Can you name the reagents?

created by Chef_BoyAndy
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  • Chapters 8, 9, 10, 11
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ProcessReagentExtra Info
AlkylationAttachment of an R group to a terminal alkyne
Alkene addition of OH groupMarkovnikov, allows carbocation rearrangement
Alkyne into Aldehyde
Hydrohalogenationanti-Markovnikov
Replace a OH with a ClPrimary and Secondary
Secondary Alcohol into a Ketone
Alkene Dihydroxylationsyn addition
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Multiple Oxygen atoms involved. Leaves other pi bonds alone.
EliminationZaitsev
Reduction of a Ketone/AldehydeDoes not reduce carboxylic acid or esters. Leaves other pi bonds alone.
Alkyne into trans-Alkene
Alkyne into Ketone
Alkene Dihydroxylationanti-addition
Alkene Ozonolysis
Primary Alcohol into Carboxylic Acid
HydrohalogenationMarkovnikov, use one equivalent per pi bond that you want broken
Radical Halogenation
Protected Alcohol back to Alcohol
Alkyne Ozonolysis
ProcessReagentExtra Info
Hydrogenation
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Does not leave other pi bonds alone.
Alkene Halohydrin Formationanti-addition
EliminationHofmann
Alcohol into Grignard
Attaching an R group to an Ester
Converts OH into a Good Leaving Group
Replace a OH with a ClPrimary Only
Primary Alcohol into a Aldehyde
Alkene addition of OH groupanti-Markovnikov, syn-addition
Reduction of a Ketone/AldehydeReduces carboxylic acid and esters. Only one Oxygen atom involved. Leaves other pi bonds alone.
Alkene addition of OH groupMarkovnikov, no carbocation rearrangement
Replace a OH with a BrPrimary and Secondary
Name of a protected Alcohol
Alkyne into cis-Alkene
Attaching an R group to a Ketone/Aldehyde
Halogenationanti-addition, use one equivalent per pi bond that you want broken
Elimination into AlkyneExample: X-C-C-X
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Organic Chemistry Reagents Quiz

  1. by Chef_BoyAndy
  • Created Feb 12, 2012 in Science
  • Game Plays 13

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