The purpose of methodology is to maintain the most accurate results by conserving the temperatures of each sample of potato. By wrapping the potatoes in tin foil, it not only maintains the heat of each, but it also allows them to have close to almost the same temperature with each other when they are trapped with the same heat. This makes sure that the hot potatoes do lose their heat and that the cold potatoes remain cold. Maintaining the same temperature for each potato prevents the results of the trials for the same potato from being different from one another. The control group consists of having the same type of potato, washing all the potatoes in the same water to get rid of grime, having about the same sized potato pieces, using 150 mL …show more content…
Eighth, wrap each group of potatoes in a 12 by 12 inch, or in a size that covers the group of potatoes entirely, piece of tin foil. For example, all the hot potatoes are wrapped together and same goes for the other potato samples. For step nine, place each of the tinfoil wraps in individual ziplock bags to secure the temperature of each potato even more. Now that the prep work is finished and all the materials are accessible, the actual experiment can begin. First, grab four beakers that have dashes that mark the up to at least 200 milliliters. Second, take one of the ziplock bags and remove the tinfoil to take the potatoes out from it. It is suggested to do the hot or cold potatoes first, so their temperatures are less likely to be lost. Third, measure the temperature of each potato using a food thermometer. For step four, place each potato of the one temperature into individual beakers, where each beaker has one potato sample that is the same temperature as the other three beakers. Fifth, pour 150 mL of hydrogen peroxide inside each beaker to. Sixth, leave the potato in the beaker for 5 minutes and watch the reaction
Procedure: Variables: Controlled- water and size of potatoes. Manipulated variables- potatoes growth based on contents of solution.
Purpose: To determine the concentration of solute in the potato’s cytoplasm by measuring the change
Students will label 3 test tubes hot, cold, and room temperature and place potato cub (3X3X3 cm)
However one beaker received 100 mL of Deionized water with a molarity of 0.0. Afterwards a cork borer was pushed through the potato and was twisted back and forth. Once the borer was filled it was removed from the potato. Pushing the potato cylinder out of the borer, this this step was repeated six more times in order to get seven undamaged potato cylinders. Using a sharp razor blade, the potato cylinders were both cut to a uniform length of about 5cm, and were removed of their potato skins. The potato pieces were also cut in half to give the cells a greater surface area in which it was easier to absorb the solution. After the cylinders were weighed on a balance and the data was recorded in Table 4. Using the razor blade each potato was cut lengthwise into two long halves. Then the potato pieces were transferred to the water beaker and the time they were submerged was recorded. This step was repeated for all potato cylinders in which the pieces were placed in solutions 0.1 to 0.6 M. The potatoes were incubated for ninety minutes. At the end of the incubation period the time was recorded. Then the potato piece was removed form the first sample. Next potato pieces were weighed the and the final weight was recorded in Table 4. This procedure was repeated until all samples had been weighed and recorded in the chronological order they were initially placed in the test solution. Afterwards the table was completed by recording the
The hypothesis for this experiment was that at 0m and at .2m the potato core was going to swell making the surroundings it was in hypotonic. For .4m it was stated that the potato core would stay the same, making the surroundings it was in isotonic. For that last three solutions, .6m, .8m, and 1m, it was thought that they would shrink, so that would mean that that the environment that they were placed in was hypertonic. Although these
8. Use the plastic forceps to remove the potato cylinders from the beakers (keep them together in the same group), and blot off the excess solution weight on them with the paper towels.
Using different sizes of potato could show us whether the concentration of enzyme affect the rate of reaction. However, this would not be a practical independent variable as the S.A to volume ratio would not be proportional and the size of the potato to get significant results would be very hard to change. It would be very hard to cut the potato tubers to exact measurements and that could lead to the results becoming inaccurate. An option could be to cut the potato tube into small 1 cm bits and pile then up on top of each other in the test tube, but this again would prove to be impractical as then not all of the surface area of the potato would be exposed to the substrate and this would make my results unreliable. It may also prove to be impractical as having the tuber bits piled on top of each
First I gather all my materials needed for the experiment (see materials list). Second I peel and slice potatoes weigh each potato in grams. Get these slices to weigh the same in mass because if they vary to much in mass that could affect the results of the experiment. Third I place each potato in its own beaker. Fourth once the potatoes are placed in beakers I make sure to place enough solution to fully cover the potato. Each beaker should have a different amount of
Small slices of potato are placed in six concentrations of sucrose: 0.0 M, 0.1 M, 0.2 M, 0.3 M, 0.4 M, and 0.5 M. The initial mass of potato is noted before being placed in the solution. The potato remained in the solution for one hour then the potato was removed from the solution and dried off before the final mass was noted. The null hypothesis is that the solutions of different molarities of sucrose will not affect the
There were three test tubes in which the experiment was held. A relatively equal sized portion of raw potato (this contained the enzyme [a biological catalyst] hydrogen peroxidase) was placed in each tube. Then, enough water to cover the potato was added. Proceeding this, each of the test tubes were assigned a temperature; cold, room temperature or warm (this was written on the tag so that they were not confused). The test tube destinated ‘cold’ was placed in a ice bath for five minutes. At the same time, the ‘hot’ test tube was placed in a hot water bath for five minutes. Meanwhile, the room temperature test tube sat at room temperature for five minutes. When the five minutes were over, the test tubes were returned to the rack (so that they were able to be observed). Then, the test tubes were allowed to sit at room temperature for five more minutes. Once that period of time was over, 2 ml of hydrogen peroxide (the substrate) was added to each tube.
You may have observed the reaction of naturally-occurring catalase in tissue from either liver of potato. Design an experiment to determine if the amount of catalase varies from tissue to tissue (e.g. 200 g of liver compared to 200 g of potato).
Measure and add 5cm3 of buffer solution using a measuring cylinder with the pH 3 into a test tube using a pipette and place the potato cylinders into the test tube.
There are 3 potential states that the cell could be in depending on the type of solution:
out the potato and dry it to ensure excess water is not added to the
Then, each group of students received the necessary materials to complete the experiment. When the students received the cups, they labeled cups to distinguish between the salt solution, distilled water, and control group. After weighing the cups and finding the mass of the cucumbers, the students poured 50 ml of water in one cup, 50 ml of salt solution in the other, and left the control cup empty. Then, the students placed the cucumbers into the cups and waited 30 minutes for the results. After the 30 minutes, the students removed the cucumbers from each solution and dried the cucumbers with paper towels. The students then weighed the cucumbers again and recorded their results. Lastly, the students found the difference from the original mass of the cucumbers and recorded their results.