Mesomeric Effect | Easy Trick of Mesomeric Effect | Organic Chemistry

I will teach you super easy trick to learn mesomeric effect.
To learn more, watch this lecture till the end.
Inductive effect: • Inductive Effect | Org...
Hyperconjugation: • Hyperconjugation in Or...
Electromeric effect: • Electromeric Effect | ...
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10M ❤

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I watched a lot of videos about mesomeric effects, this ist the best one !!!! Thx

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For the sixth compound in the example, CH3 is alkyl group so doesn't it exhibit + I effect ?

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[@VelvetVortex-0479]

small error: 16:10 ch3 is an alkyl group so it has +i effect sir

[@mizlolia]

Thank you so much for this sir. In the 6th example also, the one with CH3. (Toluene) isn't it safe to say that it is +I since it's an alkyl group?? And -M since no lone pair

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Read the second condition for mesomeric effect there should be at least one functional group along with carbon atoms

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Sir in the case of Benzene with CH3 there is +I effect. isn't it

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Teacher: what is Resonance? Me: Shifting of football between 3 brothers 💀

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I have a doubt : 16:12 there is a alkyl group then there should be a +I effect......?

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Hello sir , thank you so much for explaining this concept ❤, but I've a doubt sir in 6th one don't we have +I effect sir?

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We have +I effect on them

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if there is -M and -I then what effect it will give?

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[@subashtripathy2069]

At 16:23 sir the 6th one I.e methylbenzene cannot go under mesomeric effect but it can surely under +I effect cuz it is itself an alkyd group I guess... Plss rectify if there is any mistake.. Thank-you

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I too had the same doubt

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+I and only resonance happens

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Why No2 doesn't have lone pair electrons

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I didn't understand why is it that electrons moved from oxygen towards the unsaturated carbon. Where as oxygen is more electro negative than carbon. But in the second molecule it left from carbon to oxygen

[@user-ed3vt3js3l]

The donation of electrons from oxygen to carbon in certain resonance structures can seem counterintuitive considering oxygen's higher electronegativity. However, it's important to understand that resonance involves the delocalization of electrons within a molecule, allowing for the formation of multiple resonance structures. In the case of the hydroxyl group (-OH), the lone pair of electrons on oxygen can participate in resonance, leading to the delocalization of electron density. This delocalization can stabilize the molecule overall by distributing electron density more evenly. Additionally, while oxygen is more electronegative than carbon, it doesn't mean that it cannot donate electrons at all. The electronegativity difference between oxygen and carbon isn't so large that it completely prohibits electron donation, especially in the context of resonance effects where electron delocalization occurs.