The structure data file (SDF/MOL File) contains the information about the atoms, bonds, connectivity and coordinates of Anthracene-maleic anhydride diels-alder adduct molecule. It starts with a header block, followed by "connection table’, which describes the structural relationships and properties of the atoms.

5443-16-3 - PSKVQQJLLWSBFV-UHFFFAOYSA-N - Anthracene-maleic anhydride diels-alder adduct - Similar structures search, synonyms, formulas, resource links, and other chemical information.

Formula: C 18 H 12 O 3; 2,5-furandione adduct; Anthracene,maleic anhydride adduct; endo-9,10-(α,β-Succinic The Anthracene-maleic anhydride diels-alder adduct images of 3-dimensional (3D) molecular structures, molecular surfaces, molecular orbitals, and an optimized 3D structure datafile (SDF/MOL File) are readily accessible for purchase, which have been generated on the basis of data derived from quantum mechanical computations under DFT (Density Functional Theory) - B3LYP functional with 6-31G The Diels-Alder Reaction of Anthracene with Maleic Anhydride Microscale Diels-Alder Reaction Leah Monroe March 6, 2003 Organic Chemistry Lab II Experiment performed on February 25 and 27, 2003 Abstract: This experiment involved a reaction between anthracene and maleic anhydride via a Diels Alder reaction to yield 9, 10-dihydroanthracene-9,10-, -succinic anhydride. Anthracene-maleic anhydride diels-alder adduct Other names: 9,10(3',4')-Furanoanthracene-12,14-dione; 9,10-Dihydroanthraceno-9,10-endo-«alpha»,«beta»-succinic The Diels-Alder Reaction of Anthracene with Maleic Anhydride 1 The Diels-Alder Reaction of Anthracene with Maleic Anhydride Microscale Diels-Alder Reaction Leah Monroe March 6, 2003 Organic Chemistry Lab II Experiment performed on February 25 and 27, 2003 Abstract: This experiment involved a reaction between anthracene and maleic anhydride via The Diels-Alder Reactionof Anthracene withMaleic Anhydrideprepared by L. G. Wade, Jr., Whitman College. Use the Diels-Alder reaction to form a bridged polycyclic anhydride.Recrystallize the product and characterize it by using melting point andinfrared spectroscopy. Reactants and Products Compoun d Name Anthracene Maleic Anhydride Xylene Pentane Anthracene-maleic anhydride diels-alder adduct Structure State Solid (s) Solid (s) Liquid (l) Liquid (l) Solid (s) Amount Used 1.0 g 0.55 g 30 mL 10 mL portions Product Formula C 14 H 10 C 4 H 2 O 3 C 8 H 10 C 5 H 10 C 18 H 12 O 3 Molecular weight 178.23 g/mol 98.06 g/mol 106.16 g/mol 72.15 g/mol 276.291 g/mol The Anthracene-maleic anhydride diels-alder adduct (5443-16-3) products are most popular in India, Pakistan, Vietnam, Indonesia, Brazil, Russia, Mexico, United States, Turkey, Germany, etc. You can ensure product safety from certified suppliers certified to the relevant standards.

Anthracene-maleic anhydride diels-alder adduct

It starts with a header block, followed by "connection table’, which describes the structural relationships and properties of the atoms. 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 The mass of the crude Anthracene-maleic anhydride diels-alder adduct was 1.02g, whereas the theoretical yield came out to be 1.55g. Giving a crude yield percentage of 65.81%. Executive Summary. High-quality images and the structure datafile of Anthracene-maleic anhydride diels-alder adduct based on a decent quantum mechanical calculation have been prepared on this webpage, which are useful not only for further scientific research and development but also for preparing professional reports, articles, presentations, webpages, books, etc. More specifically, bomb-calorimetric experiments have been carried out on the Diels-Alder adduct of anthracene and maleic anhydride (DAAMA), thus providing enthalpies of formation of value in predictive computational-chemistry models. DAAMA has the structure: 9,10,11,12-tetrahydro- 9,10r [3',4']-furanoanthracene-13,15-dione.

Reactants to form this NMR by diels-alder reaction are Anthracene,… H NMR Spectra of the Diels -Alder Adduct from anthracene and maleic anhydride.

This is because Jun 2, 2009 Anthracene is the diene and maleic anhydride is the dienophile. Others Diels- Alder adduct are of maleic anhydride and 1,3-cyclohexadiene, n- Good EWGs include ketone, aldehyde , nitrile, nitro, and trifluoromethyl groups. Maleic anhydride is an excellent dienophile. Comment.

The Anthracene-maleic anhydride diels-alder adduct (5443-16-3) products are most popular in India, Pakistan, Vietnam, Indonesia, Brazil, Russia, Mexico, United States, Turkey, Germany, etc. You can ensure product safety from certified suppliers certified to the relevant standards.

The Diels-Alder reaction is a member of a class of reactions called cycloadditions. The reaction involves three π bonds, two from the diene and one from the dienophile in a concerted reaction to form a six-membered ring. Since the reaction involves four π electrons in the diene and two π electrons from the dienophile, it is sometimes referred to as a 4 + 2 cycloaddition. Although there are four stereogenic centres in the product only two diastereoisomers can be formed, any others are impossibly strained.

Yield, melting point and appearance Table 1. FAQ; Credits; More documentation; Anthracene-maleic anhydride Diels-Alder adduct. 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.
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The Anthracene-maleic anhydride diels-alder adduct (5443-16-3) products are most popular in India, Pakistan, Vietnam, Indonesia, Brazil, Russia, Mexico, United States, Turkey, Germany, etc. 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).

Learn more about Anthracene-maleic anhydride diels-alder adduct chemical formula at Mol-Instincts. The Anthracene-maleic anhydride diels-alder adduct molecule consists of 12 Hydrogen atom (s), 18 Carbon atom (s) and 3 Oxygen atom (s) - a total of 33 atom (s).
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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

Remember that the sand in the sand bath will be very hot. Do not touch the sand or sand bath until it The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. Since the reaction involves the formation of a cyclic product via a cyclic transition state, it is also referred to as a Although there are four stereogenic centres in the product only two diastereoisomers can be formed, any others are impossibly strained.

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Anthracene acts as the diene and maleic anhydride functions as the dienophile. commonly known as “adduct” and reaction is known as Diels- Alder reaction.

The percent yield of the crude product was 69.03%.