Organic Chemistry Reagents

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Can you name the reagents?

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

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