Synthesis of aspirin

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Aspirin is synthesized from salicylic acid and acetic anhydride using concentrated sulfuric acid as the catalyst. The purity of the synthesized aspirin is measured using the ferric chloride test as well as obtaining an FTIR spectrum.
The following lab techniques are demonstrated:
Using a warm water bath
Scratching glass to induce crystallization
Vacuum filtration
Recrystallization
Ferric chloride (FeCl3) test for phenol
FT-IR analysis

Опубликовано:

29 дек 2020

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Комментарии : 24

@alaaali6883 3 года назад

That scratch sound is so lovely 😂 lol

@plantinpot5712 25 дней назад

Thanks ❤

@rey-jc7yk 3 года назад

I enjoyed this thank you for the awesome content!

@RoxiHulet 3 года назад

Glad you enjoyed it!

@Anne-lg7wh 2 года назад

Hello! Can you upload the result of the FITR analysis? It would be a great help. Thank you.

@eleftheriospitsilis2988 Год назад

Hey I start working in pharmacutical company in my country your videos help me a lot thank you very much

@RoxiHulet Год назад

Congratulations!! 🎊🎈🎉

@sydneyhunt6681 3 года назад

Do you have to use the Acid Catalyst if given more time? Have subbed good information

@Harsh-vx6pg 2 года назад

Indian student here ... enjoyed ... greatly done

@user-ew7ih2of8o 7 месяцев назад

Organic Chemistry 2B. Sierra College Rocklin California

@hadjernoui8335 3 года назад

لماذا أضفنا الماء المثلج؟

@rohitjoshi4559 6 месяцев назад

Industrial scale, may I know the temperature at which the reaction is carried out?? Please reply ASAP

@hadjernoui8335 3 года назад

Pourquoi ajoute-t-on de l'cau

@Brumbrumauto 2 года назад

why doesnt aspirin dissolve completey in water like the medicine does? wouldthe acetic anhydride react with the water and form acetic acid?

@RoxiHulet 2 года назад

Aspirin isn’t very soluble in water. You can only dissolve about 0.3 g aspirin in 100 mL of water. When you dissolve an aspirin tablet in water, what you observe is mostly just the binder material dissolving, not the actual aspirin molecule. And yes, acetic anhydride will form acetic acid when combined with water. I don’t use water in this reaction.

@anakin1028 3 года назад

Professor Smith, thank you! Can we skip the water bath and put it directly on the hot plate?

@RoxiHulet 3 года назад

It depends on how much water or aqueous solvent you have in the flask. If there is only a small amount of aqueous substance in the flask, putting it directly on the hot plate may cause the reactants to heat up too fast and decompose. This is why a water bath is used for this particular synthesis. If there is a lot of aqueous solvent, the high heat capacity of water makes it safe to put the flask directly on the hot plate without worrying about decomposition of your reactants.

@anakin1028 3 года назад

@@RoxiHulet I see! You explained it so well. Thank you so much, have a nice day! 💖