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The electron cloud in a σ-bond between two unlike atoms is not uniform and is slightly displaced towards the more electronegative of the two atoms. This causes a permanent state of bond polarization, where the more electronegative atom has a slight negative charge (δ–) and the other atom has a slight positive charge (δ+). If the electronegative atom is then joined to a chain of atoms, usually carbon, the positive charge is relayed to the other atoms in the chain. This is the electron-withdrawing inductive effect, also known as the effect. Some groups, such as the alkyl group, are less electron-withdrawing than hydrogen and are therefore considered as electron-releasing. This is electron releasing character and is indicated by the effect. In short, alkyl groups tend to give electrons, leading to induction effect.
As the induced change in polarity is less than the original polarity, the inductive effect rapidly dies out and is significant only over a short distance. Moreover, the inductive effect is permanent but feeble since it involves the shift of strongly held σ-bond electrons and other stronger factors may overshadow this effect.
Relative inductive effects have been experimentally measured with reference to hydrogen, in decreasing order of -I effect or increasing order of +I effect, as follows:
–NH3+ > –NO2 > –SO2R > –CN > –SO3H > –CHO > CO > –COOH > –COCl> –CONH2 > –F > –Cl > –Br > –I > –OR > -OH > –NH2 > –C6H5 > –CH=CH2 > –H
The strength of inductive effect is also dependent on the distance between the substituent group and the main group that react; the greater the distance, the weaker the effect.
Inductive effects can be measured through the Hammett equation, which describes the relationship between reaction rates and equilibrium constants with respect to substituents.
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. Similarly, if an atom has a negative charge and is attached to a +I group its charge becomes 'amplified' and the molecule becomes more unstable. In contrast, if an atom has a negative charge and is attached to a −I group its charge becomes 'de-amplified' and the molecule becomes more stable than if I-effect was not taken into consideration. Similarly, if an atom has a positive charge and is attached to a +I group its charge becomes 'de-amplified' and the molecule becomes more stable than if I-effect was not taken into consideration. The explanation for the above is given by the fact that more charge on an atom decreases stability and less charge on an atom increases stability.
The inductive effect also plays a vital role in deciding the acidity and basicity of a molecule. Groups having +I effect attached to a molecule increases the overall electron density on the molecule and the molecule is able to donate electrons, making it basic. Similarly, groups having -I effect attached to a molecule decreases the overall electron density on the molecule making it electron deficient which results in its acidity. As the number of -I groups attached to a molecule increases, its acidity increases; as the number of +I groups on a molecule increases, its basicity increases.
- Carboxylic acids
In acids, the electron-releasing inductive effect of the alkyl group increases the electron density on oxygen and thus hinders the breaking of the O-H bond, which consequently reduces the ionization. Greater ionization in formic acid when compared to acetic acid makes formic acid (pKa=3.74) stronger than acetic acid (pKa=4.76). Monochloroacetic acid (pKa=2.82), though, is stronger than formic acid, since the electron-withdrawing effect of chlorine promotes ionization.
In benzoic acid, the carbon atoms which are present in the ring are sp2 hybridised. As a result, benzoic acid (pKa=4.20) is a stronger acid than cyclohexanecarboxylic acid (pKa=4.87). Also, in aromatic carboxylic acids, proton-withdrawing groups substituted at the ortho and para positions can enhance the acid strength.
- Important publications in organic chemistry
- Baker–Nathan effect: the observed order in electron-releasing basic substituents is apparently reversed.
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