Comments on: How To Determine Hybridization: A Shortcut https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/ Thu, 15 Aug 2024 08:41:43 +0000 hourly 1 https://wordpress.org/?v=6.6.2 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.

]]> 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….

]]> 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

]]> By: How To Determine Hybridization: A Shortcut | Straight A Mindset https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-674737 Tue, 17 Oct 2023 23:18:54 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-674737 […] Some Simple Worked Examples Of The Hybridization Shortcut […]

]]> 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.

]]> 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

]]> By: Hybridization involving s, p and d-Orbitals - Overall Science https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/#comment-629007 Thu, 02 Jun 2022 16:45:58 +0000 https://www.masterorganicchemistry.com/?p=11195#comment-629007 […] i) https://www.masterorganicchemistry.com/2018/01/16/a-hybridization-shortcut/ […]

]]> 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!

]]> 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

]]> 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.

]]>