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Topic: help !!! Nitration Of Naphthalene  (Read 8855 times)

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Offline saint_john

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help !!! Nitration Of Naphthalene
« on: October 12, 2010, 03:44:56 PM »
When Napthalene is nitrated the products are either 1-nitronaphthalene or 2- nitronaphthalene.

1-nitronaphthalene is the major product but why is this so ?

can someone explain
« Last Edit: October 12, 2010, 04:11:19 PM by saint_john »

Offline kryptoniitti

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Re: help !!! Nitration Of Naphthalene
« Reply #1 on: October 12, 2010, 05:41:10 PM »
This is a textbook case of kinetic vs thermodynamic reaction. Dig into that and you'll get full disclosure.

Offline orgopete

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Re: help !!! Nitration Of Naphthalene
« Reply #2 on: October 12, 2010, 07:59:17 PM »
The explanation I prefer is due to the stability of the two different arenium ions. The one better stabilized by resonance while maintaining aromaticity leads to the major product.

However, krypton has raised an interesting question. Is there something that I don't know here? I thought the product was 1-nitro, but other conditions or continued reaction gives the 2-nitro (or vice versa)?
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Offline saint_john

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Re: help !!! Nitration Of Naphthalene
« Reply #3 on: October 13, 2010, 02:45:52 AM »
yeah i think it would depend on the conditions, even though 1- nitro naphthalene is the kinetic product.... 2- nitronaphthalene is the thermodynamically stable product

Offline AWK

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