Science Quiz / Organic Chemistry Reagents

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Can you name the reagents?

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Score 0/37 Timer 20:00
ProcessReagentExtra Info
Alkyne into cis-Alkene
Radical Halogenation
Hydrogenation
Secondary Alcohol into a Ketone
Replace a OH with a ClPrimary Only
Alcohol into Grignard
Alkyne into trans-Alkene
Reduction of a Ketone/AldehydeDoes not reduce carboxylic acid or esters. Leaves other pi bonds alone.
Replace a OH with a ClPrimary and Secondary
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Only one Oxygen atom involved. Leaves other pi bonds alone.
Alkyne into Aldehyde
EliminationHofmann
Alkene Halohydrin Formationanti-addition
Alkyne into Ketone
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Does not leave other pi bonds alone.
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
Replace a OH with a BrPrimary and Secondary
Halogenationanti-addition, use one equivalent per pi bond that you want broken
ProcessReagentExtra Info
Alkene addition of OH groupMarkovnikov, no carbocation rearrangement
Name of a protected Alcohol
Alkyne Ozonolysis
Alkene Dihydroxylationanti-addition
Converts OH into a Good Leaving Group
AlkylationAttachment of an R group to a terminal alkyne
Alkene Ozonolysis
EliminationZaitsev
Protected Alcohol back to Alcohol
Alkene Dihydroxylationsyn addition
Hydrohalogenationanti-Markovnikov
Alkene addition of OH groupanti-Markovnikov, syn-addition
Attaching an R group to an Ester
Primary Alcohol into a Aldehyde
Alkene addition of OH groupMarkovnikov, allows carbocation rearrangement
Primary Alcohol into Carboxylic Acid
Elimination into AlkyneExample: X-C-C-X
Attaching an R group to a Ketone/Aldehyde

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