The carbon cycle has several sources including all of the following except:
1 answer:
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Answer:
Explanation:
The equation is given as:
CH3CHOHC2H4CHO + CH3OH --> CYCLIC ACETAL + H2O
This above equation is carried out in the presence of a strong acid. There are five mechanisms employed and they are:
Step 1:
Initial formation of the hemiacetal which takes several steps
Step 2:
Addition of a proton. The hemicetal is protonated on the hydroxyl group (-OH group)
Step 3:
As seen a bond is broken to give the H2O molecule and a resonance stabilized cation.
The carbonyl group on the cation is enriched with the oxygen-18 got from the H2O molecule as seen in the mechanism.
Step 4:
An attraction occurs between electrophile and nucleophile i.e the stabilised cation and the lone paids of the methanol.
Step 5:
Finally, a proton (+) is removed from the molecule by a lone pair of electron on the methanol.
Attached are the Steps 1 - 5 mechanism below
By definition, Bronsted-Lowry acid is a proton donor in the acid-base neutralization reaction. When a weak acid like acetylsalicylic acid is reacted with water, the water here acts as the Bronsted-Lowry base. This is possible because water has properties of amphoterism - can act as an acid or base. In this case, acetylsalicylic acid would have to donate its H+ atom to water, so that it would yield a hydronium ion, H₃O⁺. The complete net ionic reaction is shown in the picture.
So, in the reaction, the products yield are the acetylsalicylate ion and the hydronium ion.
So, in the reaction, the products yield are the acetylsalicylate ion and the hydronium ion.