atoms. ▪ General formula is Cn H2n+2 ▪ All alkanes have the ending –“ane” ▪ Any alkyl branches in the carbon chain have the suffix –“yl” ▪ The name of a branched alkane must indicate the point of attachment of the branch. o Alkenes ▪ A hydrocarbon that contains at least one carbon – carbon double bond. ▪ General formula is Cn H2n o Alkynes ▪ A hydrocarbon that contains at least one carbon – carbon triple bond. ▪ General formula is Cn H2n-2 ▪ In
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Fluid Catalytic Cracking Fluid catalytic cracking* (FCC) is the most important conversion process used in petroleum refineries. It is widely used to convert the high-boiling hydrocarbonfractions of petroleum crude oils into more valuable [1][2][3] gasoline‚ olefinic gases and other products. . Cracking of petroleum hydrocarbons for conversion of heavy fractions into lighter fractions was originally done by thermal cracking which has been almost completely replaced by catalytic cracking because
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fractions from the refining of petroleum Catalytic cracking is the process whereby high molecular weight fractions are broken down to low molecular weight ones. This process is used in petroleum refineries where crude oil is broken down to smaller alkenes and alkanes‚ until ethene‚ propene‚ (or both) are formed. Catalytic Cracking allows greater output of high-demand products. Identify that ethylene‚ because of the high reactivity of its double bond‚ is readily transformed into many useful products
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Chemistry Essay Butane‚ Butene and all isomers that come with them are considered to be alkanes and alkenes respectively. They differ from each other in the fact that Butane contains only single bonds‚ whereas Butene has both single and one double bond. Regardless of this difference in many situations the two molecules can display similar behaviours. For the purposes of this comparison But-1-ene will be used as ‘Butene’ unless otherwise indicated. But-1-ene is almost identical to the other
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One major observation made throughout this experiment was during the steam distillation. As the steam distillation started and the solution in the flask began heating‚ it was clear that too much stopcock grease was used around the glassware. The grease from the connecting ends of the three way connecting tube was melting and seeping into the clove and water solution in the two necked round bottom flask. The solution in the flask was immediately discarded and repeated with clean glassware and a very
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Preparation of Bromotriphenylmethane Abstract The structure of a major component of star anise oil was derived by analyzing its IR spectroscopy melting point of after oxidation and purification. From the evidence obtained‚ it was concluded that the exact structured should be p-methoxybenzoic acid. Introduction The purpose of this experiment is to determine the structure of the major component of star anise oil. It is already known that this component has a molecular formula C10H12O. This
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Stereochemistry of Dihydroxylation Reactions Question: Can the stereochemical outcome of dihydroxylation reactions be determined by thin layer chromatography? Overview: In this experiment‚ you will perform two reactions that transform alkenes into diols. While similar in functional group transformation‚ these reactions may lead to stereochemically different products. The two possible products are diastereomers of one another‚ and therefore have different physical chracteristics. After
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AS Chemistry Revision-Chemistry for Life 1. Avagadro constant‚ 6.02 x 10²³ number of particles in 1 mole of a substance 2. Empirical formula-simplest ratio of atoms of each element in a compound 3. 4. Model of an atom Particle Mass on relative atomic scale Charge Proton 1 1+ Neutron 1 0 Electron Very small (0.00055) 1- 5. Radioactive isotopes Radiation What is it? Relative charge How does the nucleus change? Stopped by? Deflection in electric field? Alpha α Helium nuclei ⁴₂He +2 2 fewer
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N11/4/CHEMI/SP2/ENG/TZ0/XX 88116105 CHEMISTRY STandaRd lEvEl PaPER 2 Monday 7 November 2011 (afternoon) 1 hour 15 minutes INSTRUCTIONS TO CANDIDATES • • • • • Candidate session number 0 0 Examination code 8 8 1 1 – 6 1 0 5 Write your session number in the boxes above. Do not open this examination paper until instructed to do so. Section A: answer all questions. Section B: answer one question. Write your answers in the boxes provided. 19 pages © International Baccalaureate Organization
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The Mole‚ Chemical Calculations‚ Acid & Bases 2. Secondary Four Topics- Salts‚ Oxidation & Reduction‚ Metals‚ Electrolysis‚ The Periodic Table‚ Energy Changes‚ Speed of Reaction‚ Ammonia‚ The Atmosphere & environment‚ Organic Chemistry‚ Alkanes‚ Alkenes‚ Alcohols & Carboxylic Acids‚ Macromolecules Physics 1. Secondary Three Topics- Measurement‚ Kinematics‚ Forces‚ Mass Weight & Density‚ Turning Effects of Forces‚ Energy Work & Power‚ Pressure‚ Temperature‚
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