"Nitrating acetanilide methyl benzoate electrophilic aromatic" Essays and Research Papers

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    acetanilide lab

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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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    Methyl Orange

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    In this experiment the initial mass of the sodium carbonate used was 2.69g. In each titration‚ 3 drops of methyl orange was added to the sodium carbonate solution. With this information the titration can begin‚ and the results obtained are shown below: Titration readings Titration Rough 1 2 3 4 5 Initial 0.00 4.30 22.00 21.00 15.00 25.90 Final 4.30 22.00 38.60 37.60 32.60 42.20 Titre (cm3) 4.30 17.70 16.60 16.60 17.60 16.30 Therefore‚ the average titre would be calculated as follows;

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    Nomenclature of Aromatic Compounds Aromatic Compounds- possess a ring shaped structure Benzene (C6H6)- aka. naphtha - unsaturated cyclic compound - simplest aromatic HC - all C to C bonds are identical; each C has a H atom - substitution reactions occur instead of addition reaction - delocalized pi bonding in benzene imparts stability (aromaticity); responsible for resistance to addition reactions (involve breaking delocalized bonding) Benzene Derivatives- produced when one or more H atoms on benzene

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    Methyl Lab

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    Glen Huang Period 9 Synthesis of Isopentyl Acetate Purpose: To prepare isopentyl acetate from isopentyl alcohol and acetic acid by the Fischer esterification reaction. Materials: West condenser‚ 250 mL round bottomed flask‚ two 250 mL flasks‚ heating mantle‚ boiling chips‚ graduated cylinder‚ sodium bicarbonate‚ isopentyl alcohol‚ glacial acetic acid‚ concentrated sulfuric acid‚ separatory funnel Procedure: 1. Place 50 mL of isopentyl alcohol in a 250 mL round bottom flask and add 60 mL

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    methyl acetate uses

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    Eastman solvents—Technical tip Using Eastman methyl acetate in cleaning applications Introduction Considerations Eastman Chemical Company‚ the world’s leading producer of methyl acetate‚ offers this solvent in two grades to suit a variety of application needs: Wide formulation latitude •  Regular (industrial) grade offers a minimum assay of 96%‚ a maximum methanol content of 2.5%‚ and a maximum water content of 1.5%. •  High purity grade offers a minimum assay of 99.5%‚ a maximum

    Free Solvent Acetic acid Ethanol

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    Synthesis of Methyl Stearate The purpose of this lab was the convert liquid methyl oleate to solid methyl stearate by catalytic hydrogenation. Firstly‚ we produced hydrogen gas using solid mossy zinc and sulfuric acid. Using the hydrogen produced in the previous reaction‚ we were able to convert the liquid methyl oleate to solid crystals of methyl stearate. A mineral oil was also used to bubbler was used to maintain the hydrogen pressure slightly above the atmospheric pressure and to prevent back-diffusion

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    2-((6‚8-dibromo-2-(4-chlorophenyl)quinazolin-4-yloxy)methyl)-5-methyl-1‚3‚4-oxadiazole (IX) : A mixture of the hydrazide VII (0.01 mol) and acetic anhydride (30mL) was refluxed for 6h. The precipitated solid formed upon cooling‚ was filtered and recrystallized from ethanol‚ m.p. 155oC‚ 80% yield. Analysis calculated for C18H11Br2ClN4O2; Calcd.: %C‚ 42.34; H‚ 2.17; N‚ 10.97‚ Found: % C‚ 42.30; H‚ 2.14; N‚ 10.90. IR: υmax./cm-1 3000 (C-H aromatic)‚ 1610 (C=N) and at 1600 (C=C). 1H-NMR (DMSO-d6‚ ppm):

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    Objective To synthesis methyl orange by coupling diazotised sulphanilic acid with N‚N-dimethylaniline. Materials (Chemicals) Sulfanilic acid‚ 2.5% aqueous sodium carbonate solution‚ sodium nitrite‚ concentrated hydrochloric acid‚ N‚N-dimethylaniline‚ glacial acetic acid‚ 10% aqueous sodium hydroxide‚ saturated sodium chloride solution Apparatus 50 mL Erlemeyer flask‚ 250 mL beaker‚ test tube‚ hot plate‚ Buchner funnels Procedure In a 50 mL Elermenyer flask 1.2 g of sulfanilic acid and

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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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    Benzoic Acid and Benzoates in Food‚ Drinks and Medicines Benzoic acid and benzoates are common additives to food‚ drinks‚ medicines and cosmetics‚ and they also occur naturally in many plants. They are useful chemicals in manufactured products because they kill or inhibit both bacteria and fungi and can act as preservatives. Benzoic acid and benzoates are considered to be safe chemicals for humans when they’re used in small quantities‚ but there are at least two situations in which even small

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