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Complete Organic Chemistry for NEET & JEE 2025 in One Shot | Gun shot by ABK Sir | #neet2025 #neetkakajee #abksir #jee2025
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Timestamps :
00:01 Intro
05:51 Important Msg by ABK Sir
09:08 How to study organic Chemistry
19:08 Ionic & Organic Reactions
34:23 Basic Script of Organic Chemistry
1:19:47 Intermediates
1:22:26 Carbon
2:00:33 Bonding Process
2:15:16 Electron Distribution
2:28:16 Carbene
3:33:32 Inductive Effect
3:44:29 Order of +I Effect
4:47:49 Application of Inductive Effect
4:57:55 Compare Acidic Strength
5:36:14 Anion (-ve Charge)
5:49:26 Basic Strength
6:05:57 Basic Strength of amines
6:44:42 Stability of Intermediates
6:51:34 Grignard Reagent
6:58:47 Exception of Inductive Effect
7:02:19 Resonance
8:04:34 Delocalisation
8:15:25 How to draw Resonation Structure
8:42:55 Acidic Strength order
8:58:22 Question Practice
9:25:35 Organic Reactions
9:50:41 Attacking Species
10:31:41 Relative Stability of Resonation Structure
11:45:52 Rules of Writing Resonating Structures
12:02:42 Cyclic Compound
14:23:56 Addition Reaction
14:26:33 Substitution Reaction
14:36:17 Elimination Reaction
14:43:21 Oxidation Reaction
14:43:35 Reduction Reaction
14:46:31 Some other Reaction
15:29:15 Wurtz Reaction
15:32:51 Fitting Reaction
15:34:07 Wurtz-Fitting Reaction
15:35:03 Ullmann Reaction
15:57:23 Dimerisation
15:59:28 Disproportionation
16:05:31 Kolbe’s Electrolysis
16:09:13 Electrolysis
16:52:30 Hundsdicker Reaction
17:01:45 (Free Radical Addition Reaction
17:08:09 Stereochemistry of Reaction
17:14:27 Free Radical Substitution Reaction
17:31:13 Markonikov’s Rule
17:34:33 Anti- Markonikov’s Rule
17:55:53 Electrophilic Addition Reaction of Benzene
17:56:47 Introduction of Reaction with HX
18:11:10 Reaction with X2
18:30:55 Reaction with H2O
18:41:23 Reaction with X2+H2O
18:58:47 Electrophilic Addition Reaction of Benzene
19:00:53 Alkylation & Acylation
19:05:46 Machsims of ESR
19:21:37 Friedel Crafts Reaction
20:17:23 Nitration of Benzene
20:16:47 Introduction of Sulphonation of Benzene
20:18:30 Introduction of Halogenation of Benzene
20:46:36 Sulphonation of Benzene
20:52:19 Halogenation of Benzene
21:18:13 Oxidation of Benzene
21:35:23 Elimination Reaction
21:48:03 Introduction of E1 Reaction
21:51:03 E2 Reaction
22:02:23 E1CB Reaction
22:11:39 E1 Reaction
22:37:46 Hoffmann Rule
22:55:25 Hoffmann Product
23:25:45 Dehydration of Alcohol
24:05:59 Carbonyl Compounds
24:16:20 Elimination Reaction
24:28:49 Carbonyl Compounds
24:38:35 Aldol Reaction
24:51:09 Simple Aldol Reaction
25:36:16 Cross Aldol Reaction
25:45:25 Intramolecular Aldol Reaction
26:11:48 Cannizaro’s Reaction
26:20:41 Simple Cannizaro’s Reaction
26:35:51 Types of Cannizaro’s Reaction
26:49:52 Oxygen Containing Compounds
26:57:29 Oxidation
27:14:28 Oxidation reactions of Carbonyl Compounds
27:37:41 Oxidation reactions of Alcohol
28:10:19 Baeyer’s Reagent
28:18:21 Fehling solution
29:04:46 Birch Reduction
29:29:18 Bouvealt - Blanc Reduction
29:44:34 Stephen’s Reduction
29:56:03 Clemmensen Reduction
30:17:43 Metal Hydrides
31:22:33 Aldehyde + LialH4
31:43:09 Red P+Hi
31:54:19 NAR
31:59:08 Carbonyl Compounds
32:12:41 Reactivity for NAR
32:17:58 Reaction with HCN
32:38:38 Reaction with NaHSO3
32:58:02 Reaction with R-OH
33:11:22 Reaction with Alcohol
33:32:50 NAR
33:33:56 Snae
33:34:29 Arsn
33:37:46 SN1 Reaction
33:39:09 SN2 Reaction
33:54:48 NSR
34:03:59 Example of NSR
34:11:40 Example of SN1
34:25:08 Example of SN2
35:02:01 Solvent
35:13:33 Lucas Reagent
35:17:58 Rosenmund Reduction
35:22:41 Acidic Oxide
35:30:58 Differentiation of carboxylic acid & phenols
35:49:30 Benzene diazonium chloride
35:58:19 Gattererman Reaction
35:58:49 Sandmeyer’s Reaction
36:12:20 Gattermann - Koch Aldehyde synthesis
36:22:00 Esterification
36:31:27 Alkyl halides
36:47:19 Primary / Secondary / Tertiary Amines
36:50:29 Acylation
40:07:17 Hinsberg’s Reagent
37:22:15 Reaction with HNo2
37:42:05 ESR of Aniline
37:47:00 ESR of Phenol
37:55:47 B.D.C as Electrophiles
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