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What turns OH into Cl
SOCl3
What makes double bond O and OH
O3 + oxidative (KMNO4 or AcOH + H2O2)
What attaches cl group to cyclic molecule?
AlCl3
H2SO4 or D2SO4 Catalyst
Froms carbocation on benzene ring
NaH
Removes proton usually most acidic C-H bond
Alkene reacts with Br2 and MeOH
MeO on more substituted Br on other side pi bond gone
Br added allylic position
NBS and delta or Br2 and hv
Add OH group to replace alkene
H3o+ and H2o
Add double bond O and just hydrogen
O3 and Sme2
Adds Br to benenze ring
Br3 FeBr3
Remove all pi bonds ever
H2 excess (Rh-pt oxide)
Add OH anti markovnikov
BH3 / NaOH H2O2
Forms epoxides
CF3Co3H
Removes double bonded O
Zn/Hg HCl
what does N2H2 do
Its just lindlars catalyst
Na + Thing
Swap a chloride or good leaving group
Kmno4 + MeOH + h2o + Naoh
pi bond gone, two oh groups on either end
BH with antlers and then NaOH h2o2 and alkyne
Adds a double-bonded O and an H
NaH and alkyne
Makes the 3 lines have a minus at the end and can then attach to Br
Hg (Oac 2) and H3o+ and water
Markovnikov double bonded O with tripple pi bond and then just a carbon on the end
Remove double bonded oxygen
zn/ hg Hcl
How to form a carbon triangle
Carbene (2hcn2
Add methyl group at the end of a tripple bond
NaH (remove proton) MeI add extra line
Benzene ring and at least one branch with kmno4
keeps ring and branch adds double bonded O and OH
Benzene and fuming H2SO4
Adds SO3H to ring
Benzene and X2, Fex3
Adds X to ring
Adds NO2 group to benzene
Use NO2BF4 or HNO3, H2SO4
Turn NO2 on benzene into NH2
H2/pdc, or Sn HCl or H2o naoh
Turn NH2 on benzene into No2
CF3CO3H
Turn NH2 on benzene into N2+
NaONO and HCl
turn N2 into benzene ring
H3PO2
Turn N2+ on benzene ring into either Cn, Cl, or Br
Cux, KI or Nabf4
Remove all bonds in benzene ring
H2 Pt/Rh oxides
OH reacts with NaOH
H goes away negative oxygen is formed and will fuse with br