Tonight's Labor |
Enolate Reactions
Answers
What will this problem set teach you?
- LDA/THF will produce the kinetic enolate product - the alkene will be the less substituted of the two possibilities (if there are two possibilities).
- Usually when H3O+ and heat are used in one step, there's a good chance you're extruding CO2 gas from the system.
- Often times, chemists will use Sodium Ethoxide in Ethanol as a strong base to promote the formation of enolates. Remember, Sodium Ethoxide is a good base because Ethanol is a terrible alcohol. Furthermore, it's more useful as a base than a nucleophile because Oxygen is very electronegative!
I highly recommend doing this problem set, more so than the other one's I've posted here.
Today's Tune: The Best of Bach
Great for doing organic chemistry before bedtime.
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