attached to the carbon chain than alkanes. Are alkenes with double bonds. Are alkynes with triple bonds. 1 Structure of Alkenes Alkenes (and alkynes) are unsaturated hydrocarbons Alkenes have one or more double bonds The two bonds in a double bond are different: - one bond is a sigma () bond; these are cylindrical in shape and are very strong - the other is a pi (π) bond; these involve sideways overlap of p-orbitals and are weaker than bonds Alkenes are flat and have a trigonal planar
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Alkanes are saturated hydrocarbons. They contain only carbon-carbon and carbon-hydrogen single bonds. They are the least reactive of the organic compounds. The main source is crude oil. Hydrocarbon- a compound consisting only of hydrogen and carbon Saturated- Contain single carbon -carbon bonds only Unsaturated-contains a C=C bond Petroleum fraction- mixture of hydrocarbons with a similar chain length and boiling range The general formula for is CnH2n+2 (for ring alkanes is CnH2n)
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Cyclic ( Open chain) Alicyclic Aromatic Alkanes Alkenes Alkyne Cycloalkanes Cycloalkenes Cycloalkynes Alkanes:- Paraffins General formula CnH2n+2 sp3 hybridisation C–C bond length 1.15 4 A0 Chemically unreactive Show chain‚ position and optical isomerism. Heptane has 9 isomer‚ Octane 18 and Decane 75. Nomenclature: 164 Preparation:- Wurtz reaction:- Follow mainly free radical mechanism Useful in preparing an alkane containing even number of carbon atoms Stepping
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Alkanes The reaction between alkanes and fluorine This reaction is explosive even in the cold and dark‚ and you tend to get carbon and hydrogen fluoride produced. It is of no particular interest. For example: The reaction between alkanes and iodine Iodine doesn’t react with the alkanes to any extent - at least‚ under normal lab conditions. The reactions between alkanes and chlorine or bromine There is no reaction in the dark. In the presence of a flame‚ the reactions are
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| | Alkanes: Alkanes are saturated hydrocarbons (this means that there are NO double bonds in the molecule). They contain Hydrogen and Carbon atoms only. There are an immense number of possibilities. The simplest being methane with just ONE atom of Carbon.You should be able to see ONE atom of Carbon and FOUR atoms of Hydrogen. In ethane there are TWO atoms of Carbon and SIX atoms of Hydrogen. In propane there are THREE atoms of Carbon and EIGHT atoms of Hydrogen. In butane there are FOUR atoms
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would die in seconds. Glucose‚ the most important carbohydrate‚ not only has a carbonyl group but is an aldehyde. Another common carbohydrate is fructose‚ fruit sugar‚ this compound is a ketone. These compounds are more reactive than your typical alkane‚ the question you may ask is why? The answer lies in the location of the electrons in the carbonyl group. First‚ look at the hybridization of a carbonyl carbon. A carbon connected to three other molecules must be doubly bonded to one of those molecules
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Experiment 23: Synthesis of an Alkene April 5‚ 2013 Purpose: Results and Discussion The weight of our n-Butyl Bromide sample (actual yield) was 0.09g. The percent yield was found to be 4.38%. Only 0.09g of the theoretical 2.055g yield was obtained. The boiling point was 104° C‚ which is higher than the literature value of 101° C. This is due to the sample being somewhat impure‚ as impurities tend to increase boiling point. When IR spectroscopy was performed‚ there were no OH stretches
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Experiment #2: Stereochemistry of Alkenes and Molecular Modeling By: Nouhad Mokdad Section: 53 TA’s: Sheida and Ryan Mills Lab Partner: David Wilson Date of Experiment: October 7th‚ 2008 Purpose: The purpose is to study the difference between the stereochemistry of the two isomers‚ maleic and fumaric acid. The first part of the experiment called for the conversion of maleic acid into fumaric acid with the addition of a proton using the acid-catalyzed isomerisation‚ vacuum filtration‚
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Experiment #3 Mark A. Bruder 07. T.A. Michael Hall Alkanes: Chlorination Introduction: The purpose of this experiment is to determine the reactivity of hydrogen atoms on a carbon chain using free radical chlorination. In this experiment 1-chlorobutane will be chlorinated with the combination of sulfuryl chloride and ABCN as an initiator to produce the chlorine radicals. The combination of 1-chlorobutane and sulfur chloride will produce four dichlorobutane
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Preparation and Characterization of Alkene Balacanao‚ Gladys A.1‚ Miranda‚ MarilynI2 1 Student (s)‚ Subject/Section‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology; 2 Professor‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology [pic] ABSTRACT The purpose of this experiment is to prepare cyclohexene form cyclohexanol‚ and know the properties of alkene. The first part of this experiment is preparation of cyclohexene
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