Organic Chemistry Reagents

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Can you name the reagents?

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ProcessReagentExtra Info
EliminationHofmann
HydrohalogenationMarkovnikov, use one equivalent per pi bond that you want broken
Alkene addition of OH groupMarkovnikov, allows carbocation rearrangement
Alkene addition of OH groupMarkovnikov, no carbocation rearrangement
Alcohol into Grignard
Elimination into AlkyneExample: X-C-C-X
AlkylationAttachment of an R group to a terminal alkyne
Primary Alcohol into Carboxylic Acid
Replace a OH with a BrPrimary and Secondary
Protected Alcohol back to Alcohol
Primary Alcohol into a Aldehyde
Alkyne into Aldehyde
Attaching an R group to a Ketone/Aldehyde
Alkene Ozonolysis
Radical Halogenation
Replace a OH with a ClPrimary and Secondary
Alkene Dihydroxylationanti-addition
Halogenationanti-addition, use one equivalent per pi bond that you want broken
Alkyne into cis-Alkene
ProcessReagentExtra Info
Secondary Alcohol into a Ketone
Converts OH into a Good Leaving Group
Alkene Halohydrin Formationanti-addition
Alkene Dihydroxylationsyn addition
Name of a protected Alcohol
Alkene addition of OH groupanti-Markovnikov, syn-addition
Hydrohalogenationanti-Markovnikov
Alkyne Ozonolysis
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Multiple Oxygen atoms involved. Leaves other pi bonds alone.
EliminationZaitsev
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Does not leave other pi bonds alone.
Alkyne into Ketone
Alkyne into trans-Alkene
Replace a OH with a ClPrimary Only
Reduction of a Ketone/AldehydeDoes not reduce carboxylic acid or esters. Leaves other pi bonds alone.
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Only one Oxygen atom involved. Leaves other pi bonds alone.
Attaching an R group to an Ester
Hydrogenation

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