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From: moroney@world.std.spaamtrap.com (Michael Moroney)
Newsgroups: sci.physics
Subject: Re: BJ And John Support Terrorists
Date: Tue, 22 Mar 2016 19:32:02 +0000 (UTC)
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john <johnsefton288@gmail.com> writes:

>turning/precessing discs. The proof
>is here- Benzene is ABSOLUTELY 
>SYMMETRICAL; there are no
>"delocalized  electrons".
>http://users.accesscomm.ca/john/BenzeneE.GIF

How is that a proof of anything?  Can it explain benzene's chemical
reactivity the way standard models can?  Why does cyclohexene react with
bromine or KMnO4 yet benzene doesn't, unless catalysts and heat are
supplied? Can you model benzene derivitives, such as naphthalene? Why does
benzene normally undergo substitution reactions instead of addition
reactions when it does react?

These are questions that chemists can answer by addressing the pi bonds of
benzene.  You don't even have any idea WTF I am talking about, but you
think "it has precessing spinny things, so it must be correct!"