Organic Chemistry Reagents

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Can you name the reagents?

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

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