Publications – Page 479 – Department of Environmental Science

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Publications – Page 479 – Department of Environmental Science

You can ensure product safety from certified suppliers certified to the relevant standards. The Anthracene-maleic anhydride diels-alder adduct molecule contains a total of 33 atom(s). There are 12 Hydrogen atom(s), 18 Carbon atom(s) and 3 Oxygen atom(s). A chemical formula of Anthracene-maleic anhydride diels-alder adduct can therefore be written as: C18H12O3 Anthracene-maleic anhydride diels-alder adduct structure data file available for download. It can be imported to most of the chemistry software for further analysis.

Anthracene-maleic anhydride diels-alder adduct

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This is because although the hydrogens of the maleic anhydride must be cis in the product, there are two possible arrangements where this is true. The actual product formed is the ‘endo’ adduct. Density (g/cm 3 ) Anthracene 178 216 340 1. Maleic Anhydride 98 55 202 1. Diels-Alder Adduct 276 261 485 1.

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17-oxapentacyclo[6.6.5.0~2,7~.0~9,14 Other names: Anthracene, 2,5-furandione adduct; Anthracene,maleic anhydride adduct; endo-9,10-(α,β-Succinic anhydride)anthracene; 9,10(3',4')-Furanoanthracene-12,14-dione; 9,10-Dihydroanthraceno-9,10-endo-α,β-succinic anhydride; 9,10-Ethanoanthracene-11,12-dicarboxylic anhydride Permanent link for this species. Use this link for bookmarking Find more compounds similar to Anthracene-maleic anhydride diels-alder adduct.

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Xylene is highly flammable and should be kept away from open flames.

Use this link for bookmarking Find more compounds similar to Anthracene-maleic anhydride diels-alder adduct. Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.
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Anthracene-maleic anhydride diels-alder adduct

This experiment involved a reaction between anthracene and maleic anhydride via a Diels Alder reaction to yield 9, 10-dihydroanthracene-9,10-α, β-succinic anhydride.

The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data. The purpose of this experiment is to form 9,10-dihydroanthracene-9,10-α,β-succinic anhydride by way of a Diels Alder reaction between anthracene and maleic anhydride, as shown in the reaction below. Anthracene acts as the diene and maleic anhydride functions as the dienophile.
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x 276.29 g Diels− Alder Addu product was an adduct of both anthracene and maleic anhydride, and thus that the experiment was successful. The Diels-Alder Reaction of Anthracene with Maleic  I'm wondering why maleic anhydride adds to the middle cycle of anthracene, and not the outer two.