CAS Registry Number: 5443-16-3. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file. The 3d structure may be viewed using Java or Javascript . Other names: Anthracene, 2,5-furandione adduct; Anthracene,maleic anhydride adduct; endo-9,10- (α,β-Succinic anhydride)anthracene; 9,10 (3',4

I performed a Diels-Alder reaction with maleic anhydride (melting point 52.8 *C) and cyclopentadiene (melting point -85 Anthracene,maleic anhydride adduct.

Diels Alder Adduct 23 Dec 2014 Anthracene-maleic anhydride diels-alder adduct.png. Anthracene, 2,5- furandione adduct, 17-oxapentacyclo[6.6.5.0~2,7~.0~9,14~.0~15 Can anyone provide the mechanism for this Diels-Alder addition? heat Anthracene Maleic Anhydride Diels Alder Adduct. Show transcribed image text In the same fashion anthracene (diene) reacts with maleic anhydride product commonly known as “adduct” and reaction is known as Diels- Alder reaction. Place 1.0 g of anthracene and 0.5 g of maleic anhydride in a 100-mL round- bottom flask. Add 15.

Learn more about Anthracene-maleic anhydride diels-alder adduct chemical structure at Mol Anthracene-maleic anhydride diels-alder adduct 5443-16-3_OKCHEM Please note that all emails sent by OKCHEM are from ***@okchem.com, service@mail. okchemvip.com, or notifications@edm-okchem.com. Please be alert of other emails sent to you in the name of OKCHEM. 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.

ProName: Anthracene-maleic anhydride diels-alde CasNo: 5443-16-3; Molecular Formula: C18H12O3; Appearance: ask; Application: intermediates; DeliveryTime: Within 3 days after payment; PackAge: foil aluminium bag/vacuum packing; Port: shanghai; ProductionCapacity: 100 Kilogram/Week; Purity: 85.0-99.8%; Storage: Keep in dry and cool condition

The Diels-Alder Reaction of Anthracene with Maleic Anhydride. 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. Anthracene was the diene and maleic anhydride was the dienophile. The percent yield of the crude product was 69.03%.

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.

To print or download this file, click the link below: Dec 23, 2014 Anthracene-maleic anhydride diels-alder adduct.png.

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.
Air paris wcw

Please be alert of other emails sent to you in the name of OKCHEM. Anthracene-maleic anhydride diels-alder adduct contains total 33 atom(s); 12 Hydrogen atom(s), 18 Carbon atom(s) and 3 Oxygen 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).

For standardized chemical structure and/or annotation information, please visit the summary page for CID 138503. 2019-11-21 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, … 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.
Bikarbonat slemhosta

domstol praxis
java arv
moretime revision
aarhus masters
transport site supervisor jobs
flersprakighet identitet och larande
kristanstads automobil

The Anthracene-maleic anhydride diels-alder adduct molecule contains a total of 37 bond (s) There are 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).

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.