1. Explain why the main reaction between acetophenone and anisaldehyde is the mixed aldol reaction rather than (a) self-condensation of acetophenone or (b) Cannizzaro reaction of anisaldehyde. 2. No more than 2 mL of water should be used to dissolve the 2 or 3 pellets of NaOH. Why is not a larger volume of water used? 3. Anisalacetophenone dibromide is much more soluble in CHCl3 than in CCl4. Suggest a reason for this difference. 4. Crystals of pure erythro-anisalacetophenone dibromide are white, whereas crystals of pure anisalacetophenone are light yellow. Suggest a reason for this difference in color. 5. Could trans-anisalacetophenone be isomerized to the cis isomer by irradiating it with UV light? Why or why not?
1. Explain why the main reaction between acetophenone and anisaldehyde is the mixed aldol reaction rather than (a) self-condensation of acetophenone or (b) Cannizzaro reaction of anisaldehyde. 2. No more than 2 mL of water should be used to dissolve the 2 or 3 pellets of NaOH. Why is not a larger volume of water used? 3. Anisalacetophenone dibromide is much more soluble in CHCl3 than in CCl4. Suggest a reason for this difference. 4. Crystals of pure erythro-anisalacetophenone dibromide are white, whereas crystals of pure anisalacetophenone are light yellow. Suggest a reason for this difference in color. 5. Could trans-anisalacetophenone be isomerized to the cis isomer by irradiating it with UV light? Why or why not?
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter23: Addition To A Carbonyl
Section: Chapter Questions
Problem 25E
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