22.65 When the following acid chloride is treated with AICI3, followed by HCl and Zn(Hg), a product is formed whose 'H NMR and IR spectra are shown here. Draw the product and propose a complete, detailed mechanism for the first of these two reactions. 1. AICI3 2. HCI, Zn(Hg) 100- 80- ? 60- 40- * 20- 7 6 4 3 2 1 4500 4000 3500 3000 2500 2000 1500 1000 500 Chemical shift (ppm) Wavenumbers (cm-1) % Transmittance

22.65 When the following acid chloride is treated with AICI3, followed by HCl and Zn(Hg), a product is formed whose 'H NMR and IR spectra are shown here. Draw the product and propose a complete, detailed mechanism for the first of these two reactions. 1. AICI3 2. HCI, Zn(Hg) 100- 80- ? 60- 40- * 20- 7 6 4 3 2 1 4500 4000 3500 3000 2500 2000 1500 1000 500 Chemical shift (ppm) Wavenumbers (cm-1) % Transmittance

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter22: Reactions Of Benzene And Its Derivatives

Section: Chapter Questions

Problem 22.50P: Following is the structure of miconazole, the active antifungal agent in a number of...

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22.65 When the following acid chloride is treated with AICI3, followed by HCl and Zn(Hg), a product is formed whose 'H NMR and IR spectra are shown here. Draw the product and propose a complete, detailed mechanism for the first of these two reactions. .CI 1. AICI3 2. HCI, Zn(Hg) 100 80- ? 60 40- * 20- 7 4 3 1 4500 4000 3500 3000 2500 2000 1500 1000 500 Chemical shift (ppm) Wavenumbers (cm-1)
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