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Afina-wow [57]
3 years ago
14

What is the purpose of reacting 2.0mL of HNO3 with 2.0 mL of H2SO4 in a separate test tube, prior to adding it to the solution c

ontaining the substrate
Chemistry
1 answer:
jok3333 [9.3K]3 years ago
4 0

The question is incomplete, the complete question is;

What is the purpose of reacting 2.0mL of HNO3 with 2.0 mL of H2SO4 in a separate test tube, prior to adding it to the solution containing the substrate? more than one answer is possible

A) The release of a water molecule that acts as an electrophile in the reaction with methyl benzoate.

B) The formation of nitronium ion, which acts an electrophile in the reaction with methylbenzoate.

C)The formation of bisulfate (hydrogen sulfate), which acts as an electrophile in the reaction with methylbenzoate.

D)The release of a water molecule that acts as a nucleophile in the reaction with methyl benzoate.

Answer:

B) The formation of nitronium ion, which acts an electrophile in the reaction with methylbenzoate.

Explanation:

The benzene ring is known to be stable hence it can only undergo a substitution reaction with the aromatic ring still intact. When the substitution reaction involves an electrophile we refer to the process as electrophillic aromatic substitution. Electrophilic aromatic substitution is a useful synthetic route for many organic compounds.

In the electrophilic substitution of methyl benzoate using the 1:1 volume ratio mixture of H2SO4/HNO3, the nitronium ion (NO2+) is the electrophile generated in the test tube. It is this NO2+ that now reacts with the methyl benzoate to yield the reaction product.

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Answer:

See explanation below (Brainlist please)

Explanation:

First of all, we need to understand what is an acidic hydrogen.

An acidic hydrogen, is the atom of hydrogen which is more propense to undergo an acid base reaction, and form a stable ion or molecule in the process.

In other words, is the hydrogen that is more vulnerable to get substracted in an acid base reaction to form another compound.

Knowing this information, gives us an idea of how a molecule can be formed and which kind of compound is formed.

Now, in this question, we have 5 molecules. Each of them is either a ketone or aldehyde, so this mean that we have the carbonile group (C = O), which means that is easier to identify the acidic hydrogen. This is because the Carbonile group is an attractor group, so, it will attract the charges by inductive effect (in some cases by resonance), and the molecule is more stable.

This can be shown by drawing the enolate ion that is formed once the molecule undergo the acid base reaction. As it's an enolate form that we are looking for, then it means that the ketone or aldehyde is undergoing an electrofilic attack with a base. This base will substract the most acidic hydrogen to form a better and stable enolate. The acidic hydrogen and the enolate form can be seen in the attached picture.

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b) Propanal happens something similar to acetaldehyde, the terminal hydrogen cannot be substracted, and carbon 3, once the hydrogen is gone, the negative charge cannot be stabilized by resonance, so hydrogens of carbon 2 can do this.

c) in the case of acetone, is easier to look because we only have the C = O between two methyl group, so you can use either carbon 1 or 3 to do the job.

d) 4 heptanone the most acidic hydrogen would be carbon 3 or 5, because they are closer to the C=O and the ion can be stabilized by resonance.

e) Finally in ciclopentanone, the most acidic hydrogen would be carbon 2 or 5.

See picture for a better understanding.

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