Hydrocarbons
40 lessons, pages 1986–2025.
- Hydrocarbon Families and Formulas — Classifying alkanes, alkenes, alkynes and arenes
- Alkane Structure and Sigma Bonds — Tetrahedral carbon and saturated carbon frameworks
- Naming Branched Alkanes — Selecting the parent chain and numbering substituents
- Constitutional Isomers of Alkanes — Different carbon connectivity at one molecular formula
- Physical Properties of Alkanes — Intermolecular forces, boiling points and solubility
- Sources and Preparation of Alkanes — Petroleum fractions and laboratory reduction routes
- Alkane Combustion — Complete and incomplete oxidation of hydrocarbons
- Free-Radical Halogenation of Alkanes — Initiation, propagation and termination in substitution
- Ethane Conformations — Staggered and eclipsed arrangements about a C–C bond
- Butane Conformations — Anti, gauche and eclipsed Newman projections
- Cycloalkane Rings and Strain — Bond-angle and torsional effects in small rings
- Cyclohexane Chair Conformation — Axial and equatorial bonds and ring flipping
- Alkene Structure and Pi Bonding — Planar double-bond carbons and restricted rotation
- Alkene Nomenclature and Position Isomers — Locating the carbon-carbon double bond in a parent chain
- Geometric Isomerism of Alkenes — Different substituent arrangements across a double bond
- Alkene Stability and Substitution — Comparing substituted double bonds and heat of hydrogenation
- Preparation of Alkenes — Elimination routes and reaction conditions
- Electrophilic Addition to Alkenes — Pi-electron attack and bond formation across a double bond
- Hydrogen Halide Addition to Alkenes — Regioselectivity and carbocation pathway
- Markovnikov Orientation — Predicting products from unsymmetrical alkene addition
- Peroxide Effect in HBr Addition — Radical-chain anti-Markovnikov addition under suitable conditions
- Alkene Hydration and Alcohol Formation — Acid-catalyzed addition of water and product orientation
- Alkene Halogenation and Halohydrins — Addition of halogen and halogen-water reagents
- Alkene Hydrogenation and Oxidation — Reduction to alkanes and selected oxidative transformations
- Alkene Polymerization — Addition polymer formation from double-bond monomers
- Alkyne Structure and Nomenclature — Linear triple-bond carbons and locating the bond
- Preparation of Alkynes — Double elimination and carbon-carbon bond formation routes
- Acidity of Terminal Alkynes — Acetylide formation and carbon hybridization
- Addition Reactions of Alkynes — Stepwise reactions across a carbon-carbon triple bond
- Hydration and Reduction of Alkynes — Carbonyl formation and selective hydrogenation
- Benzene Structure and Aromaticity — Cyclic conjugation and delocalized pi electrons
- Huckel Rule and Aromatic Systems — Four-n-plus-two pi electron criterion and its conditions
- Aromatic Stabilization and Benzene Reactivity — Why substitution is favored over ordinary addition
- Electrophilic Aromatic Substitution — Electrophile attack, sigma complex and aromaticity restoration
- Nitration and Halogenation of Benzene — Electrophile generation and aromatic substitution products
- Sulfonation and Friedel-Crafts Reactions — Introducing sulfonyl, alkyl and acyl groups to benzene
- Directing Effects in Aromatic Substitution — Ortho, meta and para orientation from existing substituents
- Activating and Deactivating Aromatic Groups — Electron donation, withdrawal and reaction rate
- Aromatic Hydrocarbons and Side-Chain Reactions — Toluene, fused rings and benzylic transformations
- Hydrocarbons Review and Synthesis — Connecting structure, naming, mechanisms and reactivity