Organic Chemistry Chapter 14,17,18

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

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