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mechanisms

TermDefinition
H2SO4 or TsOH or H3PO4 (acids) with secondary and tertiary alcohols dehydration elimination through E1
POCl3 and pyridine with secondary or tertiary alcohols dehydration elimination through E2
HX (HBr, HCl) with secondary or tertiary alcohols substitution through SN1
SOCl2 with secondary or teritirary alcohols substitution through SN2
PBr3 and pyridine with secondary or teritirary alcohols substitution through SN2
H2SO4 or TsOH or H3PO4 (acids) with primary alcohols dehydration elimination through E2
POCl3 and pyridine with primary alcohols dehydration elimination through E2
HX (HBr, HCl) with primary alcohols substitution through SN2
SOCl2 with primary alcohols substitution through SN2
PBr3 and pyridine with primary alcohols substitution through SN2
TsOH elimination
H2SO4 elimination
H3PO4 elimination
POCl3 with pyridine elimination
HX (HCl, HBr) substitution
SOCl2 substitution
PBr3 and pyridine substitution
NaNH2 elimination
SH with alkyl halides SN2
OTs SN2 or E2 (bulky base)
BH3 with H2O2 and OH on an alkene -addition of one OH -syn addition -OH on the least subsitutated carbon -produces enantiomers
H2SO4, H3PO4, TsOH (acids) with H20 on an alkene -addition of one OH -syn and anti addition -produces two sets of enantiomers -OH on the most substituated carbon
Br2, Cl2 on an alkene -addition of both alkyl halides -anti addition -produces enantiomers
Br2, Cl2 with H2O on an alkene -addition of one alkyl halide and an OH -enantiomers
NaOH with water on an epoxide adds two OH groups (diol)
HBr, HCl with an epoxide adds alkyl halide and OH group
 

 



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