Search results
Results From The WOW.Com Content Network
The mesomeric effect as a result of p-orbital overlap (resonance) has absolutely no effect on this inductive effect, as the inductive effect has purely to do with the electronegativity of the atoms and their topology in the molecule (which atoms are connected to which). Specifically the inductive effect is the tendency for the substituents to ...
Parallel resonance or near-to-resonance circuits can be used to prevent the waste of electrical energy, which would otherwise occur while the inductor built its field or the capacitor charged and discharged. As an example, asynchronous motors waste inductive current while synchronous ones waste capacitive current.
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.
This effect is the peak natural resonance frequency of the circuit and in general is not exactly the same as the driven resonance frequency, although the two will usually be quite close to each other. Various terms are used by different authors to distinguish the two, but resonance frequency unqualified usually means the driven resonance frequency.
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.
In accordance with new definition (6), the value of the inductive coupling coefficient of resonant LC-circuits is expressed by formula (4) as before. It has a positive value when L m > 0 {\displaystyle L_{m}>0} and a negative value when L m < 0. {\displaystyle L_{m}<0.}
Resonant inductive coupling or magnetic phase synchronous coupling [4] [5] is a phenomenon with inductive coupling in which the coupling becomes stronger when the "secondary" (load-bearing) side of the loosely coupled coil resonates. [5]
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.