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

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