(Diels-Alder reaction of anthracene with malice anhydride)
Calculate the percent recovery for the recrystallization. (Started with 100 mg anthracene and 55 mg maleic anhydride)
product before recrystallization: 0.083 g product after recrystallization: 0.038 g
(Diels-Alder reaction of anthracene with malice anhydride) Calculate the percent recovery for the recrystallization. (Started with...
(Diels-Alder reaction of anthracene with malice anhydride) Calculate the percent yield of your product before and after recrystallization. Compare the percent yields and explain why they are not the same. 100 mg anthracene 55 mg maleic anhydride product before recrystallization: 0.083 g product after recrystallization: 0.038 g
Calculate the theoretical yield of the Diels-Alder reaction between anthracene (100 mg) and maleic anhydride (55 mg). Which is the limiting reagent ? Show all calculation steps.
Finding the theoretical yield of the Diels-Alder Adduct with maleic anhydride and anthracene. amount of anthracene used: 0.20 grams amount of maleic anhydride used: 0.11 grams molar weight of anthracene: 178.23 g/mol molar weight of maleic anhydride: 98.06 g/mol molar weight of Diels-Alder adduct: 276.29 g/mol
Reaction is Diels-Alder Reaction: 0.6 g (Anthracene) + 0.3 g (maleic anhydride) --> product [9,10-dihydroanthreceno-9,10-endo- α, β-succinic anhydride] 0.70 grams obtained. When vacuumed, xylened and isolated, the product yielded 0.70 grams product. Please show how to calculate % yield with the weights above (Theoretical + Actual).
How many g of anthracene would you need to react with 9.8 g of maleic anhydride in a Diels-Alder reaction? (Assume a 1:1 molar ration of anthracene to maleic anhydride.) 2 - If you started lab using 0.221 g of anthracene and 0.652 g of maleic anhydride, and obtained 0.182 g of product, what is the percent yield?
Write a reaction scheme and structures for the diels-alder reaction to 0.8 g of anthracene and 0.40g of maleic anhydride and add 10 mL of p-xylene
Diels-alder reaction lab Reaction: anthracene+ maleic anhydride <---> 9,10-Dihydroanthracene-9,10-α,β-succinic acid anhydride How would raising the temperature of the experiment affect product isolation? Would more or less product be expected, and why?
What is the complete Infrared Spectrum of 9,10-dihydroanthracene-9,10-α,β-succinic anhydride, in the diels-alder reaction of Anthracene With Maleic Anhydride?
I did an organic chemistry lab using the Diels-Alder reaction with anthracene-9-methanol, N-methylmaleimide, and water. I started with 0.066 g of anthracene-9-methanol, 25 mL of deionized water, and 0.070 g of N-methylmaleimide. How would I calculate the percent recovery of the product? (not the percent yield)
Identify products peaks A-D in Diels-Alder reaction where we
used Anthracene and Maleic anhydride to produce Diels-Alder Product
7.41 7.40 7.26 odds 7.34 1-7.34 7.33 1.7.22 7.21 -7.21 17.20 17.20 17.18 6621 17.39 SE2 44.83 14.83 SRB 3.60 3.58 3.56 3.50 3.48 3.46 C (dd) 7.45 7.40 735 3.54 3.52 11 (ppm) 730 725 11 ppm) 720 7.15 7.10 B (da) A (dt) 7.397.20 E dd) 3.53 1.98 1,93 4.00 2.01 6.6 6.4 6.2 6.0 5.8 5.6 5.4 5.2 5.0...