Properties of Solutions Part 2
Properties of Solutions Part 2
SOLUTIONS
(Part II)
By: Mrs. Maria Niña C. Cabrera
LEARNING COMPETENCIES (WEEK 4)
• Perform stoichiometric calculations for reactions in
solution.
REACTANT PRODUCT
SIDE SIDE
H atoms 2 3
N atoms 2 1
H 2(g) + N 2(g) → 2NH 3(g)
3H 2(g) + N 2(g) → 2NH 3(g)
TITRATION
• Turmeric • Onion
• Red Cabbage • Beetroot
• Grape juice
• Cherries
ACID-BASE NEUTRALIZATION
REACTION
In an acid-base neutralization reaction, it is
important to note the relationship between
the number of moles of the acid and the
base at the completion of the reaction. This
is called the equivalent point.
Remember: A permanent color change
indicates the end of the reaction.
MONOPROTIC ACID
• This is an acid that donates only one proton or
hydrogen atom per molecule to an aqueous
solution.
• Examples: nitric acid (HNO 3 ), hydrochloric acid
(HCl), hydrobromic acid (HBr), acetic acid
(CH 3COOH)
MONOBASIC BASE
• A base that will accept just one hydrogen
ion per formula unit
• Examples: sodium hydroxide (NaOH),
potassium hydroxide (KOH), ammonia
(NH 3)
MONOPROTIC ACID vs MONOBASIC BASE
nacid = nbase
We can express the number of moles, n, of the
standard solution as the product of its concentration
(expressed in terms of molarity, M), and the volume, V,
used in titration. Choosing the base standard solution
for this example,
= 0.5 M KOH x 60 mL
1 M HCl
Vstd sol = 30 mL
1) Find moles:
(4.49g CuCl2) x 1 mole CuCl2
134.45 grams
= 0.033395 moles CuCl2
Solution:
∆Tf = mKf
∆Tf = mKf
Where m is the molal concentration of the solution.
Kf is the freezing point depression constant of the
solvent
Tf is the change in freezing point = Tfsolution - Tfsolvent
FREEZING POINT
It is the temperature at
which the liquid starts to
become solid.
3. OSMOTIC PRESSURE
It is the pressure that has to be applied
to pure solvent to prevent the solvent
from passing into a given solution by
the process of osmosis.
Mathematically, it can be expressed
as:
𝝅 = MRT
𝝅 = MRT
Where 𝝅 is the osmotic pressure in atmosphere
M is the concentration of solution in molarity
R is the universal gas constant = 0.082 atm-L
mole-K
T is the temperature in Kelvin scale
OSMOSIS
It is process by which solvent tends to pass
through a semipermeable membrane from a
less concentrated solution into a more
concentrated one, to attain equilibrium on
each side of the membrane.
4. VAPOR PRESSURE LOWERING
It is the pressure of a vapor in contact with
its liquid or solid. Between 1887 and 1888, a
French c hemist, Francois-Marie Raoult,
showed that the vapor pressure of a
solution is equal to the mole of the solvent
multiplied by the vapor pressure of the
pure liquid knows as Raoult’s law.
P’ =XsolventP0
P’ =XsolventP0
Where P’ is the vapor pressure of
solution
Xsolvent is the mole fraction of solvent
P0 is the vapor pressure of pure
solvent
SAMPLE PROBLEM 1
Given:
Molar mass C6H12O6 =180 g/mol
msolvent =800 g (1kg/1000g) =0.80 kg solvent
msolute =68.0 g solute
m =68g/180g/mole =0.47 molal
0.80 kg solvent
ΔTb =mKb =0.47m(0.5120C/molal) =0.240C
Bpt of soln =100 +0.24 =100.240C
ΔTf =mKf =0.47 (1.860C/molal) =0.870C
FPt of soln =0 - 0.87 =- 0.870C
Remember:
Given: Required:
mass of C aC l2 =41.10 g Tf soln=?
mass of water =500 g Tb soln=?
Kf of H2O =1.860C /molal
Kb of H2O =0.5120C /molal
ΔTb =imKb
ΔTb = 3 (41.10g/110.90g/mol)(0.5120C/molal) =1.140C
0.5 kg solvent
Therefore, Tbsoln =1000C +1.14 0C = 101.14 0C
SAMPLE PROBLEM 4
Given:
Required: Molar mass =?
msolute =2.00 g
msolvent =40 g (1kg/1000g) =0.04 kg FPt of soln =- 0.4650C
ΔTf = 0.465 0 C
Molal = mole solute/kg solvent
ΔTf=mKf
ΔTfsoln = Tfsolvent - Tfsoln
0 - (-0.465 0 C)
- 0.4650C = 2.00 g / x (1.860C/n solute/kg solvent)
0.04 kg solvent
Given: Required:
msolute =4.00 g Vapor pressure of soln, P’
Vwater =mwater =500 g Molar mass of NaOH
=23+16+1
T=250C
=40g/mol
P0 =23.80 torr (water vapor exerts a pressure of 23.80 torr at 250C)
P’ =Xsolvent P0
Xsolvent = nsolvent
n solute +n solvent
P’ = 500 g/18g/mole
4.0g/40g/mole +500g/18g/mole (23.80 torr)
P’ =23.71 torr vapor pressure of solution at 250C