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Diels-Alder Reaction: Preparation of cis-Norbornene-5,6-endo-dicarboxylic Anhydride (University of Colorado, Boulder, Dept of Chem and Biochem.) The Diels-Alder reaction is an important addition reaction.

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Related content

Maleic anhydride - the NIST WebBook
Breslauer and Kabakoff, 1974. Breslauer, K.J.; Kabakoff, D.S., Enthalpy of the Diels-Alder...
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Chemistry 210 Experiment 9
In this experiment you will react cyclopentadiene (the diene) with maleic anhydride (the...
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Frontier molecular orbital theory - gaz.wiki
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In this experiment you will react cyclopentadiene (the diene) with maleic anhydride (the dienophile) to produce the bicyclic compound, endo-bicyclo[2.2. 1]hept-5-ene-2,3-dicarboxylic anhydride.

The Diels‐Alder reaction is a cycloaddition reaction between a conjugated diene and an alkene. This reaction produces a 1,4‐addition product. A typical example is the reaction of 1,3‐butadiene with maleic anhydride.

The Diels-Alder reaction is a conjugate addition reaction of a conjugated diene to an alkene or alkyne (the dienophile) to produce a cyclohexene.

Furan and maleic anhydride react to form a bicyclic Diels-Alder adduct. The bicyclic product can have either endo or exo stereochemistry. In Diels-Alder reactions the endo product forms faster - it has a lower energy transition state due to favorable pi orbital overlap.

The Diels-Alder reaction between cyclopentadiene and maleic anhydride can produce two possible products, the 'endo' and the 'exo' adducts. 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.

Cyclopentadiene is the limiting reagent by a small margin. A 100% theoretical yield should be 0.00303 mols of product since cyclopentadiene gets fully consumed first. The actual yield is 0.00228 mols .

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 "cycloaddition".

The Diels‐Alder reaction is a cycloaddition reaction between a conjugated diene and an alkene. This reaction produces a 1,4‐addition product. A typical example is the reaction of 1,3‐butadiene with maleic anhydride.

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Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
Privacy Notice
Legal Hub
Content Takedown Policy
Bug Bounty Program
About Us
Help Portal
Legal Resources
Blog
Affiliates
Contact Us
Delete My Account
Site Map
Industries
Forms in Spanish
Localized Forms
State-specific Forms
Forms Kit
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate WorkFlow
DocHub
Instapage
Social Media
Call us now toll free:
+1 833 426 79 33
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232