Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: HCl + H2O Gibbs free energy Question
SunriseSunset
Hazard to Self
**




Posts: 82
Registered: 9-6-2015
Location: USA
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 13:02
HCl + H2O Gibbs free energy Question


I calculated Gibbs free energy of HCl(aq) -> H+(aq) & Cl-(aq)

And got a positive number. (38650.6) Which would indicate that it's not a favorable reaction.. Yet we know that HCl dissolves readily with water.

So I calculated gibbs free energy of
NaOH(s) -> Na+(aq) & OH-(aq)
and got -37.8, which indicates a favorable reaction. Which is true, dissolving NaOH in water definitely gives off heat. So I wanted to see what would happen when I calculated dissolving HCl in water, since I know no real heat is given off, yet it's definitely a strong acid. Wanted to see what the gibbs free energy calculation would look like, and for some reason, it's saying it's not favorable. Why is that?

Nvm. I didn't convert J/mole for entropy to KJ/mole... I wish I could delete my own topic. My mistake!

[Edited on 2-11-2015 by SunriseSunset]




Why do chemists call helium, curium and barium the medical elements?
because if you cant helium or curium, you barium! - Heimerdinger
View user's profile View All Posts By User
blogfast25
International Hazard
*****




Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 13:33


Quote: Originally posted by SunriseSunset  
I calculated Gibbs free energy of HCl(aq) -> H+(aq) & Cl-(aq)



How did you calculate ΔG here?

Hint: H<sup>+</sup>(aq) doesn't really exist, protons is water are fully solvated as H<sub>3</sub>O<sup>+</sup>(aq).

The dissolution of HCl(g) into water is exothermic, by the way.

[Edited on 1-11-2015 by blogfast25]




View user's profile View All Posts By User
SunriseSunset
Hazard to Self
**




Posts: 82
Registered: 9-6-2015
Location: USA
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 13:51


I did originally attempt to use H3O+ ion, but every thermodynamic data chart that I could find only had H+ values.

Ultimately for HCl(aq) + H2O -> H+ & Cl-, I got..

delta G* = -38.65 KJ/mole

Quote:
The dissolution of HCl(g) into water is exothermic, by the way.


After just thinking about it some more for a second, that could make sense bcuz HCl aqueous solns. are already pre-dissolved and diluted. If I were to take 99% HCl and add it to water, things would be quiet obvious... Lol

[Edited on 1-11-2015 by SunriseSunset]




Why do chemists call helium, curium and barium the medical elements?
because if you cant helium or curium, you barium! - Heimerdinger
View user's profile View All Posts By User
blogfast25
International Hazard
*****




Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 15:27


You chose a particular example that probably deserves explaining.

In the electrochemical series the 'centre point' (so to speak) the half reaction H<sup>+</sup>/1/2 H<sub>2</sub> has been chosen conventionally to be +0 V. This means that in accordance with Nernst we have to put the Standard ΔG for the H<sup>+</sup>/1/2 H<sub>2</sub> reaction (oxidation or reduction makes no difference here: + 0 V = - 0 V) also at 0 kJ/mol. And since as the Standard ΔG of Formation for H<sub>2</sub> is also conventionally set to 0 kJ/mol, the Standard ΔG of Formation for H<sup>+</sup> must also be zero.

Now, as ALL SRPs are relative to H<sup>+</sup>/1/2 H<sub>2</sub>, it matters not one iota: we really are interested in changes in Gibbs Free Energy of actual reactions and these the system used predicts perfectly well.


[Edited on 1-11-2015 by blogfast25]




View user's profile View All Posts By User
SunriseSunset
Hazard to Self
**




Posts: 82
Registered: 9-6-2015
Location: USA
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 16:34


This might be an obviously bad question, but what's the way to find out the delta "G", delta "H", or "S"'s at other varying temperatures besides standard room temp data from the charts?

If it requires calculus, i'll be biting the dust for weeks. lol

[Edited on 2-11-2015 by SunriseSunset]




Why do chemists call helium, curium and barium the medical elements?
because if you cant helium or curium, you barium! - Heimerdinger
View user's profile View All Posts By User
blogfast25
International Hazard
*****




Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 16:50


Take a simple reaction:

A + B === > C

You already know how to calculate these values at STP (298 K), so how do we calculate it at any T different from 298 (Kelvin)?

You need to calculate the increase in ΔG (or ΔH or S) to get A and B from 298 K to T and simply add these increases to their STP values.

Then calculate the increase in ΔG (or ΔH or S) to get C from 298 K to T and simply subtract that increase from C's STP value.

Then carry out the summation as you would at 298 K.

NIST webbook provides a large database of data of ΔH or S in function of temperature for many compounds.

For watery species these data are harder to find but how often do you watery chemistry at 200 C? ;)


[Edited on 2-11-2015 by blogfast25]




View user's profile View All Posts By User
SunriseSunset
Hazard to Self
**




Posts: 82
Registered: 9-6-2015
Location: USA
Member Is Offline

Mood: No Mood

[*] posted on 1-11-2015 at 20:14


This looks nice and useful to calculate Gibbs free energies of reactions at other temperatures than STP. Too bad it's calculus. I'll see if I can't learn it real quick tho

Gibbs–Helmholtz equation

OH! I understand what you were saying. Basically, T variable can be changed, and it works fine to figure out a new delta G according to any temperature.

[Edited on 2-11-2015 by SunriseSunset]




Why do chemists call helium, curium and barium the medical elements?
because if you cant helium or curium, you barium! - Heimerdinger
View user's profile View All Posts By User

  Go To Top