2. Explain why the synthetic process used here allows one to carry the reaction to t eaöuht of wa...
Working on the questions at the end of this lab report (see above). I need help answering questions 2, 3, and 4 completely and thoroughly. Thank you! s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
2. Was benzene present as a side product in the GC? If so, try to identify it (there is likely no standard for comparison in our lab facility because of benzene's toxicity). 3. What steps were taken to keep the system water free? Name each precaution taken. 139 4. Illustrate the mechanism for the desired reactions pas electrons. 5. How does your IR compare with the standard library match? 6. Why is THF a better solvent than diethyl ether for...
2. Briefly explain why ethanol, and not hexane, was used as a solvent in this reaction? 3. Why it is necessary to filter the crude coupling product through a column of anhydrous MgSO4? 4. Briefly explain why aryl bromides and iodides, rather than aryl chlorides or fluorides, are typically used as substrates in Pd-catalyzed coupling reactions. 5. Propose a synthesis for the molecule A shown below, using benzene, phenyl boronic acid, tert-butyl bromide and any inorganic reagents needed. A retrosynthetic...
Why did you wash the ether solution with sodium bicarbonate? Write chemical equations for the reactions that took place. b. At which purification steps was the unreacted methanol removed in the reaction? Some of it may have been removed in more than one place. c. Three-Step Synthesis of Methyl Anisate (Step 3) 0 CHOH. Н.so, cat.) Wear gloves. Methanol is poisonous. Ether is an anesthetic, so don't breathe it. Sulfuric acid is a strong corrosive acid. Wash any you spill...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
please answer all these questions, thank you. CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...
Please explain what is going on in this lab for STEP 3. what are some important factors? Multistep Synthesis Preparation of 4,4-Diphenyl-3-buten-2-one! This experiment illustrates se multistep synthesis, in which the the next. This process is very common iment illustrates several important concepts of organic synthesis. It is a synthesis, in which the product of one reaction becomes the starting material of This process is very common in industry and research, and demands careful to vields and techniques. The experiment...
i need help with the postlab questions please Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
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,...