December 22, 2024, 11:13:14 AM
Forum Rules: Read This Before Posting


« previous next »
Pages: [1]   Go Down

Topic: Hydrolysis of 4-Hydroxy-(N-ethanoyl-aminobenzene)  (Read 4430 times)

0 Members and 1 Guest are viewing this topic.

Offline zilalti

  • Regular Member
  • ***
  • Posts: 46
  • Mole Snacks: +2/-2
  • Gender: Male
  • I'm a mole!
Hydrolysis of 4-Hydroxy-(N-ethanoyl-aminobenzene)
« on: November 03, 2005, 04:58:48 PM »
If i were to hydrolize paracetemol (4-Hydroxy-(N-ethanoyl-aminobenzene) with sulphuric acid would the C-C bond be broken to leave a methyl group or N-C bond to leave a ketone?
Logged

Offline AWK

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 7976
  • Mole Snacks: +555/-93
  • Gender: Male
Re:Hydrolysis of 4-Hydroxy-(N-ethanoyl-aminobenzene)
« Reply #1 on: November 04, 2005, 05:47:15 AM »
During hydrolysis you can break C-N bond
Logged
AWK

Offline FeLiXe

  • Theoretical Biochemist
  • Chemist
  • Full Member
  • *
  • Posts: 462
  • Mole Snacks: +34/-7
  • Gender: Male
  • Excited?
    • Chemical Quantum Images
Re:Hydrolysis of 4-Hydroxy-(N-ethanoyl-aminobenzene)
« Reply #2 on: November 05, 2005, 09:17:34 AM »
you break the amide bond. I am afraid I am not allowed to tell you the answer: So look up what an amide is an then it's pretty obvious how the water works in splitting it. It's the opposite to its formation.
Logged
Math and alcohol don't mix, so... please, don't drink and derive!
Pages: [1]   Go Up
« previous next »
Sponsored Links