Can you name the reagents?

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