In this video the synthesis of cinnamaldehyde from benzaldehyde and acetaldehyde is shown. Patreon: / randomexperimentsinter... Buy Stock Footage: sellfy.com/science-stock-footage
Very nice! I synthesized p-Methoxy-Cinnamic Acid from Benzaldehyde via Knoevenagel reaction as part of my undergraduate organic chemistry lab course - I'm specialising in inorganic chemistry, but that synthesis was one of my favourites. This one seems more challenging, at least for getting a good yield, but still very interesting to see!
Sir Can you please make a synthesis of di iodomethane? It is the heaviest organic solvent and it can float an piece of aluminum I think that's why I really like it
Complex synthesis, since it's a challenge to separate benzaldehyde, acetaldehyde and cinnamaldehyde, and they are easily undergo oxidation, the yield was so so, 23%
Usually, I clean everything with soap and water, then with acetone and at the end with air or just letting it sit over night, before I use it again for the next distillation.
Yes, it's a general procedure. As long as there are no other functional groups, the Aldehyde and CH-acidic compound can be substituted by anything and it's highly likely to work.
Thank you, brother, but I want you to have the necessary ingredients. I want the ingredients to make a kilo of Bakelite. How much phenol, formaldehyde and hydrochloric acid should I put?