Organic Chemistry Chapter 14,17,18

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

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