BrainChildren Chemistry
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jeffrey Moore
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3D Views to Represent Conformation
A Carbonyl's Alpha Hydrogens are Acidic: Tautomerization
A Frontier Orbital Analysis (4.7)
A Schematic Representation of LCAO
Acetals and Ketals: jeffrey Moore
Acid-Base Equilibria in Organic Chemistry
Acid-Catalyzed Addition of Water to Alkenes
Activated Alcohols: A Good Leaving Group from a Poor One
Acyl Substitution Followed by Addition
Acyl Substitution: jeffrey Moore
Addition of Br2 to an Alkene
Addition of Br2 to an Alkyne
Addition of HBr to an Alkene: jeffrey Moore
Addition of Nucleophiles to Ketone and Aldehyde Carbonyls
Addition Reactions that Proceed Non-Stereospecifically
Addition to Alkenes by the Radical Chain Mechanism
Aldol Condensation: Dehydration of the Aldol Addition Product
Alkylation and Acylation Using Enamine Nucleophiles
An Example of Carbocation Ring Expansion
Anti and Gauche Conformational States
Aromatic Substituents: Directing and Activating Trends
Aromatic Substitution Pathways
Aromatic Substitution via Diazonium Chemistry
Aromatic Substitution: Mechanistic Details & Frontier Orbitals
Atom Classification Lingo
Atom Connectedness
Atomic Trends and the Periodic Table
Atoms in Molecules are in Motion
Benzyne: jeffrey Moore
Beyond Pairwise AO Combinations (s/p mixing)
Bimolecular Photochemical Reactions
Bond Energy Changes
Bromonium Ion Formation: jeffrey Moore
Calculating Formal Charge: jeffrey Moore
Carbocation Rearrangements in the x [SN1] Pathway
Carbocation Ring Expansion in MarvinSketch
Carbocations: jeffrey Moore
Carbonyl Functional Groups
CHEM 332 Wiki Tour (4)
Chiral vs. Achiral Objects
Chromophore-Chromophore Interactions (5)
Classes of Chemical Transformations
Classification of Stereoisomers
Common Hydrocarbon Fragments
Common Mistakes Made in Drawing Resonance Contributors
Comparing the x [SN1] and x [SN2] Substitution Pathways
Conventions & Terms in Writing Chemical Equations
Curved Arrows and Resonance Contributors
Dan Pink on Autonomy
Dan Pink on Education and Motivation
Dan Pink on Grades
Dan Pink on Mastery
Dan Pink on Rigor
Dan Pink Two Questions
Dan Pink: Mastery as a Motivational Driver
Decarboxylation of beta-Carbonyl Acids
Direct vs. Conjugate Addition
Disallowed Pairwise Orbital Combinations
Drawing Conventions
Electrocyclic Reactions are Stereospecific (8.2)
Electron Configuration and the Origins of the Octet Rule
Electron Donating and Electron Withdrawing Groups
Electron Pairs and Electron Pair Domains
Electronic Transitions in Organic Molecules (4)
Electrophile Additions to Unsymmetrical Alkenes
Electrophiles and Reactivity
Electrophilic Addition to an Alkyne
Electrophilic Aromatic Substitution: jeffrey Moore
Electrophilic Aromatic Substitution: Product Prediction
Electrostatics, Electron Density Distributions & Chemical Bonding
Elements of Symmetry: jeffrey Moore
Elimination Reactions & Alkene Stability
Enolate and Enol Nucleophiles
Enolate Anion Formation Using LDA
Ethane MOs by LCAO (3)
Ethylene MOs by LCAO (4)
Examples of Frontier Orbital Interactions
Examples of the Substitution-Addition Mechanism
Exceptions to the Octet Rule: jeffrey Moore
Excited State Electron Configurations
Exploring the Conformations of Some Cycloalkanes
Factors that Influence Carbonyl Reactivity
Fluorescence and Molecular Probes (6)
FMO Analysis for Electrocyclic Ring Opening (8.3)
FMO Analysis for Electrocyclic Ring-Closing (8.4)
FMO Analysis for the x [1,j] Sigmatropic Reactions (8.6)
FMO Analysis for the x [3,3] Sigmatropic Reactions (8.7)
FMO Theory Only Describes the Initial Stages of a Reaction (4.3)
Force-Activated Electrocyclic Rearrangements (8.8)
Friedel-Crafts Alkylation and Acylation: jeffrey Moore
Frontier Orbital Interactions Are Most Important (4.5)
Frontier Orbitals and Resonance
Frontier Orbitals: Filled
Frontier-Controlled Reactions (4.6)
Functional Groups: jeffrey Moore
Generalized Sigma- and Pi-Type Interactions
Geometry Depends on the Number of Electron Pair Domains
Grignard Reagents and Other Carbon-Based Nucleophiles
Halogenation of the Carbonyl alpha-Carbon
Homolytic Fragmentation: jeffrey Moore
Hybrid Atomic Orbitals: jeffrey Moore
Hydrogen MOs by LCAO (1)
Hydrogenation of Alkenes and Alkynes
Imine and Enamine Formation: jeffrey Moore
Instruction to Atoms
Interconversion of Carboxylic Acid Derivatives
Intermediates in Carbonyl Chemistry & Their Interconversion
Interpreting the MO Diagram of Carbon Monoxide
Intro to Electrocyclic and Sigmatropic Reactions (8.1)
Introduction to Frontier Molecular Orbital Theory (4.2)
LCAO Involving Polarized Bonds (5)
Lewis Structures from Crystallographic Models
Linear Combination of Atomic Orbitals: jeffrey Moore
Mechanism Calculator Example
Mechanism, pH and Charge: General Considerations
Mechanisms of Amide Reduction by LiAlH4
Mechanisms of Ester Formation: pH & Acyl Substitution
Methane MOs by LCAO (2)
Mixed Aldol Reactions
MO Diagrams, Energy & Orbital Interactions
Molecular Models
Molecular Orbitals from Hybrid Atomic Orbitals
Molecular Orbitals of Butadiene (3)
Molecular Structure, Energy & Reactivity
Molmodac Overview (5.1)
Mono and Disubstituted Cyclohexanes
Notation for Sigmatropic Reactions (8.5)
Nucleophile Addition to alpha, beta-Unsaturated Carbonyls
Nucleophiles and Electrophiles: jeffrey Moore
Nucleophiles and Reactivity
Nucleophilic & Electrophilic Sites from MO Diagrams
Nucleophilic Aromatic Substitution: jeffrey Moore
On the Acidity of the Alpha Carbon
On the Importance of Models in Science (4.1)
Orbital Energy Levels and Light Absorption (1)
Orbital Interactions Involving the Excited State
Orbitals Are Represented as Isosurfaces
Other Photoinduced Pericyclic Reactions
P38AM901jsm
Pairwise AO Combinations Resulting in Pi MOs
Pairwise AO Combinations Resulting in Sigma MOs
Pathways for Electrophile Addition to an Alkene
Photoaddition Reactions: jeffrey Moore
Photochemical Reaction Pathways
Photocycloaddition Reactions: jeffrey Moore
Photofragmentation & Photoelimination Reactions
Photoinduced Energy & Electron Transfer Reactions
Photosubstitution Reactions
Pigments and Chromophores in Nature (7)
Polar Bonds Result from Energy Mismatched Atomic Orbitals
POTDs for Cycloaddition Reactions Q7
Practical Guidelines for Generating Resonance Contributors
Practice Curved Arrows and Resonance in MarvinSketch
Radical Combination Results in Termination
Radical Propagation
Reactions at sp3 Carbon: Leaving Group Ability & pKa
Reactivity Trends for Carboxylic Acid Derivatives
Reading Scientific Literature
Recognizing Acids and Bases in Organic Chemistry
Reductive Amination: Mechanism & Examples
Retrosynthetic Analysis: jeffrey Moore
RPMS
Shortcomings of the Lewis Model
Stereochemistry of the x [E2] Pathway
Stereochemistry of the x [SN2] Pathway
Stereoisomers and Addition Reactions
Stereoisomers and the Time Scale of Interconversion
Stereoisomers: jeffrey Moore
Stereospecific Addition of Bromine to an Alkene
Structure-Reactivity Relationships
Structures Having More Than One Stereocenter
Substitution at sp3 Carbon: Examples
Substitution Involving Epoxides
Substitution of the Carbonyl Oxygen in Aldehydes and Ketones
Symmetry and Reactivity
Symmetry, Stereochemistry & Reactivity: An Introduction
Tautomers, Enols and Enamines
The 10 Unique, Pairwise AO Combinations
The Acidity of Terminal Alkynes
The Aldol Addition Reaction: jeffrey Moore
The Building Blocks of Organic Chemistry
The Claisen Condensation: jeffrey Moore
The Conformations of Cycloalkanes
The Conformations of Cyclohexane
The Cyclohexane Ring-Flip
The Eigenvector Table Explained
The Elements of Organic Chemistry
The Eleven Octet Configurations
The Energy of Atomic Orbitals
The Intramolecular Aldol Reaction: jeffrey Moore
The Language of Organic Chemistry
The Mechanism Calculator Tool
The Michael Reaction: jeffrey Moore
The MO Diagram of Carbon Monoxide
The Molecular Orbital Diagram of Fluorine
The MOs of Ethylene
The Proton Transfer Step on a Reaction Coordinate Diagram
The Reaction Coordinate Diagram
The Rules of Resonance
The Significance of Resonance Contributors
The Stereocenter
The Transfer of Energy from Light to Molecule
The Wittig Reaction: jeffrey Moore
The x [E1] Elimination Mechanism
The x [E2] Elimination Mechanism
The x [E2] Pathway in Acyclic Compounds
The x [E2] Pathway in Cyclic Compounds
Tools for Estimating pKa
Transition State Structures: jeffrey Moore
Types of Carbonyl Reactions
Types of Orbital Interactions (4.4)
Typical Acids & Bases Used in Organic Chemistry
VFTD
Wavefunctions Are Additive
WebMO Demonstration
When Will the Less Substituted Alkene Be Favored?
Working with Line-Angle Drawings
x [1,2R]
x [AdN]
x [AE]
x [E2] x [Ebeta] & x [DE]
x [Ebeta] Elementary Step & Mechanisms of Acyl Substitution
x [pt] The Proton Transfer Step
x [SN1] & x [SN2] Structure-Reactivity: The Electrophile
x [SN1] & x [SN2] Structure-Reactivity: The Nucleophile
x [SN2] x [AN] and x [DN]
x 3-Atom Pi Systems (2)