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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]
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.
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.
Download as PDF; Printable version; In other projects ... Appearance. move to sidebar hide. EDG may refer to: Science and medicine Electron donating group, a ...
Examples of Lewis bases based on the general definition of electron pair donor include: simple anions, such as H − and F −; other lone-pair-containing species, such as H 2 O, NH 3, HO −, and CH 3 −; complex anions, such as sulfate; electron-rich π-system Lewis bases, such as ethyne, ethene, and benzene
You may be familiar with the Environmental Working Group (EWG) because they release a list of the most pesticide-filled produce every year called The Dirty Dozen. They also establish the produce ...
Gen Z has come up with yet another pop culture phrase to baffle anyone born before the year 2000. On the Feb. 2 edition of Hoda & Jenna, the hosting duo puzzled over a popular Gen Z slang term ...
The EWG withdraws electron density by resonance and effectively stabilizes the negative charge that is generated. The corresponding plot will show a positive rho value. In the case of a nucleophilic acyl substitution the effect of the substituent, X, of the non-leaving group can in fact accelerate the rate of the nucleophilic addition reaction ...