Explain the inductive effect with a suitable example.

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(N/A) The inductive effect is the permanent displacement of shared electron pairs along a carbon chain due to the difference in electronegativity between the carbon atom and an attached atom or group.
$1$. It is a permanent effect and operates through $\sigma$-bonds.
$2$. It decreases rapidly as the distance from the source of the effect increases.
$3$. Groups that withdraw electrons are called $-I$ groups (e.g.,$-Cl, -NO_2$),while groups that donate electrons are called $+I$ groups (e.g.,$-CH_3, -C_2H_5$).
Example: In $CH_3-CH_2-CH_2-Cl$,the chlorine atom is more electronegative than carbon. It pulls the shared electron pair of the $C-Cl$ bond towards itself,creating a partial negative charge $(\delta^-)$ on $Cl$ and a partial positive charge $(\delta^+)$ on the $C_1$ atom. This polarization is transmitted to $C_2$ $(\delta\delta^+)$ and $C_3$ $(\delta\delta\delta^+)$,but the effect weakens significantly with distance.

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In which of the following organic compounds are all effects (i.e.,mesomeric effect,hyperconjugation effect,and inductive effect) present?

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Show the polarisation of the carbon-magnesium bond in the following structure: $CH_3-CH_2-CH_2-CH_2-MgX$.

Match List $I$ with List $II$:
$(A)$. Inductive effect$(I)$. Delocalization of $\pi$ electrons
$(B)$. Hyper-conjugation$(II)$. Displacement of $\pi$ electrons
$(C)$. Resonance effect$(III)$. Delocalization of $\sigma$ electrons
$(IV)$. Displacement of $\sigma$ electrons
Choose the correct answer from the options given below:

The functional group that shows negative resonance effect ($-R$ effect) is:

The interaction between $\pi$ bond and lone pair of electrons present on an adjacent atom is responsible for

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