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Acetanilide Lab Report

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Hazards The substances used during the experiment have some hazardous drawbacks. Some hazards of working with Acetanilide are irritation to the skin and serious eye damage, when in contact (Acetanilide). This compound is combustible. Some hazards of working with P-toluic acid are a skin, eye, and throat irritant (4-Methylbenzoic acid). This compound is combustible. Some hazards of working with P-tert-butylphenol are irritation to the eyes, nose and skin (4-tert-butylphenol). This compound is combustible. Some hazards of working with Tert-butyl methyl ether are irritation to the tissues of external organs and toxic vapors (Tert-Butyl methyl ether). This compound is combustible and highly flammable. Some hazards of working with Sodium Bicarbonate …show more content…

First, the students set up a separatory funnel on a support ring over a 150mL beaker labeled carboxylic acid. 2. They then added 25mL of a premixed solution containing acetanilide and tert-butyl methyl ether to the separatory funnel and mixed the solution with 10mL of sodium bicarbonate. The gaseous emission was carefully released while mixing. 3. The aqueous solution on the bottom layer was drained into the 150mL beaker. 4. Steps 2 and 3 was repeated two more times and the final mix was with 5mL of water, then the aqueous solution on the bottom layer was drained into the 150mL beaker. 5. The carboxylic acid was mixed with enough HCl to precipitate and was put on a vacuum filtration apparatus. The weight of the residue was recorded. 6. They then mixed the original solution with 10mL of sodium hydroxide. The gaseous emission was carefully released while …show more content…

The aqueous solution on the bottom layer was drained into another 150mL beaker labeled phenol. 8. Steps 5 and 6 was repeated two more times and the final mix was with 5mL of water, then the aqueous solution on the bottom layer was drained into the 150mL beaker. 9. The phenol was mixed with enough HCl to precipitate and placed in an ice bath to form crystal. After 10 minutes, it was put on a vacuum filtration apparatus. The weight of the residue was recorded. 10. After, Na2SO4 was added to the separatory funnel and left for 5 minutes while occasionally mixed. The residue was taken out. 11. The mixture was poured into a 150mL pot and heated until all the aqueous solution evaporated, leaving acetanilide in the pot. 12. The mass of the pot before and after the reaction was recorded. 13. The observations were recorded and the lab was concluded by cleaning the fume

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