. Flashcards
describe SN2 rxns
d
describe SN1 rxns
Describe E2 rxns
describe E1 rxns
internal alkynes from terminal alkynes
describe addition of X2
carbocation stability
none of the cis-product
backside attack
describe addition of X and OH
CL2 or Br2 with H2O
make enantiomers
describe addiiton of H and OH
strong acid with first with the H - attaches to the less substituted carbon
H2O gives OH to the most substituted carbon
descruve addition of BH3
gives oppostie of markovnikovs product
1. BH3 with 2.H2O2, NaOH
Addition of H2 and partial reduction
H2 with a catalysis Pd/c or Pt (PtO2)
partial reduction with quinoline (Lindlar’s catalysis)
explain fomation of epoxides
using mCPBA, H+, H2O
formation of expocises with OsO4 and KMnO4
- same thing with OsO4 and NaHSO3 and H2O