Organic Chemistry Chapter 14,17,18

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

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