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
BenzeneCarboxylic acid group
Opening an EpoxideRO group 2 steps
Sulfide to Sulfone
Disulfide to Thiols
Allylic Alcohol to EpoxideEpoxide on bottom, after orienting correctly
Crown Ether that Solvates Potassium
Opening an Epoxide X group, 1 step
Opening an EpoxideH group
Opening an EpoxideOH group 1 step
Opening an EpoxideSH group
Opening an EpoxideR group
Crown Ether that Solvates Lithium
Opening an EpoxideSH group, 1 step
Thiols to Disulfide
BenzeneNH2 group
BenzeneEthyne
Benzene1,4
Breaking an Ether
Sulfide to Sulfoxide
Question/DefinitionReagentExtra Info
Alkene to Epoxide
Benzene1,2
Benzene1,3
Opening an EpoxideCN group
BenzeneOCH3 group
Alkene addition of RO group Markovnikov, no carbocation rearrangement
Opening an EpoxideRO group 1 step
Crown Ether that Solvates Sodium
BenzeneKetone group
Allylic Alcohol to EpoxideEpoxide on top, after orienting correctly
BenzeneCH3 group
BenzeneReduction
Opening an EpoxideOH group 2 steps
BenzeneOH group
Alkyl Halide to ThiolInversion of configuration
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
Thiol to Sulfide
BenzeneAldehyde group

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