Comments on: The Mesomeric Effect And Aromatic Amines https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/ Wed, 21 Sep 2022 02:26:15 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: James Ashenhurst https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-636607 Mon, 29 Aug 2022 18:04:02 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-636607 In reply to Anjana.

I am glad you found it useful, Anjana

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By: Anjana https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-636588 Mon, 29 Aug 2022 14:29:02 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-636588 Thank u so much for the explanation

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By: James Ashenhurst https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-589234 Wed, 09 Dec 2020 17:59:08 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-589234 In reply to ayesha.

Inductive effects. The methyl group donates electron density into the ring, which increases the resulting electron density of the nitrogen, resulting in increased basicity. Installing a CF3 on the other hand would reduce basicity.

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By: ayesha https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-589034 Sat, 05 Dec 2020 05:16:37 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-589034 sir! why the basicity of 4 methyl pyridine is greater than pyridine

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By: Moataz https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-588517 Sat, 21 Nov 2020 10:10:30 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-588517 Thanks to you very much I understood organic chemistry from your explanation mr.james

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By: James Ashenhurst https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-578419 Tue, 24 Mar 2020 21:04:21 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-578419 In reply to Deepak.

Ah yes. Thanks for pointing that out.

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By: Deepak https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-578382 Mon, 23 Mar 2020 04:04:55 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-578382 You did not explained the steric inhibition of resonance(SIR effect) which is one of the key factor in identifying basic strength of amines

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By: James Ashenhurst https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-567835 Wed, 16 Oct 2019 16:04:54 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-567835 In reply to Rameshwar.

Yes it can, but it will result in a charged species.

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By: Rameshwar https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-567752 Wed, 16 Oct 2019 04:50:10 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-567752 Can tertiary amine acts as nucleophile ?

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By: James Ashenhurst https://www.masterorganicchemistry.com/2017/04/28/the-mesomeric-effect-and-aromatic-amines/#comment-557535 Fri, 05 Jul 2019 15:13:15 +0000 https://www.masterorganicchemistry.com/?p=10719#comment-557535 In reply to Harish Kumar.

Glad to hear it Harish. Thank you.

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