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ORGANIC CHEMISTRY • FREE LECTURE SERIES

Name Reactions Complete Lecture Series

Master important Organic Chemistry name reactions, enolate chemistry, carbonyl condensations, rearrangements and olefination methods through a structured, exam-oriented series by Chiral Academy.

✓ CSIR NET ✓ GATE Chemistry ✓ IIT JAM ✓ SET & MSc Entrances
ORGANIC TRANSFORMATION
Aldol Wittig Claisen Michael
19 Structured Lectures
29+ Hours of Learning
4 Learning Modules
PDF Lecture Notes
01
Concept to Application Mechanisms, reagents and product prediction
02
Exam-Oriented Learning Designed for major Chemistry examinations
03
Lecture PDFs Attach downloadable notes with every lecture

Learn Name Reactions in a Logical Sequence

The series begins with carbanions and enolates, then progresses through carbonyl reactions, rearrangements, eliminations and advanced olefination.

Module 01

Enolate Chemistry

Carbanions, tautomerism, enolates, alkylation and asymmetric synthesis.

L-01 to L-08
Module 02

Carbonyl Reactions

Aldol, Michael, Claisen, Dieckmann and other important condensations.

L-09 to L-13
Module 03

Rearrangements & Eliminations

Favorskii, Benzilic Acid, HVZ, Chugaev and related transformations.

L-14 to L-16
Module 04

Olefination & Advanced Reactions

Julia, Wittig, HWE, Peterson and advanced alkene-forming methods.

L-17 to L-19

All Name Reactions Lectures

19 lectures displayed

L-01 1:28:06
Enolate Chemistry

Carbanions and Their Reactions

Master carbanion structure, stability, generation and important synthetic reactions used in competitive-examination Organic Chemistry.

Carbanions Stability Reactivity
L-02 1:35:32
Enolate Chemistry

Tautomerism and Enolization

Understand tautomerism, keto–enol equilibrium, enol formation and the factors controlling enolization.

Tautomerism Enolization Keto–Enol
L-03 1:56:23
Enolate Chemistry

Enolates and Their Generation

Learn enolate formation, kinetic and thermodynamic control, regioselectivity and the key factors governing enolate generation.

Enolates Kinetic Control Thermodynamic Control
L-04 2:01:10
Enolate Chemistry

Alkylation of Enolates – Part 1

Study the principles of enolate alkylation, carbon–carbon bond formation and the factors controlling reaction selectivity.

Alkylation Enolates C–C Bond
L-05 1:24:09
Enolate Chemistry

Alkylation of Enolates – Part 2

Continue enolate alkylation with advanced examples, regioselectivity, stereochemical aspects and exam-oriented applications.

Alkylation Regioselectivity Stereochemistry
L-06 1:17:25
Enolate Chemistry

Equivalents of Enolates

Explore important enolate equivalents and their use in selective carbon–carbon bond-forming reactions.

Enamines Silyl Enol Ethers Enolate Equivalents
L-07 1:35:43
Enolate Chemistry

Asymmetric Alkylation of Enolates – Part 1

Begin asymmetric enolate alkylation with chiral-control concepts, stereochemical models and important synthetic strategies.

Asymmetric Synthesis Chiral Control Enolates
L-08 1:25:12
Enolate Chemistry

Asymmetric Alkylation of Enolates – Part 2

Continue asymmetric enolate alkylation through advanced stereoselective examples and competitive-exam applications.

Stereoselectivity Alkylation Advanced Practice
L-09 1:41:29
Carbonyl Reactions

Aldol Condensation and Michael Addition

Understand aldol condensation and Michael addition, including mechanism, selectivity and synthetic applications.

Aldol Michael Addition Mechanism
L-10 56:35
Carbonyl Reactions

Michael Addition

Study Michael donors, Michael acceptors, conjugate-addition mechanisms and important problem-solving approaches.

Conjugate Addition Michael Donor Michael Acceptor
L-11 2:05:40
Carbonyl Reactions

Stereoselectivity of Aldol Reaction and Zimmerman–Traxler Model

Master aldol stereoselectivity using the Zimmerman–Traxler model and predict syn/anti product formation.

Aldol Selectivity Zimmerman–Traxler Syn/Anti
L-12 1:33:12
Carbonyl Reactions

Knoevenagel, Stobbe, Henry, Nef, Mannich, Haloform and Perkin Reactions

Cover seven important carbonyl and name reactions with mechanisms, reagents, products and exam-oriented comparisons.

Knoevenagel Mannich Perkin
L-13 1:43:09
Carbonyl Reactions

Claisen and Dieckmann Condensation

Learn intermolecular Claisen and intramolecular Dieckmann condensations, mechanisms and synthetic applications.

Claisen Dieckmann Condensation
L-14 1:31:51
Rearrangements

Reformatsky Reaction, Favorskii Rearrangement and Darzens Reaction

Study Reformatsky, Favorskii and Darzens reactions with mechanisms, rearrangement pathways and product prediction.

Reformatsky Favorskii Darzens
L-15 1:08:50
Rearrangements

Cannizzaro Reaction, Benzilic Acid Rearrangement and Benzoin Condensation

Master three important carbonyl reactions with their mechanisms, substrate requirements and synthetic significance.

Cannizzaro Benzilic Acid Benzoin
L-16 1:46:31
Eliminations

HVZ Reaction, Pyrolytic Syn Elimination and Chugaev Elimination

Understand HVZ α-halogenation and important pyrolytic syn eliminations, including the Chugaev reaction.

HVZ Syn Elimination Chugaev
L-17 1:33:01
Olefination

Julia Olefination, Shapiro, Bamford–Stevens and Peterson Olefination

Compare four important alkene-forming reactions through mechanisms, reagents, stereoselectivity and applications.

Julia Shapiro Peterson
L-18 1:36:47
Olefination

Wittig, HWE and Schlosser Wittig Reactions

Study Wittig and related olefination methods, including HWE and Schlosser modifications for alkene synthesis.

Wittig HWE Schlosser
L-19 1:08:29
Advanced Reactions

Corey–Winter, Julia–Kocienski, Ramberg–Bäcklund and Neber Rearrangement

Complete the series with advanced olefination and rearrangement reactions frequently tested in competitive examinations.

Corey–Winter Julia–Kocienski Neber

Build Strong Command over Organic Transformations

Identify suitable substrates, reagents and reaction conditions.
Understand stepwise mechanisms and reactive intermediates.
Predict major products, regioselectivity and stereoselectivity.
Compare similar reactions and avoid common examination mistakes.
RECOMMENDED METHOD

How to Use This Series

  1. Watch the lectures in sequence.
  2. Download and revise the lecture PDF.
  3. Write each mechanism independently.
  4. Practise PYQs after completing every module.

Begin with Carbanions and Build Step by Step

Follow the complete sequence to strengthen Organic Chemistry for CSIR NET, GATE, IIT JAM, SET and MSc entrance examinations.

Watch Lecture 01
Lecture 02 1:35:32

Tautomerism & Enolization

Learn the concepts of Keto-Enol Tautomerism, Enolization, acidity of α-hydrogen, factors affecting enol formation, and reaction mechanisms essential for CSIR NET, GATE, IIT JAM, SET and MSc Entrance examinations.

Tautomerism Enolization Organic Chemistry CSIR NET
Lecture 03 1:56:23

Enolates and Their Generation

Understand the formation of Enolates, kinetic and thermodynamic enolates, strong bases, reaction mechanisms and their applications in Organic Chemistry for CSIR NET, GATE, IIT JAM, SET and MSc Entrance examinations.

Enolates Generation Organic Chemistry CSIR NET
Lecture 04 2:01:10

Alkylation of Enolates (Part 1)

Learn the principles of Enolate Alkylation, SN2 reactions, regioselectivity, reaction mechanisms and synthetic applications important for CSIR NET, GATE, IIT JAM, SET and MSc Entrance.

Alkylation Enolates SN2 Reaction CSIR NET
Lecture 05 1:24:09

Alkylation of Enolates (Part 2)

Continue with advanced concepts of Enolate Alkylation, reaction selectivity, stereochemical considerations and problem-solving techniques for competitive chemistry examinations.

Alkylation Advanced Enolates Organic Chemistry GATE
Lecture 06 1:17:25

Equivalents of Enolates

Explore various Enolate Equivalents, synthetic strategies, reaction mechanisms and their role in modern Organic Chemistry for competitive examinations.

Enolate Equivalents Synthetic Methods Organic Chemistry CSIR NET
Lecture 07 1:35:43

Asymmetric Alkylation of Enolates (Part 1)

Learn the fundamentals of Asymmetric Enolate Alkylation, chiral auxiliaries, stereoselective synthesis and reaction mechanisms for CSIR NET, GATE, IIT JAM, SET and MSc Entrance examinations.

Asymmetric Synthesis Enolates Stereochemistry CSIR NET
Lecture 08 1:25:12

Asymmetric Alkylation of Enolates (Part 2)

Continue learning Asymmetric Alkylation of Enolates with advanced stereochemical concepts, chiral auxiliaries, reaction mechanisms and competitive exam oriented problem solving.

Asymmetric Alkylation Enolates Stereochemistry CSIR NET
Lecture 09 1:41:29

Aldol Condensation & Michael Addition

Master the mechanisms of Aldol Condensation and Michael Addition, including reaction pathways, synthetic applications and previous year question concepts for competitive exams.

Aldol Condensation Michael Addition Carbonyl Chemistry CSIR NET
Lecture 10 56:35

Michael Addition

Learn the complete mechanism of Michael Addition, conjugate addition reactions, nucleophilic additions and their importance in Organic Chemistry for competitive examinations.

Michael Addition Conjugate Addition Organic Chemistry GATE
Lecture 11 2:05:40

Stereoselectivity of Aldol Reaction (Zimmerman–Traxler Model)

Understand Stereoselective Aldol Reactions, the Zimmerman–Traxler Model, transition state analysis and stereochemical outcomes for CSIR NET and GATE Chemistry.

Aldol Reaction Zimmerman-Traxler Stereochemistry CSIR NET
Lecture 12 1:33:12

Knoevenagel, Stobbe, Henry, Nef, Mannich, Haloform & Perkin Reactions

Learn important Organic Chemistry name reactions including Knoevenagel, Stobbe, Henry, Nef, Mannich, Haloform and Perkin Reactions with mechanisms, applications and exam-oriented concepts.

Knoevenagel Mannich Perkin Haloform
Lecture 13 1:43:09

Claisen Condensation & Dieckmann Condensation

Master the mechanisms of Claisen Condensation and Dieckmann Condensation, reaction conditions, synthetic applications and previous year questions for CSIR NET, GATE, IIT JAM, SET and MSc Entrance.

Claisen Dieckmann Condensation CSIR NET
Lecture 14 1:31:51

Reformatsky Reaction, Favorskii Rearrangement & Darzens Reaction

Learn Reformatsky Reaction, Favorskii Rearrangement and Darzens Reaction with complete mechanisms, stereochemistry and important competitive exam applications.

Reformatsky Favorskii Darzens Organic Chemistry
Lecture 15 1:08:50

Cannizzaro Reaction, Benzilic Acid Rearrangement & Benzoin Condensation

Study the mechanisms of Cannizzaro Reaction, Benzilic Acid Rearrangement and Benzoin Condensation with detailed examples for CSIR NET and GATE Chemistry.

Cannizzaro Benzoin Benzilic Acid CSIR NET
Lecture 16 1:46:31

HVZ Reaction, Pyrolytic Syn Elimination & Chugaev Elimination

Understand the Hell–Volhard–Zelinsky (HVZ) Reaction, Pyrolytic Syn Elimination and Chugaev Elimination with complete mechanisms and exam-oriented concepts.

HVZ Chugaev Syn Elimination GATE
Lecture 17 1:33:01

Julia Olefination, Shapiro Reaction, Bamford–Stevens Reaction & Peterson Olefination

Learn important carbon–carbon double bond formation reactions including Julia Olefination, Shapiro Reaction, Bamford–Stevens Reaction and Peterson Olefination with complete mechanisms and exam-oriented applications.

Julia Olefination Shapiro Peterson CSIR NET
Lecture 18 1:36:47

Wittig Reaction, Horner–Wadsworth–Emmons (HWE) Reaction & Schlosser Wittig Reaction

Master the Wittig Reaction, Horner–Wadsworth–Emmons (HWE) Reaction and Schlosser Wittig Reaction, including mechanisms, stereoselectivity and synthetic applications for competitive chemistry exams.

Wittig HWE Schlosser Organic Chemistry
Lecture 19 1:08:29

Corey–Winter Reaction, Julia–Kocienski Olefination, Ramberg–Backlund Rearrangement & Neber Rearrangement

Complete the Name Reactions series by learning the Corey–Winter Reaction, Julia–Kocienski Olefination, Ramberg–Backlund Rearrangement and Neber Rearrangement with detailed mechanisms and competitive exam applications.

Corey-Winter Julia-Kocienski Ramberg-Backlund Neber
FREQUENTLY ASKED QUESTIONS

Frequently Asked Questions

Find answers to the most common questions about the Name Reactions Complete Lecture Series.

Name Reactions are important organic reactions named after the scientists who discovered them. These reactions are frequently asked in CSIR NET, GATE, IIT JAM, SET, MSc Entrance and other chemistry competitive examinations.

Yes. All 19 lectures are available free of cost along with downloadable PDF notes provided by Chiral Academy.

This course is useful for CSIR NET Chemical Sciences, GATE Chemistry, IIT JAM, SET, MSc Entrance and other university entrance examinations.

Yes. Every lecture includes downloadable PDF notes that summarize important concepts, mechanisms and reactions.

The course contains 19 complete lectures covering more than 50 important Organic Chemistry Name Reactions from basic to advanced level.

Yes. The course starts with the fundamentals of Carbanions, Enolization and Enolates before progressing to advanced Name Reactions, making it suitable for both beginners and advanced learners.

Yes. The lectures are designed with an exam-oriented approach and include reaction mechanisms, shortcuts and concepts frequently asked in previous year papers.

After completing this course, you should continue with General Organic Chemistry (GOC), Organic Reaction Mechanism, Stereochemistry, Named Reagents and Spectroscopy for complete Organic Chemistry preparation.

This course covers more than 50 important Organic Chemistry Name Reactions including Aldol Condensation, Michael Addition, Mannich Reaction, Knoevenagel Condensation, Claisen Condensation, Dieckmann Condensation, Perkin Reaction, Cannizzaro Reaction, Benzoin Condensation, Benzilic Acid Rearrangement, Reformatsky Reaction, Favorskii Rearrangement, Darzens Reaction, Hell–Volhard–Zelinsky (HVZ) Reaction, Chugaev Elimination, Julia Olefination, Julia–Kocienski Olefination, Shapiro Reaction, Bamford–Stevens Reaction, Peterson Olefination, Wittig Reaction, Horner–Wadsworth–Emmons (HWE) Reaction, Schlosser Wittig Reaction, Corey–Winter Reaction, Ramberg–Backlund Rearrangement, Neber Rearrangement and many more. The course starts with the fundamentals of Carbanions, Enolization and Enolates before progressing to advanced name reactions.

There is no official list of Name Reactions prescribed for CSIR NET Chemical Sciences or GATE Chemistry. Students should prepare all important Organic Chemistry Name Reactions because questions can be asked from any standard reaction involving reaction mechanism, reagents, stereochemistry, selectivity or synthetic applications.

The important Name Reactions include: Aldol Condensation, Michael Addition, Claisen Condensation, Dieckmann Condensation, Knoevenagel Condensation, Stobbe Condensation, Henry (Nitroaldol) Reaction, Nef Reaction, Mannich Reaction, Perkin Reaction, Haloform Reaction, Cannizzaro Reaction, Benzoin Condensation, Benzilic Acid Rearrangement, Reformatsky Reaction, Darzens Reaction, Favorskii Rearrangement, Hell–Volhard–Zelinsky (HVZ) Reaction, Chugaev Elimination, Julia Olefination, Julia–Kocienski Olefination, Wittig Reaction, Horner–Wadsworth–Emmons (HWE) Reaction, Schlosser Wittig Reaction, Peterson Olefination, Shapiro Reaction, Bamford–Stevens Reaction, Corey–Winter Reaction, Ramberg–Backlund Rearrangement, Neber Rearrangement, Beckmann Rearrangement, Pinacol Rearrangement, Baeyer–Villiger Oxidation, Wolff Rearrangement, Curtius Rearrangement, Hofmann Rearrangement, Schmidt Reaction, Lossen Rearrangement, Fries Rearrangement, Claisen Rearrangement, Cope Rearrangement, Oxy-Cope Rearrangement, Wagner–Meerwein Rearrangement, Stevens Rearrangement, Sommelet–Hauser Rearrangement, Brook Rearrangement, Pummerer Rearrangement, Fischer Indole Synthesis, Paal–Knorr Synthesis, Skraup Synthesis, Friedel–Crafts Alkylation, Friedel–Crafts Acylation, Clemmensen Reduction, Wolff–Kishner Reduction, Birch Reduction, Rosenmund Reduction, Meerwein–Ponndorf–Verley Reduction, Oppenauer Oxidation, Swern Oxidation, PCC Oxidation, Jones Oxidation, Sharpless Epoxidation, Sharpless Dihydroxylation, Mitsunobu Reaction, Sandmeyer Reaction, Gattermann Reaction, Gattermann–Koch Reaction, Reimer–Tiemann Reaction, Kolbe–Schmitt Reaction, Williamson Ether Synthesis, Gabriel Phthalimide Synthesis, Suzuki Coupling, Heck Reaction, Sonogashira Coupling, Stille Coupling, Negishi Coupling, Kumada Coupling, Ullmann Coupling, Wurtz Reaction, Wurtz–Fittig Reaction, Finkelstein Reaction, Hunsdiecker Reaction, Gomberg–Bachmann Reaction, Buchwald–Hartwig Amination, Diels–Alder Reaction, Ene Reaction, Prilezhaev Epoxidation, Robinson Annulation, Nazarov Cyclization, Simmons–Smith Reaction, Eschweiler–Clarke Reaction, Birch Reduction, Mukaiyama Aldol Reaction, Tebbe Olefination, Nozaki–Hiyama–Kishi Reaction, Mitsunobu Reaction , along with the fundamental concepts of Carbanions, Enolization and Enolate Chemistry.

Studying these reactions with their mechanisms, stereochemistry, reagents, intermediates and synthetic applications is sufficient for almost all questions asked in CSIR NET, GATE, IIT JAM, SET and MSc Entrance examinations.

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