Question

In: Chemistry

Calculate the atom economy and reaction efficiency for the Diels Alder reaction.


Calculate the atom economy and reaction efficiency for the Diels Alder reaction. For the reagents, consider only the mass Mol. wt. of the 9-anthracenemethanol and N-methylmaleimide. Use proper significant figures, units and show all work. 


Atom economy (Mol, wt, desired product/combined Mol, wt. of all reagents) 

Reaction efficiency = atom economy x percent yield

Solutions

Expert Solution


Related Solutions

Diels Alder reaction Draw the Diels Alder reaction between cyclopentadiene and maleic anhydride in ethyl acetate.what...
Diels Alder reaction Draw the Diels Alder reaction between cyclopentadiene and maleic anhydride in ethyl acetate.what would happen if it is run inwater? draw the reaction and explain it.
1. Explain the principle synthetic value of the Diels-Alder reaction 2. The Diels-Alder reaction proceeds well...
1. Explain the principle synthetic value of the Diels-Alder reaction 2. The Diels-Alder reaction proceeds well in nonpolar solvents. Why are polar solvents not required?
what statement about Diels-Alder reaction is wrong? a. a diels alder reaction has translation state b....
what statement about Diels-Alder reaction is wrong? a. a diels alder reaction has translation state b. a diels alder reaction has an intermidiate state c. a diesk alder reaction is concerted d all of above What statement about diels alder reaction is true a. a typical diels-alder reaction forms potentially two new sterocenters. b. a typical diels-alder reaction is thermodynamically controlled. c.a typical diels-alder reaction forms potentially 4 new sterocenters. d. a typical diels-alder reaction forms potentially 6 new sterocenters.
A Diels-Alder reaction of 2,5-dimethylfuran and maleic anhydride
A Diels-Alder reaction of 2,5-dimethylfuran and maleic anhydride gives a compound A that undergoes acid- catalyzed dehydration to give 3,6-dimethylphthalic anhydride. (a) Deduce the structure of compound A. Draw all non-bonding electrons (as applicable) (b) Give a curved-arrow mechanism for the conversion of A into 3,6-dimethylphthalic anhydride. The catalyst H2SO4 is abbreviated as "H-B" below and its conjugate base is abbreviated as B Follow the directions above each drawing box. First step: Delete/Add bonds to form A,  Add 2 curved arrows to give...
synthesis of Ethanol by fermentation (a) Calculate the atom economy and reaction efficiency of your ethanol...
synthesis of Ethanol by fermentation (a) Calculate the atom economy and reaction efficiency of your ethanol synthesis. (b) Describe some green features of your synthesis, and any that aren't so green.
The product of a Diels Alder reaction is often a pair of enantiomers. Does the reaction...
The product of a Diels Alder reaction is often a pair of enantiomers. Does the reaction of 9 10-dihydroanthracene-9 10-a b-succinic anhydride produce enantiomers? If yes, please draw each enantiomer. If your answer is no explain why using accurate structural drawings.
In the procedure for the synthesis of hexaphenylbenzene, a Diels-alder reaction occurs and we needed to...
In the procedure for the synthesis of hexaphenylbenzene, a Diels-alder reaction occurs and we needed to ensure all the starting materials were dry. After the reaction, we also washed with hexanes and toluene. What is the purpose of this two things? also worth mentioning Silicon oil was used as a solvent
The Diels-Alder reaction is one of the most useful in organic chemistry because it allows for...
The Diels-Alder reaction is one of the most useful in organic chemistry because it allows for the formation of rings: The reactor initially has only the diene and the dienophile. The product stream has 55 mole% of the ring and 17 mole% of diene. Calculate the fractional conversion of the limiting reactant and the percentage by which the other reactant is in excess. If we assume that we can do this reaction continuously, pick a basis for the feed and...
In a Diels-Alder reaction why doesn't the carboxylic acid attack the ester to reform the acid...
In a Diels-Alder reaction why doesn't the carboxylic acid attack the ester to reform the acid anhydride?
In a Diels-Alder reaction, why doesn't the carboxylic acid attack the ester to reform the acid...
In a Diels-Alder reaction, why doesn't the carboxylic acid attack the ester to reform the acid anhydride? Why this Diels-Alder provides the cis-ring juncture instead of the trans?
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT