Synthesis of Salicylic Acid Experimental Data: 1. Mass of methyl salicylate used: 0.232 g 2. Theoretical yield of salicylic acid: 0.211 g 3. Volume H2SO4 added‚ with units (drops or mL): 3mL 4. Mass of crude salicylic acid obtained: 0.250 g 5. Volume of water used as recrystallizing solvent: 2 mL 6. Mass of purified salicylic acid: 0.134 g 7. Percent yield of purified salicylic acid from reaction: 63.5% 8. Melting point of purified product: 158-160 oC 9. Name of NMR solvent used and
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Starting with the weight of .198 g of salicylic acid‚ the moles of the reactant was determined to be 1.43 x 10-3‚ as shown in Equation 3. The purified aspirin product was a white powder that had a weight of .140 g. The number of moles of the purified aspirin product after extraction was 7.77 x 10-4 as shown in Equation 4. These two moles calculated a chemical yield of 54.3% as shown in Equation 5. The melting point of the pure aspirin product was ranged at 117.8-125.2C as shown in Table 1.
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evaporates from a warm surface and condenses as a solid on a cold surface. The crude naphthalene had a melting point range of 85°-90° C while the 35.4% yield of pure naphthalene had a melting point range of 70°-76° C. Recrystallization was used to purify the salicylic acid. Recrystallization is the process of dissolving the original solid in a hot solvent and then allowing the solution to cool to let the solid crystallize again. The crude salicylic acid had a melting point range of 150°-153° C while
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component of Panacetin. This is answering question 2 of the two questions that were to be answered in experiment 2. The equation of this reaction is as follows (and is the same as that found in experiment 2):  During this experiment‚ we used recrystallization methods in order to help in the purification of the unknown solid‚ as well as drying and vacuum filtration. We then ground the unknown and combined it with different chemicals (such as acetanilide or phenacetin) and used the melting point ranges
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Nor Amirah Farhana Nawawi Organic Chemistry Lab Report Bo Shen Title: Nucleophillic Substitution Reaction Introduction: This lab experimented on the reactions of the chemicals that undergoes SN1 or SN2 reaction. Nine different compounds were given to be examined with two reagents - NaI in acetone and AgNO3 in ethanol. The SN1 reaction happens in AgNO3 in ethanol reagents‚ and SN2 reaction is in NaI in acetone. Procedure: Following the lab manual. Results: compound NaI /acetone (SN2) AgNO3/ethanol
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Title: Acetanilide Synthesis Objective: To synthesize Acetanilide by recrystallization. To check its purity by calculating its percent yield. Introduction: Aniline is a primary aromatic amine and weak base which forms salts with mineral acids. In acidic solution‚ nitrous acid converts aniline into a diazonium salt that is an intermediate in the preparation of a great number of dyes and other organic compounds of commercial interest. When aniline is heated
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Lide‚ David R. “Physical Constanst of Chemical Compounds”. CRC Handbook of Chemistry and Physics 88th Edition (Internet Version 2008. CRC Press/Taylor and Francis. Boca Raton‚ FL. (2008). [4] Milligan‚ G. St.Martin’s University: Separation by Recrystallization. <http://homepages.stmartin.edu/fac_staff/gmilligan/>. (2007). Accessed May 19‚ 2008.
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Abstract In this experiment‚ 4-(4-chlorophenyl)-3‚4-dihydropyrimidine-2-one is synthesized in a solvent-free reaction‚ where urea‚ ethyl acetoacetate‚ 4-chlorobenzaldehyde are used as the reactants and p-toluenesulfonic acid is used as the catalyst. This reaction is similar to the original synthesis of DHPM by Pietro Bignelli‚ as it incorporates a single step. Due to its environmentally friendly conditions‚ such as the use of solar energy as a heat source and the lack of solvent‚ this synthesis of
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VI. Results and Discussion In this exercise‚ the goal was to produce acetylsalicylic acid through the organic synthesis from the reaction of salicylic acid to acetic anhydride‚ the starting materials. Instead of using acetic acid‚ acetic anhydride was used as solvent since the anhydride reacting with water to form acetic acid tends to drive the reaction to the right. It results from the elimination of a molecule of water from two molecules of acetic acid (see Fig. 11.2). Figure 11.3 below
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SUPPLEMENTARY MATERIAL (#2000-0709) SOAP FROM NUTMEG: AN INTEGRATED INTRODUCTORY ORGANIC CHEMISTRY LABORATORY EXPERIMENT Marcio C.S. de Mattos and David E. Nicodem Departamento de Química Orgânica‚ Instituto de Química‚ Universidade Federal do Rio de Janeiro‚ Caixa Postal 68545 21945-970‚ Rio de Janeiro‚ Brazil 1) Written material used by students 2) Instructor notes 3) Chemical abstract registry number of chemicals 1) Written material used by students Soaps
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