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  2. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    The effect of the sigma electron displacement towards the more electronegative atom by which one end becomes positively charged and the other end negatively charged is known as the inductive effect. The - I effect is a permanent effect & generally represented by an arrow on the bond.

  3. Electron-withdrawing group - Wikipedia

    en.wikipedia.org/wiki/Electron-withdrawing_group

    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.

  4. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    The inductive effect is the transmission of charge through covalent bonds and Bent's rule provides a mechanism for such results via differences in hybridisation. In the table below, [ 26 ] as the groups bonded to the central carbon become more electronegative, the central carbon becomes more electron-withdrawing as measured by the polar ...

  5. Field effect (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Field_effect_(chemistry)

    If induction was the dominant effect in these compounds, acidity should increase linearly with the number of available inductive pathways (linkers). However, the experimental data shows that effect on acidity in related octanes and cubanes is very similar, and therefore the dominant effect must be through space.

  6. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    In general, the resonance effect of elements in the third period and beyond is relatively weak. This is mainly because of the relatively poor orbital overlap of the substituent's 3p (or higher) orbital with the 2p orbital of the carbon. Due to a stronger resonance effect and inductive effect than the heavier halogens, fluorine is anomalous.

  7. Taft equation - Wikipedia

    en.wikipedia.org/wiki/Taft_equation

    where ⁡ is the ratio of the rate of the substituted reaction compared to the reference reaction, ρ* is the sensitivity factor for the reaction to polar effects, σ* is the polar substituent constant that describes the field and inductive effects of the substituent, δ is the sensitivity factor for the reaction to steric effects, and E s is ...

  8. Electronic effect - Wikipedia

    en.wikipedia.org/wiki/Electronic_effect

    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. The term polar effect is ...

  9. Induction - Wikipedia

    en.wikipedia.org/wiki/Induction

    Induction or inductive may refer to: Biology and medicine ... Inductive cleavage, in organic chemistry; Inductive effect, change in electron density;