Science / Organic Chemistry Reagents

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Can you name the reagents?

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

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