Organic Chemistry Chapter 14,17,18

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

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