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In organic chemistry, the inductive effect in a molecule is a local change in the electron density due to electron-withdrawing or electron-donating groups elsewhere in the molecule, resulting in a permanent dipole in a bond. It is present in a σ (sigma) bond, unlike the electromeric effect which is present in a π (pi) bond.
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effect inductive molecule charge atom groups bond acid atoms electron acidity group effects also electron-withdrawing stronger pka alkyl ionization electronegative
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| the more rapid nitration of toluene compared to benzene | instance of | results | 0.80 | text |
| were deduced as being due to an inductively donating effect of alkyl groups | instance of | results | 0.80 | text |
| the lower acidity of alcohols | instance of | Effects | 0.80 | text |
| higher basicity of substituted amines further deepened the misunderstanding | instance of | Effects | 0.80 | text |
| despite this being due to solvent or polarisability effects.As the induced change in polarity is less than the original polarity | instance of | Effects | 0.80 | text |
| the inductive effect rapidly dies out | instance of | Effects | 0.80 | text |
| is significant only over a short distance | instance of | Effects | 0.80 | text |
| Inductive effect | has effect | Relative | 0.60 | section |
| Inductive effect | has effect | Although | 0.60 | section |
| Inductive effect | has effect | For | 0.60 | section |
| Inductive effect | has effect | This | 0.60 | section |
| Inductive effect | has effect | The | 0.60 | section |
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