Uploaded September 2021 | Updated September 2026, 1 week ago
The mechanism for a Julia olefination reaction in which phenyl sulfones are reacted with aldehydes or ketone in order to produce an alkene. The first step in this reaction produces an alcohol intermediate which then goes through an in-situ esterification. Reductive elimination then takes place with sodium amalgam in order to produce the desired alkene.
Music by Ryan Little
Song: Beach House
Link: youtu.be/xOH9Lbe8gdo
The mechanism for a Julia olefination reaction in which phenyl sulfones are reacted with aldehydes or ketone in order to produce an alkene. The first step in this reaction produces an alcohol intermediate which then goes through an in-situ esterification. Reductive elimination then takes place with sodium amalgam in order to produce the desired alkene.
Music by Ryan Little
Song: Beach House
Link: youtu.be/xOH9Lbe8gdo
![L-Selectride Reduction Mechanism | Organic Chemistry
The mechanism for the reduction of a ketone to an alcohol using L-Selectride. There are multiple reagents that have the formula M[HB(sec-Bu)3] which are all used as reducing agents. There are three different cations with these reducing agents and they are L-Selectride (lithium), N-Selectride (sodium), and K-Selectride (potassium). Due to the sec butyl groups on these reducing agents, these reagents are sensitive to steric influences which has the potential to allow for stereoselective reactions.
Music: Gray Clouds – Infraction L-Selectride Reduction Mechanism | Organic Chemistry](https://i.ytimg.com/vi/oEoTzkAP0ak/mqdefault.jpg)








![N-Selectride Reduction Mechanism | Organic Chemistry
The mechanism for the reduction of a ketone to an alcohol using N-Selectride. There are multiple reagents that have the formula M[HB(sec-Bu)3] which are all used as reducing agents. There are three different cations with these reducing agents and they are L-Selectride (lithium), N-Selectride (sodium), and K-Selectride (potassium). Due to the sec butyl groups on these reducing agents, these reagents are sensitive to steric influences which has the potential to allow for stereoselective reactions.
Music: Abstract Wall – Infraction N-Selectride Reduction Mechanism | Organic Chemistry](https://i.ytimg.com/vi/sTgbTyXcB2s/mqdefault.jpg)
