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Reductions

  1. 1. LAH 2.H3O+ and Ketone
    C=O turns to C-OH
  2. 1. LAH 2.H3O+ and Carboxylic acid
    primary alcohol
  3. 1. LAH 2.H3O+ and Acid Halide
    primary alcohol
  4. 1. LAH 2. H3O+ and Ester
    two alcohols based off of R groups
  5. 1. LAH 2. H3O+ and Amide
    turns C=O to C-H2
  6. 1. LAH 2. H3O+ and Nitrile
    primary amine (NH2)
  7. 1. LAH 2. H3O+ and Anhydride
    2 R-OH depending on R groups
  8. 1. NaBH4 2. H3O+ and Ketone
    Turns C=O to C-OH
  9. 1. NaBH4 2. H3O+ and Carboxylic acid
    NR
  10. 1. NaBH4 2. H3O+ and Acid halide
    NR
  11. 1. NaBH4 2. H3O+ and Ester
    NR
  12. 1. NaBH4 2. H3O+ and Amide
    NR
  13. 1. NaBH4 2. H3O+ and Nitrile
    NR
  14. 1. NaBH4 2. H3O+ and Aldehyde
    turns C=O to C-OH
  15. 1. NaBH4 2. H3O+ and Anhydride
    breaks it in half, making a COOH and an primary alcohol
  16. 1. DIBAL 2. H3O+ and Ketone
    NR
  17. 1. DIBAL 2. H3O+ and Carboxylic acid
    aldehyde
  18. 1. DIBAL 2. H3O+ and Acid Halide
    Aldehyde
  19. 1. DIBAL 2. H3O+ and Ester
    Aldehyde and R'-OH
  20. 1. DIBAL 2. H3O+ and Amide
    Aldehyde
  21. 1. DIBAL 2. H3O+ and Nitrile
    Aldehyde
  22. 1. DIBAL 2. H3O+ and Anhydride
    Aldehyde
  23. 1. BH3/THF 2. H3O+ and Ketone
    turns C=O to C-OH
  24. 1. BH3/THF 2. H3O+ and carboxylic acid
    primary alcohol, gets rid of C=O
  25. 1. BH3/THF 2. H3O+ and Acid Halide
    NR
  26. 1. BH3/THF 2. H3O+ and Ester
    two alcohols depending on R group
  27. 1. BH3/THF 2. H3O+ and PRIMARY Amide only
    Amine
  28. 1. BH3/THF 2. H3O+ and secondary/tertiary Amide
    NR
  29. 1. BH3/THF 2. H3O+ and Nitrile
    Primary amine (NH2)
  30. 1. BH3/THF 2. H3O+ and Anhydride
    2 Alcohols depending on R groups
Author
brendanbui
ID
82483
Card Set
Reductions
Description
List of reductions
Updated

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