If the reaction mixture containing p-aminophenol, distilled water, and acetic anhydride was heated to 200 °C as opposed to 100 °C, what would have happened? (Please clearly explain the differences between the two temps the mixture is heated to)
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Q: the reaction mixture containing p-aminophenol, distilled H2O, and acetic anhydride was heated to 200…
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If the reaction mixture containing p-aminophenol, distilled water, and acetic anhydride was heated to 200 °C as opposed to 100 °C, what would have happened? (Please clearly explain the differences between the two temps the mixture is heated to)
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- If the reaction mixture containing p-aminophenol, distilled water, and acetic anhydride was heated to 200 °C (as opposed to 100 °C), what would have happened?If the reaction mixture containing p-aminophenol, distilled H2O, and acetic anhydride was heated to 200 degrees celsius what would have happened? (Originally, was heated to 95-100 degrees celsius and formed crude Acetaminophen for my Acetaminophen lab, but am unsure if heated at 200) Please help! Thanks in advance!!!What common result occurred in all of the following experimental tubes? Why? a. a mixture of hot water and egg white b. a mixture of salt and egg white c. a mixture of baking soda and egg white d. a mixture of lemon juice and egg white e. a mixture of ethyl alcohol and egg white
- Which layer (aqueous or organic) would you expect to find 3,5-dimethylaniline in the following liquid-liquid extractions? Explain. Draw chemical structures to help explain your answers. If the structure of themolecule changes in the aqueous solution, then draw the new structure. i. water and dichloromethaneii. aq. NaOH and dichloromethaneiii. aq. HCl and dichloromethaneWhy does the acetic anhydride react with the -NH2 and not the -OH group of p-aminophenolWhy is sodium benzoate soluble in cold water but benzoic acid is insoluble in cold water despite both having an aromatic ring in its structure which is non-polar in nature?
- A student decided to run the esterification reaction between p-toluic acid (p-methylbenzoic) and ethanol but found that the stockroom had only just enough ethanol left to react with her carboxylic acid, that is, a stoichiometric amount of alcohol. Furthermore, the only concentrated acid the stockroom had left was hydrochloric acid (a non-dehydrating acid ). What other method (s) could she use to drive the esterification reaction to completion ?a. Give at least three characteristics of dichloromethane that makes it a good extracting solvent for the alkaloid.b. Why is it necessary to remove a stopper from a separatory funnel when the liquid is being drained from it through a stopcock?c. What are emulsions? Why do they form during extractions? How is the formation of an emulsion minimized? How are emulsions removed?in the synthesis of benzocaine: what is the structure of the precipitate that formed after the sulfuric acid was added to the cooled mixture of p-aminobenzoic acid and pure ethanol?
- For an acid-base experiment with access to DCM, HCl & NaOH,trying to seperate a mixture of caffeine, benzoic acid and cellulose, can someone explain how this experiment can be conducted? with the chemicals included andinstrumentationGive at least three characteristics of chloroform that make it a good extracting solvent for the alkaloid.At the end of your ester synthesis, you would have had a reaction mixture (what are the compounds in this mixture). Draw a detailed separation flow scheme (chart) for the isolation of pure banana oil from the reaction mixture. Hint: think extraction and distillation.