Online courses directory (381)
Watch fun, educational videos on all sorts of Materials, how they're created and what they can do. Whats all the matter? Atoms and Molecules. What is Soap?. Flocculation: Making Clean Water. Manufacturing Processes: Hands On to Hands Off. Whats all the matter? Atoms and Molecules. What is Soap?. Flocculation: Making Clean Water. Manufacturing Processes: Hands On to Hands Off.
Everything in the universe can be measured. Under Pressure. Earth's Tilt 1: The Reason for the Seasons. Earth's Tilt 2: Land of the Midnight Sun. 2D Equilibrium -- Balancing Games. Under Pressure. Earth's Tilt 1: The Reason for the Seasons. Earth's Tilt 2: Land of the Midnight Sun. 2D Equilibrium -- Balancing Games.
Watch fun, educational videos on all sorts of Physics questions. Bridge Design and Destruction! (part 1). Bridge Design (and Destruction!) Part 2. Shifts in Equilibrium. The Marangoni Effect: How to make a soap propelled boat!. The Invention of the Battery. The Forces on an Airplane. Bouncing Droplets: Superhydrophobic and Superhydrophilic Surfaces. A Crash Course on Indoor Flying Robots.
Watch fun, educational videos on all sorts of Physics questions. Thomas Young's Double Slit Experiment. Newton's Prism Experiment. Bridge Design and Destruction! (part 1). Bridge Design (and Destruction!) Part 2. Shifts in Equilibrium. The Marangoni Effect: How to make a soap propelled boat!. The Invention of the Battery. The Forces on an Airplane. Bouncing Droplets: Superhydrophobic and Superhydrophilic Surfaces. A Crash Course on Indoor Flying Robots. Heat Transfer. Thomas Young's Double Slit Experiment. Newton's Prism Experiment. Bridge Design and Destruction! (part 1). Bridge Design (and Destruction!) Part 2. Shifts in Equilibrium. The Marangoni Effect: How to make a soap propelled boat!. The Invention of the Battery. The Forces on an Airplane. Bouncing Droplets: Superhydrophobic and Superhydrophilic Surfaces. A Crash Course on Indoor Flying Robots. Heat Transfer.
Topics covered in college organic chemistry course. Basic understanding of basic high school or college chemistry assumed. Representing Structures of Organic Molecules. Naming Simple Alkanes. Naming Alkanes with Alkyl Groups. Correction - 2-Propylheptane should never be the name!. Common and Systematic Naming-Iso, Sec and Tert Prefixes. Organic Chemistry Naming Examples 1. Organic Chemistry Naming Examples 2. Organic Chemistry Naming Examples 3. Organic Chemistry Naming Examples 4. Organic Chemistry Naming Examples 5. Naming Alkenes Examples. Naming Alkyl Halides. sp3 Hybridized Orbitals and Sigma Bonds. Pi bonds and sp2 Hybridized Orbitals. Newman Projections. Newman Projections 2. Chair and Boat Shapes for Cyclohexane. Double Newman Diagram for Methcyclohexane. Introduction to Chirality. Chiral Examples 1. Chiral Examples 2. Cahn-Ingold-Prelog System for Naming Enantiomers. R,S (Cahn-Ingold-Prelog) Naming System Example 2. Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds. Cis-Trans and E-Z Naming Scheme for Alkenes. Entgegen-Zusammen Naming Scheme for Alkenes Examples. Introduction to Reaction Mechanisms. Markovnikov's Rule and Carbocations. Addition of Water (Acid-Catalyzed) Mechanism. Polymerization of Alkenes with Acid. Sn2 Reactions. Sn1 Reactions. Steric Hindrance. Sn2 Stereochemistry. Solvent Effects on Sn1 and Sn2 Reactions. Nucleophilicity (Nucleophile Strength). Nucleophilicity vs. Basicity. E2 Reactions. E1 Reactions. Zaitsev's Rule. Comparing E2 E1 Sn2 Sn1 Reactions. E2 E1 Sn2 Sn1 Reactions Example 2. E2 E1 Sn2 Sn1 Reactions Example 3. Free Radical Reactions. Alcohols. Alcohol Properties. Resonance. Ether Naming and Introduction. Cyclic ethers and epoxide naming. Ring-opening Sn2 reaction of expoxides. Sn1 and Sn2 epoxide opening discussion. Aromatic Compounds and Huckel's Rule. Naming Benzene Derivatives Introduction. Electrophilic Aromatic Substitution. Bromination of Benzene. Amine Naming Introduction. Amine Naming 2. Amine as Nucleophile in Sn2 Reaction. Amine in Sn2 part 2. Sn1 Amine Reaction. Aldehyde Introduction. Ketone Naming. Friedel Crafts Acylation. Friedel Crafts Acylation Addendum. Keto Enol Tautomerization. Carboxlic Acid Introduction. Carboxylic Acid Naming. Fisher Esterification. Acid Chloride Formation. Amides, Anhydrides, Esters and Acyl Chlorides. Relative Stability of Amides Esters Anhydrides and Acyl Chlorides. Amide Formation from Acyl Chloride. Aldol Reaction.
alcohols, ethers, epoxides, thiols, sulfides. Alcohols. Alcohol Properties. alcohol nomenclature. physical properties of alcohols and preparation of alkoxides. preparation of alcohols using NaBH4. preparation of alcohols using LiAlH4. synthesis of alcohols using grignard reagents I. synthesis of alcohols using grignard reagents II. oxidation of alcohols I: mechanism and oxidation states. oxidation of alcohols II: examples. biological redox reactions. formation of nitrate esters. preparation of alkyl halides from alcohols. Ether Naming and Introduction. Ether nomenclature. Properties of ethers and crown ethers. williamson ether synthesis. acidic cleavage of ethers. Cyclic ethers and epoxide naming. nomenclature and preparation of epoxides. preparation of epoxides: stereochemistry. Ring-opening Sn2 reaction of expoxides. Sn1 and Sn2 epoxide opening discussion. ring-opening reactions of epoxides: strong nucleophiles. ring opening reactions of epoxides: acid-catalyzed. preparation of sulfides. Alcohols. Alcohol Properties. alcohol nomenclature. physical properties of alcohols and preparation of alkoxides. preparation of alcohols using NaBH4. preparation of alcohols using LiAlH4. synthesis of alcohols using grignard reagents I. synthesis of alcohols using grignard reagents II. oxidation of alcohols I: mechanism and oxidation states. oxidation of alcohols II: examples. biological redox reactions. formation of nitrate esters. preparation of alkyl halides from alcohols. Ether Naming and Introduction. Ether nomenclature. Properties of ethers and crown ethers. williamson ether synthesis. acidic cleavage of ethers. Cyclic ethers and epoxide naming. nomenclature and preparation of epoxides. preparation of epoxides: stereochemistry. Ring-opening Sn2 reaction of expoxides. Sn1 and Sn2 epoxide opening discussion. ring-opening reactions of epoxides: strong nucleophiles. ring opening reactions of epoxides: acid-catalyzed. preparation of sulfides.
naming alkanes and cycloalkanes, conformations of alkanes and cycloalkanes, and free radical reactions. Representing Structures of Organic Molecules. Naming Simple Alkanes. Naming Alkanes with Alkyl Groups. Correction - 2-Propylheptane should never be the name!. Common and Systematic Naming-Iso, Sec and Tert Prefixes. Organic Chemistry Naming Examples 1. Organic Chemistry Naming Examples 2. Organic Chemistry Naming Examples 3. Organic Chemistry Naming Examples 4. Organic Chemistry Naming Examples 5. Newman Projections. Newman Projections 2. Chair and Boat Shapes for Cyclohexane. Double Newman Diagram for Methcyclohexane. alkane and cycloalkane nomenclature I. alkane and cycloalkane nomenclature II. alkane and cycloalkane nomenclature III. bicyclic compounds. naming cubane. conformations of ethane and propane. conformations of butane. conformations of cyclohexane I: chair and boat. conformations of cyclohexane II: monosubstituted. conformations of cyclohexane III: disubstituted. conformations of cyclohexane IV: trisubstituted. Free Radical Reactions. Representing Structures of Organic Molecules. Naming Simple Alkanes. Naming Alkanes with Alkyl Groups. Correction - 2-Propylheptane should never be the name!. Common and Systematic Naming-Iso, Sec and Tert Prefixes. Organic Chemistry Naming Examples 1. Organic Chemistry Naming Examples 2. Organic Chemistry Naming Examples 3. Organic Chemistry Naming Examples 4. Organic Chemistry Naming Examples 5. Newman Projections. Newman Projections 2. Chair and Boat Shapes for Cyclohexane. Double Newman Diagram for Methcyclohexane. alkane and cycloalkane nomenclature I. alkane and cycloalkane nomenclature II. alkane and cycloalkane nomenclature III. bicyclic compounds. naming cubane. conformations of ethane and propane. conformations of butane. conformations of cyclohexane I: chair and boat. conformations of cyclohexane II: monosubstituted. conformations of cyclohexane III: disubstituted. conformations of cyclohexane IV: trisubstituted. Free Radical Reactions.
naming alkenes and alkynes, reactions of alkenes and alkynes, synthesis. Naming Alkenes Examples. Cis-Trans and E-Z Naming Scheme for Alkenes. Entgegen-Zusammen Naming Scheme for Alkenes Examples. Introduction to Reaction Mechanisms. Markovnikov's Rule and Carbocations. Addition of Water (Acid-Catalyzed) Mechanism. Polymerization of Alkenes with Acid. Alkene intro and stability. Alkene nomenclature. cis/trans and the E/Z system. hydrogenation. hydrohalogenation. hydration. halogenation. halohydrin formation. hydroboration-oxidation. epoxide formation and anti dihydroxylation. syn dihydroxylation. Ozonolysis. alkyne nomenclature. alkyne acidity and alkylation. preparation of alkynes. reduction of alkynes. hydrohalogenation of alkynes. hydration of alkynes. hydroboration-oxidation of alkynes. halogenation and ozonolysis of alkynes. synthesis using alkynes. Naming Alkenes Examples. Cis-Trans and E-Z Naming Scheme for Alkenes. Entgegen-Zusammen Naming Scheme for Alkenes Examples. Introduction to Reaction Mechanisms. Markovnikov's Rule and Carbocations. Addition of Water (Acid-Catalyzed) Mechanism. Polymerization of Alkenes with Acid. Alkene intro and stability. Alkene nomenclature. cis/trans and the E/Z system. hydrogenation. hydrohalogenation. hydration. halogenation. halohydrin formation. hydroboration-oxidation. epoxide formation and anti dihydroxylation. syn dihydroxylation. Ozonolysis. alkyne nomenclature. alkyne acidity and alkylation. preparation of alkynes. reduction of alkynes. hydrohalogenation of alkynes. hydration of alkynes. hydroboration-oxidation of alkynes. halogenation and ozonolysis of alkynes. synthesis using alkynes.
aromatic compounds, naming derivatives of benzene, electrophilic aromatic substitution reactions. Naming Benzene Derivatives Introduction. naming benzene derivatives. Aromatic Compounds and Huckel's Rule. Aromatic Stability I. aromatic stability II. aromatic stability III. aromatic stability IV. aromatic stability V. Aromatic Heterocycles I. Aromatic Heterocycles II. Resonance. Electrophilic Aromatic Substitution. Bromination of Benzene. Friedel Crafts Acylation. Friedel Crafts Acylation Addendum. Electrophilic Aromatic Substitution Mechanism. Halogenation. Nitration. Sulfonation. Friedel-Crafts Alkylation. Friedel-Crafts Acylation. Ortho-Para Directors I. Ortho-Para Directors II. Ortho-Para Directors III. Meta Directors I. Meta Directors II. Multiple Substituents. Birch Reduction I. Birch Reduction II. Reactions at the Benzylic Position. Synthesis of Substituted Benzene Rings I. Synthesis of Substituted Benzene Rings II. Nucleophilic Aromatic Substitution I. Nucleophilic Aromatic Substitution II. Naming Benzene Derivatives Introduction. naming benzene derivatives. Aromatic Compounds and Huckel's Rule. Aromatic Stability I. aromatic stability II. aromatic stability III. aromatic stability IV. aromatic stability V. Aromatic Heterocycles I. Aromatic Heterocycles II. Resonance. Electrophilic Aromatic Substitution. Bromination of Benzene. Friedel Crafts Acylation. Friedel Crafts Acylation Addendum. Electrophilic Aromatic Substitution Mechanism. Halogenation. Nitration. Sulfonation. Friedel-Crafts Alkylation. Friedel-Crafts Acylation. Ortho-Para Directors I. Ortho-Para Directors II. Ortho-Para Directors III. Meta Directors I. Meta Directors II. Multiple Substituents. Birch Reduction I. Birch Reduction II. Reactions at the Benzylic Position. Synthesis of Substituted Benzene Rings I. Synthesis of Substituted Benzene Rings II. Nucleophilic Aromatic Substitution I. Nucleophilic Aromatic Substitution II.
naming carboxylic acids, formation of carboxylic acid derivatives. Carboxlic Acid Introduction. Carboxylic Acid Naming. Fisher Esterification. Acid Chloride Formation. Amides, Anhydrides, Esters and Acyl Chlorides. Relative Stability of Amides Esters Anhydrides and Acyl Chlorides. Amide Formation from Acyl Chloride. Carboxlic Acid Introduction. Carboxylic Acid Naming. Fisher Esterification. Acid Chloride Formation. Amides, Anhydrides, Esters and Acyl Chlorides. Relative Stability of Amides Esters Anhydrides and Acyl Chlorides. Amide Formation from Acyl Chloride.
conjugation, conjugated dienes, addition reactions of conjugated dienes, diels-alder reaction, MO theory, color. addition reaction of conjugated dienes I: mechanism. addition reaction of conjugated dienes II: example. addition reaction of conjugated dienes III: control. diels-alder I: mechanism. diels-alder II: endo vs exo. diels-alder III: stereochemistry of dienophile. diels-alder IV: stereochemistry of diene. diels-alder V: regiochemistry. diels-alder VI: more regiochemistry. diels-alder VII: intramolecular. intro to molecular orbital (MO) theory. MO theory for butadiene. MO theory for Diels-Alder. intro to color theory. conjugation and color. color in organic molecules. addition reaction of conjugated dienes I: mechanism. addition reaction of conjugated dienes II: example. addition reaction of conjugated dienes III: control. diels-alder I: mechanism. diels-alder II: endo vs exo. diels-alder III: stereochemistry of dienophile. diels-alder IV: stereochemistry of diene. diels-alder V: regiochemistry. diels-alder VI: more regiochemistry. diels-alder VII: intramolecular. intro to molecular orbital (MO) theory. MO theory for butadiene. MO theory for Diels-Alder. intro to color theory. conjugation and color. color in organic molecules.
A review of hybrid orbitals, dot structures, electronegativity, and polarity. sp3 Hybridized Orbitals and Sigma Bonds. Pi bonds and sp2 Hybridized Orbitals. dot structures I: single bonds. dot structures II: multiple bonds. sp3 hybrid orbitals. tetrahedral bond angle proof. sp2 hybrid orbitals. sp hybrid orbitals. more hybridization. electronegativity. electronegativity and intermolecular forces. sp3 Hybridized Orbitals and Sigma Bonds. Pi bonds and sp2 Hybridized Orbitals. dot structures I: single bonds. dot structures II: multiple bonds. sp3 hybrid orbitals. tetrahedral bond angle proof. sp2 hybrid orbitals. sp hybrid orbitals. more hybridization. electronegativity. electronegativity and intermolecular forces.
bond-line structures, functional groups, formal charges, resonance structures, oxidation and reduction, acid/base chemistry. bond-line structures. 3-D bond-line structures. structural (constitutional) isomers. functional groups I. functional groups II. formal charge I. formal charge II. resonance structures I. resonance structures II. resonance structures III. oxidation states I. oxidation states II. Acid/Base Definitions. Ka and pKa Derivation. Stabilization of Conjugate Base I. Stabilization of Conjugate Base II. Stabilization of Conjugate Base III. Stabilization of Conjugate Base IV. bond-line structures. 3-D bond-line structures. structural (constitutional) isomers. functional groups I. functional groups II. formal charge I. formal charge II. resonance structures I. resonance structures II. resonance structures III. oxidation states I. oxidation states II. Acid/Base Definitions. Ka and pKa Derivation. Stabilization of Conjugate Base I. Stabilization of Conjugate Base II. Stabilization of Conjugate Base III. Stabilization of Conjugate Base IV.
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