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The inductive effect can be used to determine the stability of a molecule depending on the charge present on the atom and the groups bonded to the atom. For example, if an atom has a positive charge and is attached to a - I group its charge becomes 'amplified' and the molecule becomes more unstable.
The most dominant effect is clear when looking at the ratio of R to F. For example, a tungsten complex was shown to alkylate allyl carbonates A and B. The ratio of products A1 and B1 can be attributed to the para substituent, X (Fig. 3). Using Swain–Lupton parameters (σ = 0.2F + 0.8R) a ρ value of -2.5 was found to be the slope.
Electron-withdrawing groups exert an "inductive" or "electron-pulling" effect on covalent bonds. The strength of the electron-withdrawing group is inversely proportional to the pKa of the carboxylic acid. [2] The inductive effect is cumulative: trichloroacetic acid is 1000x stronger than chloroacetic acid.
Due to the electronegativity difference between carbon and oxygen / nitrogen, there will be a slight electron withdrawing effect through inductive effect (known as the –I effect). However, the other effect called resonance add electron density back to the ring (known as the +M effect) and dominate over that of inductive effect.
A field effect is the polarization of a molecule through space. The effect is a result of an electric field produced by charge localization in a molecule. [1] This field, which is substituent and conformation dependent, can influence structure and reactivity by manipulating the location of electron density in bonds and/or the overall molecule. [2]
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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.
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