anthracene and maleic anhydride product nmr


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PDF A Neat Diels-Alder Reaction: 910-dihydroanthracene-910

The Diels-Alder reaction is a concerted [4+2] cycloaddition between a diene and a dienophile (which is often an alkene) The reaction simultaneously forms two C-C single bonds The reaction you will carry out is between anthracene (the diene) and maleic anhydride (the dienophile): O + heat

PDF 1H NMR Spectra of the Diels -Alder Adduct from anthracene and

O O O a a b c a b c 1 H NMR Spectra of the Diels -Alder Adduct from anthracene and maleic anhydride

PDF Experiment 20 — Pericyclic reactions

anthracene and maleic anhydride The Diels-Alder cycloaddition is a concerted 6-electron reaction that involves a 4-π-e– component usually a diene and a 2-π-e– component called the dienophile The text has several examples; one additional example the reaction of cyclopentadiene and maleonitrile is illustrated below CN CN CN CN CN CN

PDF Chem 2229: Exp  The Diels-Alder Reaction of Anthracene

Chem 2229: Exp #3 The Diels-Alder Reaction of Anthracene with Maleic Anhydride (bolonc tbone updated 8-16-22) 3 Table 1: Molar Masses and Melting Points of Reactants and Products Substance Molar Mass (g/mole) MP (oC)___ BP (oC)___ anthracene 178 23 216-218 maleic anhydride 98 06 54-56

  • How do you mix anthracene and maleic anhydride?

    Be sure to wear gloves and avoid contact with these compounds. In a dry round-bottom flask, combine 1.0g of anthracene and 0.5 g of maleic anhydride, add 12 ml of xylenes (a mixture of dimethylbenzenes), and reflux the reaction mixture for about 30 min. Use an IR lamp as the heat source. Allow the mixture to cool to room temperature.

  • Why do we need NMR spectroscopy for anthracene synthesis?

    Because many of these applications involve the incorporation of anthracene into a much larger macromolecule mainly through a Diels Alder reaction, monitoring such transformations using NMR techniques requires an accurate appreciation of the chemical shifts of protons and carbons in these materials.

  • What is 1H NMR spectra of Diels-Alder adduct?

    1H NMR Spectra of the Diels -Alder Adduct from anthracene and maleic anhydride O O O a a b c a b c 1 H NMR Spectra of the Diels -Alder Adduct from anthracene and maleic anhydride Title

  • How are 9 substituted anthracene derivatives obtained?

    9-substituted derivative (2) were obtained by reacting the corre- sponding anthracene derivative with 1-octylmaleimide as de- scribed in Scheme 1. The two other compounds (3 and 4) are Diels –Alder adducts of 9- substituted anthracene, obtained by reacting the corresponding anthracene derivative with maleic anhydride (Scheme 2).

Reaction Thermochemistry Data

Go To: Top, References, Notes Data compilation copyrightby the U.S. Secretary of Commerce on behalf of the U.S.A.All rights reserved. Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein Note: Please consider using thereaction search for this species. This page allows searchingof all reactions involving this species. A general

References

Go To: Top, Reaction thermochemistry data, Notes Data compilation copyrightby the U.S. Secretary of Commerce on behalf of the U.S.A.All rights reserved. Kiselev, Mavrin, et al., 1982 Kiselev, V.D.; Mavrin, G.V.; Konovalov, A.I.,Thermodynamic principles of the occurrence of a Diels-Alder reaction in the presence of a Lewis acid,Zh. Org. Khim., 1982,

Notes

Go To: Top, Reaction thermochemistry data, References 1. Symbols used in this document: 2. Data from NIST Standard Reference Database 69:NIST Chemistry WebBook 3. The National Institute of Standards and Technology (NIST)uses its best efforts to deliver a high quality copy of theDatabase and to verify that the data contained therein havebeen selecte

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