First, I gathered the necessary equipment:
Thermostatically controlled water baths
Photographic film (b/w)
Test tube rack
O.1% trypsin made in pH7 buffer solution
I then decided on the range of results and temperatures I was to investigate. I decided to observe 20º, 30º, 40º, 50º, 60º, 70º and 80º. 3.
Next, I label each test tube with the temperature to be investigated and then added 2.5cm3 of Trypsin solution. 4.
I ensured that I cut the necessary pieces of film using a ruler and a pair of scissors. I cut pieces that were 2cm in length, and 1.6cm in width each. 5.
The only water baths of my choice that were running were at 30º and 60º. I therefore had to use the Bunsen burner etc. for the rest of the temperatures (excluding 20º). I kept each test tube heated for 5 minutes. 6.
I added the photographic film pieces just before I placed the test tubes in the water baths/ Bunsen burners, and ensured that they submerged fully before I began timing. 7.
I carefully and frequently examined each test tube for the time that the film became transparent and listed the result
Time taken (minutes)
Time taken (seconds)
Rate of Reaction -(1/time in mins) 4.d.p
It is evident from the graph and the table above, that as the temperature is increased, the amount of light passing through the tested solutions is decreased, and therefore the amount of pigment released from the beetroot samples is increased. The results produce a graph with negative correlation, a curve that has a negative gradient. The graph shows that as the temperature is increased, the colorimeter reading is decreased. The structure of my results proves my theory correct. The increase in...
Please join StudyMode to read the full document