April 25, 2024, 06:42:53 AM
Forum Rules: Read This Before Posting


Topic: most rapid sulfonation upon treatment with fuming sulfuric acid?  (Read 6959 times)

0 Members and 1 Guest are viewing this topic.

Offline madscientist

  • Full Member
  • ****
  • Posts: 225
  • Mole Snacks: +14/-7
  • University of New England Australia
Ive got a question ive been working on and cannot find an answer.

Question states: Which of the following undergoes the most rapid sulfonation upon treatment with fuming sulfuric acid?

a.) benzoic acid

b.) benzonitrile

c.) benzene

d.)nitrobenzene

my working so far: I couldnt think of any other way of answering this question besides determining the activation/ deactivation abilitys of the substituants, for eg,  the NO2 substituant on nitrobenzene is deactivating, the COOH group on benzoic acid is also deactivating, the CN group on benzonitrile I am not sure whether or not this is activating or deactivating.

I can only guess that benzene (c.) is the correct answer?

I am very very lost with this q and any help would be appreciated.

cheers,

madscientist  :albert:
« Last Edit: October 27, 2005, 01:59:32 AM by Mitch »
The only stupid question is a question not asked.

Offline Winga

  • Chemist
  • Full Member
  • *
  • Posts: 510
  • Mole Snacks: +39/-10
Re:Sulfonation
« Reply #1 on: October 16, 2005, 05:40:15 AM »
Cyano group is a deactivator and a meta director.
« Last Edit: October 16, 2005, 05:41:47 AM by Winga »

Offline madscientist

  • Full Member
  • ****
  • Posts: 225
  • Mole Snacks: +14/-7
  • University of New England Australia
Re:Sulfonation
« Reply #2 on: October 16, 2005, 08:30:15 AM »
Thanks very much for your helpfull reply Winga

cheers,

madscientist
The only stupid question is a question not asked.

Sponsored Links