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 Epoxide X group, 1 step
Crown Ether that Solvates Potassium
BenzeneReduction
Williamson Ether Synthesis Starts with R-OH. Beware steric hinderance.
Opening an EpoxideSH group
Opening an EpoxideCN group
Thiol to Sulfide
Opening an EpoxideOH group 1 step
BenzeneOH group
BenzeneKetone group
Allylic Alcohol to EpoxideEpoxide on bottom, after orienting correctly
Sulfide to Sulfoxide
BenzeneCH3 group
Adding a R Group to a SulfidePlaces positive charge on Sulfur atom. Great alkylating agent
Opening an EpoxideH group
Opening an EpoxideOH group 2 steps
BenzeneNH2 group
Alkyl Halide to ThiolInversion of configuration
Crown Ether that Solvates Sodium
Question/DefinitionReagentExtra Info
Opening an EpoxideSH group, 1 step
Benzene1,3
BenzeneAldehyde group
Benzene1,2
Alkene addition of RO group Markovnikov, no carbocation rearrangement
Opening an EpoxideR group
Allylic Alcohol to EpoxideEpoxide on top, after orienting correctly
BenzeneEthyne
Alkene to Epoxide
Crown Ether that Solvates Lithium
Disulfide to Thiols
Breaking an Ether
BenzeneOCH3 group
BenzeneCarboxylic acid group
Benzene1,4
Sulfide to Sulfone
Opening an EpoxideRO group 2 steps
Opening an EpoxideRO group 1 step
Thiols to Disulfide

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