1. A. Predict the products for the following reaction and write a rational mechanism. OCH3 (CH3CO20...
1. C. A student reacted anisole with acetic anhydride in dichloromethane using aluminum chloride as a catalyst. The student used the experimental procedure as described in the laboratory manual. At the end of the experiment the student failed to get 4 methoxyacetophenone. Give reasons for the student's failure to get the product.
m. A. Predict the products for the following reaction and write a rational mechanism. HO -NH2 (CH3CO)20 Mechanism: M. B. The reaction of 5.30g of p-aminophenol with 15.20 g of acetic anhydride produced 4.35 g of acetaminophen. Calculate the percent yield of acetaminophen. m. C. How did you purify the crude acetaminophen? Briefly explain.
predit the products for the followig reaction and write a rational mechanism 1. A. Predict the products for the following reaction and write a rational mechanism. OCH (CH3CORO AICI: Mechanism:
Please help with questions 1-5. I have attached the additional lab information pages for help if you are unclear on anything please review those. We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
QUESTIONS 1. What is the purpose of the sulfuric acid (yes, it's a catalyst, but why is it a catalyst? What is it doing that makes the reaction possible? Would the reaction just go slower without it, or would the reaction not go at all? Why?) 2. If isobutyl alcohol (2 methyl propanol) is used instead of tert butyl alcohol, a mixture of products is obtained. One the products is the same as the product obtained with the tert butyl...
The following questions are from an experiment titled Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are pictures attached of the lab manual. 2) Is this method a good route for the preparation of p-sec-butyltoulene? Give reasons for your answer. 3) Why do you use a large excess of toulene. What are its functions? 4) What is the purpose for adding the hydrochloric acid to the water in the separatory funnel in step 5? Hint: If no acid is added,...