Uploaded January 2022 | Updated September 2026, 1 week ago
The mechanism for the addition of a Methoxymethyl (MOM) ether group which is generally used to protect the hydroxyl group. However, it is also used to protect amino groups. MOM groups have the potential to be cleaved by refluxing in methanol or under acidic conditions.
Music: Gray Clouds – Infraction
The mechanism for the addition of a Methoxymethyl (MOM) ether group which is generally used to protect the hydroxyl group. However, it is also used to protect amino groups. MOM groups have the potential to be cleaved by refluxing in methanol or under acidic conditions.
Music: Gray Clouds – Infraction
![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)









