Write down one paragraph (with proper equations) the steps for synthesizing a sample of Aspirin.

What is the name of the reaction

1. Write all steps in the hydrolysis of tert-bútyl chloride to tert-butanol.

PURPOSE: • To synthesize esters and to identify the odor of each ● To write chemical equations for the formation of each ester APPARATUS AND MATERIALS: test tubes 400 mL beaker hotplate SAFETY: Note: ethanoic acid I;is labelled Glacial Acetic Acid PROCEDURE: Lab - MAKING ESTERS drop bottles of: Sulfuric acid is extremely corrosive. Avoid direct contact. If any touches your skin, wash it off immediately. Note the eyewash station. Alcohols and carboxylic acids are flammable. Use caution. TEST TUBE concentrated sulfuric acid methanol ethanol 1-octanol A B C D E 1. Prepare a hot water bath using the 400mL beaker and hotplate. Adjust the heating control to maintain a water temperature of about 70°C. 2. Label 5 test tubes A to F. Place the test tubes on a test tube rack 3. In the appropriate test tube, add 0.5 mL (10 drops) of alcohol followed by 0.5 mL (10 drops) of the carboxylic acid according to the table below. CARBOXYLIC ACID 0.25 g salicylic acid 0.5 mL ethanoic acid 0.5 mL butanoic…

1. Draw the chemical structures of both Amiodarone and Levothyroxine. Label all of the organic chemical reactions between them (you can use arrows, etc to do this). Aswell as explain Goitre in your own words, the increased iodine from the Amiodarone and why TSH may increase and T3, T4 remain normal etc. -0-CH2 -CH2-N Amiodarone C;H5 CH2)3 CH3 но NH2 Levothyroxine HO. HO. ÑH2

4 uv/vis spectrum obtained by my TA

Examine the following 12 organic compounds and answer the following questions. Answer by writing the letter associated with the correct compounds to the right of each question. A.) Indicate the compounds may serve only as H-bond acceptor? B.) Indicate the compounds that serve both as H-bond acceptors and donors? C.) Indicate the compounds that will not participate in H-bonding?

Could I please have help with number 5: Show the full structure of the salt that forms when triethylamine reacts with hydrochloric acid

shawl the detailed beland the neaction Label each спе of the reaction the ardor listed belanu. of part of the defalled mechanism wing of the terms listed.. - ester hydrolysis decarboxylaton Keto- endi tautomensin reaction. mechanism proceeds in •OCN3 OH 1130 + он '+' CH 3 CH + CO₂