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ahrayia [7]
3 years ago
6

Consider the reaction below.

Chemistry
1 answer:
patriot [66]3 years ago
6 0

Answer:

HI and I-

Explanation:

Hello there!

In this case, according to the acid ionization of hydroiodic acid:

HI+H_2O\rightarrow I^-+H_3O^+

Now, since the acid, HI, results in the conjugate base, I- and the base, H2O in the conjugate acid, H3O+, it is correct to assert that the acid-conjugate base pair is HI and I-

Best regards!

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g Write a molecular equation for the precipitation reaction that occurs (if any) when the following solutions are mixed. If no r
Mrac [35]

Answer:

CuBr₂(aq) + Pb(CH₃COO)₂(aq) → Cu(CH₃COO)₂(aq) + PbBr₂ (s)↓

Explanation:

We identify the reactants:

CuBr₂ and Pb(CH₃COO)₂

The products will be: Cu(CH₃COO)₂ and PbBr₂

You may know these information:

Salts from acetate are soluble.

Bromide can make solid salts with these cations: Ag⁺, Pb²⁺, Hg₂²⁺, Cu⁺

PbBr₂ is formed, so this will be our precipitate

The equation is:

CuBr₂(aq) + Pb(CH₃COO)₂(aq) → Cu(CH₃COO)₂(aq) + PbBr₂ (s)↓

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3 years ago
Which of these elements is the most ductile?
Inessa05 [86]
The answer is going to be mercury
8 0
3 years ago
Read 2 more answers
Identify the most acidic hydrogens in each of the following molecules. Give the structure of the enolate ion arising from deprot
san4es73 [151]

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.

a) In the case of acetaldehyde, the most acidic will be the hydrogen of carbon 2, because the hydrogen from the carbonile, once it's substracted, the charge of the carbon cannot be stabilized by resonance. Carbon 2 hydrogens, can do this job easily.

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.

Hope it helps.

7 0
3 years ago
What are some synonyms for dissolved
Luba_88 [7]
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Hope it helps! Brainliest answer, PLZ? :)
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Yanka [14]

Answer:

tendons and ligaments

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