H2(g) + MgC4H2O4
I'm doing the same problem..are u in my chm206 lab? lol anyway..maleic anhydride reacts with water from the toluene to form maleic acid.
Maleic Anhydride.
Put the maleic anhydride into the appropriately marked hazardous waste container.
it will react to make water and carbon dioxide
It's illegal.
I'm doing the same problem..are u in my chm206 lab? lol anyway..maleic anhydride reacts with water from the toluene to form maleic acid.
The product of the reaction between anthracene and maleic anhydride is known as anthracene-maleic anhydride adduct. This adduct is commonly used in the synthesis of dyes, polymers, and other organic compounds.
Maleic Anhydride.
Put the maleic anhydride into the appropriately marked hazardous waste container.
it will react to make water and carbon dioxide
Maleic acid and fumaric acid are cis-trans isomers of each other.
Side reactions would be the reaction of cyclopentadiene with itself (dimerization) into dicyclopentadiene, as well as the formation of the exo-product along with the usual endo-product (cis-norbornene-5,6-endo-dicarboxylic anhydride).
It's illegal.
C4H2O3
1. Maleic anhydride is hydrated. This produces maleic acid. 2. Maleic acid is isomerised in the presence of a catalyst. 3. Fumaric acid is produced. Easy as that! (Except the temperature and pressure have to be kept controlled throughout)
Molecular Weight: 98.06
If maleic anhydride were planar, then it would actually be ANTIaromatic, because one of the lone pairs on the cyclic oxygen would participate in the cyclic pi-bonding. For this reason, maleic anhydride is NOT planar. The cyclic oxygen actually sticks out about .3 Angstroms, which breaks antiaromaticity. So, short answer: no.