<span>Planck’s constant relates the
joules of energy absorbed/released by matter to the wave frequency f. the
plancks constant was first recognized in 1900 by Max Planck. The equation that
relates the joules of energy absorbed/released by matter to the wave frequency
f is called the plancks-eintein relation, E = hf</span>
<span>Solubility product constant (Ksp) is </span>applied to the saturated ionic solutions<span> which are in equilibrium with its
solid form. The solid is partially dissociated into its ions.</span><span>
For the BaF, the dissociation as follows;
BaF</span>₂(s) ⇄ Ba²⁺(aq)
+ 2F⁻(aq)
<span>
Hence,
Ksp = [Ba</span>²⁺(aq)] [F⁻(aq)]²
Balanced Eqn
2
C
2
H
6
+
7
O
2
=
4
C
O
2
+
6
H
2
O
By the Balanced eqn
60g ethane requires 7x32= 224g oxygen
here ethane is in excess.oxygen will be fully consumed
hence
300g oxygen will consume
60
⋅
300
224
=
80.36
g
ethane
leaving (270-80.36)= 189.64 g ethane.
By the Balanced eqn
60g ethane produces 4x44 g CO2
hence amount of CO2 produced =
4
⋅
44
⋅
80.36
60
=
235.72
g
and its no. of moles will be
235.72
44
=5.36 where 44 is the molar mass of Carbon dioxide
hope this helps
The ph of the best buffer is 4.74
The given acetic acid is a weak acid
The equation of the pH of the buffer
pH = pKa + log ( conjugate base / weak acid ).
For best buffer the concentration of the weak acid and its conjugate base is equal.
pH = pKa + log 1
pH = pKa + 0
pH = pKa
given Ka = 1.8 × 10⁻⁵
pKa = - log ka
pH = -log ( 1.8 × 10⁻⁵ )
pH = 4. 74
Hence the pH of the best buffer is 4.74
Learn more about the pH on
brainly.com/question/22390063
#SPJ4
Answer : The value of
for the reaction is -959.1 kJ
Explanation :
The given balanced chemical reaction is,

First we have to calculate the enthalpy of reaction
.

![\Delta H^o=[n_{H_2O}\times \Delta H_f^0_{(H_2O)}+n_{SO_2}\times \Delta H_f^0_{(SO_2)}]-[n_{H_2S}\times \Delta H_f^0_{(H_2S)}+n_{O_2}\times \Delta H_f^0_{(O_2)}]](https://tex.z-dn.net/?f=%5CDelta%20H%5Eo%3D%5Bn_%7BH_2O%7D%5Ctimes%20%5CDelta%20H_f%5E0_%7B%28H_2O%29%7D%2Bn_%7BSO_2%7D%5Ctimes%20%5CDelta%20H_f%5E0_%7B%28SO_2%29%7D%5D-%5Bn_%7BH_2S%7D%5Ctimes%20%5CDelta%20H_f%5E0_%7B%28H_2S%29%7D%2Bn_%7BO_2%7D%5Ctimes%20%5CDelta%20H_f%5E0_%7B%28O_2%29%7D%5D)
where,
= enthalpy of reaction = ?
n = number of moles
= standard enthalpy of formation
Now put all the given values in this expression, we get:
![\Delta H^o=[2mole\times (-242kJ/mol)+2mole\times (-296.8kJ/mol)}]-[2mole\times (-21kJ/mol)+3mole\times (0kJ/mol)]](https://tex.z-dn.net/?f=%5CDelta%20H%5Eo%3D%5B2mole%5Ctimes%20%28-242kJ%2Fmol%29%2B2mole%5Ctimes%20%28-296.8kJ%2Fmol%29%7D%5D-%5B2mole%5Ctimes%20%28-21kJ%2Fmol%29%2B3mole%5Ctimes%20%280kJ%2Fmol%29%5D)

conversion used : (1 kJ = 1000 J)
Now we have to calculate the entropy of reaction
.

![\Delta S^o=[n_{H_2O}\times \Delta S_f^0_{(H_2O)}+n_{SO_2}\times \Delta S_f^0_{(SO_2)}]-[n_{H_2S}\times \Delta S_f^0_{(H_2S)}+n_{O_2}\times \Delta S_f^0_{(O_2)}]](https://tex.z-dn.net/?f=%5CDelta%20S%5Eo%3D%5Bn_%7BH_2O%7D%5Ctimes%20%5CDelta%20S_f%5E0_%7B%28H_2O%29%7D%2Bn_%7BSO_2%7D%5Ctimes%20%5CDelta%20S_f%5E0_%7B%28SO_2%29%7D%5D-%5Bn_%7BH_2S%7D%5Ctimes%20%5CDelta%20S_f%5E0_%7B%28H_2S%29%7D%2Bn_%7BO_2%7D%5Ctimes%20%5CDelta%20S_f%5E0_%7B%28O_2%29%7D%5D)
where,
= entropy of reaction = ?
n = number of moles
= standard entropy of formation
Now put all the given values in this expression, we get:
![\Delta S^o=[2mole\times (189J/K.mol)+2mole\times (248J/K.mol)}]-[2mole\times (206J/K.mol)+3mole\times (205J/K.mol)]](https://tex.z-dn.net/?f=%5CDelta%20S%5Eo%3D%5B2mole%5Ctimes%20%28189J%2FK.mol%29%2B2mole%5Ctimes%20%28248J%2FK.mol%29%7D%5D-%5B2mole%5Ctimes%20%28206J%2FK.mol%29%2B3mole%5Ctimes%20%28205J%2FK.mol%29%5D)

Now we have to calculate the Gibbs free energy of reaction
.
As we know that,

At room temperature, the temperature is 500 K.


Therefore, the value of
for the reaction is -959.1 kJ