What's the relationship between aspirin and salicylic acerbic?
I just learned that aspirin can be prepared by the esterification of the phenolic hydroxyl group of salicylic acid. What does this mingy? The stuff I use for acne treatment contains salicylic acid, just how is it related to the aspirin drug surrounded by plain english?
Answers:
Aspririn is acetylsalicylic acid. Basically, an acetic acid is combined with the salicylic sharp so that when it gets disolved in your stomach it does not tear through the protective pool liner as much (in other words, give you an ulcer)
The uncatalyzed BrO^sub 3^^sup -^-O-acetylsalicylic acid (aspirin) reaction in aqueous H^sub 2^SO^sub 4^ exhibits oscillatory behavior. The induction time observed before the onset of oscillations depends on the extent of hydrolysis of aspirin. The rate constant of hydrolysis of aspirin was determined indirectly from the merit of induction period. When aspirin undergoes hydrolysis, the degradation products are salicylic acerbic and acetic acid. Salicylic acid may play a role of "active" substrate responsible for the oscillations. Aspirin^A(R) (Bayer) generates also oscillations near bromate.
same thing
Salicylic acid is an ingredient in aspirin. Its probably much stronger contained by the acne medication but Aspirin contains salicylic acid.
The chemical name of aspirin is acetylsalicylic acid. Its chemical structure is very similar to plain dated salicylic acid, except it has an acetyl group stuck to it. This 'acetyl group' is simply an older describe for what nowadays chemists call a 'phenolic hydroxyl' group. The overall structure is quite complicated, unless you've studied A-level chemistry.
Hope this help ;)
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Answers:
Aspririn is acetylsalicylic acid. Basically, an acetic acid is combined with the salicylic sharp so that when it gets disolved in your stomach it does not tear through the protective pool liner as much (in other words, give you an ulcer)
The uncatalyzed BrO^sub 3^^sup -^-O-acetylsalicylic acid (aspirin) reaction in aqueous H^sub 2^SO^sub 4^ exhibits oscillatory behavior. The induction time observed before the onset of oscillations depends on the extent of hydrolysis of aspirin. The rate constant of hydrolysis of aspirin was determined indirectly from the merit of induction period. When aspirin undergoes hydrolysis, the degradation products are salicylic acerbic and acetic acid. Salicylic acid may play a role of "active" substrate responsible for the oscillations. Aspirin^A(R) (Bayer) generates also oscillations near bromate.
same thing
Salicylic acid is an ingredient in aspirin. Its probably much stronger contained by the acne medication but Aspirin contains salicylic acid.
The chemical name of aspirin is acetylsalicylic acid. Its chemical structure is very similar to plain dated salicylic acid, except it has an acetyl group stuck to it. This 'acetyl group' is simply an older describe for what nowadays chemists call a 'phenolic hydroxyl' group. The overall structure is quite complicated, unless you've studied A-level chemistry.
Hope this help ;)
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