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

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