Oxidation Reactions and Reactants
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What is the reactant?
What is the mechanism?
HBr —>
SN2
What is the reactant?
What is the mechanism?
HCl —>
SN1
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16 Terms
What is the reactant?
What is the mechanism?
HBr —>
SN2
What is the reactant?
What is the mechanism?
HCl —>
SN1
What is the reactant?
What is the mechanism?
(Works well with tertiary carbons)
HBr —>
SN1
What is the reactant?
(Works well with primary and secondary carbons)
Inversion!!!
PBr3 —> CH2Cl2
What is the reactant?
(Works well with primary and secondary carbons)
Inversion!!!
SOCl2 —> pyridine
What is the reactant?
H3PO4 —> heat
What is the reactant?
Removes OH and converts the other OH to double bonded O
H2SO4 —> H2O
What is the reactant?
H2CrO4 —> H2O, Acetone
What is the reactant?
H2CrO4 —> Acetone
What is the reactant?
PCC —> CH2Cl2
What reactants can be used to oxidize secondary alcohols into ketones?
H2CrO4 —> Acetone
PCC —> CH2Cl2
1) COCl2, DMSO —> 2) Et3N
What is the reactant?
1) (COCl)2, DMSO —> 2) Et3N
What is the reactant?
HIO4 —>
What is the reactant?
TsCl —> pyridine
Oxidizing secondary alcohols into ketones and primary alcohols into carboxylic acids (2):
K2Cr2O7 —> H2SO4 H2O
CrO3 —> H2SO4 H2O
Reduces aldehydes into primary alcohols and ketones into secondary alcohols
NaBH4 —> CH3OH