Comments on: How To Determine Hybridization: A Shortcut https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/ Sat, 18 Apr 2026 02:14:33 +0000 hourly 1 https://wordpress.org/?v=6.9.4 By: Lovvic Isacvy https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-725102 Mon, 27 Jan 2025 09:57:36 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-725102 🤔"what's the difference between attached atoms and lone pairs???"]]> Thanks for the explanation.But am confused 🤔🤔”what’s the difference between attached atoms and lone pairs???”

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By: Henry Austine Ugbomah https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-710021 Fri, 04 Oct 2024 01:44:00 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-710021 Henry Ugbomah;
The view that geometry determines hybridization, and not otherwise is quite taken. Amine enantiomers are unsuccessful because, at room temperature, they undergo inversion is also interesting. However, the literature states, that catalysts can induce hybridization, by changing the electronic environment surrounding atoms.

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By: xiao liu https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-703284 Thu, 15 Aug 2024 08:41:43 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-703284 The direction of the equal sign may be wrong in the image below this sentence.

Better orbital overlap allows for stronger pi-bonding between the nitrogen lone pair and the carbonyl p-orbital, which results in an overall lowering of energy.

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By: om agrawal https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-682288 Sat, 13 Jan 2024 05:52:39 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-682288 i am in love with this site….. explains so clear and good….. really man i was irritated because i was not able to understand but now i understand it just because of this site….

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By: Nidhi https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-676443 Fri, 10 Nov 2023 02:55:39 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-676443 Sir thankyou so much for your explain , i was able to get a lot of things I couldn’t understand earlier, thanks a lot ,but I have a doubt about the last note ….how did it go from antiaromatic to aromatic in coelentrazine

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By: Harith Al-Masoodi https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-660044 Thu, 29 Jun 2023 20:04:56 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-660044 Thank you for the great post, as usual.

I think there is a typo in the first section of point 5 and its picture; the geometry is trigonal pyramidal instead of tetrahedral.

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By: Ayush sharma https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-647754 Fri, 10 Feb 2023 09:25:56 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-647754 very helpful thanks a lot SIR

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By: Gilllian https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-626589 Wed, 04 May 2022 15:35:20 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-626589 thank youuuuu!!! your discussions really helped my laboratory report in organic chemistry which is due tomorrow. can you have a discussion about the effect of pi systems? i’m looking forward to it!

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By: James Ashenhurst https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-626536 Wed, 04 May 2022 03:20:25 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-626536 In reply to Gilllian.

Pentane, C5H12 ? Tetrahedral carbons, sp3 hybridized

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By: Gilllian https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-626533 Wed, 04 May 2022 03:00:37 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-626533 may i ask for the carbon hybridization of pentane and the effects of the pi system.

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