Alkene reactions practice problems

    • [DOC File]CHM 331 : General Organic Chemistry

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      • Most reactions occur via 2-electron mechanisms (e.g. H–Br + alkene) ... Example problems: give the major organic products of the following reactions ... • note however, that in practice this reaction is only really useful if there is an obvious radical site that is more stable that any others, otherwise there will be multiple products ...

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    • [DOC File]Alkenes (Module 1)

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      If the alkene is also a gas, you can simply mix the gases. If the alkene is a liquid, you can bubble the hydrogen halide through the liquid. Addition to unsymmetrical alkenes. Orientation of addition. If HCl adds to an unsymmetrical alkene like propene, there are two possible ways it could add. However, in practice, there is only one major product.

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    • [DOC File]Organic Nomenclature - Alkanes, Alkenes, Alkynes

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      The alkene family uses the -ene ending. The double bond is stronger than a single bond, and the bond length between the carbon atoms is shorter in the double bond. It is also more reactive than a single bond since the ( bond (the second pair of electrons) is farther from the nuclei.

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    • CHAPTER 24- Practice Exercise

      CHAPTER 24- Practice Exercise A. Kweyete Organic Chemistry. 1. Which of the following is (are) a saturated hydrocarbon? (underline your choice) alkane alkyne alkene cycloalkane cycloalkene aromatic hydrocarbon. 2. Identify the following general formulas as alkanes, alkenes, alkynes, and cycloalkanes. CnHn CnH2n CnH2n+2 CnH2n-2

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    • [DOC File]THE CARBON-CARBON DOUBLE BOND - THE CHEMISTRY OF …

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      Work through the practice problem on p. 200 of McMurry (5th Ed.) and problems 6.9 to 6.11 on p. 201. Industrial Preparation of Alkenes: Thermal 'cracking' of high molecular weight alkanes: Laboratory Preparation of Alkenes: There are four standard laboratory methods for preparing alkenes from non-alkene starting materials: (1)

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    • [DOC File]CHE 235 Unit 1 - Chemistry Solutions

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      Predict and explain the stereochemistry of E2 eliminations reactions to form alkenes. Predict the products of addition, oxidation, reduction, and cleavage of alkenes with proper regio and stereochemistry. Use retrosynthetic analysis to solve multi-step synthesis problems with alkenes as reagents, intermediates, or products.

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