3. Solid iodine in 1 mL of alcohol is slightly more soluble. Residue still remains on the bottom and alcohol changed to an orange red color. 4. Solid iodine in 1 mL of mineral oil is slightly soluble.
Part B: The graduated pipet’s average density at 22.3 °C was determined to be 0.9785g/mL with a percentage error of 1.89% shows the graduated pipet to be more accurate and precise. Part C: Density of an unknown NaCl solution was measured and a calibration curve used to determine the percentage of NaCl by mass in the solution. y=0.007x + 0.998 which concluded that the concentration of the sodium chloride solution was 3.14%. INTRODUCTION Anything that you can see, touch, taste or smell, occupies space and has mass, it is called matter. Matter can be a gas, a liquid,
Wait 90 seconds for the light source to warm up, then fill a cuvette with distilled water and clean the flat, clear sides on the cuvette with a Kimwipe, removing dust and fingerprints before putting the cuvette into the instrument. Orient the cuvette so that the clear sides line up with the white arrow on the top of the spectrometer. Click “Finish Calibration”, then “OK”. Next, fill a cuvette with the “yellow” sample, repeating the steps to clean the clear sides of the cuvette with a Kimwipe to remove fingerprints and dust. Place the clean cuvette containing the “yellow” sample into the spectrometer, orienting the cuvette so that the clear sides of the cuvette line up with the white arrow in the cuvette.
Use your 4 markers to draw a different colored dot on each of the pencil marks on the paper strip. Allow the markers ink to dry, and then go back recolor each dot. 5. Prepare the saltwater mixture by mixing 1/8 teaspoon of salt and three cups of water in a clean 2-liter bottle. Stir or shake the solution until it is dissolved.
The streak plate technique is done to isolate a colony formed by a single cell from a mixture containing millions of cells. The streak plate technique was also used to obtain pure cultures of the bacteria using a trypticase soy agar (TSA) plate and was incubated at 37 ̊ for 48 hours. Secondly a Gram stain was performed as directed from exercise 6in the lab manual (Kleyn 37) and was found to be Gram negative Rods. The Gram stain is important to do because it reveals the morphology of the organism and the arrangement of the cells; if an organism appears purple under a microscope then it is said to be Gram positive, and if it
Name: ___________________________________ Date: ______________ Practice Test #3 ____ 1. When a precipitation reaction occurs, the ions that do not form the precipitate A) evaporate B) are cations only C) form a second insoluble compound in the solution D) are left dissolved in the solution E) none of these 2. An aqueous solution of potassium chloride is mixed with an aqueous solution of sodium nitrate. The complete ionic equation contains which of the following species (when balanced in standard form)? A) B) C) D) E) ____ 3.
EXPERIMENT: TECH 0704, Distillation, macroscale technique only, simple and fractional: Substitute a mixture of 25 mL ethanol and 25 mL water for the toluene/cyclohexane mixture. Record the temperature at 2 mL intervals of distillate. Use glass beads to pack the fractionating column. Construct a graph of temperature vs volume for each distillation in your lab notebook. Compare the efficiencies of the two distillation methods in your lab notebook.
In well A2: Place 10 drops of Magnesium Sulfate, MgSO4 c. In well A3: Place 10 drops of Zinc Nitrate, Zn(NO3)2 d. In well A4: Place 10 drops of Iron (III) Chloride, FeCl3 e. In well A5: Place 10 drops of Copper (II) Sulfate, CuSO4 3. Take the metal solids from your LabPaq; there should be one piece each of magnesium, zinc, and iron plus two pieces of lead. NOTE: Magnesium and lead oxidize very easily and an almost invisible oxidation layer may coat the metal. To insure good reactions you should scrape the surface of those metals with a pocketknife or remove the oxidation layer by rubbing the metal pieces with steel wool or something similar. Evidence that a reaction is taking place is the formation of bubbles or a coating on the metal immersed into the solution.
Then you put the remaining liquid (neutral component mixture) through the suction filtration funnel to isolate the crystals. After 10-15 minutes, the crystals will be dry and you can weigh them and find their melting point. How is the neutral component of your 3-compound mixture isolated from the final methylene chloride solution? 16 of 22 4/16/12 9:15 PM StudyBlue Flashcard Printing of Lab Final 2211L UGA http://www.studyblue.com/servlet/printFlashcardDeck?deckId=... Name the four active ingredients that we will be testing for in the TLC of Analgesics lab: Ibuprophen Caffeine Acetaminophen Acetylsalicylic acid What solvent system will you be using to dissolve the common analgesics (power) in preparation for TLC spotting? Methylene chloride: ethanol (1:1 solution) What solvent system will you be using to "develop" your TLC plates in the TLC of Analgesics lab?
After donning the appropriate safety gear I began by placing 3 separate sets of 10 drops of distilled water into an unused well of the 24 well plate. I added the following chemicals into one of the three sets of distilled water creating three separate chemical mixtures: HCI, Ammonia, and Sodium Hydroxide. I mixed all thoroughly with a toothpick and then sucked the mixtures into separate pipets. These were placed into the 24 well plate for later use. Using the 96 well plate I combined various chemicals together to observe the chemical changes that were created.