Organic Chemistry II – Aromatic Reactions and Carbonyls!

Organic Chemistry II – Aromatic Reactions and Carbonyls!, available at $59.99, has an average rating of 4.75, with 70 lectures, 33 quizzes, based on 26 reviews, and has 351 subscribers.

You will learn about Carbonyl Chemistry (Type I and Type II) Carbonyls as Nucleophiles (Aldol, Claisen, Michael, Malonic Ester, etc…) Benzene Reactions and Aromaticity How to Apply Fundamental Principles to situations instead of Tedious Memorization! How to use Numbering, Lettering, and Coloring to help keep track of atom movement! How to draw Electron Flow for Mechanisms How to Dominate Synthesis problems This course is ideal for individuals who are OChem II students who need supplemental content to round out their current knowledge or OChem II students who might be having a hard time following their current instructor and would like more approachable lectures or Gen Chem students who want to prep for a future OChem Course It is particularly useful for OChem II students who need supplemental content to round out their current knowledge or OChem II students who might be having a hard time following their current instructor and would like more approachable lectures or Gen Chem students who want to prep for a future OChem Course.

Enroll now: Organic Chemistry II – Aromatic Reactions and Carbonyls!

Summary

Title: Organic Chemistry II – Aromatic Reactions and Carbonyls!

Price: $59.99

Average Rating: 4.75

Number of Lectures: 70

Number of Quizzes: 33

Number of Published Lectures: 70

Number of Published Quizzes: 23

Number of Curriculum Items: 103

Number of Published Curriculum Objects: 93

Original Price: $199.99

Quality Status: approved

Status: Live

What You Will Learn

Carbonyl Chemistry (Type I and Type II)
Carbonyls as Nucleophiles (Aldol, Claisen, Michael, Malonic Ester, etc…)
Benzene Reactions and Aromaticity
How to Apply Fundamental Principles to situations instead of Tedious Memorization!
How to use Numbering, Lettering, and Coloring to help keep track of atom movement!
How to draw Electron Flow for Mechanisms
How to Dominate Synthesis problems

Who Should Attend

OChem II students who need supplemental content to round out their current knowledge
OChem II students who might be having a hard time following their current instructor and would like more approachable lectures
Gen Chem students who want to prep for a future OChem Course

Target Audiences

OChem II students who need supplemental content to round out their current knowledge
OChem II students who might be having a hard time following their current instructor and would like more approachable lectures
Gen Chem students who want to prep for a future OChem Course

In this course, I’ll walk you through some of the major topics that are covered in Organic Chemistry II courses. Each topic is covered in detail with background and practice problems. I’ll warn you about common stumbling blocks and mental hurdles students normally face, and I’ll give you practical problem solving tips and tricks! You’re going to do AWESOME! 🙂

Course Curriculum

Chapter 1: Type I Carbonyls

Lecture 1: Type I Carbonyls and Substitution

Lecture 2: Type II Carbonyls and Addition

Lecture 3: Type I Mechanism (Tetrahedral Intermediate)

Lecture 4: Reactivity of Different Type I Carbonyls

Lecture 5: Leaving Group Ability Affects Reactivity

Lecture 6: Carboxylic Acid Substitution – The Fischer Esterification

Lecture 7: Activating Carboxylic Acids for Other Substitutions

Lecture 8: Trans-Esterification of Esters

Lecture 9: Hydrolysis of Esters and Amides

Chapter 2: Type II Carbonyls – Super Strong Nucleophiles

Lecture 1: Type II Carbonyls – Nucleophile Strength

Lecture 2: Grignards – Part I

Lecture 3: Grignards – Part 2

Lecture 4: Grignards from sp2 Carbons

Lecture 5: Limitations on Grignards

Lecture 6: Final Products of Grignards + Type II Carbonyls

Lecture 7: Grignards + Type I Carbonyls

Lecture 8: Turning Alcohols into Grignards (2 steps)

Lecture 9: Type II Carbonyls + Hydrides

Lecture 10: NaBH4 (Sodium Borohydride)

Lecture 11: LiAlH4 (Lithium Aluminum Hydride)

Lecture 12: DIBAL-H

Lecture 13: Hydrides + Carboxylic acids/Amides

Lecture 14: LiAlH4 Mechanism

Chapter 3: Type II Carbonyls – Less Strong Nucleophiles

Lecture 1: Primary Amines + Type II Carbonyls

Lecture 2: Secondary Amines + Type II Carbonyls

Lecture 3: Secondary Amines + Type II Carbonyls – Part II

Lecture 4: Reductive Amination

Lecture 5: Reductive Amination – Secondary Amines

Lecture 6: Alcohols + Ketones = Hemi-Ketals/Ketals

Lecture 7: Alcohols + Aldehydes = Hemi-Acetals/Acetals

Lecture 8: Prelude to Protection with Alcohols

Lecture 9: Alcohols Protect Type II's from Reducing Agents

Lecture 10: Deprotecting Ketals/Acetals

Chapter 4: Carbonyls as Nucleophiles

Lecture 1: Nucleophilic alpha carbons

Lecture 2: Incomplete deprotonation

Lecture 3: The Aldol reaction

Lecture 4: The Aldol with multiple alpha carbons

Lecture 5: The Aldol dehydration

Lecture 6: The Mixed Aldol – Part I

Lecture 7: The Mixed Aldol – Part II

Lecture 8: The More efficient Aldol

Chapter 5: Aromaticity and Anti-Aromaticity

Lecture 1: Reactions on Benzene

Lecture 2: Aromatic Criteria – Part I

Lecture 3: Aromatic Criteria – Part II

Lecture 4: Determining Aromaticity – Part I

Lecture 5: Determining Aromaticity – Part II

Lecture 6: Determining Aromaticity – Part III

Lecture 7: Anti-Aromaticity

Lecture 8: How Benzene Reacts – Part I

Lecture 9: How Benzene Reacts – Part II

Chapter 6: Benzene Reactions

Lecture 1: Halogenation and Nitration – Part I

Lecture 2: Halogenation and Nitration – Part II

Lecture 3: Other Benzene Reactions – Part I

Lecture 4: Other Benzene Reactions – Part II

Lecture 5: Other Benzene Reactions – Part III

Lecture 6: Rates of EAS – Part I

Lecture 7: Rates of EAS – Part II

Lecture 8: Positioning of EAS – Part I

Lecture 9: Positioning of EAS – Part II

Lecture 10: Speed for EAS -Part I

Lecture 11: Speed for EAS – Part II

Lecture 12: Esters are Chameleons

Lecture 13: Activators and Deactivators

Lecture 14: Disubstituted Benzenes

Lecture 15: Steric Blockade

Lecture 16: Limitations on Friedel Crafts

Lecture 17: Limitations on Friedel Crafts – Part II

Lecture 18: Arene Diazonium Salts

Lecture 19: SnAR and Benzynes

Lecture 20: Benzyne Reactions

Instructors

Jason Crumpton
Organic Chemistry Professor with 15+ years experience

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3 stars: 2 votes
4 stars: 10 votes
5 stars: 14 votes

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