| Subject | chemistry | Medium | ENGLISH |
|---|---|---|---|
| Faculty | VKP Sir | Status | AVAILABLE |
| Category | COMPLETE COURSE | Lecture | 112 |
| Target | XI XII XIII | Books | QUESTION BANK ATTACHED |
| You May Pay in Installments through Credit Card | |||
| Product Type | Prices | Validity | |
|---|---|---|---|
| USB | 6000 10%OFF 5400 | 2 year |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Definition of isomerism, Classification of isomerism, Chain isomerism, Positional isomerism | 45 Minutes |
| 02 | Functional isomerism, Ring-chain isomerism, Metamerism | 40 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Introduction, Classification of stereoisomerism, Geometrical Isomerism (G.I.) | 20 Minutes |
| 02 |
G.I. in C=C system , G.I. in Ring system , G.I. due to double bond inside the ring , Cummulenes |
55 Minutes |
| 03 | G.I. in C=N system, E/Z Nomenclature | 55 Minutes |
| 04 | Number of geometrical Isomers, Cummulenes, Spiranes, Cycloalkylidenes, Diphenyl system, Physical properties of geometrical isomers | 58 Minutes |
| 05 | Optical Isomerism , Plane polarised light , Chiral centre , Chirality ' Assymmetric molecules , Dissymmetric molecules , Plane of symmetry (POS), Centre of symmetry (COS) | 1 Hr 09 Minutes |
| 06 | POS, COS. Chirality, Optical activity | 55 Minutes |
| 07 | Wedge-Dash projection fromula , Fischer–Projection formula , Absolute configuration (R/S-configuration) , CIP-Rule | 52 Minutes |
| 08 | Enantiomers , Diastereomers , Axis of symmetry (AOS) | |
| 09 | Erythro enantiomers, Threo enatiomers, D/L- Configuration (Relative configuration) , Number of stereoisomers , Pseudo chiral carbon (PCC), Racemic mixture (or, R/S-mixture) , Polarimeter , Functioning of polarimeter , Percentage enantiomeric excess (%EE), Optical purity | 58 Minutes |
| 10 | Optical Resolution , Tertiary amine optical activity , Optical activity in absence of chiral centre , Cummulenes , Spiranes , Cycloalkylidene, Diphenyls , Alternating axis of symmetry (AAOS) , Conformational Isomerism | Minutes |
| 11 | Conformational isomers , Newmann projection formula , Dihedral angle (DHA) , Tortional strain (T.S.) , Vander waals strain (V.S.) , Angle strain (A.S.) , Definition of conformational isomers, Conformational analysis , Sawhorse projection formula | 57 Minutes |
| 12 | Conversion of Fischer to Newmann, Conformational analysis of cyclohexane , Energy profile | 51 Minutes |
| 13 | Conformational analysis of dimethyl cyclohexane | 15 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Structural Identification, Degree of unsaturation (DU), Catalytic hydrogenation H2/cat, Monochlorination Cl2/hn | 29 Minutes |
| 02 | Structural Identification , Monochlorination Cl2/hv , Ozonolysis , Reductive ozonalysis , Oxidation ozonalysis , Practical organic chemistry (POC), POC-I , Lassaigne’s test, Elemental analysis | 54 Minutes |
| 03 | Elemental anlaysis , Test of unsaturation, Test of terminal alkyne , Test of alcohols , Test of carbonyl compounds , Tests of aldehydes | 35 Minutes |
| 04 | Iodoform Test, Sodium metal test | 19 Minutes |
| 05 | Sodiumbicarbonate test (NaHCO3), Test of phenols and enols , Test of nitro compounds , Test of amines , Hinseberg’s test , POC-II | 33 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Electornic effect , Inductive effect | 36 Minutes |
| 02 | Applications of I-Effect , Resonance , Conjugated system | 47 Minutes |
| 03 | When double bond is in conjugation with vacant -p , When double bond is in conjugation with fully filled -p | 28 Minutes |
| 04 | When double bond is in conjugation with fully filled -p, When double bond is in conjugation with half filled-p , When +ve charge and lone pair are adjacent , d-orbital resonance , Conditions of Resonance, Mesomeric effect (M) | 53 Minutes |
| 05 | Stability of resonating structures (R.S), Steric Inhibition of Resonance (SIR) , Equivalent R.S. | 35 Minutes |
| 06 | Equivalent R.S. , Hyperconjugation HC , Hyperconjugation in carbocations , Hyperconjugation in Alkenes , Heat of hydrogenation (HOH) | 54 Minutes |
| 07 | Hyperconjugation in Toluene, Hyperconjugation in Free Radicals, Electromeric effect (E), Applications of electronic effects , Dipole moment, Bond length , Aromaticity , Benzenoids and Non-benzenoids | 38 Minutes |
| 08 | Examples of aromatic compounds , Heterocyclic aromatic compounds | 27 Minutes |
| 09 | M.O. Diagram, Polycyclic aromatic compounds | 24 Minutes |
| 10 | Examples of aromatic systems, [n] Annulenes , NMR- definition of Aromaticity , Resonance energy (RE) | 37 Minutes |
| 11 | Acidic strength of acids , Acidic strength of dicarboxylic acids | 44 Minutes |
| 12 | Aromatic acids , Ortho effect, Acidic strength of phenols , Feasibility of reactions , Sodium bicarbonate test of acids | 52 Minutes |
| 13 | Basic strength , Organic Nitrogenous bases. | 12 Minutes |
| 14 | Basic strngth of Aliphatiec amines , Aromatic amines | 43 Minutes |
| 15 | Basic strength of Amidines , Basic strength of Guanidines, Proton sponges, Site of protonation , Feasibility of Reaction | 31 Minutes |
| 16 | Carbanions (C-), Reactions in which carbanions are formed , Organometallic compounds, Active methylene group., Tautomerism, Types of Tautomerism | 38 Minutes |
| 17 | Enolisable –H, Keto-enol Tautomerism, Mechanism of keto-enol Tautomerism | 23 Minutes |
| 18 | Stability of enol (Percentage enol-content), Racemisation due to enolisation | 43 Minutes |
| 19 | D-Excharge , Tautomerism in phenols , Ring-chain Tautomerism , Unsymmetrical alpha-hydroxy ketones | 37 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Basic organic chemistry, Definition of organic compound , Representation of organic compound , Hybridisation | 12 Minutes |
| 02 | Number of Sigma and PI bonds , Degree of carbon , Degree of hydrogen , Degree of Alkyl halides, Degree of Alcohols , Degree of Amines , Degree of unsaturation (DU) , Calculation of DU , Fundamental definition of DU, Homologous series (H.S.) | 46 Minutes |
| 03 | Classification of organic compound , Aromatic compounds , Homocyclic compounds , Heterocyclic compounds , IUPAC- Nomenclature , Scheme of IUPAC, Naming of Alkanes | 38 Minutes |
| 04 | Scheme of IUPAC, Naming of alkanes , Retained Names , Naming of alkenes | 59 Minutes |
| 05 | Naming of Alkene, Naming of Alkynes , Naming of cycloalkanes | 33 Minutes |
| 06 | Naming of cycloalkenes , Alkylidenes , Naming of cycloalkynes , Naming of Bicyclo compounds | 42 Minutes |
| 07 | Functional Groups (F.G.), Naming of carboxylic acids, Special Name of carboxylic acids , Naming of dicarboxylic acids | 33 Minutes |
| 08 | Naming of sulphonic acid , Naming of Alcohols , Naming of Amines , Naming of thioalcohols, Naming of Aldehydes , Special name of Aldehydes | 49 Minutes |
| 09 | Naming of Ketones , Naming of cyanides , Special name of cyanides , Naming of isocyanides , Naming of Amides , Special name of amides , Naming of acid halides | 46 Minutes |
| 10 | naming of acid halide, naming of acid anhydride, naming of esters, special name of ester | 41 Minutes |
| 11 | Naming of haloalkanes , Naming of Nitro compounds , Naming of Nitroso compounds , Naming of Aromatic compound , Benzene , Other aromatic compound | 38 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Carbocations C+, Hybridisation of carbocations , Stability of carbocations , Rearrangement of carbocations , Type of shifts , Migratory aptitude | 36 Minutes |
| 02 | Migratory aptitude of aromatic group , Rearrangement in cyclic carbocations , Ring expansion (RE), Ring contracting (RC) , Cyclopropyl methyl carbocations (CPM–C+), Stability order of carbocations , Some extra ordinary stable carbocations, CPM carbocation , Aromatic carbocations | 42 Minutes |
| 03 | Rearrangement of carbocation, Reaction mechanism , Solvents , Polar protic solvents (PPS), Polar aprotic solvents (PAs) , Reagents , Nucleophiles, Nu, Electrophilic E+ | 35 Minutes |
| 04 | Electrophiles, E+, Nucleophiles, Nu, Nucleophilicity , Experimental order of Nu, Strong Nu with weak basic character , Strong Nu with strong basic character, Weak Nu with weak basic character , Solvation of Nu | 47 Minutes |
| 05 | Leaving group (l.g.), Leaving group ability , Unimolecular nucleophilic substitution reaction of first order (for R–X) i.e SN1 of R–X , Kinetics of SN1, Stereo of SN1, PE- diagram of SN1, SN1 with rearrangement in C+, Rate of SN1 reaction | 36 Minutes |
| 06 | SN1 or R–X, Solvolysis reaction , Factors affecting the rate of SN1 reactions , SN1 of alcohol R–OH | 50 Minutes |
| 07 | SN1 of R–OH, Lucas reaction , SN1 of ethers , Hydrolysis of ethers , SN2 reaction of (R–X), Kinetics of SN2 reaction , Stereochemistry of SN2 Rxn , PE-diagram of SN2 Rxn | 43 Minutes |
| 08 | Walden's experiment , Walden Inversion , Factors affecting the rate of SN2 Rxn , Halogen exchange reaction , Finkelstien reaction , Swart's reaction , SN2 Rxn of alcohol (R–OH), SNi reaction of alcohol with SOCl2 | 48 Minutes |
| 09 | SN2 of ether , Reaction of epoxides , Williamson's ether synthesis | 29 Minutes |
| 10 | Intramolecular SN2 reactions , Neighbouring group participation (NGP) , Comparison between SN1 and SN2 , SN1 Vs SN2 | 41 Minutes |
| 11 | Elimination Reaction , E1 elimination (of R–X), Saytzeff's rule , Regioselectivity , E1 of Alcohols, Acid catalysed dehydroation of alcohol, Dienone- Phenol rearrangement , Pinacol - Pinacolone rearrangement , Semipinacol- Pinacolone rearrangement | 51 Minutes |
| 12 | E2 Rxn of (R–X), Stereoselectivity and sterospecificity , Reagents of E–2 Reaction , Order of Rate of E–2, Major Hofmann Alkene | 37 Minutes |
| 13 | Summary of SN1/ SN2/E1/E2, Stereo selectivity of E–2 reaction , E1CB reaction , Cases when Hofmann Alkene is the major product | 40 Minutes |
| 14 | Tetraalkyl ammonium hydroxide , E–2 Rxn, Didehalogenation , Stereoselectivity , Isotope effect (KH/KD) | 24 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Organometallic compounds , Preparation of G.R. | 12 Minutes |
| 02 | Preparation of GR, Solvents of GR, Reaction of GR, Acid-base reaction of GR, Zerewitinoff's active hydrogen determination | 33 Minutes |
| 03 | Nucleophilic addition reaction of GR, SN2- Th reaction of GR | 30 Minutes |
| 04 | Unstable GR, Mono GR is not possible with dihalide , Reaction of GR with CO2, Reaction of GR with O2, Reaction of GR with RCN, Digrignard reagent , Reactions of digrignard reagent | 40 Minutes |
| 05 | Attack of GR on weak bond, 1,2-addtion & 1,4-additon , Reaction of GR with metal halides , REDUCTION , Definition of reduction , Table of reducing agents , Catalytic hydrogenation | 42 Minutes |
| 06 | Catalylic hydrogenation , Stereoselectivity ,) Partial hydrogenation , Lindlar's catalyst , P-2 catalyst (Nickle Boride), Birch reduction | 44 Minutes |
| 07 | Hydroboration Reduction (HBR), Transfer Hydrogenation, Clemmensen reduction , Wolf-Kishner reduction, Lithium aluminium hydride (LiAlH4) | 54 Minutes |
| 08 | Sodiumboro hydride (NaBH4) (SBH), Triphenyltin hydride Ph3SnH (TPH), DiBAl-H- Diisobutyl Aluminium hydride , Red –P + HI, Mozingo reduction , MPV- reduction , Oppeneaus Oxidation , Bauvealt-Blanc reduction , ALKANES, Free Radicals , Formation of free radicals , F.R. Catalyst/ Initiators / Promotors , F.R. Inhibitors/ Scavangers/Poisons , Stability of free radicals , Reactions of free radicals , Combination Reactions , Disproportionation reaction | 53 Minutes |
| 09 | Reactions of Free radicals , Stability of free radicals , Preparation of Alkanes , Wurtz Reaction (WR), Wurtz-Fitting reaction , Fitting reaction , Frankland reaction , Kolbe's Electrolytic synthesis (KES), Corey-House Reaction | 41 Minutes |
| 10 | Corey House reaction, Decarboxylation , Decarboxylation by soda lime , Decarboxylation by heating | 40 Minutes |
| 11 | Properties of Alkanes , Chemical properties of Alkanes , Free Radical substitution reaction , PE-diagrams , Reactivity order , Conditions of halogenation | 25 Minutes |
| 12 | reactivity and selectivity , Percentage yield , Quantum yield , Isomerisation reaction of alkanes , Aromatisation reaction of alkanes , Petroleum , Physical Properties of alkanes | 39 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Alkenes , Preparation of Alkene , Pyrolysis of ester , Pyrolysis of xanthates (Chaugave reaction ) , Cope reaction , Didehalogenations | 37 Minutes |
| 02 | Chemical reactions of Alkenes , Electrophilic addition reaction (AE Rxn), Classical carbocation mechanism , Non-Classical carbocation mechanism , Markowni Koff's rule , Addition of H–X, Antimarkowni Koff's rule | 52 Minutes |
| 03 | Addition of H2O on Alkenes , Acid-catalysed hydration of Alkenes , Oxymercuration- Demercuration reaction (OM/DM), Hydroboration -oxidation (HBO), Alkoxymercuration Demercuration , Addition of X2 on Alkenes | 47 Minutes |
| 04 | Addition of HOX on alkenes , Stereoselectivity , Order of rate of addition of X2 on alkene , Chemical reaction of Alkynes , Addition of H-X on alkynes , Addition of H2O on alkynes , Hydration of alkyne with dil H2SO4 and HgSO4, Hydroboration – Oxidation | 48 Minutes |
| 05 | Addition of HOX on alkynes , Preparation of alkynes , Isomerisation | 24 Minutes |
| 06 | Isomerisation mechanism , Reaction of terminal alkynes , Dienes , Conjugated diene , Addition NOCl on alkene , Allylic substitution , NBS- N-bromosuccinimide | 35 Minutes |
| 07 | Reaction of NBS, MnO2- Oxidising agent , Carbenes , Sources of carbenes , Types of carbenes | 21 Minutes |
| 08 | Reaction of carbene , Reimmer-Tiemann reaction , Carbyl amine reaction , OXIDATION , definition of oxidation , Oxidation of alkenes and alkynes , Ozonolysis of Alkenes and alkynes , Oxidation of Ketone , Perhydroxylation of Alkenes (Formation of diols), Baiyer reaction – Baeyer's reagent , Osmium tetraoxide (OsO4), Epoxidation by per acid | 49 Minutes |
| 09 | Oxidation-strong oxidising agent , Potassium dichromate K2Cr2O7/H2SO4, Alkaline KMnO4/ OH-, H2CrO4 or CrO3 + H2O, Table of oxidising agents , Oxidation of alcohols , Mild oxidising agents , Oxidation of periodic acid HIO4, Oxidation of aldehydes , Oxidation with NBS, Tollen's reagent , Fehling's Reagent , Benedict's solution , Schiff's reagent | 38 Minutes |
| 10 | Oxidation of seleniumdioxide SeO2, Side-Chain oxidation | 13 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Aromaticity , Benzenoids and Non-Benzenoids , NMR-definition of Aromaticity , Anti Aromaticity , Polycyclic aromatic compound , Azulenes , Reaction of AgNO3 and Na-metal , (n)-Annulenes , Peripheral aromaticity | 44 Minutes |
| 02 | Electrophilic aromatic substitution reaction , Halogenation of Benzene , Baltz-Schiemann reaction , Nitration of benzene , Kinetic Isotope effect , Sulphonation of benzene , Friedel-Craft reaction (F.C. Rxn), F.C. Alkylation | 49 Minutes |
| 03 | Ring-Closure at C-1 and C–2, Dehydrogenation , Limitations of F.C. reaction , Friedel Craft Acylation , Ring closure , Directive influence or Directive effect , Table of activating and deactivating groups | 44 Minutes |
| 04 | Ortho-para ratio , Direction effect on disubstituted benzene , Directive influence in monosubstituted benzene , Directive influence in naphthalene , Directive influence in diphenyl , Directive influence in Anthracene and phenanthrene, Directive influence in pyridine & pyrrole , SN2 Ar reaction , PHENOL, Preparation of phenol | 37 Minutes |
| 05 | Preparation of phenol from acid hydrolysis of cumene , Chemical reaction of phenol , Halogenation of phenol , Protection of –OH group, Nitration of Phenol , Sulphonation of Phenol, Reimer-Tiemann Reaction , Reimer-Tiemann formylation , Reimer-Tiemann carboxylation , Comparison of Reimer-Tiemann and carbyl amine reactions , Kolbe-Schmidt reaction , Some medicinally important compounds , Aspirine, Salol, Oil of winter green | 39 Minutes |
| 06 | Nitrosation of phenol , Use of phenol as nucleophile, ANILINE, Preparation of aniline from reduction of nitrobenzene , Selective reduction , Chemical reactions of aniline , Halogenation of Aniline , Nitration of Aniline, Sulphonation of Aniline | 26 Minutes |
| 07 | Fries rearrangment reaction in Phenol , Claisen rearrangement , Diazotisation of Aniline , Reaction of Benzene diazonium chloride (BDC) , Sandmeyer reaction , Baltz-scheimann reaction , Experimental evidence of formation of phenyl cation , Amination – Deamination | 43 Minutes |
| 08 | AMINES, Preparation of Amines , Hofmann Bromamide reaction , Hofmann methylation , Gabriel phthalimide reaction , Coupling reaction of BDC | 32 Minutes |
| 09 | Test of Amines ,Isocyanide Test of 1º Amine , Test with nitrous acid HNO2, CYANIDES and ISOCYANIDES , Preparation of cyanides and isocyamide , Hydrolysis of cyanides and isocyanides , IPSO-Substitution | 23 Minutes |
| 10 | Basic Strength, Definition of bases , Scales of basic strength , Organic Nitrogenous bases | 12 Minutes |
| 11 | Basic strength of Aliphatic amines , Basic strength of Aromatic amines , SH of H2O, SIR effect on Aromatic amines , Basic strength of pyridine and pyarole | 43 Minutes |
| 12 | Amidine-basic strength , Guanidine- basic strength , Kb order , Proton sponges , Site of protonation , Feasibility of reaction | 31 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Preparation of aldehydes & Ketones , Dehydrogenation , Hydrolysis of gem. dihalide , From dry distillation of Col. salt of fatty acid , From acid chloride (Rossenmund's) , Formylation of benzene (Gattermann Koch Ald. Synthesis) , Chemical reaction of carbonyl compound , Nucleophilic addition reaction , Addition of H2O (Formation of hydrates) | 41 Minutes |
| 02 | Addition of R–OH (Formation acetal/Ketal), Addition of G.R., Addition of HCN (Formation of cyanohydrin), Addition of NH3, Addition of Ammonia derivative | 35 Minutes |
| 03 | Addition of NaHSO3 (Sodium bisulphite) , Backmann rearrrangment , Cyclic Ketone | 29 Minutes |
| 04 | Condensation reaction , Aldol condensation reaction , Cross Aldol , Intramolecular Aldol reaction | 40 Minutes |
| 05 | Perkin condensation reaction , Classen Ester condenstion , Cross-Claisen , Intramolecular claisen (Dieckmann's reaction ) , knoevenagel reaction | 22 Minutes |
| 06 | Reformatsky reaction , Favorskii reaction , Cannizaro reaction | 23 Minutes |
| 07 | Cross Aldol , Cross Cannizaro , Intramolecular cannizaro , Tischenko reaction , Alpha-Halogenation , Haloform reaction , Iodoform test | 44 Minutes |
| 08 | Baeyer - Villiger Oxidation , Benzil - Benzilic acid Rearrangement , D-exchange reaction , Witting reaction , Benzoin condensation | 33 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Carboxylic acid preparation , Arndt-Eistert reaction (Homologation of acid), Chemical reactions of carboxylic acids , Hunsdiecker reaction | 18 Minutes |
| 02 | Decarboxylication reaction , Decarboxylation of acids by soda lime (SL), Decarboxylation by heating , Hell-Volhard-Zelinsky (HVZ) reaction , Acid derivatives , Preparation of acid derivatives , SN2 Th reaction , Esters- preparation , Type-I mechanism of esterification, Type-II mechanism of esterification | 44 Minutes |
| 03 | Examples of esterification, Hydrolysis of ester , Acid hydrolysis of ester and saponification , Acid amide , Hofmann Bromamide reaction , Curtius reaction , Schmidt reaction , Lossen reaction | 28 Minutes |
| Lecture# | Description | Duration |
|---|---|---|
| 01 | Carbohydrates , definition , Classification of carbohydrates , Based on number of units , Based on water solubility , Based on reducing properties | 18 Minutes |
| 02 | Monosaccharides - Aldoses and Ketoses, D/L-configuration (Relative configuration) , Glucose , Cyclic hemiacetal structure of glucose , ANOMERS , EPIMERS , Haworth structure of glucose- glucopyranose structure, Formation of methyl-O-glucoside , Mutarotation, FRUTOSE , cyclic hemiacetal structure of fructose , Haworth structure of fructose- Fructofuranose structure | 47 Minutes |
| 03 | SUCROSE, Inversion of sugar , Glycosidic linkage , Maltose ,Lactose , Starch , Amylose and amylopectin , Cellulose , Reaction of carbohydrates , Osazone formation of glucose and fructose | 45 Minutes |
| 04 | Amino acids , Types of Alpha-Amino acids (AA), Neutral Alpha-AA, Acidic Alpha-AA, Basic Alpha-AA, Zwitter ion , Iso-electric point (pI), Calculation of pI value | 21 Minutes |
| 05 | Peptides , Dipeptides , Peptide link, Polypeptides , Protein , Examples of Amino acids | 18 Minutes |
| 06 | Polymerisation , Classification of polymer , Based on source , Base on Intermolecular force of attraction , Elastromers , Fibres , Thermoplastics, Thermosettings , Polyethylene , Nylon-6, Nylon-6,6, Natural Rubber , Synthetic Rubber- Neoprene , Buna-S, Buna-N , Dacron , Low density polyethylene (LDPE) | 33 Minutes |
| 07 | High density polyethylene (HDPE) , Polypropylene , Poly isobutylene , Poly vinyl chloride (PVC), Poly tetrafluoro ethylene (PTFEW Tefflon) , Poly acrylonitrile (PAN or orlon), Poly styrene , Poly methyl methanacrylate (PMMA or Lucite) or (Plexiglas or prespex), Natural Rubber- Polyisoprene , Gutta-percha, Vinylidene chloride- Vinyl chloride polymer , Lexan-Poly carbonate , Glyptal , Bakelite (or phenol- formaldehyde Resin), Melamine- formaldehyde (Melmac) , Polyurethane | 33 Minutes |