To determine which order of the reaction it is, first we need to calculate the rate of change of moles.
the data is as follows
time 0 40 80 120 160
moles 0.100 0.067 0.045 0.030 0.020
Q1)
for the first 40 s change of moles ;
= -d[A] / t
= - (0.067-0.100)/40s
= 8.25 x 10⁻⁴ mol/s
for the next 40 s
= -(0.045-0.067)/40
= 5.5 x 10⁻⁴ mol/s
the 40 s after that
= -(0.030-0.045)/40 s
= 3.75 x 10⁻⁴ mol/s
k - rate constant
and A is the only reactant that affects the rate of the reaction
rate = k [A]ᵇ
8.25 × 10⁻⁴ mol/s = k [0.100 mol]ᵇ ----1
5.5 x 10⁻⁴ mol/s = k [0.067 mol]ᵇ -----2
divide the 2nd equation by the 1st equation
1.5 = [1.49]ᵇ
b is almost equal to 1
Therefore this is a first order reaction
Q2)
to find out the rate constant(k), we have to first state the equation for a first order reaction.
rate = k[A]ᵇ
As A is the only reactant thats considered for the rate equation.
Since this is a first order reaction,
b = 1
therefore the reaction is
rate = k[A]
substituting the values,
8.25 x 10⁻⁴ mol/s = k [0.100 mol]
k = 8.25 x 10⁻⁴ mol/s /0.100mol
= 8.25 x 10⁻³ s⁻¹
Answer:
see note under explanation
Explanation:
When describing system and surroundings the system is typically defined as the 'object of interest' being studied and surroundings 'everything else'. In thermodynamics heat flow is typically defined as endothermic or exothermic. However, one should realize that the terms endothermic and exothermic are in reference to the 'system' or object of interest being studied. For example if heat is transferred from a warm object to a cooler object it is imperative that the system be defined 1st. So, with that, assume the system is a warm metal cylinder being added into cooler water. When describing heat flow then the process is exothermic with respect to the metal cylinder (the system) but endothermic to the water and surroundings (everything else).
Answer:
A communicable disease
Explanation:
Diseases that can be transferred are known as communicable diseases.
<u>Answer:</u> The value of 
of the reaction is 28.38 kJ/mol
<u>Explanation:</u>
For the given chemical reaction:
- The equation used to calculate enthalpy change is of a reaction is:
![\Delta H^o_{rxn}=\sum [n\times \Delta H^o_f_{(product)}]-\sum [n\times \Delta H^o_f_{(reactant)}]](https://tex.z-dn.net/?f=%5CDelta%20H%5Eo_%7Brxn%7D%3D%5Csum%20%5Bn%5Ctimes%20%5CDelta%20H%5Eo_f_%7B%28product%29%7D%5D-%5Csum%20%5Bn%5Ctimes%20%5CDelta%20H%5Eo_f_%7B%28reactant%29%7D%5D)
The equation for the enthalpy change of the above reaction is:
![\Delta H^o_{rxn}=[(1\times \Delta H^o_f_{(SO_2Cl_2(g))})]-[(1\times \Delta H^o_f_{(SO_2(g))})+(1\times \Delta H^o_f_{(Cl_2(g))})]](https://tex.z-dn.net/?f=%5CDelta%20H%5Eo_%7Brxn%7D%3D%5B%281%5Ctimes%20%5CDelta%20H%5Eo_f_%7B%28SO_2Cl_2%28g%29%29%7D%29%5D-%5B%281%5Ctimes%20%5CDelta%20H%5Eo_f_%7B%28SO_2%28g%29%29%7D%29%2B%281%5Ctimes%20%5CDelta%20H%5Eo_f_%7B%28Cl_2%28g%29%29%7D%29%5D)
We are given:
Putting values in above equation, we get:
![\Delta H^o_{rxn}=[(1\times (-364))]-[(1\times (-296.8))+(1\times 0)]=-67.2kJ/mol=-67200J/mol](https://tex.z-dn.net/?f=%5CDelta%20H%5Eo_%7Brxn%7D%3D%5B%281%5Ctimes%20%28-364%29%29%5D-%5B%281%5Ctimes%20%28-296.8%29%29%2B%281%5Ctimes%200%29%5D%3D-67.2kJ%2Fmol%3D-67200J%2Fmol)
- The equation used to calculate entropy change is of a reaction is:
![\Delta S^o_{rxn}=\sum [n\times \Delta S^o_f_{(product)}]-\sum [n\times \Delta S^o_f_{(reactant)}]](https://tex.z-dn.net/?f=%5CDelta%20S%5Eo_%7Brxn%7D%3D%5Csum%20%5Bn%5Ctimes%20%5CDelta%20S%5Eo_f_%7B%28product%29%7D%5D-%5Csum%20%5Bn%5Ctimes%20%5CDelta%20S%5Eo_f_%7B%28reactant%29%7D%5D)
The equation for the entropy change of the above reaction is:
![\Delta S^o_{rxn}=[(1\times \Delta S^o_{(SO_2Cl_2(g))})]-[(1\times \Delta S^o_{(SO_2(g))})+(1\times \Delta S^o_{(Cl_2(g))})]](https://tex.z-dn.net/?f=%5CDelta%20S%5Eo_%7Brxn%7D%3D%5B%281%5Ctimes%20%5CDelta%20S%5Eo_%7B%28SO_2Cl_2%28g%29%29%7D%29%5D-%5B%281%5Ctimes%20%5CDelta%20S%5Eo_%7B%28SO_2%28g%29%29%7D%29%2B%281%5Ctimes%20%5CDelta%20S%5Eo_%7B%28Cl_2%28g%29%29%7D%29%5D)
We are given:
Putting values in above equation, we get:
![\Delta S^o_{rxn}=[(1\times 311.9)]-[(1\times 248.2)+(1\times 223.0)]=-159.3J/Kmol](https://tex.z-dn.net/?f=%5CDelta%20S%5Eo_%7Brxn%7D%3D%5B%281%5Ctimes%20311.9%29%5D-%5B%281%5Ctimes%20248.2%29%2B%281%5Ctimes%20223.0%29%5D%3D-159.3J%2FKmol)
To calculate the standard Gibbs's free energy of the reaction, we use the equation:
where,
= standard enthalpy change of the reaction =-67200 J/mol
= standard entropy change of the reaction =-159.3 J/Kmol
Temperature of the reaction = 600 K
Putting values in above equation, we get:
Hence, the value of of the reaction is 28.38 kJ/mol
