To solve this problem, we should recall that
the change in enthalpy is calculated by subtracting the total enthalpy of the reactants
from the total enthalpy of the products:
ΔH = Total H of products – Total H of reactants
You did not insert the table in this problem, therefore I
will find other sources to find for the enthalpies of each compound.
ΔHf CO2 (g) = -393.5 kJ/mol
ΔHf CO (g) = -110.5 kJ/mol
ΔHf Fe2O3 (s) = -822.1 kJ/mol
ΔHf Fe(s) = 0.0 kJ/mol
Since the given enthalpies are still in kJ/mol, we have to
multiply that with the number of moles in the formula. Therefore solving for ΔH:
ΔH = [<span>3 mol </span><span>( − </span><span>393.5 </span>kJ/mol<span>) + 1 mol (</span>0.0
kJ/mol)<span>] − [</span><span>3 mol </span><span>( − </span><span>110.5 </span>kJ/mol<span>) + </span><span>2 mol </span><span>( − </span><span>822.1 </span>kJ/mol<span>)]</span>
ΔH = <span>795.2
kJ</span>
Answer:
I think it is 100 if I guess
D because these are the biggest particles, and are therefore, the most dense.
Answer:
I'm a bit confused on where the question is. Perhaps re-write it in the comments? I'd love to help but this seems more like an answer than a question xD
Explanation:
Answer:
Phenols do not exhibit the same pka values as other alcohols;
They are generally more acidic.
Using the knowledge that hydrogen acidity is directly related to the stability of the anion formed, explain why phenol is more acidic than cyclohexane.
Explanation:
According to Bromsted=Lowry acid-base theory,
an acid is a substance that can release 
ions when dissolved in water.
So, acid is a proton donor.
If the conjugate base of an acid is more stable then, that acid is a strong acid.
In the case of phenol,
the phenoxide ion formed is stabilized by resonance.
The resonance in phenoxide ion is shown below:
Whereas in the case of cyclohexanol resonance is not possible.
So, cyclohexanol is a weak acid compared to phenol.
