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

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