5) Complete the following reaction. 5) Compound below was synthesized using a Wi

Question

5) Complete the following reaction. 5) Compound below was synthesized using a Williamson ether synthesis; provide a stepwise mechanism which accounts for its formation. Show electron flow and all the intermediates involved. 6) Why is acetaminophen soluble in 5% aqueous sodium hydroxide while phenacetin is not? Explain using a relevant chemical equation or words. For number 5, the first reaction would the product be a benzene ring with an O-Na attached?? Could someone please answer all of these Im not sure I am understanding them correctly. I understand the second reaction in number 5 would yield an ester though.

Explanation / Answer

a)cyclohexanol with a strong base sodium ethoxide undergoes elimination by E1CB mechanism though the yields might be verypoor, since there is no strong

Related Questions

Navigate

• Browse (All)
• Browse 5
• Subjects

---

---

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