Organic Chemistry Synthesis Reactions
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8.3. - Anti-Markovnikov Addition of H and OH
8.3. - Anti-Markovnikov Addition of H and OH
8.3. - Anti-Markovnikov Addition of H and OH
8.4. - Anti-Markovnikov Addition of H and Br
8.4. - Anti-Markovnikov Addition of H and Br
8.4. - Anti-Markovnikov Addition of H and Br
8.5. - Markovnikov Addition of H & X
8.5. - Markovnikov Addition of H & X
8.5. - Markovnikov Addition of H & X
8.5. - Markovnikov Addition of H & X
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9.1. - Addition of Br2 to an Alkene (trans)
9.1. - Addition of Br2 to an Alkene (trans)
9.1. - Addition of Br2 to an Alkene (trans)
9.1. - Addition of Br2 to an Alkene (trans)
9.2. - Oxidation of an Alkene to an Epoxide
9.2. - Oxidation of an Alkene to an Epoxide
9.2. - Oxidation of an Alkene to an Epoxide
9.3. - Anti-Markovnikov Epoxide Ring Opening (Basic Conditions)
9.3. - Anti-Markovnikov Epoxide Ring Opening (Basic Conditions)
9.3. - Anti-Markovnikov Epoxide Ring Opening (Basic Conditions)
9.3. - Anti-Markovnikov Epoxide Ring Opening (Basic Conditions)
9.4. Markovnikov Ring Opening (Acidic Conditions)
9.4. Markovnikov Ring Opening (Acidic Conditions)
9.4. Markovnikov Ring Opening (Acidic Conditions)
9.4. Markovnikov Ring Opening (Acidic Conditions)
9.5. - Markovnikov Addition of Br and OR to an Alkene
9.5. - Markovnikov Addition of Br and OR to an Alkene
9.5. - Markovnikov Addition of Br and OR to an Alkene
9.5. - Markovnikov Addition of Br and OR to an Alkene
10.2. - Catalytic Hydrogenation
10.2. - Catalytic Hydrogenation
10.2. - Catalytic Hydrogenation
10.3. - Stereoselective Alkene Reductions
10.3. - Stereoselective Alkene Reductions
10.3. - Stereoselective Alkene Reductions
10.4. - Stereoselective Alkene Reductions
10.4. - Stereoselective Alkene Reductions
10.4. - Stereoselective Alkene Reductions
10.5. - Stereoselective Alkene Reductions
10.5. - Stereoselective Alkene Reductions
10.5. - Stereoselective Alkene Reductions
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10.6. - Oxidation of Primary Alcohol to an Aldehyde
10.6. - Oxidation of Primary Alcohol to an Aldehyde
10.6. - Oxidation of Primary Alcohol to an Aldehyde
10.7. - Oxidation of Secondary Alcohol to Ketone
10.7. - Oxidation of Secondary Alcohol to Ketone
10.7. - Oxidation of Secondary Alcohol to Ketone
10.8. - Oxidation of a Primary Alcohol or Aldehyde to Carboxylic Acid
10.8. - Oxidation of a Primary Alcohol or Aldehyde to Carboxylic Acid
10.8. - Oxidation of a Primary Alcohol or Aldehyde to Carboxylic Acid
10.9. - Syn Addition of 2 OH Groups to a Pi Bond (a cold, dilute KMnO4 solution followed by KOH (aq) can be used in place of the highly toxic OsO4.
10.9. - Syn Addition of 2 OH Groups to a Pi Bond
10.9. - Syn Addition of 2 OH Groups to a Pi Bond
10.10. Cleavage of a C=C bond via Ozonolysis
10.10. Cleavage of a C=C bond via Ozonolysis
10.10. Cleavage of a C=C bond via Ozonolysis
10.12. - Cleavage of a C=C Double Bond using Permanganate
10.12. - Cleavage of a C=C Double Bond using Permanganate
10.12. - Cleavage of a C=C Double Bond using Permanganate
Note 
Flashcards (315)