Chapter =IUPAC Nomenclature

Video -1 (12 min)

(1) Basic organic chemistry
(2) Definition of organic compound
(3) Representation of organic compound
(4) Hybridisation

Video -2 [46 min]

(1) Number of ​σ​ and ​π​ bonds
(2) Degree of carbon
(3) Degree of hydrogen
(4) Degree of Alkyl halides
(5) Degree of Alcohols
(6) Degree of Amines
(7) Degree of unsaturation (DU)
(8) Calculation of DU
(9) Fundamental definition of DU
(10) Homologous series (H.S.)

Video -3 [37.38 min]

(1) Classification of organic compound
(2) Aromatic compounds
(3) Homocyclic compounds
(4) Heterocyclic compounds
(5) IUPAC- Nomenclature
(6) Scheme of IUPAC
(7) Naming of Alkanes

Video -4 [58.45 Min]

(1) Scheme of IUPAC
(2) Naming of alkanes
(3) Retained Names
(4) Naming of alkenes

Video -5 [32.25 Min]

(1) Naming of Alkene
(2) Naming of Alkynes
(3) Naming of cycloalkanes

Video -6 [41.44 Min]

(1) Naming of cycloalkenes
(2) Alkylidenes
(3) Naming of cycloalkynes
(4) Naming of Bicyclo compounds

Video -7 [32.32 Min]

(1) Functional Groups (F.G.)
(2) Naming of carboxylic acids
(3) Special Name of carboxylic acids
(4) Naming of dicarboxylic acids
Video -8 [48.33 Min]
(1) Naming of sulphonic acid
(2) Naming of Alcohols
(3) Naming of Amines
(4) Naming of thioalcohols
(5) Naming of Aldehydes
(6) Special name of Aldehydes
Video -9 [46.09 Min]
(1) Naming of Ketones
(2) Naming of cyanides
(3) Special name of cyanides
(4) Naming of isocyanides
(5) Naming of Amides
(6) Special name of amides
(7) Naming of acid halides
Video-10 [41min]
(1) naming of acid halide
(2) naming of acid anhydride
(3) naming of esters
(4) special name of ester
Video -11 [37.43 Min]
(1) Naming of haloalkanes
(2) Naming of Nitro compounds
(3) Naming of Nitroso compounds
(4) Naming of Aromatic compound
(5) Benzene
(6) Other aromatic compound
 Chapter =Reaction mechanism
(R–X), (R–OH), (R–O–R)
Video -1 [36.05 Min]
(1) Carbocations C​⊕
(2) Hybridisation of carbocations
(3) Stability of carbocations
(4) Rearrangement of carbocations
(5) Type of shifts
(6) Migratory aptitude

Video -2 [41.32 Min]

(1) Migratory aptitude of aromatic group
(2) Rearrangement in cyclic carbocations
(3) Ring expansion (RE)
(4) Ring contracting (RC)
(5) Cyclopropyl methyl carbocations (CPM–C​⊕​)
(6) Stability order of carbocations
(7) Some extra ordinary stable carbocations
(8) CPM carbocation
(9) Aromatic carbocations

Video - 3 [34.57 Min]

(1) Rearrangement of carbocation
(2) Reaction mechanism
(3) Solvents
(4) Polar protic solvents (PPS)
(5) Polar aprotic solvents (PAs)
(6) Reagents
(7) Nucleophiles, Nu
(8) Electrophilic E​⊕

Video - 4 [46.52 Min]

(1) Electrophiles, E​⊕
(2) Nucleophiles, Nu
(3) Nucleophilicity
(4) Experimental order of Nu
(5) Strong Nu with weak basic character
(6) Strong Nu with strong basic character
(7) Weak Nu with weak basic character
(8) Solvation of Nu

​Video - 5 [35.51 Min]

(1) Leaving group (g)
(2) Leaving group ability
(3) Unimolecular nucleophilic substitution reaction of first order (for R–X) i.e SN​1​ or R–X
(4) Kinetics of SN​1
(5) Stereo of SN​1
(6) PE- diagram of SN​1
(7) SN​1​ with rearrangement in C​⊕
(8) Rate of SN​1​ reaction

Video - 6 [49.16 Min]

(1) SN​1​ or R–X
(2) Solvolysis reaction
(3) Factors affecting the rate of SN​1​ reactions
(4) SN​1​ of alcohol R–OH

Video - 7 [42.49 Min]

(1) SN​1​ of R–OH
(2) Lucas reaction
(3) SN​1​ of ethers
(4) Hydrolysis of ethers
(5) SN​2​ reaction of (R–X)
(6) Kinetics of SN​2​ reaction
(7) Stereochemistry of SN​2​ Rxn
(8) PE-diagram of SN​2​ Rxn

Video - 8 [47.11 Min]

(1) Walden's experiment
(2) Walden Inversion
(3) Factors affecting the rate of SN​2​ Rxn
(4) Halogen exchange reaction
(5) Finkelstein reaction
(6) Swart's reaction
(7) SN​2​ Rxn of alcohol (R–OH)
(8) SN​1​ reaction of alcohol with SOCl​2

Video - 9 [28.46 Min]

(1) SN​2​ of ether
(2) Reaction of epoxides
(3) Williamson's ether synthesis

Video - 10 [40.29 Min]

(1) Intramolecular SN​2​ reactions
(2) Neighbouring group participation (NGP)
(3) Comparison between SN​1​ and SN​2
(4) SN​1​ Vs SN​2
Video - 11 [50.45 Min]
(1) Elimination Reaction
(2) E​1​ elimination (of R–X)
(3) Saytzeff's rule
(4) Regioselectivity
(5) E1 of Alcohols
(6) Acid catalysed dehydration of alcohol
(7) Dienone- Phenol rearrangement
(8) Pinacol - Pinacolone rearrangement
(9) Semi Pinacol- Pinacolone rearrangement

Video - 12 [36.21 Min]

(1) E​2​ Rxn of (R–X)
(2) Stereoselectivity of stereospecificity
(3) Reagents of E​–2​ Reaction
(4) Order of Rate of E​–2
(5) Major Hofmann Alkene

Video - 13 [39.57Min]
(1) Summary of SN​1​/ SN​2​/E​1​/E​2
(2) Stereoselectivity of E2 reaction
(3) E​1​CB reaction
(4) Cases when Hofmann Alkene is the major product

Video - 14 [23.15 Min]

(1) Tetraalkyl ammonium hydroxide
(2) E–2 Rxn
(3) Didehalogenation
(4) Stereoselectivity
(5) Isotope effect (K​H​/K​D​)
 Chapter-GR, Alkane, Reduction
Video - 1 [11.19 Min]
(1) Organometallic compounds
(2) Preparation of G.R.

Video - 2 [32.32 Min]

(1) Preparation of GR
(2) Solvents of GR
(3) Reaction of GR
(4) Acid-base reaction of GR
(5) Zerewitinoff active hydrogen determination

Video - 3 [29.32 Min]

(1) Nucleophilic addition reaction of GR
(2) SN2 the reaction of GR

Video - 4 [39.13 Min]

(1) Unstable GR
(2) Mono GR is not possible with dihalide
(3) Reaction of GR with CO​2
(4) Reaction of GR with O​2
(5) Reaction of GR with RCN
(6) Grignard reagent
(7) Reactions of grignard reagent

Video - 5 [41.29 Min]

(1) Attack of GR on weak bond
(2) 1,2-addition & 1,4-addition
(3) Reaction of GR with metal halides
(4) REDUCTION
(5) Definition of reduction
(6) Table of reducing agents
(7) Catalytic hydrogenation

Video - 6 [43.47 Min]

(1) Catalytic hydrogenation
(2) Stereoselectivity
(3) Partial hydrogenation
(4) Lindlar's catalyst
(5) P-2 catalyst (Nickel Boride)
(6) Birch reduction

Video - 7 [53.26 Min]

(1) Hydroboration Reduction (HBR)
(2) Transfer Hydrogenation
(3) Clemmensen reduction
(4) Wolf-Kishner reduction
(5) Lithium aluminium hydride (LiAlH​4​)

Video - 8 [52.55 Min]

(1) Sodium Borohydride (NaBH​4​) (SBH)
(2) Triphenyltin hydride Ph3SnH (TPH)
(3) DiBA-H- Diisobutyl Aluminium hydride
(4) Red –P + H​Ι
(5) Mozingo reduction
(6) MPV- reduction
(7) Oppenauer Oxidation
(8) Bouveault-Blanc réduction
(9) ALKANES
(10) Free Radicals
(11) Formation of free radicals
(12) F.R. Catalyst/ Initiators / Promoters
(13) F.R. Inhibitors/ Scavengers/Poisons
(14) Stability of free radicals
(15) Reactions of free radicals
(16) Combination Reactions
(17) Disproportionation reaction

Video - 9 [40.26 Min]

(1) Reactions of Free radicals
(2) Stability of free radicals
(3) Preparation of Alkanes
(4) Wurtz Reaction (WR)
(5) Wurtz-Fittig reaction
(6) Fitting reaction
(7) Frankland reaction
(8) Kolbe's Electrolytic synthesis (KES)
(9) Corey-House Reaction

Video - 10 [39.19 Min]

(1) Corey House reaction
(2) Decarboxylation
(3) Decarboxylation of soda lime
(4) Decarboxylation of heating

Video - 11 [24.53 Min]

(1) Properties of Alkanes
(2) Chemical properties of Alkanes
(3) Free Radical substitution reaction
(4) PE-diagrams
(5) Reactivity order
(6) Conditions of halogenation

Video - 12 [00.00 Min]

(1) reactivity and selectivity
(2) Percentage yield
(3) Quantum yield
(4) Isomerisation reaction of alkanes
(5) Aromatisation reaction of alkanes
(6) Petroleum
(7) Physical Properties of alkanes
Chapter ​→​ Alkene, Alkyne, Oxidation
Video - 1 [36.30 Min]
(1) Alkanes
(2) Preparation of Alkene
(3) Pyrolysis of ester
(4) Pyrolysis of xanthates (charge +ve reaction )
(5) Cope reaction
(6) Dehalogenation S

Video - 2 [51.59 Min]

(1) Chemical reactions of Alkenes
(2) Electrophilic addition reaction (A​E​ Rxn)
(3) Classical carbocation mechanism
(4) Non-Classical carbocation mechanism
(5) Markownikoff's rule
(6) Addition of H–X
(7) Anti Marconi Koff's rule
Video - 3 [46.52 Min]
(1) Addition of H​2​O on Alkenes
(2) Acid-catalysed hydration of Alkenes
(3) Oxymercuration- Demercuration reaction (OM/DM)
(4) Hydroboration -oxidation (HBO)
(5) Alkoxymercuration Demercuration
(6) Addition of X​2​ on Alkenes

Video - 4 [47.13 Min]

(1) Addition of HOX on alkenes
(2) Stereoselectivity
(3) Order of rate of addition of X​2​ on alkene
(4) Chemical reaction of Alkynes
(5) Addition of H-X on alkynes
(6) Addition of H​2​O on alkynes
(7) Hydration of alkyne with dil H​2​SO​4​ and HgSO​4
(8) Hydroboration – Oxidation

Video - 5 [23.46 Min]

(1) Addition of HOX on alkynes
(2) Preparation of alkynes
(3) Isomerisation

Video - 6 [34.13 Min]

(1) Isomerisation mechanism
(2) Reaction of terminal alkynes
(3) Dienes
(4) Conjugated diene
(5)Addition NOCl on alkene
(6) Allylic substitution
(7) NBS- N-bromosuccinimide

Video - 7 [20.22 Min]

(1) Reaction of NBS
(2) MnO2- Oxidising agent
(3) Carbenes
(4) Sources of carbenes
(5) Types of carbenes

Video - 8 [48.15 Min]

(1) Reaction of carbene
(2) Reimer-Tiemann reaction
(3) Carbylamine reaction
(4) OXIDATION
(5) definition of oxidation
(6) Oxidation of alkenes and alkynes
(7) Ozonolysis of Alkenes and alkynes
(8) Oxidation of Ketone
(9) Per Hydroxylation of Alkenes (Formation of diops)
(10) Baiyer reaction – Baeyer's reagent
(11) Osmium tetroxide (OsO​4​)
(12) Epoxidation by per acid

Video - 9 [38.07 Min]

(1) Oxidation-strong oxidising agent
(2) Potassium dichromate K​2​Cr​2​O​7​/H​2​SO​4
(3) Alkaline KMnO​4​/ OH​Θ
(4) H​2​CrO​4​ or CrO​3​ + H​2​O
(5) Table of oxidising agents
(6) Oxidation of alcohols
(7) Mild oxidising agents
(8) Oxidation of periodic acid HIO​4
(9) Oxidation of aldehydes
(10) Oxidation with NBS
(11) Tollen's reagent
(12) Fehling's Reagent
(13) Benedict's solution
(14) Schiff's reagent

Video - 10 [12.44 Min]

(1) Oxidation of selenium dioxide SeO​2
(2) Side-Chain oxidation
Chapter – Aromatic compound

Video - 1 [43.11 Min]

(1) Aromaticity
(2) Benzenoids and NOn-Benzenoids
(3) NMR-definition of Aromaticity
(4) Anti Aromaticity
(5) Polycyclic aromatic compound
(6) Azulenes
(7) Reaction of AgNO​3​ and Na-metal
(8) (n)-Annulenes
(9) Peripheral aromaticity

Video - 2 [49.03 Min]

(1) Electrophilic aromatic substitution reaction
(2) Halogenation of Benzene
(3) Balz-Schiemann reaction
(4) Nitration of benzene
(5) Kinetic Isotope effect
(6) Sulphonation of benzene
(7) Friedel-Craft reaction (F.C. Rxn)
(8) F.C. Alkylation

Video - 3 [43.45 Min]

(1) Ring-Closure at C- and C–2
(2) Dehydrogenation
(3) Limitations of F.C. reaction
(4) Friedel Craft Acylation
(5) Ring closure
(6) Directive influence or Directive effect
(7) Table of activating and deactivating groups

Video - 4 [37.06 Min]

(1) Ortho-para ratio
(2) Direction effect on disubstituted benzene
(3) Directive influence in monosubstituted benzene
(4) Directive influence in naphthalene
(5) Directive influence in diphenyl
(6) Directive influence in Anthracene and phenanthrene
(7) Directive influence in pyridine & pyrrole
(8) SN​2​ Ar reaction
(9) PHENOL
(10) Preparation of phenol
Video - 5 [38.16 Min]
(1) Preparation of phenol from acid hydrolysis of cumene
(2) Chemical reaction of phenol
(3) Halogenation of phenol
(4) Protection of –OH group
(5) Nitration of Phenol
(6) Sulphonation of Phenol
(7) Reimer-Tiemann Reaction
(8) Reimer-Tiemann formylation
(9) Reimer-Tiemann carboxylation
(10) Comparison of Reimer-Tiemann and carbyl amine reactions
(11) Kolbe-Schmitt reaction
(12) Some medicinally important compounds
(13) Aspirine, Salol, Oil of wintergreen

Video - 6 [26.09 Min]

(1) Nitrosation of phenol
(2) Use of phenol of nucleophile
(3) ANILINE
(4) Preparation of aniline from reduction of nitrobenzene
(5) Selective reduction
(6) Chemical reactions of aniline
(7) Halogenation of Aniline
(8) Nitration of Aniline
(9) Sulphonation of Aniline

Video - 7 [42.47 Min]

(1) Fries rearrangement reaction in Phenol
(2) Claisen rearrangement
(3) Diazotization of Aniline
(4) Reaction of Benzene diazonium chloride (BDC)
(5) Sandmeyer reaction
(6) Balz-schiemann reaction
(7) Experimental evidence of formation of phenyl cation
(8) Amination – Deamination

Video - 8 [31.25 Min]

(1) AMINES
(2) Preparation of Amines
(3) Hofmann Bromamide reaction
(4) Hofmann methylation
(5) Gabriel phthalimide reaction
(6) Coupling reaction of BDC
Video - 9 [22.58 Min]
(1) Test of Amines
(2) Isocyanide Test of 1º Amine
(3) Test with nitrous acid HNO​2
(4) CYANIDES and ISOCYANIDES
(5) Preparation of cyanides and isocyanides
(6) Hydrolysis of cyanides and isocyanides
(7) IPSO-Substitution

Video - 10 [11.51 Min]

(1) Basic Strength
(2) Definition of bases
(3) Scales of basic strength
(4) Organic Nitrogenous bases

Video - 11 [42.11 Min]

(1) Basic strength of Aliphatic amines
(2) Basic strength of Aromatic amines
(3) SH of H​2​O
(4) SIR effect on Aromatic amines
(5) Basic strength of pyridine and pyrrole

Video - 12 [31.09 Min]

(1) Amidine-basic strength
(2) Guanidine- basic strength
(3) K​b​ order
(4) Proton sponges
(5) Site of protonation
(6) Feasibility of reaction
 Chapter- Carbonyl Compound

Video - 1 [40.34 Min]

(1) Preparation of aldehydes & Ketones

(2) Dehydrogenation

(3) Hydrolysis of gem. dihalide

(4) From dry distillation of Col. salt of fatty acid

(5) From acid chloride (Rosenmunds)

(6) Formylation of benzene (Gattermann Koch Ald. Synthesis)

(7) Chemical reaction of carbonyl compound

(8) Nucleophilic addition reaction

(9) Addition of H​2​O (Formation of hydrates)

Video - 2 [34.36 Min]

(1) Addition of R–OH (Formation acetal/Ketone

(2) Addition of G.R.

(3) Addition of HCN (Formation of cyanohydrin)

(4) Addition of NH​3

(5) Addition of Ammonia derivative

Video - 3 [29.04 Min]

(1) Addition of NaHSO​3​ (Sodium bisulphite)

(2) Beckmann rearrangement

(3) Cyclic Ketone

Video - 4 [40.09 Min]

(1) Condensation reaction

(2) Aldol condensation reaction

(3) Cross Aldol

(4) Intramolecular Aldol reaction

Video - 5 [21.20 Min]

(1)Perkin condensation reaction

(2) Claisen Ester condensation

(3) Cross-Clauses

(4) Intramolecular claisen (Dieckmann reaction )

(5) knoevenagel reaction

Video - 6 [22.35 Min]

(1) Reformatsky reaction

(2) Favorskii reaction

(3) Cannizzaro reaction

Video - 7 [43.51 Min]

(1) Cross Aldol

(2) Cross Cannizzaro

(3) Intramolecular cannizzaro

(4) Tishchenko reaction

(5) ​α​-Halogenation

(6) Haloform reaction

(7) Iodoform test

Video - 8 [32.52 Min]

(1) Baeyer - Villiger Oxidation

(2) Benzil - Benzilic acid Rearrangement

(3) D-exchange reaction

(4) Wittig reaction

(5) Benzoin condensation

Chapter- Carboxylic acid & their derivatives

Video - 1 [17.53 Min]

(1) Carboxylic acid preparation

(2) Arndt-Eistert reaction (Homologation of acid)

(3) Chemical reactions of carboxylic acids

(4) Hunsdiecker reaction

Video - 2 [43.28 Min]

(1) Decarboxylation reaction

(2) Decarboxylation of acids by soda lime (SL)

(3) Decarboxylation by heating

(4) Hell-Volhard-Zelinsky (HVZ) reaction

(5) Acid derivatives

(6) Preparation of acid derivatives

​ reaction
(7) SN​2​ Th​

(8) Esters- preparation

(9) Type-I mechanism of etherification

(10) Type-II mechanism of etherification

Video - 3 [27.40 Min]

(1) Examples of metrification

(2) Hydrolysis of ester

(3) Acid hydrolysis of ester and specification

(4) Acid amide

(5) Hofmann Bromamide reaction

(6) Curtius reaction

(7) Schmidt reaction

(8) Lossen reaction

Chapter-Polymer
Video - 1 [33.02 Min]
(1) Polymerisation
(2) Classification of polymer
(3) Based on source
(4) Base on Intermolecular force of alteration
(5) Elastomers
(6) Fibres
(7) Thermoplastics
(8) Thermosettings
(9) Polyethylene
(10) Nylon-6
(11) Nylon-6,6
(12) Natural Rubber
(13) Synthetic Rubber- Neoprene
(14) Buna-S
(15) Buna-N
(16) Dacron
(17) Low density polyethylene (LDPE)

Video - 2 [33.09 Min]

(1) High density polyethylene (HDPE)
(2) Polypropylene
(3) Poly isobutylene
(4) Poly vinyl chloride (PVC)
(5) Polytetrafluoroethylene (PTFE Teflon)
(6) Poly acrylonitrile (PAN or orlon)
(7) Poly styrene
(8) Poly methyl methacrylate (PMMA or Lucite) or (Plexiglass or perspex)
(9) Natural Rubber- Polyisoprene
(10) Gutta-percha
(11) Vinylidene chloride- Vinyl chloride polymer
(12) Lexan-Polycarbonate
(13) Glyptal
(14) Bakelite (or phenol- formaldehyde Resin)
(15) Melamine- formaldehyde (Melmac)
(16) Polyurethane

Chapter-Biomolecular

Video - 1 [00.00 Min]

(1) Carbohydrates
(2) definition
(3) Classification of carbohydrates
(4) Based on number of units
(5) Based on water solubility
(6) Based on reducing properties
Video - 2 [46.50 Min]
(1) Monosaccharides - Aldoses and Ketoses
(2) D/L-configuration (Relative configuration)
(3) Glucose
(4) Cyclic hemiacetal structure of glucose
(5) ANOMERS
(6) EPIMERS
(7) Haworth structure of glucose- glucopyranose structure
(8) Formation of methyl-O-glucoside
(9) Mutarotation
(10) FRUTOSE
(11) cyclic hemiacetal structure of fructose
(12) Haworth structure of fructose- Fructofuranose structure
Video - 3 [45.09 Min]
(1) SUCROSE
(2) Inversion of sugar
(3) Glycosidic linkage
(4) Maltose
(5)Lactose
(6) Starch
(7) Amylose and amylopectin
(8) Cellulose
(9) Reaction of carbohydrates
(10) Osazone formation of glucose and fructose
Video - 4 [20.45 Min]
(1) Amino acids
(2) Types of ​α​-Amino acids (AA)
(3) Neutral ​α​-AA
(4) Acidic ​α​-AA
(5) Basic ​α​-AA
(6) Zwitterion
(7) Isoelectric point (p​Ι​)
(8) Calculation of p​Ι​ value
Video - 5 [17.57 Min]
(1) Peptides
(2) Dipeptides
(3) Peptide link
(4) Polypeptides
(5) Protein
(6) Examples of Amino acids

(I) Structural isomerism

Video –I– 45 min
(1) Definition of isomerism
(2) Classification of isomerism
(3) Chain isomerism
(4) Positional isomerism

Video -2–40.03 min

(1) Functional isomerism
(2) Ring-chain isomerism
(3) Metamerism

Chapter-Stereoisomerism
Video 1- [19.25 min]
(1) Introduction
(2) Classification of stereoisomerism
(3) Geometrical Isomerism (G.I.)

Video -2 – duration 55 min

(1) G.I. in C=C system
(2) G.I. in Ring system
(3) G.I. due to double bond inside the ring
(4) Cumulenes
Video –3 [54.48 min]
(1) G.I. in C=N system
(2) E/Z Nomenclature

Video –4 [58 min]

(1) Number of geometrical Isomers
(2) Cumulenes
(3) Spiranes
(4) Cycle Alkylidenes
(5) Diphenyl system
(6) Physical properties of geometrical isomers

Video–5[1:08:40]
(1) Optical Isomerism
(2) Plane polarised light
(3) Chiral centre
(4) Chirality
(5) Asymmetric molecules
(6) Dissymmetric molecules
(7) Plane of symmetry (POS)
(8) Centre of symmetry (COS)

Video–6 [54.30]min
(1) POS, COS
(2) Chirality, Optical activity

Video–7 [51:56] min

(1) Wedge-Dash projection formula
(2) Fischer–Projection formula
(3) Absolute configuration (R/S-configuration)
(4) CIP-Rule

Video –8
(1) Enantiomers
(2) Diastereomers
(4) Axis of symmetry (AOS)

Video –9 [57.37] min

(1) Erythro enantiomers
(2) Threo enantiomers
(3) D/L- Configuration (relative configuration)
(4) Number of stereoisomers
(5) Pseudo chiral carbon (PCC)
(6) Racemic mixture (or, R/S-mixture)
(7) Polarimeter
(8) Functioning of polarimeter
(9) Percentage enantiomeric excess (%EE)
(10) Optical purity

Video–10
(1) Optical Resolution
(2) Tertiary amine optical activity
(3) Optical activity in absence of chiral centre
(4) Cumulenes
(5) Spiranes
(6) Cyclo Alkylidene
(7) Biphenyls
(8) Alternating axis of symmetry (AAOS)
(9) Conformational Isomerism

Video–11 [56.19]min
(1) Conformational isomers
(2) Newman projection formula
(3) Dihedral angle (DHA)
(4) Torsional strain (T.S.)
(5) Van Der waals strain (V.S.)
(6) Angle strain (A.S.)
(7) Definition of conformational isomers
(8) Conformational analysis
(9) Sawhorse projection formula

Video–12 [50.57] min

(1) Conversion of fischer to Newman
(2) Conformational analysis of cyclohexane
(3) Energy profile

Video –13 [14.25] min

(1) Conformational analysis of dimethyl cyclohexane
 Chapter –3
Structural Identification and POC
Video –1 [28.46] min
(1) Structural Identification
(2) Degree of unsaturation (DU)
(3) Catalytic hydrogenation H2/cat
(4) Monochlorination Cl2/h​ν

Video –2 [53.33] min

(1) Structural Identification
(2) Monochlorination Cl2/h​ν
(3) Ozonolysis
(4) Reductive ozonolysis
(5) Oxidative ozonolysis
(6) Practical organic chemistry (POC)
(7) POC-I
(8) Lassaigne’s test
(9) Elemental analysis

Video –3 [34.23] min

(1) Elemental analysis
(2) Test of C=C/ C​≡​C
(3) Test of terminal alkyne
(4) Test of alcohols
(5) Test of carbonyl compounds
(6) Tests of aldehydes

Video –4 [18.11] min

(1) Iodoform Test
(2) Sodium metal test

Video –5 [32.48] min

(1) Sodium Bicarbonate test (NaHCO3)
(2) Test of phenols and enols
(3) Test of nitro compounds
(4) Test of amines
(5) Hinsberg's test
(6) POC-II
 Chapter-GOC
Video –1 [35.39] min
(1) Electronic effect
(2) Inductive effect

Video – [46.37] min

(1) Applications of I-Effect
(2) Resonance
(3) Conjugated system
Video –3 [27.16]min
(1) When double bond is in conjugation with vacant -p
(2) When double bond is in conjugation with fully filled -p

Video –4 [52.42] min

(1) When double bond is in conjugation with fully filled -p
(2) When double bond is in conjugation with half filled-p
(3) When +ve charge and lone pair are adjacent
(4) d-orbital resonance
(5) Conditions of Resonance
(6) Mesomeric effect (M)

Video –5 [35.01] min

(1) Stability of resonating structures (R.S)
(2) Steric Inhibition of Resonance (SIR)
(3) Equivalent R.S.

Video –6 [54.01] min

(1) Equivalent R.S.
(2) Hyperconjugation HC
(3) Hyperconjugation in carbocations
(4) Hyperconjugation in Alkenes
(5) Heat of hydrogenation (HOH)

Video –7 [38.10] min

(1) Hyperconjugation in Toluene
(2) Hyperconjugation in Free Radicals
(3) Electromeric effect (E)
(4) Applications of electronic effects
(5) Dipole moment
(6) Bond length
(7) Aromaticity
(8) Benzenoids and Non-benzenoids

Video –8 [27.01] min

(1) Examples of aromatic compounds
(2) Heterocyclic aromatic compounds

Video –9 [23.51] min

(1) M.O. Diagram
(2) Polycyclic aromatic compounds

Video –10 [36.16] min

(1) Examples of aromatic systems
(2) [n] Annulenes
(3) NMR- definition of Aromaticity
(4) Resonance energy (RE)

Video –11 [43.36] min

(1) Acidic strength of acids
(2) Acidic strength of dicarboxylic acids

Video –12 [51.35] min

(1) Aromatic acids
(2) Ortho effect
(3) Acidic strength of phenols
(4) Feasibility of reactions
(5) Sodium bicarbonate test of acids

Video –13 [11.51] min

(1) Basic strength
(2) Organic Nitrogenous bases.

Video –14 [42.16]min

(1) Basic strength of Aliphatic amines
(2) Aromatic amines

Video –15 [31.09] min

(1) Basic strength of Amidines
(2) Basic strength of Guanidines
(3) Proton sponges
(4) Site of protonation
(5) Feasibility of Reaction
Video –16 [37.36] min
(1) Carbanions (C​Θ​)
(2) Reactions in which carbanions are formed
(3) Organometallic compounds
(4) Active methylene group.
(5) Tautomerism
(6) Types of Tautomerism

Video –17 [23.03] min

(1) Enolisable –H
(2) Keto-enol Tautomerism
(3) Mechanism of keto-enol Tautomerism

Video –18 [42.29] min

(1) Stability of enol (Percentage enol-content)
(2) Racemisation due to enolisation

Video –19 [36.46] min

(1) D-Exchange
(2) Tautomerism in phenols
(3) Ring-chain Tautomerism
(4) Unsymmetrical ​α​-hydroxy ketones