Organic Chemistry Reagents

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Can you name the reagents?

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

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