Synthesize 1-Butyl-3-Propylbenzene from 1-Chloropropane & 1-Butyne

  • Thread starter Thread starter jayashae
  • Start date Start date
  • Tags Tags
    Benzene Synthesis
AI Thread Summary
The discussion centers on synthesizing 1-butyl-3-propylbenzene using 1-chloropropane and 1-butyne as starting materials. The main challenge highlighted is how to incorporate these molecules onto the benzene ring without causing branching. There is skepticism about the effectiveness of Friedel-Crafts alkylation for this purpose. Participants express frustration over a user seeking help across multiple forums without adequately engaging with previous responses. The importance of effort and engagement in discussions is emphasized, with members indicating a preference for not providing complete answers when questions have been posed elsewhere. This reflects a broader community standard for collaborative problem-solving and knowledge sharing.
jayashae
Messages
2
Reaction score
0
Given 3 molescules: 1-chloropropane, 1-butyne, and a benzene ring, how do I synthesize 1-butyl-3-propylbenzene?

my question is, how do I get 1-chloropropane or 1-butyne on the ring without having branching? these 2 must be the starting material. I don't see how F&C alkcylation would work.
 
Chemistry news on Phys.org
help?
 
What carbon-carbon bond forming reactions have you studied?
 
i answered this pretty clearly on chemicalforums. go check my post there.
 
So, Jay... you ask the question over on ChemicalForums and when you don't get immediate gratification you post over here? Seriously? You were getting good help over there but you put absolutely no effort into answering their questions... which were actually guidance to help you. You put in the same effort over here on this forum. I'm sure you note the similarity of the kind of help you were getting from Dan, OrgoPete (on CF) and myself on this forum. There is a reason we do things in this way.

Burning... Shame on you! Giving complete answers on this forum is not our style much less pointing to other forums where you have done so!

Jay, I'm a member of CF as well as this forum. I don't answer questions that have been posted over there on our forum and don't answer questions over there that have been posted over here. ...at least when I remember to check both forums.
 
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!!
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...

Similar threads

Back
Top