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Alkene to Halide (Markovnikov)
Hydrogen Halides

2 Alkenes to 2 Halides

Alkene to Halide (Antiarkovnikov)
Free-radical addition of hydrogen bromide to alkenes

Alkene to 2 halogens

Alkane to Halogen

Alcohol to Halogen
SN1 + SN2

Alcohol to Halide
SN2

Ether to (Halide) + (Alcohol)
SN1

Ether to (Halide) + (Halide)
SN2

Alcohol to Ether
Ethers can also be synthesized via SN2 reactions or acid-catalyzed addition of alcohols to alkenes

Alkene to Alcohol (Markovnikov - Shifts)
Acid-Catalysed Hydration, alkyl + hydride shifts can occur

Alkene to Alcohol (Antimarkovnikov)
Hydroboration-Oxidation

Alkene to Alcohol (Markovnikov - no shifts)
Oxymercuration-reduction, no shifts occur

Epoxide to Alcohol
Organometallic Reagents

Halogen to MgX
Organometallic Reagent

Halogen to Li
Organometallic Reagent

Addition of carbons
Organometallic Reagent

Li to CuLi
Organometallic Reagent

Alkene to Epoxide

Halohydrin (Halogen + OH) to Epoxide
Williamson Ether Synthesis

Epoxide to alcohol + ether
Ring-opening under basic + acidic conditions

Alcohol to Sulfonate Ethers

Alcohol to Halohydrins (OH + X)

Alkene to Alkane
Hydrogenation

Alkyne to Alkane

Alkyne to Alkyne + R group

Alkene to Cyclopropane + 2 X

Alkene to Cyclopropane

Alkene to Ketone/Aldehyde
Ozonolysis

Alkyne to Carbonyl (Markovnikov)
Acid-Catalysed Hydration

Alkyne to Carbonyl (Antimarkovnikov)