Answer:
The number of lines possible for SO2 is 3
Explanation:
The following Procedure should be followed when calculating the number of vibrational modes:-
- Identify if the given molecule is either linear or non-linear
- Calculate the number of atoms present in your molecule
- Place the value of n in the formula and solve.
SO2 is a non-linear molecule because it contains a lone pair which causes the molecule to bent in shape hence, The mathematical formula for calculating the number of non-linear molecule in a infrared region is (3n - 6) here n is the number of atoms in molecule.
hence for Sulphur Dioxide (SO2), n will be 3
<u> Therefore, The number of lines possible for SO2 is (3*3) - 6 = 3</u>
Hello there!
An Atom would be considered to be the smallest unit that would make up matter. If were to ever see a picture of an atom, they would consists of a proton, neutron, electron, and a nucleus. And all this would be called a Atom.
Your answer: Atom
C is the answer hope this helps
Answer :
(1) pH = 1.27
(2) pH = 13.35
(3) The given solution is not a buffer.
Explanation :
<u>(1) 53.1 mM HCl</u>
Concentration of HCl =
As HCl is a strong acid. So, it dissociates completely to give hydrogen ion and chloride ion.
So, Concentration of hydrogen ion=
pH : It is defined as the negative logarithm of hydrogen ion concentration.
<u>(2) 0.223 M KOH</u>
Concentration of KOH = 0.223 M
As KOH is a strong base. So, it dissociates completely to give hydroxide ion and potassium ion.
So, Concentration of hydroxide ion= 0.223 M
Now we have to calculate the pOH.
Now we have to calculate the pH.
<u>(3) 53.1 mM HCl + 0.223 M KOH</u>
Buffer : It is defined as a solution that maintain the pH of the solution by adding the small amount of acid or a base.
It is not a buffer because HCl is a strong acid and KOH is a strong base. Both dissociates completely.
As we know that the pH of strong acid and strong base solution is always 7.
So, the given solution is not a buffer.
(a) One form of the Clausius-Clapeyron equation is
ln(P₂/P₁) = (ΔHv/R) * (1/T₁ - 1/T₂); where in this case:
Solving for ΔHv:
- ΔHv = R * ln(P₂/P₁) / (1/T₁ - 1/T₂)
- ΔHv = 8.31 J/molK * ln(5.3/1.3) / (1/358.96 - 1/392.46)
(b) <em>Normal boiling point means</em> that P = 1 atm = 101.325 kPa. We use the same formula, using the same values for P₁ and T₁, and replacing P₂ with atmosferic pressure, <u>solving for T₂</u>:
- ln(P₂/P₁) = (ΔHv/R) * (1/T₁ - 1/T₂)
- 1/T₂ = 1/T₁ - [ ln(P₂/P₁) / (ΔHv/R) ]
- 1/T₂ = 1/358.96 K - [ ln(101.325/1.3) / (49111.12/8.31) ]
(c)<em> The enthalpy of vaporization</em> was calculated in part (a), and it does not vary depending on temperature, meaning <u>that at the boiling point the enthalpy of vaporization ΔHv is still 49111.12 J/molK</u>.