The answer is D: Saturated.
A saturated solution is one in which the exact maximum amount of solute has been dissolved. So, new solute will not dissolve in the solution. In contrast, an unsaturated solution can hold more solute, so if that option were correct, the crystal would have dissolved.
The other two terms are a bit more complicated. A supersaturated solution is one holding an amount of solute above the sustainable limit. Because of that, when more solute is added, the solution will immediately adjust, and some solute will come out of solution in a precipitate. Because the crystal isn't growing, we can eliminate this option.
A concentrated solution is one holding a relatively large amount of solute. However, you can have concentrated solutions that are saturated and unconcentrated (the word for this is dilute) solutions that aren't saturated. Therefore, we can say that because the crystal doesn't dissolve, this solution is saturated, but we can't say with certainty that it is concentrated.
Because the first three options are invalid, as described above, while the scenario does describe a saturated solution, D is the correct answer.
Answer:
<h2>1.9</h2>
Explanation:
The pH of a solution can be found by using the formula
![pH = - log [ {H}^{+} ]](https://tex.z-dn.net/?f=pH%20%3D%20-%20log%20%5B%20%7BH%7D%5E%7B%2B%7D%20%5D)
From the question we have

We have the final answer as
<h3>1.9</h3>
Hope this helps you
Complete Question:
check the first image for complete part of the question
Answer and Explanation:
Epoxide is a three membered ring made up of two carbon atoms and one oxygen atom. Epoxides are cyclic ethers. Due to its ring size, it is highly strained and very reactive. Epoxide ring opening takes place with respect to addition of acid and base.
Ring opening of epoxide with acid:
In the presence of base, the nucleophile attacks the epoxide ring at more substituted site and inverse stereochemistry takes place.(check file 2 attached)
Ring opening of epoxide with base:
The backside attack of nucleophile takes place in less substituted site and then it undergoes protonation to form a product.
(check file 2 attached)
Answer:
D. 5 moles
Explanation:
C3H8 + 5O2 → 4H2O + 3CO2
5 mol 3 mol
So, to make 3 mol CO2 5 mol O2 are needed.