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butalik [34]
2 years ago
14

4-hydroxypentanal reacts with one equivalent of methanol to form a cyclic acetal.

Chemistry
1 answer:
quester [9]2 years ago
4 0

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

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2 years ago
What average global temperature is maintained when there is a balance in Earth’s energy budget?
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The complete combustion of propane (C3H8) in the presence of oxygen yields CO2 and H2O: C3H8 (g) + 5O2 (g) 3CO2 (g) + 4H2O (g) a
mixas84 [53]

Answer:

26.9 L is the volume of CO₂, we obtained

Explanation:

The reaction is: C₃H₈(g) + 5O₂(g)  →  3CO₂ (g) + 4H₂O (g)

Let's determine the reactants moles:

27.5 g . 1mol / 44 g = 0.625 moles

We need density of O₂ to determine mass and then, the moles.

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Let's find out the limiting reactant:

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Oxygen is the limiting reactant, we need 3.125 moles but we only have 2.009 moles

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