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
Answer:add acid
Explanation:
Methyl orange is red in acid and yellow in base. When added to distilled water and the colour turns yellow, it means it is in its anion form. The equilibrium can be shifted towards the acid form (HMO) by adding acid. The acid will protonate the indicator shifting the position of equilibrium towards the acid side and the solution turns red.
