Answer:
The change in entropy of the surrounding is -146.11 J/K.
Explanation:
Enthalpy of formation of iodine gas = 
Enthalpy of formation of chlorine gas = 
Enthalpy of formation of ICl gas = 
The equation used to calculate enthalpy change is of a reaction is:
For the given chemical reaction:

The equation for the enthalpy change of the above reaction is:
![\Delta H_{rxn}=[(2\times \Delta H_f_{(ICl)})]-[(1\times \Delta H_f_{(I_2)})+(1\times \Delta H_f_{(Cl_2)})]](https://tex.z-dn.net/?f=%5CDelta%20H_%7Brxn%7D%3D%5B%282%5Ctimes%20%5CDelta%20H_f_%7B%28ICl%29%7D%29%5D-%5B%281%5Ctimes%20%5CDelta%20H_f_%7B%28I_2%29%7D%29%2B%281%5Ctimes%20%5CDelta%20H_f_%7B%28Cl_2%29%7D%29%5D)
![=[2\times 17.78 kJ/mol]-[1\times 0 kJ/mol+1\times 62.436 kJ/mol]=-26.878 kJ/mol](https://tex.z-dn.net/?f=%3D%5B2%5Ctimes%2017.78%20kJ%2Fmol%5D-%5B1%5Ctimes%200%20kJ%2Fmol%2B1%5Ctimes%2062.436%20kJ%2Fmol%5D%3D-26.878%20kJ%2Fmol)
Enthaply change when 1.62 moles of iodine gas recast:

Entropy of the surrounding = 

1 kJ = 1000 J
The change in entropy of the surrounding is -146.11 J/K.
Answer:

Explanation:
Although the context is not clear, let's look at the oxidation and reduction processes that will take place in a Fe/Sn system.
The problem states that anode is a bar of thin. Anode is where the process of oxidation takes place. According to the abbreviation 'OILRIG', oxidation is loss, reduction is gain. Since oxidation occurs at anode, this is where loss of electrons takes place. That said, tin loses electrons to become tin cation:

Similarly, iron is cathode. Cathode is where reduction takes place. Reduction is gain of electrons, this means iron cations gain electrons and produce iron metal:

The net equation is then:

However, this is not the case, as this is not a spontaneous reaction, as iron metal is more reactive than tin metal, and this is how the coating takes place. This implies that actually anode is iron and cathode is tin:
Actual anode half-equation:

Actual cathode half-equation:

Actual net reaction:

Answer:
A, C and D are correct.
Explanation:
Hello.
In this case, since the relationship between the vapor pressure of a solution is directly proportional to the mole fraction of the solvent and the vapor pressure of the pure solvent as stated by the Raoult's law:

Since the solute is not volatile, the mole fraction of the solute is not taken into account for vapor pressure of the solution, therefore A is correct whereas B is incorrect.
Moreover, since the higher the vapor pressure, the weaker the intermolecular forces due to the fact that less more molecules are like to change from liquid to vapor and therefore more energy is required for such change, we can evidence that both C and D are correct.
Best regards.
I don’t get it. What is the question asking?
If you increase the frequency, the photon will have more energy and can therefore transfer more electrons to the other side. As such, you will have an increased current.