Organic Chemistry Reagents

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Can you name the reagents?

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

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