Curriculum
- 1 Section
- 137 Lessons
- Lifetime
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- Primera137
- 2.1Organic Chemistry – How To Draw Lewis Structures
- 2.2Ionic Bonds, Polar Covalent Bonds, and Nonpolar Covalent Bonds
- 2.3Which Bond Is More Polar?
- 2.4Formal Charge
- 2.5Predicting Bond Angles
- 2.6Kekule Structures and Condensed Structures
- 2.7VSEPR Theory – Basic Introduction
- 2.8Molecular Geometry & VSEPR Theory – Basic Introduction
- 2.9Valence Bond Theory & Hybrid Atomic Orbitals
- 2.10Bond Strength and Bond Length
- 2.11Dipole Moment, Molecular Polarity & Percent Ionic Character
- 2.12Intermolecular Forces – Hydrogen Bonding, Dipole Dipole Interactions – Boiling Point & Solubility
- 2.13pKa, Ka, and Acid Strength
- 2.14Conjugate Acids and Bases
- 2.15Using Pka Values To Predict The Position of Equilibrium & The Products of an Acid Base Reaction
- 2.16Curved Arrow Notation For Acid Base Reaction Mechanisms
- 2.17Acids and Bases – Electronegativity, Atomic Size, Hybridization, Resonance & Inductive Effect
- 2.18Lewis Acids and Bases
- 2.19Nucleophiles and Electrophiles
- 2.20The Effect of pH on Acid Structure
- 2.21Hydrocarbons – Aliphatic vs Aromatic Molecules – Saturated & Unsaturated Compounds
- 2.22Functional Groups
- 2.23Organic Chemistry Drawing Structures – Bond Line, Skeletal, and Condensed Structural Formulas
- 2.24Naming Organic Compounds – IUPAC Nomenclature of Alkanes
- 2.25Naming Alkanes With Branched Substituents – IUPAC Nomenclature
- 2.26Constitutional Isomers
- 2.27Resonance Structures
- 2.28Naming Cycloalkanes With Substituents, Cis & Trans, Bicyclo Alkane Nomenclature
- 2.29Naming Bicyclic Compounds
- 2.30Naming Ethers – IUPAC Nomenclature With Branching, Organic Chemistry Practice Problems
- 2.31Naming Alcohols – IUPAC Nomenclature
- 2.32Naming Alkyl Halides – IUPAC Nomenclature
- 2.33Naming Amines – IUPAC Nomenclature & Common Names
- 2.34Van Der Waals Forces
- 2.35Boiling Point of Organic Compounds
- 2.36Ring Flips
- 2.37Newman Projections
- 2.38Chair Conformation
- 2.39Stability of Cycloalkanes – Angle Strain
- 2.40Cis and Trans Isomers
- 2.41Finding Chirality Centers
- 2.42R and S Configuration – Stereochemistry
- 2.43Fischer Projections – Stereochemistry
- 2.44Enantiomers
- 2.45Diastereomers
- 2.46Meso Compounds
- 2.47Stereoisomers
- 2.48Specific & Observed Rotation, Optically Active, Enantiomeric Excess, Chiral & Achiral Molecules
- 2.49Naming Alkenes Using E Z System – IUPAC Nomenclature
- 2.50Degree of Unsaturation and Index of Hydrogen Deficiency
- 2.51Hydrohalogenation – Alkene Reaction Mechanism
- 2.52Hydration of Alkenes Reaction Mechanism
- 2.53Oxymercuration Demercuration Reaction Mechanism
- 2.54Alkoxymercuration Demercuration Reaction Mechanism
- 2.55Hydroboration – Oxidation Reaction Mechanism
- 2.56Halogenation of Alkenes & Halohydrin Formation Reaction Mechanism
- 2.57Epoxidation of Alkenes
- 2.58Alkene + KMnO4 Reaction
- 2.59Ozonolysis – Oxidative Cleavage of Alkenes
- 2.60Alkene Reactions – Fast Review!
- 2.61Naming Alkynes – IUPAC Nomenclature & Common Names
- 2.62Alkyne Reactions – Quick Review!
- 2.63SN2 SN1 E1 E2 Reaction Mechanisms Made Easy!
- 2.64SN2 Reaction Mechanism With Stereochemistry, Chair Conformation & Fischer Projection Problems
- 2.65SN1 Reaction Mechanism – Carbocation Rearrangements, Solvolysis & Racemic Mixtures
- 2.66Carbocation Stability – Hyperconjugation, Inductive Effect & Resonance Structures
- 2.67Polar Protic Solvents and Polar Aprotic Solvents For SN1 & SN2 Reactions
- 2.68E1 Reaction Mechanism With Alcohol Dehydration & Ring Expansion Problems
- 2.69E2 Reaction Mechanism – Hoffman Elimination vs Zaitsev’s Rule
- 2.70E2 Stereochemistry With Newman Projections
- 2.71Organic Chemistry – Reactions of Alcohols – PBr3, SOCl2, HBr & Tosylation
- 2.72E1 & E2 Dehydration of Alcohols Into Alkenes – Acid Catalyzed Elimination Reaction Mechanism
- 2.73Oxidation of Alcohols – PCC, H2CrO4 & Swern Oxidation
- 2.74Williamson Ether Synthesis Reaction Mechanism
- 2.75Ether and Epoxide Reactions
- 2.76Free Radical Reactions of Alkanes & Alkenes With NBS
- 2.77Kinetic vs Thermodynamic Product – 1,2 vs 1,4 Addition of HBr to 1,3 Butadiene
- 2.78Diels Alder Reaction
- 2.79Aromatic, Antiaromatic, or Nonaromatic – Huckel’s Rule, 4n+2 – Heterocycles & Aromaticity
- 2.80Naming Carboxylic Acids – IUPAC Nomenclature
- 2.81Naming Esters – IUPAC Nomenclature, Branches, Substituents, & Benzene Rings – Organic Chemistry
- 2.82Naming Acid Anhydrides and Nitriles – IUPAC Nomenclature
- 2.83Naming Acid Chlorides With IUPAC Nomenclature
- 2.84Naming Amides – IUPAC Nomenclature
- 2.85Carboxylic Acid Derivative Reactions
- 2.86Naming Aldehydes Explained, IUPAC Nomenclature Practice – Organic Chemistry
- 2.87Naming Ketones Explained – IUPAC Nomenclature Practice & Examples – Organic Chemistry
- 2.88NaBH4, LiAlH4, DIBAL Reduction Mechanism, Carboxylic Acid, Acid Chloride, Ester, & Ketones
- 2.89Grignard Reagent Reaction Mechanism
- 2.90Aldehydes and Ketones
- 2.91Keto Enol Tautomerism – Acid & Base Reaction Mechanism, Tautomerization, Organic Chemistry
- 2.92Alpha Halogenation of Ketones
- 2.93Imine and Enamine Formation Reactions With Reductive Amination
- 2.94Protecting Groups, Acetals, and Hemiacetals
- 2.95Wittig Reaction Mechanism
- 2.96Naming Benzene Derivatives – Aromatic Compounds
- 2.97Aromatic Halogenation Mechanism – Chlorination, Iodination & Bromination of Benzene
- 2.98Nitration of Benzene Mechanism – Electrophilic Aromatic Substitution Reactions
- 2.99Sulfonation of Benzene & Desulfonation Reaction Mechanism – Aromatic Compounds
- 2.100Friedel Crafts Acylation of Benzene Reaction Mechanism
- 2.101Gatterman Koch Reaction
- 2.102Friedel Crafts Alkylation of Benzene Reaction Mechanism – Tons of Examples!
- 2.103Clemmensen Reduction, Wolff Kishner Mechanism, Thioketal Mozingo Reaction, Organic Chemistry
- 2.104Benzene Side Chain Reactions
- 2.105Ortho Meta Para Directors – Activating and Deactivating Groups
- 2.106Nitration of MethylBenzoate and Nitration of Bromobenzene
- 2.107Ortho Para Ratio – Aromatic Nitration of Toluene
- 2.108Electrophilic Aromatic Substitution Reactions Made Easy!
- 2.109Nucleophilic Aromatic Substitution – Benzyne Intermediate and Meisenheimer Complex
- 2.110Arenediazonium Salts With Diazo Coupling and Sandmeyer Reactions
- 2.111Enolate Reactions – Direct Alkylation of Ketones With LDA
- 2.112Aldol Addition Reactions, Intramolecular Aldol Condensation Reactions, Retro Aldol & Cross Aldol Rea
- 2.113Michael Addition Reaction Mechanism
- 2.114Robinson Annulation Reaction Mechanism
- 2.115Stork Enamine Reaction Mechanism – Alkylation, Acylation, & Michael Addition
- 2.116Claisen Condensation Reaction Mechanism
- 2.117Dieckmann Condensation Reaction Mechanism
- 2.118Malonic Ester Synthesis Reaction Mechanism
- 2.119Acetoacetic Ester Synthesis Reaction Mechanism
- 2.120Decarboxylation Reaction Mechanism
- 2.121Amine Synthesis Reactions
- 2.122Aromatic Compounds & Heterocycles – Nucleophilic & Electrophilic Aromatic Substitution Reactions
- 2.123Introduction to Organometallic Compounds
- 2.124Carbohydrates – Haworth & Fischer Projections With Chair Conformations
- 2.125Organic Chemistry Reactions Summary
- 2.126Organic Chemistry – Reaction Mechanisms
- 2.127Mass Spectrometry
- 2.128Shielding and Deshielding – H NMR Spectroscopy
- 2.129Basic Introduction to NMR Spectroscopy
- 2.130How To Determine The Number of Signals In a H NMR Spectrum
- 2.131Chemical Shift In NMR Spectroscopy
- 2.132Diamagnetic Anisotropy – H NMR Spectroscopy – Organic Chemistry
- 2.133Integration of H NMR Signals – Spectroscopy – Organic Chemistry
- 2.134Spin Spin Splitting – N+1 Rule – Multiplicity – Proton NMR Spectroscopy
- 2.135How To Draw The Proton NMR Spectrum of an Organic Molecule
- 2.136Proton NMR Spectroscopy – How To Draw The Structure Given The Spectrum
- 2.137Carbon-13 NMR Spectroscopy
