Aromatic Antiaromatic and Nonaromatic Compounds | Super Easy Trick
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- Опубликовано: 5 фев 2025
- This lecture is about aromatic, nonaromatic and antiaromatic compounds. I will teach you super easy trick to find aromatic antiaromatic and nonaromatic compounds. After watching this lecture, you will master aromaticity.
#aromatic
#antiaromatic
#nonaromatic
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#chemistry
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same question
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13:58 sir the first compund will be non aromatic as the hybridisation of the lower most carbon is sp3( correct me if I'm wrong)
bro sir has said atleast 1 sp2 hybridised carbon should be there in comnpound
Kisi ek mai bhi sp2, conjugation or cyclic hai toh woh aromatic,antiaromatic hoga
Right
@@Priyanshu45516-n no complete conjugation hona chahiye and each carbon have sp2 hybridization
The structure at 12:35 with the OH group is impossible. The carbon attached to the OH cannot have 2 double bonds. This structure has a carbon with 5 total bonds which is impossible because carbon can only form 4 bonds. Also oxygen cannot form more than 1 bond but in your structure the oxygen is bonded to a H and double bonded to the carbon. Someone verify please
the oxygen atom is also very unhappy in this situation. this compound would be super unstable, if it is even possible
That might be single bonded and it would be correct only if it is single bonded
Mujhe aisha kabhi nahi samajh mai aaya tha sir thank you so much sir
13:00 The compound is not anti-aromatic because conjugation is not formed across the ring.And the latter compound is similarly non-aromatic.
You are right. I also confuse on this part of video. Thanks you for solving my doubt.
Whole explanation is great but this part who further study before/after this video. They can understand this mistakes.
And this molécules has a carbon with 5 bonds. Octet rule is broken 🤯
Right
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Please make video on acidity and bascity comparison in organic compounds.
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Please make video on inert pair effect
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16:02 !!
How do you know that the lone pair is outside of the ring in pyridine?
Why can't it be inside??
It has already formed a double bond so lone pair is not a part of conjugation
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at 13:49 the first example has a sp3 carbon at the bottom so it isnt planar? how is it aromatic?
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On 10:17 there is 2nd cyclic structure where you positive charge didn't count ,if we count positive charge too so it will be aromatic
for positive charge there is no need to count
Sir could you please upload a video for remembering exceptions in p-block elements
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at 12:50 isnt it has 4 double bond so it must be 8pi electron and should be antiaromatic? no?