Organic Chemistry Chapter 14,17,18

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Can you name the Organic Chemistry Chapter 14?

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Question/DefinitionReagentExtra Info
BenzeneOH group
Benzene1,4
Opening an EpoxideCN group
BenzeneCarboxylic acid group
Alkene addition of RO group Markovnikov, no carbocation rearrangement
Sulfide to Sulfoxide
Opening an EpoxideSH group
BenzeneNH2 group
Disulfide to Thiols
BenzeneKetone group
Benzene1,3
Allylic Alcohol to EpoxideEpoxide on bottom, after orienting correctly
Opening an EpoxideOH group 2 steps
BenzeneAldehyde group
Adding a R Group to a SulfidePlaces positive charge on Sulfur atom. Great alkylating agent
BenzeneEthyne
Opening an EpoxideSH group, 1 step
Opening an EpoxideRO group 1 step
BenzeneReduction
Question/DefinitionReagentExtra Info
BenzeneCH3 group
Crown Ether that Solvates Lithium
Opening an EpoxideH group
Opening an EpoxideOH group 1 step
Alkene to Epoxide
Crown Ether that Solvates Sodium
Thiols to Disulfide
Williamson Ether Synthesis Starts with R-OH. Beware steric hinderance.
Opening an EpoxideR group
Allylic Alcohol to EpoxideEpoxide on top, after orienting correctly
Crown Ether that Solvates Potassium
Sulfide to Sulfone
BenzeneOCH3 group
Breaking an Ether
Opening an Epoxide X group, 1 step
Opening an EpoxideRO group 2 steps
Thiol to Sulfide
Benzene1,2
Alkyl Halide to ThiolInversion of configuration

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