EE-Learning
Free radical reactions
Catogry:
Science & Engineering
Subject:
Organic Chemistry
Course:
Substitution And Elimination Reactions
Lecture List
Elimination vs substitution: tertiary substrate
Elimination vs substitution: secondary substrate
Elimination vs substitution: primary substrate
Elimination vs substitution: reagent
Regioselectivity, stereoselectivity, and stereospecificity
E2 elimination: Substituted cyclohexanes
E2 elimination: Stereospecificity
E2 elimination: Stereoselectivity
E2 mechanism: regioselectivity
E2 mechanism: kinetics and substrate
E1 mechanism: carbocations and rearrangements
E1 mechanism: stereoselectivity
E1 elimination: regioselectivity
E1 mechanism: kinetics and substrate
Sn1 vs Sn2: Summary
Sn1 vs Sn2: Solvent effects
Sn1 and Sn2: leaving group
Sn2 mechanism: stereospecificity
Sn2 mechanism: kinetics and substrate
Sn1 carbocation rearrangement (advanced)
Sn1 mechanism: carbocation rearrangement
Carbocation rearrangement practice
Carbocation stability and rearrangement introduction
Sn1 mechanism: stereochemistry
Sn1 mechanism: kinetics and substrate
Alkyl halide nomenclature and classification
Intro to organic mechanisms
Curly arrow conventions in organic chemistry
Identifying nucleophilic and electrophilic centers
E2 E1 Sn2 Sn1 reactions example 3
E2 E1 Sn2 Sn1 reactions example 2
Comparing E2, E1, Sn2, Sn1 reactions
Zaitsev's rule
E1 reactions
E2 reactions
Nucleophilicity vs. basicity
Nucleophilicity (nucleophile strength)
Free radical reactions