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

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