precipitate formed Formation of Esters a. From Carboxylic acids Acetic acid + ethanol + H2SO4 - produced a sweet smell b. From Acyl Halides Ethanol + H2O + H2SO4 - produced a sweet smell Hydroxamic acid test for the Ester group Ethyl acetate in ether + NH2OH.HCl + KOH heat effervescence + alcoholic HCl + FeCl3 – red colored solution Hydrolysis of acid derivatives H2O + Acetic anhydride 2-immiscible layer formed‚ blue litmus paper turned red‚ test tube becomes warm as
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and HNO3 the chloride ion solutions are used because silver nitrate is insoluble in HNO3. During the acetate anion test we had a positive result for solution D that proved the presence of the acetate ion. This reaction was from one drop of concentrated sulfuric acid and 1ml of ethanol and then required heating to excite the solution. Since ethyl acetate was produced we knew D contained the acetate anion‚ the fruity aroma produced after the solution was heated to release a gas proved this. This newly
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transition metal ion of Nickel(II)‚ that further more react with nickel acetate to form red crystals through condensation‚ the colour being constituded by the congugated bonds. These series of reactions synthesize the Schiff Base ligand and Nickel(II) complex of the Schiff base ligand. 0.36g of the Schiff base ligand is yielded and 0.1g of the nickel complex is yielded from the 0.36g Schiff base ligand and 0.5g nickel acetate. Introduction We perform two separate reactions in this experiment
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oils that can be used as an insecticide‚ a fragrance‚ a solvent‚ or possibly a biofuel.1 It is a somewhat non-polar hydrocarbon that can be extracted from orange rinds using a relatively non-polar solvent such as liquid carbon dioxide (CO2) or ethyl acetate. 1 CO2 exists in a gas phase at room temperature and 1 atm‚ but can also be obtained in solid phase (dry ice) for a general laboratory setting. In order to obtain liquid phase CO2 at room temperature and 1 atm‚ CO2 has to be pressurized and heated
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INTRODUCTION: Carboxylic acids are organic acids characterized by the presence of a carboxyl group‚ -COOH. This acid acts as a weak acid‚ which can react with a strong base. Carboxylic acids form hydrogen bonds with many water molecules and are more soluble with one to four carbon atoms. Also‚ it may have an R group that consist of hydrogen or an alkyl group that changes its water solubility. Carboxylic acids with low molecular weight have odor at room temperature and higher molecular weight
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Introduction: In this experiment‚ when vinyl strip and acetate strip is rubbed by tissue‚ it will charge the vinyl strip negatively and acetate strip positively caused by the transfer of electron between the strip and tissue. If molecules have non zero bond dipole‚ because polar molecule must have a non-zero molecular dipole where electron spend more of their time closer to one atomic nucleus than the other and make one end partially positive or negative than the other end. Different charge will
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except those of silver‚ lead (II)‚ and mercury (I) ions. G. Sulfides: Most sulfides are insoluble‚ except from alkali metals and ammonium ion. H. Acetates: All acetates are soluble‚ except silver acetate‚ which is slightly soluble. I. Silver salts: All silver salts are insoluble‚ except silver nitrate‚ silver nitrite‚ and silver perchlorate. Silver acetate and silver sulfate are slightly soluble. J. Carbonates: All carbonates are insoluble‚ except those of
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present on oxygen and results in the formation of a tetrahedral intermediate. The next step involves the deprotonation of the positively charged nitrogen‚ which is then followed by reformation of the oxygen-carbon double bond and the loss of the acetate
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Ethyl Acetate C4H8O2 88.11 0.897 -83.6 oC 77.1 oC Slightly soluble in water (~8.3g/100mL‚ 20 oC)‚ very miscible with alcohol‚ ether‚ acetone‚ benzene. Hexane C6H14 86.18 0.6548 -95 oC 69oC Immiscible with water Dichloro-methane CH2Cl2 84.93 -97 oC 40 oC 1.325 Slightly soluble in water (~1.3g/100mL‚ 20 oC)‚ very miscible with most organic solvent. Hazard 1. Ferrocene is highly flammable and it is harmful if swallowed. 2. Acetylferrocene is highly toxic if swallowed. 3. Ethyl acetate is irritant
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Chemical composition of the essential oil of Majorana hortensis grown in Uttaranchal Shishir Kumar Singh Abstract GLC and GC-MS Analysis was done to analyse the hydrodistilled essential oil of Majorana hortensis grown in Uttranchal state of India. The 36 compounds could be identified out of 50 by their mass spectra accounting for 93% of the oil. The major ones are trans-sabinene hydrate (41.2%)‚ terpinen-4-ol (18.5%)‚ cis-sabinene hydrate (9.3%)‚ a-terpineol (3.8%)
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