akcapr
Harmless
Posts: 21
Registered: 26-5-2005
Location: Washington
Member Is Offline
Mood: No Mood
|
|
QUestion about product of reaction
My chemistry professor proposed a question to me today, and I cant realyl figure it out. We were talkign about Nitration of aromatics, and he told me
that if you take N,N-dimethyl aniline, and add conc. sulfuric acid, and then add a mix of HNO2 and H2so4 you will get one product-
meta-nitro-N,N-dimethyl aniline.
First if find it wierd that it adds nitro, and about the spicific order of first adding just h2so4, then the mix to gain the mono nitrate product. I
rationalize that it only adds once because the nitro group is e-withdrawing, but why does it add meta? N,N-dimethyl aniline is activiating, and should
add to o and p positions, and help/thoughts? thanks
[Edited on 27-5-2010 by akcapr]
|
|
psychokinetic
National Hazard
Posts: 558
Registered: 30-8-2009
Location: Nouveau Sheepelande.
Member Is Offline
Mood: Constantly missing equilibrium
|
|
The H2SO4 is likely there to make an electrophile (NO2+), and will be 'reformed' at the end.
The meta bit I'm not sure about, sorry. Perhaps it is to do with the stereochemistry of the N(CH3)2
Perhaps also, the addition of conc H2SO4 at the beginning alters the ring's para carbon by sulfonation.
“If Edison had a needle to find in a haystack, he would proceed at once with the diligence of the bee to examine straw after straw until he found
the object of his search.
I was a sorry witness of such doings, knowing that a little theory and calculation would have saved him ninety per cent of his labor.”
-Tesla
|
|
not_important
International Hazard
Posts: 3873
Registered: 21-7-2006
Member Is Offline
Mood: No Mood
|
|
The acid converts the amino group into the corresponding substituted ammonium salt, and NR4<sup>(1+)</sup> is deactivating and meta
directing. You've got a + charge sitting out on the nitrogen, sucking at ring electrons.
It takes strongly acid conditions to insure that most to all the amine is in the salt form, adding H2SO4 first does so without any chance of the free
amine reacting.
One page 10 of the PDFF here http://www.smccd.edu/accounts/lawrencey/232_Fall09/16_Study_... is a nice graph of substitutes rank by their activating/deactivating and meta/o-p
direction; you'll see that +NR2 is about the same as NO2
|
|
akcapr
Harmless
Posts: 21
Registered: 26-5-2005
Location: Washington
Member Is Offline
Mood: No Mood
|
|
thanks i didnt think of that but it makes perfect sense!
[Edited on 27-5-2010 by akcapr]
|
|
psychokinetic
National Hazard
Posts: 558
Registered: 30-8-2009
Location: Nouveau Sheepelande.
Member Is Offline
Mood: Constantly missing equilibrium
|
|
Ok that makes more sense.
“If Edison had a needle to find in a haystack, he would proceed at once with the diligence of the bee to examine straw after straw until he found
the object of his search.
I was a sorry witness of such doings, knowing that a little theory and calculation would have saved him ninety per cent of his labor.”
-Tesla
|
|