Organic Chemistry

Includes reactions for alkenes, alkynes and alcohols, SN1/SN2/E1/E2 reactions, table of strong/weak nucleophiles and strong/weak bases, conditions for each type of substitution/elimination reaction to occur, how to form hoffman/zeitseff product, Radical reactions, R/S configurations and chair conformations.

Basics for organic chemistry

Organic Chemsitry Post Lab Elimination Reaction

Most notes are types and structure drawn with chemdraw, some mechanism, and quite cheat sheet are shown in neat handwriting produced on ipad. Most reactions show detailed step-wise mechanism (with electron transfer arrows) Material covered are as shown below Carbonyl rearrangements: Schmidt, Beckmann, Curtius, Wolff Enols and Enolates: ketone deuteration, alpha-halogenations, alpha-alkylations, enamine alkylations, decarboxylation Aldol Reaction: general, condensation, Cross Aldol condensation, ...

Most notes are types and structure drawn with chemdraw, some mechanism, and quite cheat sheet are shown in neat handwriting produced on ipad. Most reactions show detailed step-wise mechanism (with electron transfer arrows) Material covered are as shown below Carbonyl: reversible addition, acetal synthesis(anomeric effect), acetal and hemiacetals Protecting group(PG): carbonyl PG, alcohol PG Imines/Enamines(reversible carbonyl addition), organometallics (irreversible carbonyl addition) Alcohol ox...

Most notes are types and structure drawn with chemdraw, some mechanism, and quite cheat sheet are shown in neat handwriting produced on ipad. Most reactions show detailed step-wise mechanism (with electron transfer arrows) Material covered are as shown below Aromaticity: Aromatic, non-aromatic, anti-aromatic Benzylic reactivity: SN1, SN2, Bromination (radical), Chemoselective oxidation Electrophilic aromatic substitution (EAS): halogenation, other activating agents, Friedel-Crafts Rearrangement ...