DOC PREVIEW
UT Arlington CHEM 1465 - Cell Potential

This preview shows page 1 out of 2 pages.

Save
View full document
View full document
Premium Document
Do you want full access? Go Premium and unlock all 2 pages.
Access to all documents
Download any document
Ad free experience
Premium Document
Do you want full access? Go Premium and unlock all 2 pages.
Access to all documents
Download any document
Ad free experience

Unformatted text preview:

Chem 1465 1st Edition Lecture 18Outline of Last Lecture 1. Redox reactions A. TermsB. Balancing a redox equation Outline of Current Lecture1. Cell notation2. Cell potential A. Galvanic cellsB. Measuring cell potentialC. Standard reduction potentials D. Nonstandard conditions3. Cell potential and equilibrium Current Lecture1. Cell notation- General notation:Anode │ electrolyte of anode ││ cathode │ electrolyte of cathode- Components of anode go on the left and the components of the cathode go on the right (the spectator ions are left out)- Vertical lines spate phase boundaries and commas spate components in the same phase- The electrodes are contained on the outsides- Double vertical lines separate the half cells and represent the salt bridgeThese notes represent a detailed interpretation of the professor’s lecture. GradeBuddy is best used as a supplement to your own notes, not as a substitute.2. Cell potentialA. Galvanic cells have potential: for the cells there are 2 components, with one component “pulling” electrons through the wire- Ecell = the cell potential, the “pull”- Units are emf or voltage- Spontaneous when Ecell is positive B. Measuring cell potential- There are no absolute values for potentials, therefore we must compare relative to each other- SHE- standard hydrogen electrode where 2H+ + 2e- → H2 and Ecell = 0 volts C. Standard reduction potentials- Convention: it is common to write all half reactions as reductions - Therefore- only reactants are oxidizing agents and only the products are reducing agents- The value of Eᵒ give us important information: the higher or larger the value of Eᵒ, the reaction goings forward; the smaller the value of Eᵒ, the reaction goes in reverse- Eᵒhalf cell is an intensive property- it does not depend on the amount- To calculate cell potential: Eᵒcell =Eᵒreduced - Eᵒoxidized D. Nonstandard conditions- The standard state is 1 molar and 1 atm; when not in standard conditions- use the Nernst equation - Nernst equation: Ecell = Eᵒcell – (RT/ nF) x (ln(q))Where q is quotient ([product] / [reactants]) F = 96,500 and R = 8.314 n = number of moles of electrons transferred 3. Cell potential and equilibrium - Since cell potential informs us on spontaneity it must be related to ΔGᵒ and K- For spontaneous reactions: ΔGᵒ is negativeK > 1Ecell is positive - For non-spontaneous reactions:ΔGᵒ is positiveK < 1Ecell is negative - How to calculate ΔGᵒ : ΔGᵒ = -nFEᵒcell Where n is the moles of electrons transferred and F =


View Full Document

UT Arlington CHEM 1465 - Cell Potential

Download Cell Potential
Our administrator received your request to download this document. We will send you the file to your email shortly.
Loading Unlocking...
Login

Join to view Cell Potential and access 3M+ class-specific study document.

or
We will never post anything without your permission.
Don't have an account?
Sign Up

Join to view Cell Potential 2 2 and access 3M+ class-specific study document.

or

By creating an account you agree to our Privacy Policy and Terms Of Use

Already a member?