E. Molarity of vinegar
i hope u get this i tried to figure it out hopefully im right
good luck!
Answer:
Zero
Explanation:
Recall that;
E = q + w
Where;
q = heat, w = work done
When heat is absorbed by the system q is positive
When heat is evolved by the system q is negative
When the system does work, w is negative
When work is done on the system w is positive
Step 1
ΔE1= 60 KJ + 40 KJ = 100KJ
Step 2
ΔE2= (-30 KJ) + (-70 KJ) = (-100) KJ
ΔE1 + ΔE2= 100KJ + (-100) KJ = 0KJ
Atmospheric
pressure<span>, sometimes also called barometric pressure, is the pressure exerted by the weight of air in
the </span>atmosphere of Earth<span> (or that of another planet)</span>
1 atm is equivalent to = 101325
Pa
= 760 mmHg
= 760 torr
= 1.01325 bar
So 1.23 atm is equal to
= 124629.8 Pa
= 934.8 mmHg
= 934.8 torr
<span>= 1.2462 bar</span>
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
Answer:
Lateral
Explanation:
Is the opposite side of the midline