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H-X
Markovnikov Hydrohalogenation - X goes on more substituted carbon of the alkene

H-X + ROOR
Anti-Markovnikov Hydrohalogenation - X goes on less substituted carbon of the alkene

H2O, H2SO4
Hydration - adds OH and H group

Hg(OAc)2, H2O
NaBH4
Oxymercuration-Demurcuration - adds OH with Hg intermediate

BH3*THF
H2O2, NaOH
Hydroboration-Oxidation (syn speecific) adds H and OH group with BH2 intermediate

H2, Pd(catalyst)
Catalytic Hydrogenation - adds H2 in syn specific addition

X-X (Br2, Cl2)
Halogenation - adds 2 X in anti addition

X-X, H2O
Halohydrin Formation

mCPBA
Epoxidation

mCPBA
H3O+
Anti-Dihydroxylation - adds 2 OH groups in anti

KMnO4 or OsO4
Syn-Dihydroxylation - adds 2 OH groups in syn

O3, DMS
Ozonolysis - separates double bond and puts O on them — creates ketone and aldehyde group
