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An electron-withdrawing group (EWG) is a group or atom that has the ability to draw electron density toward itself and away from other adjacent atoms. [1] This electron density transfer is often achieved by resonance or inductive effects.
An electron donating group (EDG) or electron releasing group (ERG, Z in structural formulas) is an atom or functional group that donates some of its electron density into a conjugated π system via resonance (mesomerism) or inductive effects (or induction)—called +M or +I effects, respectively—thus making the π system more nucleophilic.
Delocalizing the radical ion stabilizes the transition state structure. As a result, the energy of activation decreases, enhancing the rate of the overall reaction. According to the captodative effect, the rate of a reaction is the greatest when both the EDG and EWG are able to delocalize the radical ion in the transition state structure. [7]
This is attributed to the resonance contribution of the EWG to withdraw electron density thereby increasing the susceptibility for nucleophilic attack on the carbonyl carbon. A change in rate occurs when X is EDG, as is evidenced when comparing the rates between X = Me and X = OMe, and nonlinearity is observed in the Hammett plot.
The polarization of a single σ covalent bond due to the electronegativity difference. Transfer of shared π-bond electron pairs to one atom under the influence of a strong external field. Permanent effect. Temporary effect. Always observed. Only observed in the presence of an electrophilic reagent. Induced charges are partial charges (δ + or ...
The difference in charging can be seismic for defendants. A felony conviction is more likely to lead to time behind bars. And even if the case ends in probation, such a conviction or even just a ...
Simple interest vs. compound interest Simple interest refers to the interest you earn on your principal balance only. Let's say you invest $10,000 into an account that pays 3% in simple interest.
An electric effect influences the structure, reactivity, or properties of a molecule but is neither a traditional bond nor a steric effect. [1] In organic chemistry, the term stereoelectronic effect is also used to emphasize the relation between the electronic structure and the geometry (stereochemistry) of a molecule.