Cannabis Sativa October 12, 2016October 12, 2016 thcscience_admin Basic reaction mechanismsNucleophilic substitutions Unimolecular nucleophilic substitution (SN1) Bimolecular nucleophilic substitution (SN2) Nucleophilic aromatic substitution (SNAr) Nucleophilic internal substitution (SNi) Nucleophilic acyl substitution (SNAcyl) Electrophilic substitutions Electrophilic aromatic substitution (SEAr) Elimination reactions Unimolecular elimination (E1) E1cB-elimination Bimolecular elimination (E2) Ei elimination Addition reactions Electrophilic addition (AE) Nucleophilic addition (AN) Free-radical addition Cycloaddition Oxidative addition Unimolecular reactions Intramolecular reaction Isomerization Photodissociation Lindemann–Hinshelwood mechanism RRKM theory Electron/Proton transfer reactions Redox Harpoon reaction Grotthuss mechanism Marcus theory Inner sphere electron transfer Outer sphere electron transfer Medium effects Solvent effects Cage effect Matrix isolation Related topics Elementary reaction Reaction dynamics Reactive intermediate Radical (chemistry) Molecularity Stereochemistry Catalysis Collision theory Arrow pushing Potential energy surface More O'Ferrall–Jencks plot Chemical kinetics Rate equation Equilibrium constant Rate-determining step Reaction coordinate Energy profile (chemistry) Transition state theory Activation energy Activated complex Arrhenius equation Eyring equation Michaelis–Menten kinetics Diffusion-controlled reaction