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This Concept Map, created with IHMC CmapTools, has information related to: CHEM232Fa12, Halogenation of the Carbonyl alpha-Carbon The Michael Reaction, [E2] [Ebeta] & [DE] - Elementary Steps for Elimination The [E2] Elimination Mechanism, Structure-Reactivity Relationships Bond Energy Changes, Conventions & Terms in Writing Chemical Equations Classes of Chemical Transformations, The Elements of Organic Chemistry Atomic Trends and the Periodic Table, Alkylation and Acylation Using Enamine Nucleophiles Halogenation of the Carbonyl alpha-Carbon, The Conformations of Cyclohexane The Cyclohexane Ring-Flip - A Minimum Energy Pathway, The Energy of Atomic Orbitals MO Diagrams, Energy & Orbital Interactions, Pairwise AO Combinations Resulting in Pi MOs The 10 Unique, Pairwise AO Combinations, Nucleophiles and Reactivity Electrophiles and Reactivity, Beyond Pairwise AO Combinations (s/p mixing) Interpreting the MO Diagram of Carbon Monoxide, Aromatic Substitution Pathways Aromatic Substitution: Mechanistic Details & Frontier Orbitals, Nucleophilic Aromatic Substitution Benzyne, Common Mistakes Made in Drawing Resonance Contributors The Significance of Resonance Contributors, The Aldol Addition Reaction Aldol Condensation: Dehydration of the Aldol Addition Product, The Significance of Resonance Contributors Shortcomings of the Lewis Model, Mechanism, pH and Charge: General Considerations [AdN] - An Elementary Step for Addition to Carbonyl Groups, Pairwise AO Combinations Resulting in Sigma MOs Disallowed Pairwise Orbital Combinations, Electrostatics, Electron Density Distributions & Chemical Bonding Orbitals Are Represented as Isosurfaces, Shortcomings of the Lewis Model Electrostatics, Electron Density Distributions & Chemical Bonding
