| |Chemistry paper | | | | | | |Class: Ten |Roll No: |Subject: Chemistry | |Student’s
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Experiment 1: TLC Analysis of Analgesic Drugs 1/23/2011 Purpose: The goal of this experiment is to test our knowledge and understanding of TLC analysis by having us do a TLC analysis of analgesics to figure out their main chemical components. Calculations: 1.) Rf = Distance spot traveled/ distance solvent traveled Results: Table 1: TLC Analysis Analgesic Drugs | Rf Value | Acetaminophen | 0.323 | Aspirin | 0.597 | Caffeine | 0.081 | Unknown 154 (Plate 1) | 0.081‚ 0.306‚ 0.597
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absorption frequencies in the spectrum‚ and associate each with a specific bond (e.g. O–H‚ C=O). Keep in mind that there are usually only one or two key bands in each spectrum‚ although in some cases you might observe up to three. Do not label the alkane C–H stretch‚ since these bands are present in most organic compounds. 2. Assign a letter from the structures given (A – J). There is only one structure per spectrum. 3. Identify the main functional group present in the structure (i.e. ketone‚ alcohol
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8.2 Chemical Earth 8.2.1 The living and non-living components of the Earth contain mixtures * Construct word and balanced formulae equations of chemical reactions as they are encountered Combustion reaction (burning) element + oxygen → oxide e.g. 4Na (S) + O2 (g) → Na2O (s) Reaction with hydrogen element + hydrogen → hydride e.g. Ca (s) + H2 (g) → CaH2 (s) Reaction between an oxide and water metallic oxide + water → hydroxide * metallic oxide is also known as “basic oxide” e.g
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classes namely: Saturated hydrocarbons and unsaturated hydrocarbons. Saturated hydrocarbons are the simplest type of organic compounds. They are hydrocarbons in which all carbon- carbon bonds are single bonds. An example of a saturated hydrocarbon is an alkane. Unsaturated hydrocarbons are hydrocarbons that contain one or more carbon-carbon multiple bonds like double bonds‚ triple bonds‚ or both. Saturated and Unsaturated hydrocarbons have similar physical properties‚ but their chemical properties are different
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Study Guide: Exam 1 1. What type(s) of molecular motion is (are) observed using infrared spectroscopy? A. Stretching and bending B. Rotation and excitation C. Spin flipping D. Fragmentation 2. The functional group region of an infrared spectrum is A. where the cations appear. B. >1500 cm-1. C. <1500 cm-1. D. >2500 cm-1. 3. Stronger bonds will be found where in the infrared spectrum? A. Higher molecular weight B. Lower molecular weight C. Lower wavenumbers D. Higher wavenumbers 4. Compared
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PPV‚ which is the abbreviated term for phenylenevinylene‚ has light emitting properties since it has a large conjugated system. This organic molecule is possible to be formed from dichloro-para-xylene which then reacts with methanol and thiolane. The nucleophile would be the thiolane. A good leaving group in this case would be chlorine. After thiolane attacks‚ it results with dithiolane-xylene. The second step is reaction with sodium hydroxide. The hydroxide it used for deprotonation upon the substituted
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Marta Gebregziabher Discussion and Conclusion: Addition reaction of Alkenes: Bromination of (E)-Stilbene 1. Addition reaction is a reaction that involved two molecules that combine to make a larger product. Addition reaction has two main types‚ electrophilic addition and nucleophilic addition. An electrophilic reaction is when the pi bond of a molecule is removed to make two covalent bonds that are bonded to two new molecules. A nucleophillic addition is a reaction that removed the pi bond
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1. An organic compound X with a molecular formula C2H6O undergoes oxidation with in presence of alkaline KMnO4 to form a compound Y. X on heating in presence of Conc. H2SO4 at 443K gives Z. Which on reaction with H2Oin presence of H2SO4 gives back `X` `Z` reacts with Br2 (aq) and decolorizes it. Identify X‚ Y‚ & Z and write the reactions involved. 2. An organic compound ‘A’ is widely used as a preservative in pickles and has a molecular formula C2H2O2. This compound reacts with ethanol to
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in case of skin contact (irritant‚ permeator)‚ of eye contact (irritant)‚ of ingestion‚ of inhalation. Slightly hazardous in case of skin contact (sensitizer). Dichloromethane (CH2Cl2) 84.93 -96.7 Soluble in water Miscible in acetate‚ alcohol‚ alkane‚ benzene‚ CCl4‚ ether‚ CHCl3 Very hazardous in case of eye contact (irritant)‚ of ingestion‚ of inhalation. Hazardous in case of skin contact (irritant‚ permeator). Inflammation of the eye is characterized by redness‚ watering‚ and itching Sodium
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