studying this unit‚ you will be able to • • name hydrocarbons according to IUPAC system of nomenclature; recognise and write structures of isomers of alkanes‚ alkenes‚ alkynes and aromatic hydrocarbons; learn about various methods of preparation of hydrocarbons; distinguish between alkanes‚ alkenes‚ alkynes and aromatic hydrocarbons on the basis of physical and chemical properties; draw and differentiate between various conformations of ethane; appreciate the role of hydrocarbons as sources of energy
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tendency to undergo evaporation on being exposed to the air even at an ambient temperature‚ they are invariably termed as volatile oils‚ essential oils or ethereal oils. They mostly contribute to the odoriferous constituents or “essences” of the aromatic plants that are used abundantly in enhancing the aroma by seasoning of eatables. Oil is "essential" in the sense that it carries a distinctive scent‚ or essence‚ of the plant. Essential oils do not form a distinctive category for any medical‚ pharmacological
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Experiment Date: 3/12/2012 Photochemistry: Photoreduction of benzophenone and rearrangement to benzpinacolone Abstract: In this experiment Benzpinacolone was synthesized in a process that contained two steps. First the photoreduction of benzophenone in 2-propanol‚ which was done by placing the flask under sunlightfor the absorption of the UV rays to carry out the reaction. Then the second part was the dehydration of benzpinacol to benzpinacolone‚ where the benzpinacol product was converted
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T2:BIOCHEMISTRY AND ANALYSIS:DETECTION OF FATS‚PROTEINS AND CARBOHYDRATES OBJECTIVE The main purpose of the experiment is to understand some general tests that detect fats‚proteins and carbohydrates in foods. INTRODUCTION Carbohydrates are also known as sacharides. There are 4 main groups of carbohydrates‚which are monosaccharides‚ disaccharides‚ oligosaccharides and polysaccharides. Carbohydrates play an important role in living organism as it is the energy storage‚ and it also plays
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Amanda Tran Date of lab: 04/25/05 Date submitted: 05/09/05 Chem 2130-3 Experiment 3: Synthesis of Co(acac-NO2)3 Introduction In this lab‚ Co(acac·NO2)3 is synthesized using the Co(acac)3 complex produced in Experiment 2. The Co(acac)3 complex is used as a reagent instead of acacH because acacH cannot be directly converted to 3-nitroacetylacetone. Since Co(acac)3 is not stable in HNO3‚ Cu(NO3)2 and acetic anhydride are used in this reaction to produce the final product
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RTECS number CY1400000 Jmol-3D images Image 1 [2] [3] [4] [5] [6] [7] [8] [9] Properties Molecular formula CH Molar mass 78.11 g mol−1 Appearance Colorless liquid Odor aromatic‚ gasoline-like 6 6 Benzene 2 Density 0.8765(20) g/cm3 Melting point 5.5 °C‚ 278.7 K‚ 41.9 °F Boiling point 80.1 °C‚ 353.3 K‚ 176.18 °F Solubility in water 1.79 g/L (15 °C) Solubility soluble in alcohol‚ chloroform
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SUMMARY OF ORGANIC REACTIONS SECTION 1 - ALIPHATIC Aldehydes and ketones |Type of reaction |Mechanism | |1. oxidation (aldehydes only): aldehyde ( carboxylic acid |n/a | | | | |reagents: potassium
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Chemistry GENERAL CHEMISTRY: Atomic Structure and elementary quantum mechanics: Blackbody radiation‚ Planck’s radiation law‚ photoelectric effect‚ Compton Effect‚ de Broglie’s hypothesis‚ Heisenberg’s uncertainty principle. Postulates of quantum mechanics‚ Schrodinger wave equation and a particle in a box‚ energy levels‚ wave functions and probability densities‚ Schrodinger wave equation for H-atom‚ Separation of variables‚ Radial and angular functions‚ hydrogen like wave functions‚ quantum numbers
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(e.g. ethyne) have carbon-carbon double or triple bonds‚ and are said to be unsaturated. Aromatic hydrocarbons are cyclic compounds whose structure is related to that of benzene‚ with six-electrons in a six-membered ring. For this experiment‚ hexane will be used as an example of saturated hydrocarbons (alkanes)‚ cyclohexene will be used as an unsaturated hydrocarbon (alkenes) and toluene as an aromatic hydrocarbon. As a precaution during these experiments‚ you should be extremely careful since
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monohydrate / triketohydrindene hydrate) | Oxidative deamination and decarboxylation; reduction of ninhydrin | free α-amino and carboxyl groups | purple-blue color solution | Yellow solution | Xanthoproteic | Conc. HNO3‚ 50% NaOH | Nitration substitution in Benzene ring | aromatic amino acids | yellow precipitate then turns orange when neutralized with NaOH | clear solution‚ no change in color | Hopkins-Cole | Hopkins-Cole reagent | Condensation of indole group with glyoxylic acid and H2SO4 | tryptophan
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