Question

The Diels-Alder Reaction of Anthracene with Maleic Anhydride. What is the theoretical yield? .80g anthracene used...

The Diels-Alder Reaction of Anthracene with Maleic Anhydride.

What is the theoretical yield?

.80g anthracene used

.40 g Maleic Anhydride used

Science   Chemistry   
0 0
Add a commentTranscribed image text
Next >

Homework Answers

Answer #1

0 0
Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Log In

Sign Up

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Calculate the theoretical yield, actual yield, and % yield of the Diels-Alder product. Amount maleic anhydride...
Calculate the theoretical yield, actual yield, and % yield of the Diels-Alder product. Amount maleic anhydride used: 0.098g Amount 3-sulfolene used: 0.261g Diels-alder adduct (MW= 152.15 g) amount recovered: 0.063g Melting point: 103C Molar mass maleic anhydride: 98.06 g/mol Molar mass 3-sulfolene: 118.15 g/mol
Diels Alder Reaction with anthracene and maleic anhydride Show the result of the hydrolysis of the...
Diels Alder Reaction with anthracene and maleic anhydride Show the result of the hydrolysis of the reactin product. Why aren't we worried about exposing the product of the reaction to atmospheric moisture during this experiment, since water will destroy the desired product? How would you distinguish whether this degradation of the product had occurred using instruments available in organic chemistry lab?
Would you expect a Diels-Alder reaction between maleic anhydride and naphthalene to require more or less...
Would you expect a Diels-Alder reaction between maleic anhydride and naphthalene to require more or less harsh conditions than the reaction performed with anthracene? Justify your answer.
Diels Alders Reaction While performing the Diels-Alder reaction between cyclopentadiene and maleic anhydride: (a) Why do...
Diels Alders Reaction While performing the Diels-Alder reaction between cyclopentadiene and maleic anhydride: (a) Why do you have to crack the diene? Draw the reaction that occurs during the cracking process   
The purpose of this experiment is to form 9,10-dihydroanthracene-9,10-α,β-succinic anhydride by way of a Diels Alder...
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. Anthracene acts as the diene and maleic anhydride functions as the dienophile. Xylene (dimethylbenzene) is used as a high boiling temperature solvent so that the reaction will proceed quickly. Give 5 observations that occurred for a Diels-Alder reaction between maleic anhydride, anthracene, and xylene and why those observations occurred (yes it is...
(1) Draw the products of Diels-Alder reaction of maleic anhydride with α-phellandrene, β- phellandrene, and α-terpinene,...
(1) Draw the products of Diels-Alder reaction of maleic anhydride with α-phellandrene, β- phellandrene, and α-terpinene, assuming that endo product is formed. In each structure, mark all chiral carbons present (if any). (2) Using a reaction of 1,3-cyclohexadiene with maleic anhydride, explain endo selectivity in Diels-Alder reaction (include a clear drawing of orbitals overlap in transition state as a part of your answer)
What is the theoretical yield in grams of the product from the Diels Alder (MW=276 g/mol)...
What is the theoretical yield in grams of the product from the Diels Alder (MW=276 g/mol) if you start with 0.123 g of anthracene (MW=178 g/mol) and 0.224 g of maleic anyhyride (MW= 98.1 g/mol). Which is the limiting reagent? *Will someone please break down stoichiometry for me.. theoretical, percent yield, & limiting reagent? I am so confused and I desperately need to learn this.
Draw the products of Diels-Alder reaction of maleic anhydride with α-phellandrene, β- phellandrene, and α-terpinene, assuming...
Draw the products of Diels-Alder reaction of maleic anhydride with α-phellandrene, β- phellandrene, and α-terpinene, assuming that endo product is formed. In each structure, mark all chiral carbons present (if any).
In a Diels-Alder reaction with benzyne and anthracene to make triptycene, why is the benzyne added...
In a Diels-Alder reaction with benzyne and anthracene to make triptycene, why is the benzyne added to the central ring of anthracene and not on the ends? Which resonance structure of anthracene is the most stable?
Diels alder reaction with anthracene 9 methanol: if the melting point of your product is below...
Diels alder reaction with anthracene 9 methanol: if the melting point of your product is below 232-235 what will be the possible reasons?
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT