During the Organic Molecules experiment, four reagents were used to test for the presence of three of the four basic categories of Organic Molecules, carbohydrates, lips, and proteins, in control substances and Cheerios. For carbohydrates, I was testing, specifically, for the presence of reducing (polysaccharides) and non-reducing sugars (monosaccharides). Carbohydrates, both reducing and non-reducing, are important to the cell because they act as an energy source and are an important factor in building and the structure of important sugars like Ribose. Monosaccharides are important, specifically, because they are sources of nutrients to cells. An example of this would be glucose. (Campbell, 2014, 68) Non-reducing sugars, such as starch, serve as storage for cells and are hydrolyzed and broken down when sugars are needed for the cell. Some polysaccharides, such as cellulose, are used for structural purposes in cells. In plants, cellulose is …show more content…
an important component to the tough cell walls in plant cells. (Campbell, 2014, 70) Lipids, which are very hydrophobic molecules, are important to cells because they store energy. (Campbell, 2014, 72) Lipids also play a major role in cell membranes. Proteins, out of all of the organic molecules, have the largest range of functions. In fact, proteins to the majority of the work in cells, accounting for more than approximately 50% of the dry mass in most cells, acting as enzymes (which are needed for every chemical reaction in the human body), transport, and even cell structure. (Campbell, 2014, 75) The four reagents that I used to test for the presence of these organic molecules in my control substances and cheerios were Benedict’s, Lugol’s, Beta Carotene, and Biuret’s. Each reagent caused a chemical reaction that turned the substances being tested, a different color, thus allowing me to determine the presence, or lack there-of, of the organic molecules in question. Benedict’s, which tests for monosaccharides, works by reacting with the carbohydrate molecules and producing a red-brown precipitate consisting of copper (I) oxide. Lugol’s, which tests for polysaccharides, produces a black-blue color when it gets stuck in the beta coils of starch. Beta Carotene, which tests for lipids, works by simply dissolving into a solution and turning it orange. Biuret’s, which tests for proteins, works by reacting with polypeptides, peptide bonds, thus producing a purple-blue color. My hypothesis, after testing the control substances, was that Cheerios would test positive for carbohydrates, lipids, and protein because I know that Cheerios contain a healthy, recommended amount of protein, carbohydrates, and fats, which is one reason they are believed to be such a great food. In each experiment, including the one using my food, distilled water was always used for the control. To begin my experimentation, I created a stock solution, which would be used in each test.
I used Cheerios, distilled water, and a pestle and mortar. I ground the Cheerios until they had a fine, sand-like texture and consistency. I then added distilled water and mixed until I was left with a thin, runny solution, that was beige in color. Once I had the stock solution made, I was able to perform my first experiment, beginning with Benedict’s reagent. For this experiment I used a hot plate, beaker, and three test tubes, one labeled + (positive control), - (negative control), and Cheerios. Two milliliters of each solution was then added to the tubes they were labeled to go into. In this experiment, the positive control was a glucose solution. I then added two milliliters of Benedict’s reagent to each tube. Once a boiling bath had been made using water, the beaker, and the hot plate, each of the three test tubes were places, sitting upwards, into the boiling bath. A timer was set for three minutes, and I recorded the color
changes. Next, I used Lugol’s reagent to test my substance. I used three test tubes, again, also labeled + (positive control), - (negative control), and Cheerios. The positive control for this experiment was a starch solution. I added one milliliter of each substance to the appropriate, labeled tube. I then added several drops of Lugol’s reagent to each tube, gently shook each, and recorded the color change. The next experiment I did used the Beta carotene pigment. As in the last two experiments, three test tubes were used and labeled the same way. In this experiment, the positive control was oil. I added two milliliters of each solution to its respective, labeled tube and then a drop of Beta carotene to each. I recorded the solubility. For the last experiment, I used Biuret’s reagent. As in the last three experiments, three test tubes were used and labeled the same way. In this experiment, the positive control was albumin. I added two milliliters of each substance to its respective, labeled tube. I then added two milliliters of Biuret’s reagent to each tube and recorded the color changes. Results of My Organic Molecule Experiment Benedict’s Lugol’s β-carotene Biuret’s Water - - - - Glucose Solution + - N/A N/A Starch Solution - + N/A N/A Oil N/A N/A + N/A Albumin Solution N/A N/A N/A + Cheerios + + - + (Note: Any place “N/A” is marked on this table, a test was not completed using this reagent/solution combination) During the experiment using Benedict’s reagent the Cheerios solution turned from beige to brown-red in color which was similar to the color of the positive control in this test; therefore the solution contained monosaccharide molecules. During the experiment using Lugol’s reagent the solution turned from beige to black in color which was similar to the color of the positive control in the test; therefore the Cheerios solution contained polysaccharide molecules. During the experiment using the Beta carotene pigment, the pigment did not seem to dissolve at all in the Cheerios solution. It only sat at the top; therefore the Cheerios solution did not seem to include lipid molecules. During the experiment using Biuret’s reagent the Cheerios turned from beige to violet in color which was similar to the color of the positive control; therefore the solution must contain protein molecules. My original hypothesis was that my Cheerios would test positive in each of the experiments that I’d be preforming, but from the results of my experimentation, I had gathered information that would’ve lead me to believe my Cheerios contained protein, monosaccharide, and polysaccharide molecules. However, based on this experiment alone, I was left to believe that there were no lipids present in my Cheerios. Although my solution tested negative for lipids, I believe the only reason this happened was because there was too much water in it. Another flaw in my experiment was that, while I am aware of the ingredients of Cheerios, I don’t really know if my solution truly contained Cheerios in the first place because I was not given the opportunity to see and observe the original box and packaging they came in. Either way, I do know that almost all processed foods have some percentage of fat, and therefore, lipids would be present. I also checked the official website for the Cheerios brand cereal, and I noticed that they all contained some percentage of fat. The only solution to this flaw that I can come up with, would be to use a different test to test for the presence of lipids in my solution. I strongly believe that the insolubility of the beta carotene in water, along with the high percentage of water in my solution, prevented me from being able to get a real result in that test. If I were to design a new experiment to test for lipids, using the Beta carotene again, I would use less water, and I would ground my Cheerios to a finer texture. I also would use more Beta carotene and I would shake the solution, with the Beta carotene added to it, for a least a minute. This way, it would’ve been able to react with more of the Cheerio component of the solution, and perhaps, change colors. Overall, the cellular activity going on in our bodies require the nutrients that come from what we ingest. As a result of this, we need to be mindful of what we are and are not eating. This way we can be sure that we’re feeding ourselves the right, and right amount, of nutrients our bodies need.
Carbohydrates are more than just fuels for the body and have other uses. Carbohydrates are hydrocarbons containing a carbonyl group and many alcohol groups. Their polymers can complex or they be simple and contain just one repeating monosaccharide, the roles of polymers can be many such as structural, storage or even signalling. (Tymoczko et al, 2012 p. 131)
They do indeed have other macromolecules but at a low concentration that would make it difficult to test for. This can be tested the same way, following the same procedure of the Glucose test. They would have the same characteristics of the Unknown #2 solution since they both have high levels of detectable glucose. It would also have a similar range of 2.6-3.5% sugars within the solution since the test would give a similar colour change. Errors that could have altered the accuracy of this experiment would be the temperature of the water. To ensure a proper reaction and colour change to occur the water strictly has to be at 80°C. If the temperature is too high/low it could alter the reaction and give inaccurate results. To ensure that this error does not affect the accuracy the temperature can be consistently monitored to stay consistent at 80°C. Monitoring the hotplate setting could also be beneficial to make sure the temperature does not exceed the ideal temperature range causing altercations in the
There were five test solutions used in this experiment, water being the control, which were mixed with a yeast solution to cause fermentation. A 1ml pipetman was used to measure 1 ml of each of the test solutions and placed them in separated test tubes. The 1 ml pipetman was then used to take 1ml of the yeast solution, and placed 1ml of yeast into the five test tubes all containing 1 ml of the test solutions. A 1ml graduated pipette was placed separately in each of the test tubes and extracted 1ml of the solutions into it. Once the mixture was in the pipette, someone from the group placed a piece of parafilm securely on the open end of the pipette and upon completion removed the top part of the graduated pipette.
The objective of this lab is to try to separate the different compounds that are contained in cereal.
Carbohydrates are divided into two groups based on how complex their structure is.Monosaccharides is a simple carbohydrate because it has one simple sugar, disaccharides has a combination of two simple sugars.An example of disaccharides is lactose.Complex carbohydrates also known as polysaccharides are known to have multiple sugars.Polysaccharides are also used to store energy, an example of this starch.In addition, nutrients include proteins ,fats, minerals and vitamins.Multiple tests were taken like Benedict’s Solution, Lugol’s Solution, and Biuret’s Solution to test if the presence of a substance was there.
These compounds have their structures range from linear to highly branched compounds. Examples of storage polysaccharide include, starch and glycogen and structural polysaccharide include cellulose and chitin. Cellulose is a significant polysaccharide as it is the most abundant organic compound in the world. It is made up of the sturdy cell wall that surround plant cells making plant stems, roots, leaves and branches strong. Chewing of plant produce such as salad takes a lot of time and strength due to the effect of cellulose. The rigid structure gives support to the plants position. Additionally, the active nature enables the existence of the paper, lumber and cotton fabric. It is due to this strength that cellulose is used in large number of synthetic products such as carpet thickening and agents in shampoo (Salter, Tucker, & Wiseman,
3. Benedict’s test, which uses Benedict’s reagent, (usually used to test for the presence of reducing sugars) will show up positive in the presence of all monosaccharaides and some disaccharides. The test will also show a positive in the presence of aldehydes and alpha-hydroxy-ketones. Benedict’s test is not positive for sucrose because the glycosidic bond between the fructose and the glucose (the two monosaccharaides making up sucrose) prevents the isomerization of glucose into aldehydes and fructose into alpha-hydroxy-ketones. Therefore sucrose is a non-reducing sugar and these do not react with Benedict’s reagent. Since the test is designed for use with monosaccharaides glucose gives a positive result, as it is one. In conclusion glucose is a monosaccharaide sugar while sucrose is a disaccharide made of two monosaccharaide sugars.
The disaccharides were: maltose and sucrose. The monosaccharides: glucose, fructose and lactose. In the experiment, the amount of CO2 produced was recorded by a gas sensor over a period of fifteen minutes in a Nalgene bottle of 3mL yeast solution and 3mL of sugar solution. It was predicted that the disaccharide sugars would produce a higher rate of cellular respiration, however, this hypothesis was proven wrong during the experiment. The data revealed that glucose was the sugar that produced the largest amount of CO2 (236 ppm/min). It had 28.5ppm/min more than the second most efficient sugar fructose (208.3ppm/min), which is also a monosaccharide. The products of one molecule of glucose in glycolysis include six molecules of carbon, six molecules of water and energy molecules called ATP and NADP (Source
The first step taken within the experiment was to obtain and label three 400 mL beakers with the numbers 1 through 3 using a wax pencil. Once labeled, each beaker needed to be filled with a corresponding solution. The beaker marked with a “1” was filled with 200 mL of distilled water and
Significance of Carbohydrates: Massive distribution of carbohydrates in nature makes them indispensable for life. Carbohydrates like cellulose, pectin and starch serve as fundamental structural components by constituting 50-80% of dry weight of plants. Simple monomeric units such as glucose form oligosaccharides by means of a covalent connection known as glycosidic linkage. Additional linkage of these oligosaccharides results in the formation of long chain polysaccharides which not only play a pivotal role in the nutrition of humans and animals but also contribute as basic substrates in manufacturing of many fermentation products. Production of many industrial products like enzymes and antibiotics is carried through the
Cellulose is different than starch in that it is made up of β-glucose. This is a storage molecule for plants and their seed. Cellulose is the main component in the cell wall of plants. It is not broken down easily by most creatures making it work well as a biological structural material. Some animals like cows and horses are able to break cellulose down because of symbiotic bacteria and protozoa in their digestive tracts.
The phenol-sulfuric acid method is a simple and rapid colorimetric method to determine total sugar in a sample. The method detects virtually all classes of carbohydrates, including mono-, di-, oligo-, and polysaccharides. It is one of the most versatile, relatively easy and cheap approaches for determination of carbohydrate concentrations is the colorimetric method based on reaction between hydrolysed carbohydrate solution and a colouring reagent that develops colour that is detectible in the visible range of the electromagnetic spectrum. Reagents used for colorimetric detection include phenol and concentrated sulphuric acid. The furfural is allowed to develop colour by reaction with phenol and its concentration is detected by visible light absorption.
There was a presence of starch in the solution. In test tube two, there was a slight color change to yellow- orange. This proved that since glucose is a monosaccharide it doesn’t go through the color change, showing no starch present. For test tube three changed to a light blue color with a precipitate at the bottom. It didn’t change to the colors that indicated many levels of reducing sugars because there is no reaction when testing Benedict’s reagent with a polysaccharide. Therefore, my hypothesis was wrong. In test tube four, there was a color change to orange with a precipitate at the bottom. The orange color and the presence of a precipitate in the solution proved my hypothesis was correct. Glucose was broken down to reduced
Starch is often converted to commercial products of glucose, maltose syrups, and is a major enzyme application. Enzymes break down the polysaccharides into multiple sugars. They help to improve starch purity and clarity, creating greater abstractionyields, and removal of fibers. Pectin and Celluloseare insoluble substances found in plant cell walls. Pectinase and Cellulase are used to break down pectin and cellulose respectively. It helps to clear fruit juice, decrease viscosity, and create a good consistency and texture (Thakur,
Organic chemistry is the best and most interesting branch of chemistry. There are five branches of chemistry: analytical, biochemistry, physical, inorganic, and organic chemistry. However organic chemistry is the largest branch, most intriguing, and has a large impact on everyone around the world. It is the study of carbon compounds and deals with the structure, reactions, and properties of organic compounds and materials. It plays a huge role in manufacturing many products that people use everyday. “Organic chemistry explores how to change and connect compounds based on carbon atoms in order to synthesize new substances with new properties” (Chemistry). There are millions of organic compounds, much more than inorganic, and new compounds