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Author Topic: acetone for methanol, swap. Less heat  (Read 2645 times)

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cheeseboy

  • Guest
acetone for methanol, swap. Less heat
« on: May 29, 2002, 08:41:00 AM »
You think Acetone could be used instead of Methanol in the Oxone run? maybe the Acetone would keep the rxn running cooler to avoid kark happening. Anyone?
May De Sorce Bee Wit Chu-Always
EDIT:
OOPs sorry, cheese now knows that Acetone reacts with Oxone to make a truly fine epoxidizing agent called...di...di..
anyone? Oh well, cheese will read harder before asking dumb questions again.
over and out
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terbium

  • Guest
Dioxirane
« Reply #1 on: May 29, 2002, 04:19:00 PM »
Search for dioxirane and you will get numerous relevant hits.

Post 220473

(foxy2: "Re: Possible Peracetic Revision", Chemistry Discourse)

Post 220436

(foxy2: "Re: Possible Peracetic Revision", Chemistry Discourse)

Post 220198

(Rhodium: "Re: Possible Peracetic Revision", Chemistry Discourse)

Post 191173 (missing)

(Osmium: "Re: Potassium Monoperoxysulfate for spas~", Chemistry Discourse)

Post 189058

(terbium: "Re: nitroethane", Novel Discourse)
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Sunlight

  • Guest
Dangerous
« Reply #2 on: May 29, 2002, 06:53:00 PM »
Dioxirane is defined as volatile organic peroxide, what means danger.
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cheeseboy

  • Guest
Post deleted by cheeseboy
« Reply #3 on: May 29, 2002, 09:35:00 PM »
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goiterjoe

  • Guest
not really
« Reply #4 on: May 30, 2002, 02:05:00 AM »
does oxone possess the potential to oxidize acetone  to acetone all the way to acetone peroxide, or does it always stop at dioxirane?

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Rhodium

  • Guest
acetone peroxide & oxone
« Reply #5 on: June 04, 2002, 10:56:00 PM »
I know that peroxymonosulfuric acid catalyzes the formation of dimeric and trimeric acetone peroxide, but I don't have any data on its potassium salt (= Oxone).
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