Organic Chemistry Chapter 14,17,18

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Question/DefinitionReagentExtra Info
Opening an EpoxideSH group
Opening an EpoxideCN group
Thiol to Sulfide
Alkene to Epoxide
Opening an EpoxideRO group 1 step
Opening an Epoxide X group, 1 step
BenzeneOCH3 group
Adding a R Group to a SulfidePlaces positive charge on Sulfur atom. Great alkylating agent
Opening an EpoxideR group
Alkene addition of RO group Markovnikov, no carbocation rearrangement
BenzeneCH3 group
Opening an EpoxideSH group, 1 step
BenzeneKetone group
BenzeneAldehyde group
BenzeneOH group
Disulfide to Thiols
Question/DefinitionReagentExtra Info
Alkyl Halide to ThiolInversion of configuration
BenzeneCarboxylic acid group
Williamson Ether Synthesis Starts with R-OH. Beware steric hinderance.
Opening an EpoxideOH group 2 steps
Crown Ether that Solvates Potassium
Sulfide to Sulfoxide
Breaking an Ether
Crown Ether that Solvates Sodium
Allylic Alcohol to EpoxideEpoxide on bottom, after orienting correctly
BenzeneNH2 group
Sulfide to Sulfone
Opening an EpoxideOH group 1 step
Opening an EpoxideRO group 2 steps
Opening an EpoxideH group
Thiols to Disulfide
Allylic Alcohol to EpoxideEpoxide on top, after orienting correctly
Crown Ether that Solvates Lithium

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