We ran the electrophonic aromatic substitution rates with equal volumes of 0.2 M

Question

We ran the electrophonic aromatic substitution rates with equal volumes of 0.2 M arene and 0.0S M bromine solutions instead of 0.05 M arene and 0.2 M bromine solutions. We ran our Fischer etherification reaction with ethanol as the solvent instead of just adding the same number of moles of ethanol as we had of p-amino benzoic acid. Need excess otherwise to push the equilibrium tirade the product then fine , the reaction product from the product. . In the Dlels-Alder reaction we added petroleum ether after the exothermic had subsided in the dlels-Alder reaction we added petroleum ether after the exotherm had subsided. After the addition of the petroleum ether in the diels - Alder reaction , we then heated the solution.

Explanation / Answer

d. If we take 0.05 M arene and 0.2M Br2 then the product is tribromo arene which is a tri substituted product.

f. Anhydride product of Diels-Alder reaction could have possibly hydrated before extraction, causing it to be soluble in petroleum ether

g.the product is not soluble in petroleum ether, but it is in the ethyl acetate solvent, therefore it crashes out upon addition to the petroleum ether

Related Questions

Navigate

• Browse (All)
• Browse W
• Subjects

---

---

Integrity-first tutoring: explanations and feedback only — we do not complete graded work. Learn more.