Hear we have to know 2 points
* * An acid react with base gives salt
** salts soluble in water, hydrocarbons and neutral hydrocarbons soluble in organic layer.
Comming to answer
a) in our reaction mixture contains two acids those are acetic acid, sulphuric acid. So it can react with sodium bicarbonate gives salt and soluble in aquas layer. Remain isopropyl alcohol and isopropyl acetate are neutral hydrocarbons are as organic layer.
Answers b, c attached photo please check the details
Thank you.
1. The reaction mixture contains isopentyl acetate, isopentyl alcohol, water, acetic acid and sulfuric acid. a)...
In Synthesis of Isopentyl Acetate experiment, how was the acetic acid and sulfuric acid neutralized after reflux has been completed? Write two separate balanced chemical equations that show how each acid was neutralized in this experiment. Isopentyl alcohol + acetic acid -> isopentyl acetate + water The reaction is treated with concentrated Sulfuric acid
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.)
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Assume you are doing an experiment on the esterification of isopentyl acetate using 1mL of isopentyl alcohol and 1.5mL of acetic acid. Assuming complete reaction, calculate the amount of acetic acid left in the post-reaction mixture at the end of reflux Calculate the amount of 5% aq sodium bicarbonate needed to neutralize the unreacted acetic acid
In the experiment of synthesizing isopentyl acetate by reacting an excess of acetic acid with Isopentyl alcohol and using sulfuric acid as the catalyst, what was the purpose of doing a distillation after heating under reflux for an hour?
Correlate the microscale procedures needed to accomplish the given steps (1-5) to isolate pure isopentyl acetate (banana oil) from the reaction mixture. (Not all of the steps on the left are required.) 1 Granular anhydrous sodium sulfate is added to the aqueous layer. This deprotonates unreacted acetic acid, making a water soluble salt. The lower aqueous layer is removed using a Pasteur pipette and discarded. 2 This ensures that the evolution of carbon dioxide gas is complete. 3 This removes...
If the yield from the reaction of acetic acid with isopentyl alcohol is 45%, how many grams of isopentyl acetate are formed from 3.58 g of acetic acid and 4.70 g of isopentyl alcohol? The reaction is: CH3CO2H+C5H12O→C7H14O2+H2O Express your answer using two significant figures.
This experiment involved the use of Fischer Esterification to create isopentyl acetate from reacting isopentyl alcohol with acetic acid and sufluric acid. 1. Provide a balanced equation to explain the evolution of gas during the sodium bicarbonate washing step. 2. The microscale synthesis of esters often uses a Dean-Stark trap. A Dean-Stark trap separates and collects water during a reaction. How would using a Dean-Stark trap during a Fisher-Esterification affect the synthesis? 3. Esters are often used in artificial flavorings....
We made esters from carboxylic acids and alcohol. (for one of them, acetic acid + isopentyl alcohol + couple drops of sulfuric acid). Could someone please explain those. Thank you 1. Consider if we had prepared high molecular weight esters, what problems would this pose regarding our method of analysis 2. We used sulfuric acid as a catalyst, but carboxylic acids are a reagent in this reaction. Would simply using excess carboxylic acid work as efficiently as sulfuric acid to...
If 4.46 g of acetic acid and 2.19 g of isopentyl alcohol are used in the reaction, what is the limiting reagent? What is the theoretical yield? What is the percent yield if 2.50 g of isopentyl acetate are obtained? (please show all calculations!!!)