Oxymercuration reduction - Samenvattingen en Aantekeningen

Blank mechanism sheet for oxymercuration-reduction

--NO2 + Sn/HCl - Correct Answers>Clemmenson Reduction --NH2 1,2-addition conj double bonds + RMgX or LiAlH4 - Correct Answers>Nucleophiles attack the carbonyl directly. Strong nucleophiles: Gringards, NaBH4, LiAlH4 1. (2) esters CH3--C=O--OEt + NaOR, EtOH 2. H3O+ ketone + (ester) CH3--C=O--OEt + -OR + H3O+ --> - Correct Answers>Claisen Condensation enolate ion of one ester acts as nucleophile attacking another ester 1. NaOR, EtOH 2. H3O+ Anhydride for mixed 1. BH3/TH...

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.

Organic chemistry notes over oxidation and reduction methods for alkenes including ozonolysis. Includes practice problems.