This problem is providing us with the mass of hydrochloric acid and the volume of solution and asks for the pH of the resulting solution, which turns out to be 1.477.
<h3>pH calculations</h3>
In chemistry, one can calculate the pH of a solution by firstly obtaining its molarity as the division of the moles of solute by the liters of solution, so in this case for HCl we have:
Next, due to the fact that hydrochloric acid is a strong acid, we realize its concentration is nearly the same to the released hydrogen ions to the solution upon ionization. Thereby, the resulting pH is:
Which conserves as much decimals as significant figures in the molarity.
Learn more about pH calculations: brainly.com/question/1195974
Answer:
B. It would lead to an increase of global temperatures.
Explanation:
Gas burns when it is hot. Therefore the more gas that our cars consume, the hotter the air will be when the car releases those gas vapors. Causing the air to become hotter.
Hope this helped <3 :) brainliest?
Answer:
a. 59 m/atm
Explanation:
- To solve this problem, we must mention Henry's law.
- <em>Henry's law states that at a constant temperature, the amount of a given gas dissolved in a given type and volume of liquid is directly proportional to the partial pressure of that gas in equilibrium with that liquid.</em>
- It can be expressed as: C = KP,
C is the concentration of the solution (C = 1.3 M).
P is the partial pressure of the gas above the solution (P = 0.022 atm).
K is the Henry's law constant (K = ??? M/atm),
∵ C = KP.
∴ K = C/P = (1.3 M)/(0.022 atm) = 59.0 M/atm.
Answer:
The reactive nucleophile is Ketone.
Explanation:
In organic chemistry, The process of acid - catalyzed aldol condensation starts from when ketone (or any aldehyde) is converted to an -enol, after which it attacks another ketone/aldehyde that has already been activated by parbonyl oxygen protonation.
The process of this is that first of all the ketone undergoes tautomerization to form -enol. Thereafter, the other carbonyl will undergo protonation which makes the carbon activated towards attack. Now, the nucleophilic enol will be added to the carbonyl in a [1,2]-addition reaction and we will now use deprotonation to obtain the neutral Aldol product.
Now, since only the ketone can produce an -enol, thus it is the nucleophile as aldehydes are better electrophiles
I think the answer is a, volume, but I still might be wrong.
