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Shkiper50 [21]
3 years ago
9

What information can be learned from bloodstains at a crime scene?

Chemistry
1 answer:
tangare [24]3 years ago
3 0

you can learn who's blood it is, you can also see the blood patterns and how the crime maybe happened.

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Write a balanced net ionic equation to show why the solubility of Cu(OH)2(s) increases in the presence of a strong acid and calc
Helga [31]

Answer:

2.2×10^8

Explanation:

Cu(OH)2(s)<---------> Cu^2+(aq) + 2OH^-(aq) Ksp=2.2 x 10 ^-20

2H3O^+(aq) + 2OH^-(aq) <-------> 4H2O(l). Kw= 1×10^14

Cu^2+(aq) + 4H2O(l) <--------> [Cu(H2O)4]^2+(aq)

Overall ionic reaction:

Cu(OH)2(s) +2H3O^+(aq) <---------> [Cu(H20)4]^2+(aq)

Equilibrium constant for the reaction: Ksp×Kw= 2.2 x 10 ^-20 × (1/(1×10^-14))^2

Keq= 2.2×10^8

Kw= ion dissociation constant of water

3 0
3 years ago
Butanoic acid + 2 propanol
Anuta_ua [19.1K]

Answer:

Butanoic acid and 2-propanol reacts to form isopropyl butyrate.

Explanation:

brainliest plz

4 0
3 years ago
The process invented in 1864 to reduce the amount of bacteria in liquids and foods by heating them to high temperatures is calle
dlinn [17]
 The key is a process called <span>pasteurization</span>
5 0
3 years ago
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
Sixty-three percent of the number 1059 is
slega [8]
667.17 (0.63x1059) shsbsbsb
4 0
3 years ago
Read 2 more answers
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