Alkene addition reactions practice problems

    • [DOC File]ALKENES INTRODUCING

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      The problem comes with the orientation of the addition - in other words, which way around the hydrogen and the halogen add across the double bond. 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. This is in line with

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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]Chapter 1:

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      Use old study guides in addition to this study guide for help and extra practice. Be sure to focus on what this study guide covers, but those old study guides help a lot. ... An alkene? An alkyne? Which of the following are alkanes? a. C8H16 b. C7H16 c. C7H18 d.

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    • [DOC File]CHAPTER 1: ORGANIC COMPOUNDS

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      Addition reactions: the double / triple bond is broken and an atom is added to each C : add halogen get alkyl compound with 2 halogens ( halogenation ) Hydrogenation: add hydrogen gas, get alkane . unsaturated fats – have alkyl groups with many double bonds – lower mp. saturated fats – hydrogenation reactions – get fats with higher mp

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    • [DOC File]Module 1: Basic Concepts and Hydrocarbons

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      Explain existence of cis (E)-trans (Z). isomerism. Practice possible E/Z isomers of alkenes. Hybridisation not required. Candidates will not be required to use Cahn–Ingold–Prelog priority rules to identify which stereoisomer is which. Reaction mechanisms: Addition reactions of alkenes (a) describe addition reactions of alkenes, i.e. by

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    • [DOC File]Topic 13 - Groby Community College

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      ADDITION POLYMERS. i) Formation of addition polymers. Addition polymers are formed from alkenes. Alkenes can be made to join together in the presence of high pressure and a suitable catalyst. The π-bond breaks and the molecules join together. No other product is formed, and so this is known as . addition polymerisation

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    • [DOCX File]Microsoft Word - Final Exam Study Guide

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      Draw the arrow mechanism (radical halogenation, substitution, elimination, addition, rearrangements, redox, Grignard) Answer questions based on mechanisms ~1/3 reagents, reactions. Predict the major product with stereochemistry and regiochemistry. Provide the correct reagents. Multistep synthesis ~1/3 miscellaneous concepts from list below

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    • [DOC File]Chapter 1:

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      Explain why in the first step in the addition of HBr to 1,3-butadiene, the proton adds to C-1 and not C-2. Write an equation for the expected products of 1,2-addition and 1,4-addition of Br to 1,3-butadiene. Which alkene will give only acetone, (CH3)2C=O, as the ozonolysis product? Write equations for the following reactions: a. CH3C(CH + Cl2 ...

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    • [DOC File]Unit M: Organic Chemistry

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      Practice Problem#1 - Org Bkt p.28 (Using Structural Formulas EI p.40) Org Bkt p.30#1. There are 5 types of hydrocarbons (contains hydrogen and carbon): alkanes, cycloalkanes, alkenes, alkynes, and aromatic compounds. 1) Alkanes. They contain only single bonds. They are . saturated

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    • [DOCX File]Summary of Alcohol Syntheses, Ch

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      -The mechanisms for the addition and also the subsequent possibly dehydration are essentially the same as for reactions 10-12. Aldol Cyclization: Basically a crossed aldol reaction in which both carbonyls are tied together, and in which aldol reaction results in formation of a cyclic rather than an acylic …

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