Organic Chemistry Reagents

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Can you name the reagents?

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

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Created Feb 12, 2012ReportNominate
Tags:chemistry, extra, organic, process, reagent