Doing a presentation. Need some pointers.

AI Thread Summary
The discussion centers on preparing a presentation about new methods for functionalizing aromatic rings, specifically focusing on constructing C-O bonds. The initial poster seeks guidance on resources for current research in this area. A suggestion is made to approach the topic by considering it as an oxidation reaction, with phenol being a key compound. It is recommended to search for recent literature on phenol production methods, particularly referencing a review in Chemical & Engineering News from the past few years. The conversation highlights the significance of phenol as a feedstock for various chemical products and notes that its production is primarily linked to the cumene peroxidation process. The economic interdependence between phenol and cumene production is also emphasized, suggesting that innovative methods for C-O bond formation could aim to separate these economic factors.
Bladibla
Messages
357
Reaction score
1
Hi

I'm currently starting to prepare a 15 min preparation on a chemistry topic.

The topic I have been chosen to do is ''New methods of functionalizing armonatic rings; New methods for the constructing of C-O bonds to functionalize aromatic rings''

Does anyone have some pointers to this topic? I am not entirely sure of where to get resources for current researches in chemistry so I'm in a bit of a dark corner when it comes to obtaining information for this project..

Thanks.
 
Chemistry news on Phys.org
You probably won't find information by searching the literature using "''New methods of functionalizing armonatic rings; New methods for the constructing of C-O bonds to functionalize aromatic rings". One way to look at this problem is to note that it is an oxidation reaction. The simplest compound in this series would be phenol. Try searching for new methods to manufacture phenol. I seem to remember that C&E News had a review about some new chemistry sometime in the last 3 1/2 years (not in 2007, though). Start by trying to find the article in C&E News then by looking at a Kirk-Othmer Encyclopedia of Chemical Technology, specifically the chapter dealing with phenol. An excerpt I found online has this:
Phenol (hydroxybenzene) is a commercially important derivative of benzene. It is the primary feedstock for the production of epoxy resins and polycarbonates, phenolic resins and molding compounds, caprolactam, aniline, and other chemical derivatives. More than 95% of the phenol consumed is produced by the cumene peroxidation process.

So you see that this is a very important process but it depends on the manufacture of cumene (probably via a Friedel-Crafts alkylation process) and thus the economics of cumene manufacture as well. These two methods of manufacture are no doubt linked
both physically and economically and the demand/price of one drives the other. Finding a way to decouple the economics of phenol production from the vagaries of cumene production would seem a logical motivation for novel methods of aromatic C-O formation.

Hope it is helpful.
 
It seems like a simple enough question: what is the solubility of epsom salt in water at 20°C? A graph or table showing how it varies with temperature would be a bonus. But upon searching the internet I have been unable to determine this with confidence. Wikipedia gives the value of 113g/100ml. But other sources disagree and I can't find a definitive source for the information. I even asked chatgpt but it couldn't be sure either. I thought, naively, that this would be easy to look up without...
I was introduced to the Octet Rule recently and make me wonder, why does 8 valence electrons or a full p orbital always make an element inert? What is so special with a full p orbital? Like take Calcium for an example, its outer orbital is filled but its only the s orbital thats filled so its still reactive not so much as the Alkaline metals but still pretty reactive. Can someone explain it to me? Thanks!!
Back
Top