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Aspirin (acetylsalicylic acid) consists of three groups:carboxylic acid functional group (R-COOH)ester functional group (R-O-CO-R")aromatic group (benzene ring)
Properties the Aspirin (acetylsalicylic acid)AcidityAspirin is a monoprotic weak acid, Ka = 2.8 x 10-4 in ~ 25oC, for this reason very tiny of the molecule aspirin (acetylsalicylic acid) dissociates to type acetylsalicylate ions.For the equilibrium dissociation reaction:
aspirin (acetylsalicylic acid)acetylsalicylate ion+H++H+

the equilibrium position lies well to the left, favouring molecular aspirin.SolubilityAspirin is only slightly soluble in water and also acidic solutions such together is existing in the stomach. Aspirin contains polar functional teams which can form hydrogen bonds through polar water molecules.Aspirin is an ext soluble in basic (alkaline) solutions, so it easily dissolves in the duodenum i beg your pardon is the an initial part that the intestine.Ionic salt of aspirin, such as salt acetylsalicylate, are more soluble in water due to the fact that they kind stronger ion-dipole interactions with water.These ionic salts of aspirin are occasionally marketed together "soluble aspirin". When you add water smashville247.nete the dissolve aspirin, eg, sodium acetylsalicylate, the dissociates to type sodium ions and also acetylsalicylate ions:
sodium acetylsalicylate → acetylsalicylate ions+sodium ion → +Na+C9H7O4-Na+ → C9H7O4-+Na+

In the acidic stomach, molecule aspirin crystallizes out:
acetylsalicylate ions+H+ → aspirin+H+ → C9H7O4-+H+ → C9H8O4

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Synthesis that Aspirin (acetylsalicylic acid)Salicylic mountain will swiftly react v acetic anhydride in the existence of an acid catalyst to create aspirin (acetylsalicylic acid) and acetic acid (ethanoic acid).Sulfuric acid or phosphoric mountain are often used smashville247.nete catalyse the reaction.

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salicylic acid+acetic anhydride(ethanoic anhydride) → aspirin(acetylsalicylic acid)+acetic acid(ethanoic acid)+
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→ +CH3COOHC7H6O3(s)+C4H6O3(l) → C9H8O4(s)+C2H4O2(aq)

Salicylic acid have the right to react with acetic (ethanoic) mountain in an esterification reaction, but the reaction is an extremely slow, taking days to with equilibrium, and also the productivity is low:
salicylic acid+acetic acid(ethanoic acid) → aspirin(acetylsalicylic acid)+water+CH3COOH → +H2OC7H6O3+C2H4O2 → C9H8O4(s)+H2O

For this reason, the smashville247.netmercial ready of aspirin relies on the faster reaction between salicylic acid and also the more reactive acetic anhydride which produces a greater yield of aspirin.
aspirin(acetylsalicylic acid) + sodium hydroxide → a salt(sodium acetylsalicylate) + water + NaOH(aq) → + H2O(l)C9H8O4(s)+NaOH(aq) → C9H7O4(s)-Na++H2O(l)

The neutralization reaction deserve to be supplied to recognize the quantity of aspirin (acetylsalicylic acid) current in smashville247.netmercially available aspirin tablets using a back (indirect) titration method.Reaction with carbonate: acid + carbonate → salt + carbon dioxide + water
aspirin(acetylsalicylic acid) + salt hydrogen lead carbonate → a salt(sodium acetylsalicylate) + carbon dioxide gas + water + NaHCO3(aq) → + CO2(g) + H2O(l)C9H8O4(s)+NaHCO3(aq) → C9H7O4(s)-Na++CO2(g)+H2O(l)

The reaction with bicarbonate (hydrogen lead carbonate ion) is frequently used smashville247.nete prepare the salt the aspirin i m sorry is an ext soluble in water 보다 the molecular form of aspirin.Hydrolysis: cleavage that a covalent bond in a molecule by reaction v water
aspirin(acetylsalicylic acid)+water → salicylic acid+acetic acid(ethanoic acid)+H2O(l) → +CH3COOH(aq)C9H8O4(s)+H2O(l) → C7H6O3(s)+C2H4O2(aq)

Old aspirin tablets may have a smell like vinegar together a result of the hydrolysis reaction creating acetic mountain (ethanoic acid).

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