IGCSE Chemistry 2012 exam revision notes by Samuel Lees Contents: 1. The particulate nature of matter 2. Experimental techniques 2.1 Measurement 2.2 (a) Criteria of purity 2.2 (b) Methods of purification 3. Atoms‚ elements and compounds 4.1 Atomic structure and the Periodic Table 4.2 Bonding the structure of matter 3.2 (a) Ions and ionic bonds 3.2 (b) Molecules and covalent bonds 3.2 (c) Macromolecules 3.2 (d) Metallic bonding 3 Stoichiometry 4
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4th form Chemistry questionnaire 1. All of the following structures show the same molecule‚ except one. Which structure is different? H H H H A) H -- C -- C -- C --- C -- H B) CH3 CH2 CH2 CH3 H H H H H H -- C -- H CH3 C) H H D)
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Chem 230 Review Conformational analysis and cyclohexane conformations (Chpt 4): 1. Use a Newman projection‚ about the indicated bond‚ to draw the most stable conformer for the following compounds. (a) 3-methylpentane about the C2-C3 bond (b) 3‚3-dimethylhexane about the C3-C4 bond 2. Using what you know about conformational energetics of substituted cyclohexanes‚ predict which of the two decalin isomers (cis or trans) is more stable. Explain you reasoning. 3. The most stable form
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three different eluents‚ hexane‚ toluene‚ and acetone. The chromatography compared aniline‚ 2‚ 4-dinitrobromobenzene‚ and a sample from the mixture of the two reactants when the reaction first began to take place. Another thin layer chromatography used a product sample an hour after the reaction first began and the eluent that showed the best separation of molecules. Table of Rf Values Table of Rf Values | Aniline | Product | 2‚ 4-Dinitrobromobenzene | Toluene | 0.083 | 0.104 | 0.333 | 0.583
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Iodine Crystal Solvents: Distilled water Ethyl Alcohol Toluene Solutions Polar‚ Non-Polar or Ionic Attractive Forces NaCl + Distilled Water Solute NaCl Solute-solute Solute-solvent Solvent Distilled water Solvent-solvent NaCl + Ethyl Alcohol Solute NaCl Solute-solute Solute-solvent Solvent Ethyl Alcohol Solvent-solvent NaCl + Toluene Solute NaCl Solute-solute Solute-solvent Solvent Toluene Solvent-solvent Naphthalene + Distilled Water Solute Naphthalene
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The Chemistry of Fragrances From Perfumer to Consumer 2nd Edition RSC Popular Science Titles The RSC publishes series of inexpensive texts suitable for teachers and students which give a clear‚ readable introduction to selected topics in chemistry. They should also appeal to the general chemist. For further information on all available titles contact: Sales and Customer Care Department‚ Royal Society of Chemistry‚ Thomas Graham House‚ Science Park‚ Milton Road‚ Cambridge CB4 0WF‚ UK
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washed following cutting until not more colour appeared in the wash water. Materials 1. Washed cylinders of beetroot (1 cm in diameter‚ 4 cm long) in distilled water 2. 3 x test tubes 3. 1 x test tube containing distilled water‚ cyclohexane and a cylinder of beetroot‚ labelled TT4. 4. Test tube rack 5. A bottle containing 8 ml distilled water 6. A bottle containing 8 ml 50% acetone 7. A bottle containing 8 ml 100% acetone 8. Permanent marker pen 9. 1x sheet
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Grading System 2012-13 CM- 601 – Process Equipment Design - I Unit I Mechanics of materials: Stress- Strain relationships of elastic materials subjected to tensile‚ compressive and shear forces‚ Elastic and plastic deformation‚ General design considerations; Design of shell‚ bottom plates‚ self supported‚ and column supported roofs‚ wind girder‚ nozzles and other accessories. Unit II Unfired pressure vessel: Pressure vessel codes‚ classification of pressure vessels‚ Design of cylindrical and
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Carbon is denoted by the symbol C‚ is part of group 14 on the periodic table‚ and is the fourth most abundant element in the universe (by mass). Carbon has an electron configuration of 1s2‚ 2s2‚ 2p2. With 4 valance shell electrons it is expected to form 4 bonds‚ this means carbon is tetravalent. However the s orbitals do not form the same type of bond (with other atoms) as the p orbitals‚ this is because their shapes are different. For example CH4 would have the following bonds: C(s)-H(s)‚ C(s)-H(s)
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EXPERIMENT 5- A FISCHER ESTERIFICATION SYNTHESIS OF PEAR OIL One of the major uses of Esterification (C(=O)-C-R) is forming compounds with different odors which can be used to make different synthetic and natural flavorings. Using the chemical and physical properties of organic compounds‚ an ester was catalyzed from the reaction of a carboxylic acid with an alcohol‚ producing an odor similar to that of pear oil. The mechanism of this Fischer- Esterification process is outlined as follows:
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