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Organic 1 Chapters 1–11
1Periodic Table/Trends
2Bonding & Structure
- 2.1 Electron waves
- 2.2 Atomic orbitals
- 2.3 Hybrid orbitals
- 2.4 Molecular Orbitals
- 2.5 Lewis Structures
- 2.6 Formal Charges
- 2.7 Drawing Compounds
- 2.8 Geometry
- 2.9 Dipole Moment
- 2.10 Solubility
- 2.11 Intermolecular Forces
- 2.12 Types of Organic Compound
- 2.13 Functional Groups
- 2.13 Functional Group Study Cards
- 2.14 Problems
3IR and MS
4Resonance
5Acids/Bases
6Alkanes
7Stereochemistry
8Organic Reaction Basics
9Alkyl Halides SN1, SN2, E1, E2
- 9.1 Introduction
- 9.2 Nomenclature
- 9.3 Preparation of Alkyl Halides
- 9.4 Alkyl halides from alcohols
- 9.5 Reactions of Alkyl Halides
- 9.6 The SN2 Reaction (backside attack)
- 9.7 Factors that affect the SN2
- 9.8 The SN1 Reaction
- 9.9 Beta-Eliminations
- 9.10 E1 Reaction
- 9.11 E2 Reaction
- 9.12 Comparison Summary
- 9.13 Reaction Summary
- 9.14 Problems
10Alkenes/Alkynes
11Alkene & Alkyne Reactions
- 11.1 Electrophilic attack
- 11.2 Markovnikov hydrohalogenation
- 11.3 Anti-Markovnikov hydrobromination
- 11.4 Hydration of alkene
- 11.5 Hydrosulfonation
- 11.6 Triangle reactions
- 11.7 Oxymercuration/Demercuration with water
- 11.8 Oxymercuration/Demercuration with alcohol
- 11.9 Markovnikov hydration of alkynes
- 11.10 Hydroboration - Anti-Markovnikov hydration
- 11.11 Halogenation
- 11.12 Epoxidation
- 11.13 Anti-hydroxylation
- 11.14 Cyclopropanation
- 11.15 Syn-Addition
- 11.16 Hydrogenation
- 11.17 Syn-hydroxylation
- 11.18 KMnO4 oxidation of alkynes
- 11.19 Further oxidation with KMnO4
- 11.20 Ozonolysis
- 11.21 Polymers
- 11.22 Olefin Metathesis
- 11.23 Acetylide formation
- 11.24 Reactions of acetylides
- 11.25 Reaction summary
- 11.26 Problems
Organic 2 Chapters 12–22
12NMR
13Alcohols
14Alcohol Reactions
15Ethers, Epoxides, Sulfides
16Carbonyl Compounds
17Carbonyl Reactions
18Enolates
19Conjugated Alkenes
- 19.1 Color Theory
- 19.2 MO Diagrams
- 19.3 Conjugation Introduction
- 19.4 1,3-butadiene
- 19.5 UV-Visible Spectroscopy
- 19.6 Allyl Groups
- 19.7 Allyl carbocation, radical, carbanion
- 19.8 Kinetic vs. Thermodynamic reaction of HBr with 1,3-butadiene
- 19.9 Diels-Alder
- 19.10 Reaction Summary
- 19.11 Extra Problems
20Aromatic Compounds
- 20.1 Introduction
- 20.2 Annulenes
- 20.3 Molecular Orbital diagrams of annulenes
- 20.4 Aromatic, antiaromatic, nonaromatic
- 20.5 ID if aromatic, antiaromatic, nonaromatic
- 20.6 Aromatic or antiaromatic reaction intermediates
- 20.7 Heterocyclic Aromatic Rings
- 20.8 Monosubstituted Benzene Derivatives
- 20.9 Disubstituted Benzene Derivatives
- 20.10 Polyaromatic Hydrocarbons (PAHs)
- 20.11 Allotropes of carbon
- 20.12 Phenyl spectroscopy
- 20.13 Extra Problems
21Aromatic Compound Reactions
- 21.1 Introduction
- 21.2 Electrophilic Aromatic Substitution
- 21.3 Activating Groups
- 21.4 Deactivating Groups
- 21.5 Halide Group
- 21.6 Disubstituted benzenes
- 21.7 Friedel-Crafts
- 21.8 Clemmensen Reduction
- 21.9 Sandmeyer Reaction
- 21.10 Friedel-Crafts on Aniline
- 21.11 Nucleophilic Aromatic Substitutions
- 21.12 Gilman Reagents
- 21.13 Addition Reactions
- 21.14 Birch Reduction
- 21.15 Oxidation of alkyl benzenes
- 21.16 Halogenation of side chains
- 21.17 Oxidation of phenols
- 21.18 Reaction Summary
- 21.19 Problems