Answer:
- <u>The arrow labeled 4: from gas to liquid.</u>
Explanation:
<em>Dew</em> is a manifestation of water condensation.
The air that surrounds us contains water vapor (humidity) from the evaporatoin of the water in the rivers, lakes, and the water with which you water the plants of your garden.
During the night, and specially in the early morning, before dawn, the temperature of the air descends, and part of the vapor in the air condensates in tiny droplets that accumulate over the surface of the plant's leaves, and other solid surfaces like the winshields and hoods of the cars.
Then, the phase transition that occurs is from gas (vapor) to liquid, which is called condensation and represented with the arrow labeled 4 on the diagram.
Answer is: a lower freezing point has solution of K₂SO₄.
Change in freezing
point from pure solvent to solution: ΔT =i · Kf · b.<span>
Kf - molal freezing-point depression constant for water is 1.86°C/m.
b - molality, moles of solute per
kilogram of solvent.
i - </span>Van't
Hoff factor.<span>
b(K</span>₂SO₄<span>) = 0.35 m.
</span>b(KCl) = 0.5 m.
i(K₂SO₄) = 3.
i(KCl) = 2.
ΔT(K₂SO₄) = 3 · 0.35 m · 1.86°C/m.
ΔT(K₂SO₄) = 1.953°C.
ΔT(KCl) = 2 · 0.5 m · 1.86°C/m.
ΔT(KCl) = 1.86°C.
2 atoms in a molecule of RSq, TSq contains 3 different types of atoms (Sq, R, and T.)
Answer: pH=12.69
Explanation:



Initial 0.12 0 0
Eqm 0.12-x x x
![K_a=\frac{[H^+][F^-]}{[HF]}](https://tex.z-dn.net/?f=K_a%3D%5Cfrac%7B%5BH%5E%2B%5D%5BF%5E-%5D%7D%7B%5BHF%5D%7D)
(neglecting small value of x in comparison to 0.12)

Moles of 



0.06 moles of NaOH will give 0.06 moles of ![[OH^-]](https://tex.z-dn.net/?f=%5BOH%5E-%5D)
Now
moles of
will be neutralized by
moles of
and
moles of
will be left.
Molarity of 
![pOH=-\log[OH^-]=-\log[0.049]=1.31](https://tex.z-dn.net/?f=pOH%3D-%5Clog%5BOH%5E-%5D%3D-%5Clog%5B0.049%5D%3D1.31)
pH = 14 - pOH= 14 - 1.31 = 12.69
Answer:p-hydroxybenzaldehyde is stronger acid to phenol
para-cyanophenol is stronger acid to meta-cyanophenol
o-fluorophenol is stronger acid to p-fluorophenol.
Explanation:
The PKa tool relative to Ph are used to contrast the pairs.
The pKa of phenol is 10. The pKa of p-hydroxybenzaldehyde is 9.24
The pKa for meta-cyanophenol is 8.61 and the pKa for para-cyanophenol is 7.95.
The pKa value of o-fluorophenol is 8.7, while that of the p-fluorophenol is 9.9. It's obvious that the inductive effect is more dominant at ortho-position, which results in a more acidic nature
The pKa is the pH value at which a chemical species will accept or donate a proton. The lower the pKa, the stronger the acid and the greater the ability to donate a proton in aqueous solution.