Free Course Image Organic Chemistry

Free online courseOrganic Chemistry

Duration of the online course: 130 hours and 28 minutes

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Enroll in a comprehensive free online Organic Chemistry course covering basic principles, bonding, structures, reactions, nomenclature, exam reviews, and advanced topics.

In this free course, learn about

  • Foundations of Organic Structure and Bonding
  • Drawing Organic Structures and Formal Charge
  • Molecular Geometry, Hybridization, and Polarity
  • Resonance, Arrow Pushing, and Acid–Base Fundamentals
  • Hydrocarbons and Basic Nomenclature
  • Physical Properties and Conformational Analysis of Alkanes
  • Exam 1 Reviews and Stereochemistry Concepts
  • Substitution and Elimination Mechanisms (SN1, SN2, E1, E2)
  • Alkenes and Alkynes: Nomenclature and Reactions
  • Exam 2 Reviews and Alcohol / Radical Chemistry
  • Spectroscopy: IR, Mass Spec, and NMR
  • Ethers, Conjugation, and Aromaticity
  • Carboxylic Acids, Derivatives, and Carbonyl Nomenclature
  • Carbonyl Reactions: Reductions, Grignards, and Alpha Chemistry
  • Aromatic Compounds and Electrophilic Aromatic Substitution
  • Enolate and Carbonyl Condensation Chemistry
  • Amines, Organometallics, and Biomolecules
  • Comprehensive Reviews, Polymers, and Statistics Intro

Course Description

Welcome to the course "Organic Chemistry". This comprehensive course offers a deep dive into the fundamental aspects of organic chemistry, stretching over a duration of 130 hours and 28 minutes. Although there are no reviews yet, this extensive program belongs to the Basic studies category, specifically under Chemistry.

The course begins with an essential groundwork in the realm of organic chemistry, presenting a solid base in the subject with modules like "Organic Chemistry - Basic Introduction" and "Organic Chemistry - Basic Introduction - Membership." It emphasizes basic concepts such as different types of chemical bonds, namely ionic, polar covalent, and nonpolar covalent bonds, and helps elucidate which bond is more polar using electrostatic potential maps and bond polarity.

As you progress, you will learn how to draw various chemical structures such as Lewis structures, Kekule structures, and condensed structures, eventually transitioning to skeletal structures. The course also provides valuable study tips for the coming college semester and covers significant theories like VSEPR Theory and Valence Bond Theory.

The course then delves into hybridization of atomic orbitals, bond strength and length, molecular polarity, and even intermolecular forces like hydrogen bonding and dipole-dipole interactions, preparing you for an in-depth understanding of resonance structures and formal charges.

Moving further, you will explore the fascinating world of acids and bases, covering the basics, pKa values, and concepts like the inductive effect and solvating effects. Important practical topics such as predicting reactants of acid-base reactions, nucleophiles, and electrophiles are thoroughly explained.

The course introduces nomenclature of various organic compounds, including alkanes, cycloalkanes, ethers, alcohols, alkyl halides, amines, alkenes, and alkynes, integrating useful IUPAC rules. Additionally, it explores physical properties, characteristics of hydrocarbons, and concepts like homolytic and heterolytic bond cleavages.

A significant portion of the course is dedicated to stereochemistry, addressing chirality centers, enantiomers, diastereomers, and meso compounds, as well as optical activity and specific rotation. Reaction mechanisms like SN2, SN1, E1, and E2 are dissected in detail, along with concepts such as carbocation and carbanion stability, polar protic and aprotic solvents, and dehydrohalogenation.

The curriculum includes comprehensive reviews and practice problems to ensure mastery of each topic, offering a practical, hands-on approach to learning. You will explore complex reaction mechanisms, spectroscopy techniques, kinetic versus thermodynamic products, and much more, advancing your understanding of organic chemistry.

Towards the end, the course covers advanced topics like the Diels-Alder reaction, nucleophilic aromatic substitution, enolate reactions, aldol condensation, and various synthesis reactions. It also provides an introduction to organometallic compounds, carbohydrates, and polymer chemistry, complete with detailed explanations of reaction mechanisms and final exam reviews.

In summary, this course aims to provide a thorough grounding in organic chemistry, equipping you with the knowledge and skills essential for advancing in this field.

Course content

  • Video class: Organic Chemistry - Basic Introduction 41m
  • Exercise: In organic chemistry, which of the following bonds is considered the strongest?
  • Video class: Organic Chemistry - Basic Introduction - Membership 1h42m
  • Video class: Organic Chemistry Tutor - Youtube Channel Membership 03m
  • Exercise: What do you need to do to access exclusive full-length videos on this YouTube channel?
  • Video class: Ionic Bonds, Polar Covalent Bonds, and Nonpolar Covalent Bonds 11m
  • Exercise: What type of bond is present in a Lithium-Fluorine compound?
  • Video class: Which Bond Is More Polar? 10m
  • Exercise: Which bond is more polar?
  • Video class: Electrostatic Potential Maps and Bond Polarity - Organic Chemistry 25m
  • Exercise: Which statement about electrostatic potential maps is correct?
  • Video class: Organic Chemistry - How To Draw Lewis Structures 11m
  • Exercise: Which of the following elements normally forms three bonds and typically has one lone pair in a neutral organic molecule?
  • Video class: Kekule Structures and Condensed Structures 06m
  • Exercise: Identify correct calculate structure representation
  • Video class: Condensed Structures to Skeletal Structures 11m
  • Exercise: What is the skeletal structure for CH3 times 2, CH, CH2 times 2, CH3?
  • Video class: List of Organic Chemistry Videos on Patreon 03m
  • Exercise: What is an advantage of joining the Patreon membership program for organic chemistry content?
  • Video class: Functional Groups 20m
  • Exercise: What functional group has a carbon-carbon triple bond?
  • Video class: Unusual Functional Groups - Organic Chemistry 55m
  • Exercise: What is the IHD (Index of Hydrogen Deficiency) for Benzene?
  • Video class: Organic Chemistry Drawing Structures - Bond Line, Skeletal, and Condensed Structural Formulas 31m
  • Exercise: Which of the following statements is correct about the bonding preferences in organic chemistry based on valence electron requirements?
  • Video class: Formal Charge 06m
  • Exercise: What is the formal charge on the bromine atom?
  • Video class: How To Identify The Number of Lone Pairs on an Atom Using Formal Charge 15m
  • Exercise: How many lone pairs are typically found on a carbon atom with three bonds and a negative charge?
  • Video class: Studying Tips For The Next College Semester 05m
  • Exercise: What is one effective studying tip to get ahead in your next class?
  • Video class: Predicting Bond Angles 05m
  • Exercise: What is the bond angle around the central carbon atom in CH2O?
  • Video class: VSEPR Theory - Basic Introduction 13m
  • Exercise: What is the bond angle for a trigonal planar molecular structure?
  • Video class: Valence Bond Theory 10m
  • Exercise: What is the hybridization of the central carbon atom in methane (CH4), and what type of bonds are formed between carbon and hydrogen atoms?
  • Video class: Valence Bond Theory 33m
  • Video class: Hybridization of Atomic Orbitals - Sigma 10m
  • Video class: Hybridization of Atomic Orbitals - Sigma 36m
  • Video class: Bond Strength and Bond Length 14m
  • Video class: Hybridization, Orbital Overlap, and Bond Length 08m
  • Video class: Steric Number, Hybridization, 12m
  • Exercise: Which of the following statements correctly describes the steric number and hybridization of the central oxygen atom in the H2O molecule?
  • Video class: Dipole Moment, Molecular Polarity 16m
  • Video class: Intermolecular Forces - Hydrogen Bonding, Dipole Dipole Interactions - Boiling Point 10m
  • Video class: Resonance Structures 13m
  • Video class: Resonance Structures - Membership 1h03m
  • Video class: Bond Order and Resonance Structures 05m
  • Video class: Curve Arrow Notation - Electron Pushing Arrows 24m
  • Exercise: In an organic chemistry context, what is represented by a half arrow in electron pushing diagrams?
  • Video class: pKa, Ka, and Acid Strength 05m
  • Video class: Acids and Bases - Basic Introduction - Organic Chemistry 29m
  • Video class: Acids and Bases - Basic Introduction - Organic Chemistry - Membership 1h20m
  • Video class: Stability of Negative Charges Acids and Bases 28m
  • Video class: pKa Values of Acids - Organic Chemistry 21m
  • Video class: pKa Values of Acids - Organic Chemistry - Membership 57m
  • Video class: Ranking Protons in order of Increasing Acidity Using pKa Values 05m
  • Video class: Inductive Effect - Acids and Bases 11m
  • Video class: Solvating Effects - Acids and Bases 08m
  • Video class: The Leveling Effect - Acids and Bases - Organic Chemistry 23m
  • Video class: How To Predict The Reactant and Reagent of Acid Base Reactions 20m
  • Video class: Lewis Acids and Bases 06m
  • Exercise: In a Lewis acid-base reaction, which of the following combinations will result in a product where the Lewis acid has a formal negative charge?
  • Video class: Nucleophiles and Electrophiles 06m
  • Video class: Hydrocarbons - Aliphatic vs Aromatic Molecules - Saturated 10m
  • Video class: Constitutional Isomers 13m
  • Video class: IUPAC Nomenclature of Alkanes - Naming Organic Compounds 11m
  • Video class: IUPAC Nomenclature of Alkanes - Naming Organic Compounds - Membership 43m
  • Video class: Naming Cycloalkanes With Substituents, Cis 11m
  • Exercise: What is the correct IUPAC name for a cycloalkane with a six-membered ring, a chloro substituent on carbon 1, and an ethyl substituent on carbon 3?
  • Video class: Naming Bicyclic Compounds 07m
  • Video class: Naming Ethers - IUPAC Nomenclature With Branching, Organic Chemistry Practice Problems 12m
  • Video class: Naming Alcohols - IUPAC Nomenclature 10m
  • Video class: Naming Alkyl Halides - IUPAC Nomenclature 11m
  • Video class: Naming Amines - IUPAC Nomenclature 18m
  • Video class: Van Der Waals Forces 10m
  • Exercise: Which of the following halogens has the highest boiling point due to the strongest London dispersion forces?
  • Video class: Boiling Point of Organic Compounds 15m
  • Video class: Melting Points of Alkanes 05m
  • Video class: Physical Properties of Alkanes - Melting Point, Boiling Point, Density, 06m
  • Video class: Homolytic and Heterolytic Bond Cleavages 12m
  • Video class: Newman Projections 23m
  • Video class: Newman Projections - Membership 59m
  • Video class: How To Convert a Perspective Formula to a Newman Projection 05m
  • Video class: Torsional Strain and Steric Strain 10m
  • Video class: Stability of Cycloalkanes - Angle Strain 07m
  • Video class: Chair Conformation and Ring Flips 24m
  • Video class: Chair Conformations and Ring Flips - Membership 1h12m
  • Video class: Cis and Trans Isomers 06m
  • Exercise: Which of the following alkenes can exhibit cis and trans isomerism?
  • Video class: Organic Chemistry Exam 1 Review 42m
  • Video class: Organic Chemistry Exam 1 Review - Membership 2h22m
  • Video class: Organic Chemistry Tutor - YouTube Membership Program 07m
  • Video class: Organic Chemistry Exam 1 - IUPAC Nomenclature, Resonance, Acids 42m
  • Video class: Organic Chemistry Exam 1 - Part 1 - Membership 3h52m
  • Video class: Organic Chemistry Exam 1 - Part 2 - Membership 3h48m
  • Video class: Finding Chirality Centers 06m
  • Video class: Stereochemistry - R S Configuration 27m
  • Video class: Stereochemistry - R and S Configuration - Fischer Projections - Membership 1h23m
  • Video class: Enantiomers 08m
  • Video class: Diastereomers 05m
  • Video class: Meso Compounds 07m
  • Exercise: Which characteristic distinguishes a meso compound from a pair of enantiomers?
  • Video class: Stereoisomers 05m
  • Video class: Optical Activity - Specific Rotation 22m
  • Video class: Optical Activity - Specific Rotation 1h01m
  • Video class: SN2 SN1 E1 E2 Reaction Mechanisms Made Easy! 38m
  • Video class: SN2 SN1 E1 1h34m
  • Video class: SN2 Reaction Mechanisms 22m
  • Exercise: Consider the following statements about the SN2 reaction mechanism. Which one is true?
  • Video class: SN2 Reaction Mechanisms - Membership 1h04m
  • Video class: SN1 Reaction Mechanism 26m
  • Video class: SN1 Reaction Mechanisms - Membership 1h04m
  • Video class: Carbocation Stability - Hyperconjugation, Inductive Effect 11m
  • Video class: Carbanion Stability 05m
  • Video class: Polar Protic Solvents and Polar Aprotic Solvents For SN1 15m
  • Exercise: Which type of reaction is favored by polar aprotic solvents, and why?
  • Video class: E1 Reaction Mechanism With Alcohol Dehydration 12m
  • Video class: E2 Reaction Mechanism - Hoffman Elimination vs Zaitsev's Rule 12m
  • Video class: E2 Stereochemistry With Newman Projections 11m
  • Video class: SN1 SN2 E1 E2 Reaction Mechanism - Test Review 59m
  • Video class: SN1 SN2 E1 4h09m
  • Video class: Naming Alkenes Using E Z System - IUPAC Nomenclature 12m
  • Exercise: Based on IUPAC nomenclature, how would you name an alkene with a six-carbon chain where there is a double bond starting at carbon 1 and a methyl group on carbon 3?
  • Video class: Degree of Unsaturation and Index of Hydrogen Deficiency 13m
  • Video class: Alkene Reactions 1h10m
  • Video class: Alkene Reactions Part 1 - Membership 2h02m
  • Video class: Alkene Reactions Part 2 - Membership 2h00m
  • Video class: Hydrohalogenation - Alkene Reaction Mechanism 12m
  • Video class: Markovnikov's Rule 11m
  • Exercise: What is the major product when 1-butene is reacted with HBr according to Markovnikov's rule?
  • Video class: Alkene HBR ROOR - Reaction Mechanism 07m
  • Video class: Hydration of Alkenes Reaction Mechanism 20m
  • Video class: Alkene H2SO4 H2O 11m
  • Video class: Oxymercuration Demercuration Reaction Mechanism 12m
  • Video class: Alkoxymercuration Demercuration Reaction Mechanism 10m
  • Video class: Hydroboration - Oxidation Reaction Mechanism 16m
  • Exercise: In a hydroboration-oxidation reaction involving 1-methylcyclopentene reacted with B2H6 and THF followed by hydroxide, peroxide, and water, what is the major product of this reaction?
  • Video class: Halogenation of Alkenes 13m
  • Video class: Alkene Br2 H2O 05m
  • Video class: Epoxidation of Alkenes 10m
  • Video class: Alkene KMnO4 Reaction 11m
  • Video class: Ozonolysis - Oxidative Cleavage of Alkenes 12m
  • Video class: Naming Alkynes - IUPAC Nomenclature 13m
  • Exercise: In alkyne nomenclature, when an alcohol group is present alongside an alkyne group in a molecule, which group is given priority in numbering and what is the IUPAC name for a molecule with an alcohol on carbon 2 and a triple bond on carbon 3 of a hexane chain?
  • Video class: Alkyne Reactions 47m
  • Video class: Alkyne Reactions - Membership 1h30m
  • Video class: Organic Chemistry 1 Exam 2 Review 1h12m
  • Video class: Organic Chemistry 1 Exam 2 Review - Membership 3h44m
  • Video class: Patreon Membership Program - Introduction 04m
  • Video class: Organic Chemistry 1 Exam 2 Review Questions 43m
  • Exercise: Which of the following statements about SN2 reactions is correct?
  • Video class: Organic Chemistry 1 Exam 2 Review Part 1 - Membership 3h10m
  • Video class: Organic Chemistry 1 Exam 2 Review Part 2 - Membership 2h48m
  • Video class: Alcohol Reactions - HBr, PBr3, SOCl2 16m
  • Video class: Alcohol Reactions - HBr, PBr3, SOCl2 - Membership 1h01m
  • Video class: Alcohol Dehydration Reaction Mechanism With H2SO4 16m
  • Video class: Free Radical Reactions 30m
  • Exercise: In a free radical reaction, which step involves two radicals combining to form a neutral molecule?
  • Video class: Free Radical Reactions - Basic Introduction - Membership 1h32m
  • Video class: Organic Chemistry Reactions Summary 38m
  • Video class: Organic Chemistry 1 Final Exam Review 2h04m
  • Video class: Organic Chemistry 1 Final Exam Review Part 2 - Membership 2h01m
  • Video class: Organic Chemistry 1 Final Exam Review Part 3 - Membership 2h15m
  • Video class: IR Spectroscopy - Basic Introduction 15m
  • Exercise: Which functional group can be identified by a broad OH stretch between 2500 and 3300 cm⁻¹ and a strong C=O stretch around 1700 cm⁻¹ in an IR spectrum?
  • Video class: IR Spectroscopy - Practice Problems 11m
  • Video class: Mass Spectrometry 10m
  • Video class: Mass Spectrometry - Membership 38m
  • Video class: Shielding and Deshielding - H NMR Spectroscopy 11m
  • Video class: Basic Introduction to NMR Spectroscopy 11m
  • Video class: How To Determine The Number of Signals In a H NMR Spectrum 20m
  • Exercise: How many unique proton signals would you expect to see in the 1H NMR spectrum of 2-chlorobutane?
  • Video class: Chemical Shift In NMR Spectroscopy 15m
  • Video class: Diamagnetic Anisotropy - H NMR Spectroscopy - Organic Chemistry 11m
  • Video class: Integration of H NMR Signals - Spectroscopy - Organic Chemistry 05m
  • Video class: Spin Spin Splitting - N 1 Rule - Multiplicity - Proton NMR Spectroscopy 22m
  • Video class: How To Draw The Proton NMR Spectrum of an Organic Molecule 12m
  • Video class: Proton NMR Spectroscopy - How To Draw The Structure Given The Spectrum 14m
  • Exercise: Given the molecular formula C4H9Br, identify the structure that matches a proton NMR spectrum with four distinct signals. Which of the following is the correct structure?
  • Video class: Proton NMR Spectroscopy - How To Draw The Structure Given The Spectrum - Membership 1h04m
  • Video class: Carbon-13 NMR Spectroscopy 1h38m
  • Video class: Williamson Ether Synthesis Reaction Mechanism 18m
  • Video class: Ether and Epoxide Reactions 11m
  • Video class: Ether and Epoxide Reactions - Membership 29m
  • Video class: Kinetic vs Thermodynamic Product - 1,2 vs 1,4 Addition of HBr to 1,3- Butadiene 12m
  • Exercise: When reacting 1,3-butadiene with HBr at high temperatures, which product predominates due to the thermodynamic control?
  • Video class: Kinetic vs Thermodynamic Product - 1,2 vs 1,4 Addition of HBr to 1,3-Butadiene - Membership 40m
  • Video class: Diels Alder Reaction 11m
  • Video class: Diels Alder Reaction - Membership 33m
  • Video class: Aromatic, Antiaromatic, or Nonaromatic - Huckel's Rule - 4n 2 - Heterocycles 10m
  • Video class: Aromatic, Antiaromatic, or Nonaromatic - Huckel's Rule - 4n 2 - Heterocycles - Membership 41m
  • Video class: Naming Carboxylic Acids - IUPAC Nomenclature 14m
  • Exercise: What is the IUPAC name for a molecule with a six-carbon chain, a carboxylic acid group at one end, and an amino group on the fourth carbon?
  • Video class: Naming Esters - IUPAC Nomenclature, Branches, Substituents, 25m
  • Video class: Naming Acid Anhydrides and Nitriles - IUPAC Nomenclature 05m
  • Video class: Naming Acid Chlorides With IUPAC Nomenclature 05m
  • Video class: Naming Amides - IUPAC Nomenclature 11m
  • Video class: Carboxylic Acid Derivative Reactions 10m
  • Video class: Carboxylic Acid Derivative Reactions - Membership 42m
  • Video class: Naming Aldehydes - IUPAC Nomenclature 11m
  • Video class: Naming Ketones Explained - IUPAC Nomenclature 13m
  • Video class: NaBH4, LiAlH4, DIBAL Reduction Mechanism, Carboxylic Acid, Acid Chloride, Ester, 38m
  • Video class: Grignard Reagent Reaction Mechanism 12m
  • Video class: Gilman Reagent 06m
  • Video class: Aldehydes and Ketones 1h13m
  • Exercise: What is the major product when an acid chloride is reacted with lithium aluminum hydride (LiAlH4) followed by H3O+?
  • Video class: Wolff Kishner Reduction Mechanism 08m
  • Video class: Keto Enol Tautomerism - Acidic 11m
  • Video class: Alpha Halogenation of Ketones 06m
  • Video class: Imine and Enamine Formation Reactions With Reductive Amination 12m
  • Video class: Protecting Groups, Acetals, and Hemiacetals 10m
  • Video class: Wittig Reaction Mechanism 11m
  • Exercise: Which of the following statements best describes the outcome of a Wittig reaction?
  • Video class: Naming Benzene Ring Derivatives - Aromatic Compounds 17m
  • Video class: Aromatic Halogenation Mechanism - Chlorination, Iodination 12m
  • Video class: Nitration of Benzene Mechanism - Electrophilic Aromatic Substitution Reactions 05m
  • Video class: Sulfonation of Benzene 12m
  • Video class: Friedel Crafts Acylation of Benzene Reaction Mechanism 11m
  • Video class: Gatterman Koch Reaction 05m
  • Exercise: What is the primary purpose of the Gatamine formulation reaction in organic chemistry?
  • Video class: Friedel Crafts Alkylation of Benzene Reaction Mechanism - Tons of Examples! 21m
  • Video class: Clemmensen Reduction 10m
  • Video class: Benzene Side Chain Reactions 10m
  • Video class: Ortho Meta Para Directors - Activating and Deactivating Groups 16m
  • Video class: Nitration of MethylBenzoate and Nitration of Bromobenzene 14m
  • Video class: Ortho Para Ratio - Aromatic Nitration of Toluene 11m
  • Exercise: What is the expected major product when benzene with a tert-butyl group undergoes nitration with nitric acid and sulfuric acid, and why?
  • Video class: Electrophilic Aromatic Substitution Reactions Made Easy! 1h01m
  • Video class: Nucleophilic Aromatic Substitution - Benzyne Intermediate and Meisenheimer Complex 23m
  • Video class: Arenediazonium Salts With Diazo Coupling and Sandmeyer Reactions 18m
  • Video class: Enolate Reactions - Direct Alkylation of Ketones With LDA 13m
  • Video class: Aldol Addition Reactions, Intramolecular Aldol Condensation Reactions, Retro Aldol 22m
  • Video class: Cannizzaro Reaction Mechanism 05m
  • Exercise: Which of the following describes the Cannizzaro reaction mechanism when using two aldehyde molecules that contain no alpha hydrogen atoms?
  • Video class: Michael Addition Reaction Mechanism 15m
  • Video class: Robinson Annulation Reaction Mechanism 21m
  • Video class: Stork Enamine Reaction Mechanism - Alkylation, Acylation, 10m
  • Video class: Claisen Condensation Reaction Mechanism 18m
  • Video class: Dieckmann Condensation Reaction Mechanism 12m
  • Video class: Malonic Ester Synthesis Reaction Mechanism 10m
  • Exercise: In the malonic ester synthesis, which sequence of reagents is needed to transform diethyl malonate into a carboxylic acid with a single alkyl group added at the alpha position?
  • Video class: Acetoacetic Ester Synthesis Reaction Mechanism 11m
  • Video class: Decarboxylation Reaction Mechanism 05m
  • Video class: Amine Synthesis Reactions 32m
  • Video class: Aromatic Compounds 31m
  • Video class: Introduction to Organometallic Compounds 21m
  • Video class: Carbohydrates - Haworth 22m
  • Exercise: What is the most common form of glucose in aqueous solution and why?
  • Video class: Organic Chemistry - Reaction Mechanisms - Addition, Elimination, Substitution, 34m
  • Video class: Organic Chemistry 1 6h08m
  • Video class: Organic Chemistry 2 Final Exam Review 1h18m
  • Video class: Organic Chemistry 2 Final Exam Review Multiple Choice Problems - Membership 7h44m
  • Video class: Polymers - Basic Introduction 26m
  • Video class: Polymers - Condensation Polymerization 08m
  • Exercise: In condensation polymerization, which statement correctly describes the process involved in forming polymers?
  • Video class: Introduction to Statistics 16m
  • Video class: Organic Chemistry 2 Final Exam Review Multiple Choice Problems - Membership 7h44m

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