Diels-Alder adducts of tetracyanoethylene (TCNE) and polyaromatic compounds (anthracene, napthacene, pentacene and phencyclone) were synthesized and were used maleic anhydride (as a dienophile) with a number of polycyclic

IR & 1H-NMR Spectra for the Diels-Alder Experiment Reaction of 1,3-cyclopentadiene with maleic anhydride, forming endo-norbornene-cis-5,6-carboxylic anhydride. To print or download this file, click the link below:

Formula: C 18 H 12 O 3. Molecular weight: 276.2861. IUPAC Standard InChI: InChI=1S/C18H12O3/c19-17-15-13-9-5-1-2-6-10 (9)14 (16 (15)18 (20)21-17)12-8-4-3-7-11 (12)13/h1-8,13-16H. Download the identifier in a file. IUPAC Standard InChIKey: PSKVQQJLLWSBFV-UHFFFAOYSA-N. Se hela listan på webbook.nist.gov Anthracene-maleic anhydride Diels-Alder adduct. Formula: C 18 H 12 O 3; Molecular weight: 276.2861; IUPAC Standard InChI: The Diels-Alder Reaction of Anthracene with Maleic Anhydride The Diels-Alder reaction is a member of a class of reactions called cycloadditions.

Maleic anhydride is an excellent dienophile. Comment. In the Diels-Alder cycloaddition reaction, a conjugated diene reacts with an alkene to form a ring Maleic anhydride is also a very good dienophile, because the Jan 1, 2011 This year we reacted the anthracene diene with two different The Bruice Organic Chemistry textbook has the Diels-Alder reaction in two different dienophiles in addition to the classic maleic anhydride. The expe 1 day ago Solved: Heat Anthracene Maleic Anhydride Diels Alder Adduct The Diels-Alder Reaction of Anthracene with - Franklin photograph. 1 day ago Anthracene-maleic anhydride diels-alder adduct | C18H12O3 The Diels–Alder Reaction for the Synthesis of Polycyclic photograph. anthracene maleic anhydride diels alder adduct.

H NMR Spectra of the Diels -Alder Adduct from anthracene and maleic anhydride. Title: PowerPoint Presentation Author: Poche, Drew Created Date: 5/17/2016 10:05:03 AM

The percent yield of the crude product was 69.03%. Analytical & Labware. Anthracene was the diene and maleic anhydride was the dienophile.

Anthracene-maleic anhydride diels-alder adduct

Experiment 9.1E Microscale Reaction of Anthracene with Maleic Anhydride The Diels Alder Reaction Purpose: The purpose of this experiment is to synthesize anthracene, maleic anhydride in toluene to produce the products 1,4 adduct or the 9,10 adduct in a Diels Alder reaction. The product of this reaction will be isolated by vacuum filtration.

IUPAC Standard InChIKey: PSKVQQJLLWSBFV-UHFFFAOYSA-N. Se hela listan på webbook.nist.gov Anthracene-maleic anhydride Diels-Alder adduct. Formula: C 18 H 12 O 3; Molecular weight: 276.2861; IUPAC Standard InChI: The Diels-Alder Reaction of Anthracene with Maleic Anhydride The Diels-Alder reaction is a member of a class of reactions called cycloadditions.

Anthracene-maleic anhydride diels-alder adduct. (2016, September ). Retrieved. September 06, Results 1 - 18 of 18 Anthracene, 2,5-furandione adduct.
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An octylmaleimide Diels–Alder adducts of The Diels-Alder Reaction of Anthracene with Maleic Anhydride The Diels-Alder reaction is a member of a class of reactions called cycloadditions.

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.
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Diels Alder Reaction Of Anthracene With Maleic Anhydride Lab Report – A laboratory report is basically how you explain what you’ve carried out in a laboratory experiment, what you found, and the results.

Tabulate 3-5 relevant IR peaks for the Diels–Alder reaction product. Compare and contrast the IR spectra of your starting materials (anthracene and maleic anhydride) and product (9,10-dihydroanthracene-9,10-a,b-succinic anhydride) and explain how the IR data for the product confirms the formation of the Diels-Alder adduct. 2016-04-28 · DIELS-ALDER MECHANISM It is a concerted cyclization reaction which generates an adduct of the starting diene (furan) and dienophile (maleic anhydride) that contains two new "C"-"C" bonds.

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Scheme 1. Synthesis of N-octylmaleimide Diels–Alder adducts of anthracene and a derivative. Scheme 2. Synthesis of maleic anhydride Diels–Alder adducts of anthracene. Figure 1. A representation of the molecular structure of 1 and 2. Ellipsoids correspond to 50% probability level. S. K. Ayer et al.

(dienophile). The reaction is carried Printed in the United States of America 156 SYNT 717: The Diels-Alder ReaCtion of Anthracene with Maleic Anhydride ( + diene (W (Eq.l) adduct dienophile Anthracene acts as the diene and maleic anhydride functions as the dienophile.