i Preview File Edit View Go Tools Window Help 68%CI, Thu 1:57 PM a :E diels alder anthracene and maleic anhydride.pdf (page 4 of 10) When anthracene's center ring reacts as a diene, the product has two fully aromatic rings, each with six pi electrons, as shown in Equation 3. (Eq. 3) maleic anhydride (dienophile) anthracene adduct) (diene) The

Anthracene-maleic anhydride Diels-Alder adduct. 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.

4 Information Sources. Help. 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. Scheme 1. Synthesis of N-octylmaleimide Diels–Alder adducts of anthracene and a derivative. Scheme 2.

Anthracene-maleic anhydride diels-alder adduct 5443-16-3 Suppliers,provide Anthracene-maleic anhydride diels-alder adduct 5443-16-3 product and the products related with China (Mainland) Anthracene-maleic anhydride diels-alder adduct 5443-16-3 Career Henan Chemical Co China (Mainland) In the present experimental work, the energy of combustion of the crystalline Diels-Alder adduct of anthracene and maleic anhydride: C18H12O3, was measured with a model 1241 Parr automatic calorimeter and a Parr model 1710 calorimeter controller. The standard molar enthalpy of combustion of the (anthracene + maleic anhydride) adduct at po = 0.1 MPa was determined to be ΔcHmo(C18H12O3, cr, 298 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 Anthracene-maleic anhydride diels-alder adduct - chemical information, properties, structures, articles, patents and more chemical data. Anthracene-maleic anhydride diels-alder adduct contains total 37 bond(s); 25 non-H bond(s), 14 multiple bond(s), 2 double bond(s), 12 aromatic bond(s), 1 five-membered ring(s), 5 six-membered ring(s), 2 nine-membered ring(s), 4 ten-membered ring(s), 2 ester(s) (aliphatic) and 1 anhydride(s) (-thio).

Anthracene-maleic anhydride diels-alder adduct. 17-oxapentacyclo CID 138503 (Anthracene-maleic anhydride diels-alder adduct) PubChem. 4 Information Sources. Help.

Xylene is an excellent solvent for both anthracene and maleic anhydride, as evidenced by their complete solubility in the early part Substance record SID 341690678 for cis-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylic acid anhydride submitted by Springer Nature. 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.

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:

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.

S. K. Ayer et al. 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.
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It can be imported to most of the chemistry software for further analysis. Obtain SDF at Mol-Instincts. In the present experimental work, the energy of combustion of the crystalline Diels-Alder adduct of anthracene and maleic anhydride: C18H12O3, was measured with a model 1241 Parr automatic calorimeter and a Parr model 1710 calorimeter controller. The standard molar enthalpy of combustion of the (anthracene + maleic anhydride) adduct at po = 0.1 MPa was determined to be ΔcHmo(C18H12O3, cr, 298 Anthracene-maleic anhydride diels-alder adduct 5443-16-3_OKCHEM Please note that all emails sent by OKCHEM are from ***@okchem.com, service@mail.

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Figure 1.