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Section outline

        • Carbon as a building block of life Lesson
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        • Silicon-based life Lesson
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        • sp3 hybridized orbitals and sigma bonds Lesson
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        • Pi bonds and sp2 hybridized orbitals Lesson
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        • Representing structures of organic molecules Lesson
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        • Dot structures I: Single bonds Lesson
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        • Dot structures II: Multiple bonds Lesson
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        • Condensed structures Lesson
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        • Bond-line structures Lesson
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        • Three-dimensional bond-line structures Lesson
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        • Tetrahedral bond angle proof Lesson
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        • Nomenclature of carbon compounds (Including functional groups) Lesson
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        • Naming simple alkanes Lesson
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        • Naming alkanes with alkyl groups Lesson
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        • Correction - 2-propylheptane should never be the name! Lesson
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        • Common and systematic naming: iso-, sec-, and tert- prefixes Lesson
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        • Naming alkanes with ethyl groups Lesson
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        • Alkane with isopropyl group Lesson
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        • Functional groups Lesson
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        • More functional groups Lesson
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        • Identifying functional groups Lesson
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        • Organic chemistry naming examples 2 Lesson
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        • Organic chemistry naming examples 3 Lesson
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        • Naming a cycloalkane Lesson
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        • Naming two isobutyl groups systematically Lesson
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        • Organic chemistry naming examples 4 Lesson
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        • Alkane and cycloalkane nomenclature I Lesson
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        • Alkane and cycloalkane nomenclature II Lesson
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        • Alkane and cycloalkane nomenclature III Lesson
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        • Naming benzene derivatives introduction Lesson
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        • Isomers Lesson
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        • Structural (constitutional) isomers Lesson
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        • Carbocation stability and rearrangements Lesson
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        • Carbocation rearrangement practice Lesson
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        • Identifying nucleophilic and electrophilic centers Lesson
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        • Curly arrow conventions in organic chemistry Lesson
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        • Nucleophilicity (Nucleophile Strength) Lesson
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        • Nucleophilicity vs. Basicity Lesson
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        • Intro to Electronic Effects (& why should I care ?) Lesson
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        • The Inductive Effect Lesson
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        • Inductive effect and stability of intermediates-Part 1 Lesson
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        • Inductive effect and stability of reaction intermediates- Part 2 Lesson
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        • Resonance structure Lesson
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        • Resonance structure patterns Lesson
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        • Resonance structures for benzene and the phenoxide anion Lesson
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        • Common mistakes when drawing resonance structures Lesson
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        • Resonance structures and hybridization Lesson
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        • Quantity of Resonating Structures vs Quality Lesson
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        • Stability due to Resonance Lesson
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        • +R & -R groups in Resonance Lesson
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        • Relative strengths of different -R groups Lesson
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        • Resonance due to Electron Donors in a Benzyl Cation Lesson
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        • Effect of an electron withdrawing group in a benzyl cation Lesson
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        • Stability of a substituted benzyl anion Lesson
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        • Worked ex - Resonance vs Inductive Effects Lesson
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        • Hyperconjugation in a benzyl cation Lesson
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        • Hyperconjugation - Isotopic Effect Lesson
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        • Worked ex - stability due to Hyperconjugation Lesson
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        • Alkene stability Lesson
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        • Heat of hydrogenation vs stability of alkenes Lesson
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        • Worked ex : Resonance vs Hyperconjugation Lesson
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        • Elimination vs substitution: reagent Lesson
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        • Simple and fractional distillations Lesson
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        • Basics of chromatography Lesson
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        • Column chromatography Lesson
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        • Thin layer chromatography (TLC) Lesson
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        • Calculating retention factors for TLC Lesson
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        • Gas chromatography Lesson
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