Recent content by melanie55

  1. M

    Chemistry-Apirin Lab, question about phenyl salicylate

    Gosh I completely forgot about this. It was several years ago. I'm not really sure where I got it from, but I still have my bibliography from the lab. You can look through the sources to find it. 1. Aspirin Foundation of America. (2007). Aspirin Foundation Homepage. Retrieved March 6, 2007...
  2. M

    Can Protein Be Used for Energy in Glycolysis and the Krebs Cycle?

    Do you have the glycolysis and krebs cycles? If so, you've most likely been given something to determine where certain molecules enter. It should tell you where amino acids enter.
  3. M

    Chemistry-Apirin Lab, question about phenyl salicylate

    I actually found the answer yesterday, but thanks for helping :) It had something to do with turning phenol into the ionic compound sodium phenoxide. There's also another method with combining two dehydrated salicylic acid molecules (salicylic anhydride) to react with phenol and produce phenyl...
  4. M

    Chemistry-Apirin Lab, question about phenyl salicylate

    Each source I go to for the synthesis of phenyl salicylate says that it is formed by phenol and salicylic acid. Not very helpful. However one site says that it is formed by heating phenol and salicylic acid with a catalyst. This is slightly different than what the other sources are saying, and...
  5. M

    Chemistry-Apirin Lab, question about phenyl salicylate

    After sleeping on it, I'm wondering if maybe mixing the phenol with the acetylsalicylic acid may work.
  6. M

    Chemistry-Apirin Lab, question about phenyl salicylate

    Homework Statement The phenyl ester of salicylic acid, phenyl salicylate, is also a useful pharmaceutical. But phenol does not react with salicylic acid directly. Suggest a possible method to accomplish the synthesis of phenyl salicylate.Homework Equations This question has been included in...
Back
Top