Organic chemistry mechanisms
Chemistry
Basic organic chemistry mechanisms. (Some cards only reflect one step of multi-step mechanisms).
Sample Data
| Mechanism |
 |
| Product and Stereochemistry | Anti-Markovnikoff Stereorandom.
 Peroxides generate the Br. radical, which adds to the double bond in the way that will generate the most stable radical. (Most substituated carbon. Explains anti-markovnikoff). |
| Tags |
| Mechanism |
 |
| Product and Stereochemistry |
 Na is a very strong reducing agent, and will reduce alkynes (but not alkenes). Selective for the trans-alkene. The NH3 provides the hydrogens in the final product. |
| Tags | Synthesis |
| Mechanism |
 |
| Product and Stereochemistry |
 Markovnikoff. |
| Tags | Synthesis, alkyne ketone to |