exam 2 reagents

SN1
weak Nu (solvent)
SN2
strong base/Nu
E1
weak base
E2
strong base/bulky base
Reduction of Aldehyde
NaBH4/MeOH or LAH/H3O+
Reduction of Ketone
NaBH4/MeOH or LAH/H3O+
Reduction of Carboxylic acids and derivatives
LAH/ H3O+
oxidation of 1. alcohol ending in aldehyde
PCC
oxidation of 2. alcohol ends in ketone
PCC or CrO3
oxidation of 1. alcohol ends in carboxylic acid
CrO3 or KMnO4
t-butyl ether synthesis
isobutylene gas and acid catalyst
E1/dehydration
H2SO4 or H3PO4
ether clevage of ether
HBr or HI (conc)
ether clevage of t-butyl ether
CF3CO2H
synthesis of alkyl bromides
PBr3
synthesis of alkyl chlorides
SOCl2
Synthesis of tosylates
tosylates
hemiacetals/acetals formation
alcohol, H+
imine formation
primary amine, H+
synthesis of amines
H2 and Pd/C or NaBH4
Alcohol synthesis via grignard
a.R-Mg-Br
b. H3O+
formation of acid chloride
SOCl2
formation of anhydride
carboxylate anion
esterification
acid catalyst
formation of amide
hydrolysis
hydrolysis of ester
H20
synthesis of alchohols (ester end)
Alcohol
synthesis of alchohols (amide end)
Amine
Hydrolysis of amide
acid or base
reduction of amide
LAH/H3O+
SN2 of nitriles
NaCN
Hydrolysis of nitriles
acid or base
reduction of nitriles
LAH, H3O+