Bonding Changes

If the ligand possesses a 71-bonding system, then its existing n- or tc -orbitals may be of the correct symmetry for overlap with metal p or d orbitals. Furthermore, any other 

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This example again emphasizes that Hendridcson only considered the bond changes at the carbon atoms of a reaction. 

In Section 1 9 we introduced curved arrows as a tool to systematically generate resonance structures by moving electrons The mam use of curved arrows however is to show the bonding changes that take place in chemical reactions The acid-base reactions to be discussed in Sections 1 12-1 17 furnish numer ous examples of this and deserve some preliminary comment... 

Use curved arrows to show the bonding changes in the reaction of CIS 4 tert butylcyclohexyl bromide with potassium tert butoxide Be sure your drawing correctly represents the spatial relationship between the leaving group and the proton that is lost... 

FIGURE 8 2 Hybrid orbital description of the bonding changes that take place at carbon during nucleophilic substitution by the Sn2 mechanism... 

The Diels-Alder reaction is believed to proceed m a single step A deeper level of understanding of the bonding changes m the transition state can be obtained by examining the nodal properties of the highest occupied molecular orbital (HOMO) of the diene and the lowest unoccupied molecular orbital (LUMO) of the dienophile... 

What will be the product isolated after thermal decarboxyla tion of each of the following Using curved arrows represent the bond changes that take place at the transition state... 

Bonding changes dunng decarboxylation of malonic acid... 

Show the bonding changes that occur and write the structure... 

Cycloaddition involves the combination of two molecules in such a way that a new ring is formed. The principles of conservation of orbital symmetry also apply to concerted cycloaddition reactions and to the reverse, concerted fragmentation of one molecule into two or more smaller components (cycloreversion). The most important cycloaddition reaction from the point of view of synthesis is the Diels-Alder reaction. This reaction has been the object of extensive theoretical and mechanistic study, as well as synthetic application. The Diels-Alder reaction is the addition of an alkene to a diene to form a cyclohexene. It is called a [47t + 27c]-cycloaddition reaction because four tc electrons from the diene and the two n electrons from the alkene (which is called the dienophile) are directly involved in the bonding change. For most systems, the reactivity pattern, regioselectivity, and stereoselectivity are consistent with describing the reaction as a concerted process. In particular, the reaction is a stereospecific syn (suprafacial) addition with respect to both the alkene and the diene. This stereospecificity has been demonstrated with many substituted dienes and alkenes and also holds for the simplest possible example of the reaction, that of ethylene with butadiene ... 

Notice that the orbital array is of the Mobius topology with a phase change depicted between the C-1 and C-2 positions. This corresponds to an allowed photochemical process since there are six electrons involved in bonding changes. 

Use curved arrows to show the bonding changes in the reaction... 

Bonding changes during decarboxylation of a (i-keto acid... 

Show the bonding changes that occur, and write the structure oMh ntemie te formed in the thermal decarboxylation of... 

Chemistry can be divided (somewhat arbitrarily) into the study of structures, equilibria, and rates. Chemical structure is ultimately described by the methods of quantum mechanics equilibrium phenomena are studied by statistical mechanics and thermodynamics and the study of rates constitutes the subject of kinetics. Kinetics can be subdivided into physical kinetics, dealing with physical phenomena such as diffusion and viscosity, and chemical kinetics, which deals with the rates of chemical reactions (including both covalent and noncovalent bond changes). Students of thermodynamics learn that quantities such as changes in enthalpy and entropy depend only upon the initial and hnal states of a system consequently thermodynamics cannot yield any information about intervening states of the system. It is precisely these intermediate states that constitute the subject matter of chemical kinetics. A thorough study of any chemical reaction must therefore include structural, equilibrium, and kinetic investigations. 

Catalysis occurs because the catalyst in some manner increases the probability of reaction. This may result from the reactants being brought closer together [catalysis by approximation, or the propinquity effect ], or somehow assisted to achieve the necessary relative orientation for reaction. Noncovalent interactions may be responsible for the effect. Covalent bond changes may also take place in catalysis. In a formal way, the manner in which catalysis occurs can be described by schemes such as Schemes I and II. 

Electron transfer into the LUMO might also cause bonding changes. What are the CBr bonding characteristics of the LUMO in methyl bromide Is it bonding (one surface extends over the bond) or antibonding (two surfaces meet in middle of the bond) How would electron transfer from a nucleophile affect the CBr bond length ... 

The standard polymers used for rubber linings consist of materials that are cross-linkable macromolecules which, on mixing with suitable reactants that form strong chemical bonds, change from a soft deformable substance into an elastic material. These polymers include natural rubber and its corresponding synthetic, c/s-polyisoprene, styrene-butadiene rubber, polychloroprene, butyl rubber, halogenated butyl rubbers, acrylonitrile-... 

Impact tests Such tests reveal the resistance of coatings to deformation and destruction by concentrated sudden stresses. They thus throw considerable light on the integrity of the metal-coating bond. Changes in adhesion through chemical reaction at the paint/metal interface will be reflected in the impact-test values. 

First, look at the reaction and identify the bonding changes that have occurred. In this case, a C—Br bond has broken and a C-C bond has formed. The formation of the C-C bond involves donation of an electron pair from the nucleophilic carbon atom of the reactant on the left to the electrophilic carbon atom ol CH Br, so we draw a curved arrow originating from the lone pair on the negatively charged C atom and pointing to the C atom of CH3Br. At the same time the C—C bond forms, the C-Br bond must break so that the octet rule is not violated. We therefore draw a second curved arrow from the C-Br bond to Br. The bromine is now a stable Br- ion. 

The best way to understand how orbital symmetry affects pericyclic reactions is to look at some examples. Let s look first at a group of polyene rearrangements called electrocyclic reactions. An electrocyclic reaction is a pericyclic process that involves the cycli/ation of a conjugated polyene. One 7r bond is broken, the other 7t bonds change position, a new cr bond is formed, and a cyclic compound results. For example, a conjugated triene can be converted into a cyclohexa-diene, and a conjugated diene can be converted into a cyclobutene. 

The trimesityl of iridium can be made by reaction of IrCl3(tht)3 with MesMgBr, while IrMes4 can be oxidized to the cationic iridium(V) species [IrMes4]+, also tetrahedral (with concomitant slight Ir-C bond changes from 1.99-2.04 A in the neutral compound to 2.004-2.037 A in the cation). Another iridium(V) species, IrO(Mes)3 has been made [190], it has a tetrahedral structure (lr=0 1.725 A). 

The covalent nature of the chemical bond changes significantly when the... 

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