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Diels alder lab report abstract the diels alder reaction is the addition of a diene or a compound with at least two double bonds that are conjugated and a dienophile which consists of at one double bond.

For one step, the reaction forms a six membered ring from an open chain compound This browser version is no longer supported Please upgrade to a supported browser. Write your report from your lab notes or notes taken during video observations (online only), and from information gleaned from your references

Type the final report draft into the template. • when the sample is completely dry (until next lab period), determine the yield and melting point, test it for unsaturation, and set aside a small sample to hand in with your lab report #4. In this experiment, a cyclopentadiene will react with one of four possible dienophiles The identity of the dienophiles is unknown

Once identification of the product takes place, the product will be hydrolyzed to form the dicarboxylic acid.

A comprehensive lab guide school university of california, davis* *we aren't endorsed by this school course che 118 subject chemistry

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