pH Value | Aniline | 7 | Benzyl aniline | 12 | Diethylamine | 10 | Table 1: Basicity of Amines Solution | Odor of Solution | Aniline added with chloroform and alcoholic KOH | Unpleasant smell | Table 2: Carbylamine Test (odor of solution) Solution | Observations | Aniline added with concentrated H2SO4 | -Salt formation upon addition of sulfuric acid- Gelatinous‚ pale yellow solution | Table 3: Salt Formation Solution: | Residue Formation: | pH level: | Aniline added with benzenesulfonyl
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Q: Which of the ff are branches of the aortic arch? A: Brachiocephalic‚ left common carotid‚ left subclavian Q: Which of the ff are branches of the subclavian arteries? A: thyrocervical‚ internal thoracic‚ and vertebral artery Q: Where is the carotid sinus located? A: Base of the internal carotid Q: Which of the ff are branches of the internal carotid? A: middle cerebral‚ anterior cerebral‚ ophthalmic artery Q: The gastroduodemal artery is a branch from which artery? A: Common hepatic artery
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Laboratory RECRYSTALLIZATION OF ACETANILIDE USING WATER AS SOLVENT Lagarteja‚ M.C.B.; Lim‚ H.G.N.; Lizo‚ K.J.R.; *Macalino‚ M.D.L.; Macapala‚ C. 2D-Pharmacy‚ Faculty of Pharmacy‚ University of Santo Tomas Abstract Recrystallization is a technique used to purify organic solids. This method involves dissolving of a solute in a solvent and inciting the solute to produce a precipitate from a solution. In this experiment‚ acetic anhydride was added to the mixture of 2mL aniline and 20mL of distilled water
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Synthesis of p-Nitroacetanilide (electrophilic aromatic substitution) In this experiment‚ we convert acetanilide to p-nitroacetanilide. [pic] The mechanism for the nitration is that of electrophilic aromatic substitution. The nitronium ion is directed to the positions ortho and para to the acetamido (-NHCOCH3) group. This occurs because the resonance electron-releasing effect of that group increases the electron density at those positions‚ helping to stabilize the intermediates that
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Lab 3: Bromination of Acetanilide CHEM 2110 Hassan Alsaleh 0525970 Due date :11/02/2015 Q1: To find the limiting reagent we need to find the number of moles of acetanilide‚ and the number of moles of Bromine. Mass of Acetanilide used = 0.67g Molar mass of Acetanilide = 135.16g/mol[1] Number of moles of Acetanilide = (0.67g) / (135.16g/mol) = 0‚005 mols Volume of Bromine = 0.25ml Density of Bromine = 3.103 g/ml[2] Mass of Bromine = (0.25ml) X (3.103g/ml) = 0.78g Molar mass of Bromine
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Purifying Acetanilide by Recrystallization Results: Acetanillide Solubility of acetanilide in water is 5.5g/100mL at 100C 0.53g/100mL at 0C PERCENT YIELD/THEORETICAL YIELD: Discussion: Acenatilide is a synthetic organic compound introduced in therapy in 1866 as a fever-reducing drug. Its effectiveness in relieving pain was discovered soon thereafter‚ and it was used as an alternative to aspirin. The solvent that I selected to recrystallize the
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A Beautiful Mind with an Ugly Mental Disorder Submitted by: Nazila R. Salamkhail V-00410030 Psychology101-901 Instructor: Tim Donahue Virginia Commonwealth University 04/27/2011 The movie “A Beautiful Mind” is a fascinating movie. Although‚ I am not a movie watcher‚ it drew my full attention as soon as I started playing it. It displays the character of a great mathematician John Nash who is struggling with schizophrenia during his college period
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LAB REPORT FOR EXPERIMENT #2: PURIFICATION OF ACETANILIDE BY RECRYSTALLIZATION Your name TA’s name Your Partner’s name Lab Section OBSERVATIONS: A. SELECTING A RECRYSTALLIZATION SOLVENT | |Solubility Test (cold) |Solubility Test (hot) | |Water |insoluble |soluble | |pet ether |insoluble
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group. The electrophilic aromatic substitution reaction nitration is used to nitrate methyl benzoate and acetanilide with a nitronium ion. Crystallization was used to purify the product. The melting point was used to determine its purity and the regiochemistry of the products. The methyl benzoate reaction product‚ methyl nitrobenzoate‚ was determined to be meta-substituted and the acetanilide reaction product‚ nitroacetanilide‚ was determined to be para-substituted. INTRODUCTION: An electrophilic
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13‚ 2015 Answers to Questions: 1.) Arrangement of Reactivity: (fastest to slowest) - Phenol‚ Nitrophenol‚ Acetanilide‚ Benzene‚ Chlorobenzene‚ Aniline - A reaction has occurred if there’s a change in color. The nature of the substituent‚ whether electron-donating to the ring or electron-withdrawing from the ring‚ was responsible for the reactivity of the benzene. Aniline and acetanilide contain amine groups‚ which are electron-donating. Chlorobenzene contains chlorine‚ which is electron-withdrawing
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