Organic Chemistry Reagents

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Can you name the reagents?

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

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