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1.CH3CH2CH2MgBr
2.HCl
Adds whats attached to MgBr group and can create double bonded oxygen from CN.

LiAIH4, -78
PCC
carboxilic acid to aldehyde

PCC
Turns an -OH to a double bonded oxygen

1.LiAIH4, -78
2.H2O
Turns -O into -OH and can remove double bonded oxygens, also can take CN and turn into —NH2

HNO3 & H2SO4
Adds NO2 (EWG, meta)

AlCl3
H2O
Remove Cl from something and adds whats left.

Zn(Hg), HCl, HOAC, heat
Removes double bonded oxygens close to the benzene

Br2, FeBr3 (has to be on benzene)
Adds Br to ring (Br is hallogen its EWG but Ortho,Para)

CH3CHOCl, AlCl3
H2O
Adds the group with the Cl on the end

FeCl3, Cl2
Adds Cl (Cl is halogen is EWG but Ortho, Para)

SOCl2 or PCl5
adds Cl to where OH is.

1.KMnO4, KOH, heat
H3O+
Changes ALL things to carboxilic acids.

H2 Pd/C
removes double bond (alkene) can also reduce NO2 to NH2

Fe, HCl
NaOH
Changes NO2+ to NN+Cl-

Na2Cr2O7, H2SO4, H2O
adds OH onto end of ketone or the other way!

PBr3, Br2
H2O
Adds Br to a carboxilic acid on less sub side

Dilute NaOH (base) in H2O
Takes Hydrogen off and adds NaO

1.NaCN
2.H3O+ dilute
CN will replace Br and then acitify.

H2CrO4
adds double bonded oxygen, turns OH into carboxilic acid

NH3 (2 equiv)
Replaces Br with NH2

1.NaOEt , EtOH
CH3Br
tBuok, tBuOH
CH3CH2Br
adds the Br group between the 2 double bonded oxygens, must use OEt if ends are OEt and then put whatever group you want to add.

1.NaOH , H2O
H3O+
heat
kicks off original group or adds OH

1.LDA
2.C6H5CH2Br
Adds phenol group

Br2, NaOH
adds Br on more sub side (theromodynamic)

1.NaBH4
2.H2O
Turns double bonded oxygen into OH

CH3CH2OH, H3O+
takes off OH end and makes OCH2CH3 end

Br2 H3O+
add Br to more sub side

Br2, NaOH, H2O
Adds Br to less sub side

HOCH2CH2OH, H+ OR HOCH2CH3CH2OH can also be replaced with OS or similar items
Makes ring with double bonded O and connects.

NaOEt, EtOH, heat
closes ring

1.O3, -78
2.DMS
can attach to benzene pi in the middle

NaNO2, H2SO4, H2O, 0 degrees
NH2 to N2

Cu3O, Cu2+, H2O
N2 to OH

NBS, Heat
Adds a Br on less sub with extra carbon.

CN
replaces Br with CN

1.KMnO4, OH, Heat
2.HCl
adds carboxilic acid to the ends.


re do this
re do this

do this
do this
DIBAL
adds OH and H
