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

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