Organic Chemistry Reagents

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Can you name the reagents?

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

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