Acid-Catalysed Iodination of Propanone
- The iodination of propanone is carried out using a catalyst of dilute sulfuric acid
- The reaction between iodine in an acidic solution and propanone is
CH3COCH3 (aq) + I2 (aq) → CH3COCH2I (aq) + H+ (aq) + I- (aq)
- We can follow the rate of this reaction by using a continuous monitoring method and therefore we will be able to deduce the order of reaction with respect to a substance using a concentration line graph
- We can calculate the order of reaction with respect to iodine as the propanone and acid are in a large excess so their concentration do not change during the reaction
- Once a portion of the reaction mixture has been removed, we stop the reaction by adding sodium hydrogencarbonate
- Performing a titration again sodium thiosulfate(VI) solution and using starch as an indicator is used to determine the concentration of iodine
2S2O32- (aq) + I2 (aq) → 2I- (aq) + S4O62- (aq)
Results
Sample Data from the Reaction
- This graph is a straight line graph
- As the gradient is constant, the rate of reaction is constant, and therefore independent of the concentration of the iodine solution
- This means the reaction is zero order with respect to the iodine
- The rate equation for the reaction is
- Rate = k[CH3COCH3 (aq)] [H+ (aq)]
Concentration-time graphs of a zero-order reaction