Main content
Course: Class 11 Chemistry (India) > Unit 12
Lesson 10: Electron displacement effects- Intro to Electronic Effects (& why should I care ?)
- The Inductive Effect
- Inductive effect and stability of intermediates-Part 1
- Inductive effect and stability of reaction intermediates- Part 2
- Inductive effect on stability of intermediates
- Stability of intermediates (all electronic effects)
- Identify aromatic, anti-aromatic and non-aromatic molecules
- Application of aromaticity
- Resonance structures
- Resonance structure patterns
- Resonance structures for benzene and the phenoxide anion
- Common mistakes when drawing resonance structures
- Identifying the correct resonating structure.
- Resonance structures and hybridization
- Stability due to Resonance
- Quantity of Resonating Structures vs Quality
- Resonance and stability of aliphatic intermediates.
- +R & -R groups in Resonance
- Relative strengths of different +R groups
- Relative strengths of different -R groups
- Resonance due to Electron Donors in a Benzyl Cation
- Effect of an electron withdrawing group in a benzyl cation
- Stability of a substituted benzyl anion
- Resonance and stability of aromatic intermediates.
- Comparing the stabilities of aromatic and aliphatic intermediates using resonance.
- Worked ex - Resonance vs Inductive Effects
- Inductive v/s Resonance.
- Hyperconjugation in a benzyl cation
- Hyperconjugation and stability of carbocations.
- Alkene stability
- Hyperconjugation - Isotopic Effect
- Heat of hydrogenation vs stability of alkenes
- Hyperconjugation and stability of alkenes.
- Worked ex : Resonance vs Hyperconjugation
- Who wins? Resonance, Hyperconjugation or Inductive? (ADVANCED)
- Carbocation stability and rearrangement introduction
- Carbocation rearrangement practice
© 2024 Khan AcademyTerms of usePrivacy PolicyCookie Notice
Hyperconjugation in a benzyl cation
In this video how a methyl group added to different positions in a benzyl cation help in stabilising it via hyperconjugation
. Created by Shahzad Karim.