Name Lab Section GTA Station # 5. Extraction Pre-lab questions Complete the following questions and submit before beginning the experiment. 1. Which layer will be the aqueous layer when using dichloromethane (methylene chloride) as the solvent (i.e.‚ top or bottom)? Which layer will be the aqueous layer when using ether as the solvent? 2. When everything has been separated in Part D‚ which compounds will be in test tubes 1‚ 2‚ and 3?
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Recrystallization of Benzoic acid Chemistry 204-002 Date: 4/9/2011 Hector Ortega Recrystallization is a method used to purify compounds‚ and this is a very important procedure because compounds are naturally impure. Polarity and solubility play a big role in this experiment and these characteristics are exploited in order to have a crystallization of the desired compound. In this experimented benzoic acid was crystallize using ethanol and water. I chose these solvents based on part C of the experiment
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standing D ef n i itions SOLUBILITY - It is the number of parts of solvent (by volume) that will dissolve one part of solute (by weight of a solid or liquid). - It also can be defined as the amount of a solute that passes into solution - A solute will dissolve best in a solvent that has a similar polarity to itself. MISCIBILITY when the two components forming a solution are either both gases‚ solids or liquids it is more usual to talk in terms of miscibility rather than solubility. Solutions Solvent:
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for 9-fluorenone did not show any significant bonds except for at 1681 cm-1‚ the C=O stretch. To separate 4-aminobenzoate into an aqueous layer‚ HCl was added to protonate the NH2 side group and form a salt‚ creating its high solubility in water and low solubility in ether. This allowed the immiscible layers to be distinguished. The addition of NaOH after pouring out the aqueous solution allowed for aminobenzoate to reform from its salt form. However‚ while inverting the funnel to vent before
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isotonic to the blood B) molar to the blood C) hypotonic to the blood D) nontonic to the blood E) hypertonic to the blood 3) Water is a polar solvent and hexane (C6H14) is a nonpolar solvent. Which of the following correctly describes the solubility of the solute in the given solvent? A) CaCl2‚ soluble in hexane B) octane‚ soluble in water C) CCl4‚ soluble in water D) mineral oil‚ soluble in water E) NaHCO3‚ soluble in water 4) What is the concentration‚ mass/volume percent (m/v)‚ of
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This solubility can be shown by calculating the solubility product Ksp. (1) AgCl(s) => Ag+(aq) + Cl-(aq) Ksp = [Ag+(aq)]·[Cl-(aq)] = 1.6 x 10-10 While silver chloride will be in equilibrium with its ions in the solution‚ because Ksp is so small‚ the
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Experiment 2 – Identification of Inorganic Solids Jesse Galina CHM 101 Lab Monday October 1‚ 2012 Unknown Solid – 2 Identifying my cation was rather easy because of the color of the powder when it was first given to me. It was pinkish/slight red when solid and when it was grounded up even further. This observation ruled out every cation except for some hydrated Co (II) salts. After being dissolved in water‚ the solution turned pink which agrees with the statement that the cation was Co
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containing 2.0g of A and 8.0g of B is to be separated and the components purified by one crystallization from 100 mL of solvent. 4.) A mixture of three compounds‚ A‚ B‚ and C‚ is to be separated and purified by crystallization. Their solubilities in g/100 mL ethanol are given below. a. 5.) You need to perform a recrystallization using a mixed-solvent system. Which of the ff. solvents could not be used as a solvent airs for the experiment? Explain your selection. Hexane and water.
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group will devise two syntheses of the compound‚ and compare them for cost effectiveness‚ safety and potential yield of the compound. So to be more specific about the tests that will be conducted on the compound; we will do the following: -Know the solubility of our compound‚ different types of compounds will dissolve in certain amounts
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Extraction and analysis of two compounds from unknown solution C ABSTRACT Liquid C and solid C were both extracted from unknown solution by first using chemically active liquid-liquid extract‚ followed by vacuum filtration. Liquid C and solid C were then purified with the use of simple distillation and recrystallization respectively. Through the process of recrystallization‚ the percentage purity of solid C was found to be 6.01%. The melting point range of purified solid C was 117.0 – 119
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