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

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