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Background check is carried out by companies and folks to know more about a person and his existing activities, financial transactions, prison records and more. There are a lot of reasons for doing a background examine but it should be executed in detail with proper cross verification wherever necessary. <br><br>
In [[Huckel theory]], a '''Dewar reactivity number''', also known as '''Dewar number''', is a measure of the reactivity in [[Aromaticity|aromatic system]]s. It is used to quantify the difference in energy between the π-system of the original molecule and the [[Reaction intermediate|intermediate]] having the incoming [[electrophile]] or [[nucleophile]] attached. It can be used to study important transformations such as the [[nitration]] of conjugated systems  from a [[Theoretical chemistry|theoretical perspective]].


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The change in energy during the reaction can be derived by allowing the [[Molecular orbital|orbitals]] nearby the site i of attack to interact with the incoming molecule. A [[secular determinant]] can be formulated resulting in the equation:<ref>{{cite book |title=Progress in Physical Organic Chemistry |volume=2|last= Cohen|first= Saul |coauthors= Andrew Streitwieser, Robert W. Taft|year= 2009|publisher= John Wiley & Sons|isbn=9780470172018 |pages=299–300}}</ref>
 
<math>\Delta E=2\beta (a_{r}+a_{s})=\beta N_i</math>
 
where β is the Huckel interaction parameter and a<sub>r</sub> and a<sub>s</sub> are the coefficients of the highest energy molecular orbital at nearby sites r and s respectively. Dewar's reactivity number is then defined as <math>N_i=2(a_{r}+a_{s})</math>.
 
Clearly, the smaller the value of N<sub>i</sub>, the less the destabilization energy in going towards the [[transition state]] and the more reactive the site. Thus, by computation of the molecular orbital coefficients it is possible to evaluate Dewar's number for all the sites and establish which one will be the most reactive. This has been shown to correlate well with experimental results.<ref>{{cite journal |last1=Smith |first1= C. Michael|last2= Savage|first2=Philip E. |year=1991 |title= Reactions of polycyclic alkylaromatics: Structure and reactivity|journal= AlChE Journal|volume= 37|issue=11 |pages=1613–1624 |publisher= Wiley|doi=10.1002/aic.690371104 |url= http://onlinelibrary.wiley.com/doi/10.1002/aic.690371104/abstract|accessdate= 2012-05-20}}</ref>
 
The method is particularly efficient for [[alternant hydrocarbon]]s in which the coefficients of the non-bonding orbitals involved are very easy to calculate.
 
== References ==
<references/>
 
[[Category:Molecular physics]]
[[Category:Theoretical chemistry]]

Latest revision as of 15:09, 23 July 2013

In Huckel theory, a Dewar reactivity number, also known as Dewar number, is a measure of the reactivity in aromatic systems. It is used to quantify the difference in energy between the π-system of the original molecule and the intermediate having the incoming electrophile or nucleophile attached. It can be used to study important transformations such as the nitration of conjugated systems from a theoretical perspective.

The change in energy during the reaction can be derived by allowing the orbitals nearby the site i of attack to interact with the incoming molecule. A secular determinant can be formulated resulting in the equation:[1]

ΔE=2β(ar+as)=βNi

where β is the Huckel interaction parameter and ar and as are the coefficients of the highest energy molecular orbital at nearby sites r and s respectively. Dewar's reactivity number is then defined as Ni=2(ar+as).

Clearly, the smaller the value of Ni, the less the destabilization energy in going towards the transition state and the more reactive the site. Thus, by computation of the molecular orbital coefficients it is possible to evaluate Dewar's number for all the sites and establish which one will be the most reactive. This has been shown to correlate well with experimental results.[2]

The method is particularly efficient for alternant hydrocarbons in which the coefficients of the non-bonding orbitals involved are very easy to calculate.

References

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