Uploaded September 2021 | Updated September 2026, 1 week ago
The mechanism for a Tebbe olefination reaction which involves a Tebbe reagent which is a metal carbenoid. The Tebbe reagent is obtained from the reaction with titanocene dichloride and trimethyl aluminum. Then, after the addition of a catalytic amount of pyridine, the Tebbe reagent is obtained which has the ability to react with various carbonyls through a straightforward mechanism in order to obtain the desired alkenes.
Music by Ryan Little
Song: Train to Busan
Link: youtu.be/mFt7yWl1CvI
The mechanism for a Tebbe olefination reaction which involves a Tebbe reagent which is a metal carbenoid. The Tebbe reagent is obtained from the reaction with titanocene dichloride and trimethyl aluminum. Then, after the addition of a catalytic amount of pyridine, the Tebbe reagent is obtained which has the ability to react with various carbonyls through a straightforward mechanism in order to obtain the desired alkenes.
Music by Ryan Little
Song: Train to Busan
Link: youtu.be/mFt7yWl1CvI






![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.
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