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Inductive Effect Examples (Part - 29) - Organic Chemistry: Some Basic Principals & Techniques Video Lecture - Class 11

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FAQs on Inductive Effect Examples (Part - 29) - Organic Chemistry: Some Basic Principals & Techniques Video Lecture - Class 11

1. What is the definition of inductive effect in organic chemistry?
Ans. Inductive effect refers to the polarization of a covalent bond due to the presence of a more electronegative atom, leading to the displacement of electron density towards the more electronegative atom.
2. How does the inductive effect affect the stability of organic compounds?
Ans. The inductive effect can influence the stability of organic compounds by either stabilizing or destabilizing them. Electron-withdrawing groups (EWG) tend to stabilize a compound by withdrawing electron density, while electron-donating groups (EDG) destabilize a compound by donating electron density.
3. Can you provide an example of a compound stabilized by the inductive effect?
Ans. Yes, an example of a compound stabilized by the inductive effect is chlorobenzene. The chlorine atom is more electronegative than carbon, so it withdraws electron density from the benzene ring through the sigma bonds, making the compound more stable.
4. How does the inductive effect affect the acidity of organic compounds?
Ans. The inductive effect can impact the acidity of organic compounds. Electron-withdrawing groups (EWG) increase the acidity of a compound by stabilizing the negative charge on the conjugate base, while electron-donating groups (EDG) decrease acidity by destabilizing the negative charge.
5. What is the difference between the inductive effect and the resonance effect in organic chemistry?
Ans. The inductive effect involves the polarization of a covalent bond due to the electronegativity difference between atoms, while the resonance effect involves the delocalization of electrons through pi bonds. The inductive effect is a localized effect, while the resonance effect is a delocalized effect.
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