| Reaction | Example | Comments |
|---|---|---|
| Oxidation to Acid | ![]() |
1o only |
| Oxidation to aldehydes | ![]() |
1o only; PCC works also |
| Oxidation to ketones | ![]() |
Only 2o alcohols; Collins, PCC works also |
| Conversion to halides | ![]() |
Best for 3o alcohols; X = Cl, Br, I |
![]() |
1o, 2o only, because SN2 | |
![]() |
1o, 2o only, because SN2 | |
| Dehydration | ![]() |
Best for 3o alcohols; yields mostly poor |
![]() |
All alcohols; best yields | |
| Conversion to conjugate bases | ![]() |
K metal also |
![]() |
H- is very strong base |