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136KB - NZQA
136KB - NZQA

... Two products are formed in this reaction because propene is an asymmetric alkene. When another asymmetric molecule such as hydrogen chloride, HCl, is added to it, there are two possible products. One product is produced in greater quantities (the major product) than the other (minor product). The ru ...
chemistry- sch4u - final exam
chemistry- sch4u - final exam

... ____ 61. The theoretical effect of an increase in the initial concentration of a reactant can be explained in terms of collision theory because it affects I. the collision geometry involved in the reaction II. the total number of collisions that occur III. the fraction of collisions that are effecti ...
Lecture 13a - UCLA Chemistry and Biochemistry
Lecture 13a - UCLA Chemistry and Biochemistry

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polar covalent bonds.
polar covalent bonds.

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Experiment 7 — Nucleophilic Substitution
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Biochemistry 462a - Enzymes Extra Questions

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ENZYMES - SELF STUDY QUESTIONS 1. A chemical reaction has a

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... Oxidation catalysts are typically based on the highest oxidation states of a particular metal complex, e.g., OsVIIIO4, RuVIIIO4, MnVIIO4-, etc. This seems consistent since the strongest “oxidants” should most efficiently catalyze “oxidation” reactions. However, this reasoning only holds if the rate ...
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... change in color when the reaction has started. – Use your time wisely. While one partner monitors reaction 1 the other should prepare the ester for reaction 2. – Most of the Mg will dissolve during the reaction. Any remaining Mg will dissolve in the work-up (week 2). – At the end of this week’s proc ...
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org test 1

... 2. Why is Sulphuric acid not used during reaction of alcohol with KI? 3. Why is preparation of ethers by acid catalysed dehydration of 2° and 3° alcohols not a suitable method? 4. Of benzene and phenol, which is more easily nitrated and why? 5. Ethers possess a net dipole moment even if they are sym ...


... Johnson Matthey have published an informative 82-page brochure, “The Catalyst Technical Handbook”, which covers the use of catalysts for chemical reactions important in industrial synthesis. The handbook recommends platinum group metal homogeneous, heterogeneous and FibreCatm anchored homogeneous ca ...
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2.9 database - DrBravoChemistry

... Addition reactions to alkenes can result in the formation of isomeric compounds. Choose an alkene with molecular formula C4H8 which reacts with HBr to form two structural isomers. Give the structures of these two isomers and name the type of structural isomerism shown. Outline a mechanism for the fo ...
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Equilibrium 4 Noteform - IndustrialProcesses

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Microwave initiated reactions: Pechmann coumarin synthesis

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energy and rates practice test answers

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Molecular Orbital

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C h e m g u id e –... ESTERS: PREPARATION

... mixture in a flask and distil off and collect the ester as it is formed. Why does this work effectively for the small esters? 2. a) You can also make esters by reacting an acyl chloride with an alcohol. Write the general equation for this using a form similar to the one in Q1(a). b) Describe the rea ...
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1 Carbonyl Condensation Reactions (Conjugate Addition) If we look

< 1 ... 52 53 54 55 56 57 58 59 60 ... 73 >

Woodward–Hoffmann rules



The Woodward–Hoffmann rules, devised by Robert Burns Woodward and Roald Hoffmann, are a set of rules in organic chemistry predicting the barrier heights of pericyclic reactions based upon conservation of orbital symmetry. The Woodward–Hoffmann rules can be applied to understand electrocyclic reactions, cycloadditions (including cheletropic reactions), sigmatropic reactions, and group transfer reactions. Reactions are classified as allowed if the electronic barrier is low, and forbidden if the barrier is high. Forbidden reactions can still take place but require significantly more energy.The Woodward–Hoffmann rules were first formulated to explain the striking stereospecificity of electrocyclic reactions under thermal and photochemical control. Thermolysis of the substituted cyclobutene trans-1,2,3,4-tetramethylcyclobutene (1) gave only one diastereomer, the (E,E)-3,4-dimethyl-2,4-hexadiene (2) as shown below; the (Z,Z) and the (E,Z) diastereomers were not detected in the reaction. Similarly, thermolysis of cis-1,2,3,4-tetramethylcyclobutene (3) gave only the (E,Z) diastereomer (4).Due to their elegance and simplicity, the Woodward–Hoffmann rules are credited with first exemplifying the power of molecular orbital theory to experimental chemists. Hoffmann was awarded the 1981 Nobel Prize in Chemistry for this work, shared with Kenichi Fukui who developed a similar model using frontier molecular orbital (FMO) theory; because Woodward had died two years before, he was not eligible to win what would have been his second Nobel Prize for Chemistry.
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