React of K2Cr2O7 & C2H6O: Product & Difference

  • Thread starter Thread starter pivoxa15
  • Start date Start date
Click For Summary

Discussion Overview

The discussion revolves around the reaction of acidified potassium dichromate (K2Cr2O7) with ethanol (C2H6O), exploring the resultant products and the differences between acidified potassium dichromate and regular potassium dichromate. The scope includes theoretical aspects of redox reactions and half-reaction balancing.

Discussion Character

  • Technical explanation
  • Mathematical reasoning
  • Debate/contested

Main Points Raised

  • One participant inquires about the products of the reaction between acidified potassium dichromate and ethanol.
  • Another participant notes that acidification increases the oxidation potential of the dichromate ion, suggesting a standard textbook problem context.
  • Half-reactions for chromium and ethanol are proposed, with one participant questioning the placement of electrons in the half-reaction for ethanol.
  • Participants provide a balanced net reaction involving chromium and ethanol, indicating that the product of ethanol is acetic acid (CH3COOH).
  • There is a query about methods for predicting products in complex reactions, with a suggestion to refer to tables for guidance.

Areas of Agreement / Disagreement

Participants present various viewpoints on the half-reactions and the balancing process, indicating some level of disagreement or uncertainty regarding the details of the reactions and the methods for predicting products.

Contextual Notes

There are unresolved aspects regarding the balancing of half-reactions and the electron transfer in the reactions discussed. Additionally, the effectiveness of using tables for predicting products remains a point of inquiry.

pivoxa15
Messages
2,250
Reaction score
1
How does acidified potassium dichromate, K2Cr2O7 react with ethanol, C2H6O ? What is the resultant product?

And as an aside question what is the difference between acidified potassium dichromate and potassium dichromate?
 
Physics news on Phys.org
pivoxa, this is a standard textbook problem and belongs in the Homework section.

Acidified dichromate is a solution of dicromate mixed with a suitable dilute acid. Acidification increases the oxidation potential of the dichromate ion.
 
symbolipoint said:
This helps to verify result of ethanoic or acetic acid:
http://www.outreach.canterbury.ac.nz/chemistry/ethanol.shtml

I've seen this site but what are the half reactions?

For chromium, it's (Cr2O7)2- + 14H+ + 6e- -> 2Cr3+ + 7H2O

For ethanol on the surface it looks like C2H5OH + O2 -> CH3COOOH + H2O
but where is the electron in this half reaction?
 
Last edited:
C2H5OH + H2O + ---> CH3COOH + (H+) + (e-)
Balance and premultiply as required to complete.

Alternatively, to your above second reaction, add the third reaction:
H2O ---> O2 + (H+) + (e-) and balance the lot of them.
 
The two half reactions are
((Cr2O7)2- + 14H+ + 6e- -> 2Cr3+ + 7H2O ) * 2
C2H5OH + H2O -> CH3COOH + 4(H+) + 4(e-) * 3

Net reaction is:
3C2H5OH + 2(Cr2O7)2- + 16H+ --> 3CH3COOH + 4Cr3+ + 11H2O

The trick was in determing that the product of C2H5OH is CH3COOH. The rest can be done by balancing water, H+ and e-. Are there ways of working out which product will form or do people usually look at tables. FOr predicting complex reactions is the best way to look up in a table? If so is there a large table on the web? I have seen ones in the textbook but many reactions seem to be missing from them.
 

Similar threads

Replies
5
Views
6K
Replies
1
Views
3K
Replies
2
Views
4K
  • · Replies 4 ·
Replies
4
Views
23K
Replies
8
Views
3K
  • · Replies 2 ·
Replies
2
Views
6K
  • · Replies 14 ·
Replies
14
Views
15K
  • · Replies 3 ·
Replies
3
Views
6K
Replies
3
Views
4K
  • · Replies 1 ·
Replies
1
Views
2K