1/7
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
Grignard: R-X + Mg+
→ R-Mg-X
solvents: THF or Et2O
Organolithium: R-X + 2Li
→ R-Li + Li-X
solvent: hexane or Et2O
RMgX and RLi + Epoxides
this is because RMgX and RLi are good nucleophiles and can allow for nucleophilic ring opening!
They will attack the LESS substituated ring C and cause inversion of that C

Gilman/ Li Diorganocopper: 2R-Li + CuI
→ R2CuLi + Li
reagants: Et2O or THF
organohalogens and Gilmans: R2CuLi + R’-X
→ R-R’ + RCu + LiX

dichlorocarbene
:CCl2
dichlorocarbene to alkenes
solvents: CH3Cl and Ko-t-Bu

Simmons Smith
alkene + CH2I2 —ZnCu and Et2O → opening alkene
