformatsky reactions, Mechanisms of reduction with (sodium boro
hydride, LiAlH4, Woiff-Kishner and MPV) – mechanisms of haloform
reaction and Michael addition, Carboxylic Acid and their derivative reactions – Conversion of acids to their derivatives, Dicarboxylic acids –
Preparation and properties of oxalic, malonic. succinic, glutaric and adipic
acids, Malonic and acetoacetic esters characterstic reactions of active
methylene group – synthetic uses of malonic ester, acetoacetic ester and
cyanoacetic ester,Enols,
Enolates and polycarbonyl compounds Tautornerism – definition – keto-enol tautomerism (identification,
acid and bae catalysed inter – conversion mechanism, preparation and
characterstics) – amidoimidol and nitroacinitro tautomerism – (a)DOWNLOAD (b) DOWNLOAD (c) DOWNLOAD (d) DOWNLOAD (e)DOWNLOAD (f) DOWNLOAD (g) DOWNLOAD (h) DOWNLOAD
6. Alkane, Alkylation – Nomenclature, isomers,
basic chemical reactions,substitution, elimination, electrophilic addition,
alkane – From other acetylenes, from carbonyls, from olefins, from Strained
Rings, Eschenmosher Fragmentation Allenes, Alkylation – Alkylation of enolates,
enamines and hydrazones, Alkylation of heteroatom stabilized anions,
Organometallic Reagents, Sigmatropic Rearrangements, olefin reactions – Aldol
Condensation, Wittig Reaction, Peterson Olefination, Julia-Lythgoe
Olefination, Carbonyl Coupling Reactions, Tebbe Reagent, Shapiro and
Related Reaction, beta-Elimination and Dehydration, From Diols and
Epoxides, From Acetylenes, From Other Alkenes-Transition Metal Catalyzed
Cross-Coupling and Olefin Metathesis, basic chemistryproblem solving approach (a) DOWNLOAD(b) DOWNLOAD(c)DOWNLOAD (d) DOWNLOAD (e) DOWNLOAD
7. Oxidation-Reduction reactions and protecting
groups –Different oxidation
reactions, and reagents – Covers almost all the oxidation reactions and
oxidizing reagents, oxidation metal Based Reagents, Non-Metal Based
Reagents, others and Epoxidations, Different reduction reactions,
and reagents – Covers almost all the reduction reactions and reducing reagents,
Different protecting groups and reaction involving each, Hydroxyl groups,
Ketones and aldehydes, Amines and Carboxylic Acids – (a) DOWNLOAD (b)DOWNLOAD (c) DOWNLOAD (d) DOWNLOAD (e) DOWNLOAD
8. Reaction Mechanism - common organic reactions with
mechanism, writing reaction mechanism, kinds of organic reactions, homolysis,
hetrolysis, bond dissociation energy, kinetics, nucleophilic
aromaticsubstitution, alkyl halide elimination reaction, β-elimination (most
common elimination reaction), useful reaction to synthesize alkenes, alkynes,
other π bond functional groups, E1 and E2 with mechanism and example, Mechanism
and stereochemistry of E1 and E2 reaction – (a) DOWNLOAD (b)DOWNLOAD (c) DOWNLOAD (d) DOWNLOAD(e) DOWNLOAD (f) DOWNLOAD (g) DOWNLOAD (h) DOWNLOAD
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