please help calculate priduct yield and percent yield for FISCHER ESTERIFICATION OF LAURIC ACID lab Product Yield? P...
What can cause a low percent yield? In lab we did fischer esterification using benzoic acid and methanol to yield methyl benzoate. 3.05 grams of benzoic acid were used and 1.10 grams of methyl benzoate were produced. We also washed the product multiple times with water, 10% sodium bicarbonate solution, then saturated sodium chloride solution. Could the washing cause a low percent yield? If so, can you explain why?
please help identify peaks for Fischer Esterification of Lauric Acid Diamond KBS exp) mwami Mamal.be CLOSE 667BZ 1900 bact Find Pki Selch AlClear Search Lo Mgr Prev Rpl Add Ne V 8 2031.00 + 2858.13 215735 197293 1743.13 2929.98 1990.36 0012 2200 Wovenumbers (cm.) Lasystem 49626 1200
Fischer Esterification of Lauric Acid 1. Why was the majority of the ethanol boiled off prior to the extraction? 2. What impurities were removed during the column chromatography?
What is the percent yield for the following Fischer Esterification... Starting Material: 3 ml of acetic anhydride and 2 ml of 1-octanol (1 drop of sulfuric acid is also added as a catalyst) End Material: 2.00g Please include all the steps for how to find the the theoretical yield and then the percent yield. Thank you!
supplementary lab question semester 2 Organic Chemistry Fischer Esterification lab A student observed that when 4-hydroxybutanoic acid is refluxed in the presence of sulfuric acid, an ester forms. However, under the same conditions 3-hydroxycyclohexanecarboxylic acid does not yield an ester. Explain this student's observation and give the product formed in the first reaction. 5.
Fischer esterification lab question, Please help. Thank you in advance 1) In the synthesis of isopentyl ethanoate, whose reaction is shown below a) what is the purpose of the sodium bicarbonate solution in the isolation step? b) what is the purpose of adding molecular sieves to the reaction? c) what is the purpose adding sulfuric acid to the reaction? d) why is acidic acid added in excess? e) what is the purpose of conducting a semi-micro distillation in the second...
I did a lab that underwent Fischer esterification and had one of the possible alcohols and carboxylic acids. please interperet the spectra results and help identify the new product Figure 2. Potential Alcohols and Carboxylic Acids 7 ОН Мон Мон ТОН Ethanol Propanol Allyl alcohol Isobutaol о ОН ОН ОН ОН Propanoic Acid Butyric Acid Isobutyric Acid 4-Pentenoic Acid PPM 180 160 140 120 100 PPM 80 60 40 20 0 El-MS: 130.1
please help! thank you 47) Draw out the reaction mechanism for a Fischer esterification reaction with ethanol and benzoic acid in hot acidic conditions. Name the products. 48) Draw out the reaction mechanism for a Fischer esterification reaction when 5-hydroxyhexanoic acid is heated. Name the products if you feel ambitious.
In this experiment, we did a Fischer Esterification using excess acetic acid, isopentyl alcohol, and sulfuric acid to form isopentyl acetate. Then sodium bicarbonate and NaCl were used in the extraction step of the experiment. Is there another method we could have used to calculate percent yield other than using the amount of isopentyl acetate? What are the advantages and disadvantages? (Using GC is not the answer we are looking for.)
Write the mechanism for the Fischer esterification of p-aminobenzoic acid with ethanol (good handwriting).