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

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