Comments on: Alkyne Halogenation: Bromination, Chlorination, and Iodination of Alkynes https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/ Wed, 01 Mar 2023 11:06:06 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: Sawaira https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-649194 Wed, 01 Mar 2023 11:06:06 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-649194 Thank you

]]> By: Halogenation: Definition, Examples, and Mechanism https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-614495 Fri, 26 Nov 2021 12:08:29 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-614495 […] Alkyne Halogenation: Bromination, Chlorination, and Iodination of Alkynes – Masterorganicchemistry.com […]

]]> By: Ganesh https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-580388 Thu, 21 May 2020 13:25:25 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-580388 I have seen somewhere that you even get a cis product,through what other mechanism can you get a it

]]> By: ty https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-525602 Tue, 26 Dec 2017 16:35:34 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-525602 Wrong halohydrin rxn with alkyne
two halo atoms get attached

]]> By: Alkyne Addition Reactions – The “Concerted” Pathway — Master Organic Chemistry https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-150485 Sun, 29 Jun 2014 03:36:14 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-150485 […] pathways, and – you guessed it – since we’ve covered the carbocation and 3-membered ring pathways for alkynes in previous posts, this post concerns the “concerted” category. […]

]]> By: James Ashenhurst https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-51870 Sun, 01 Dec 2013 20:36:29 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-51870 In reply to Karin.

Yes, exactly!

]]> By: Karin https://www.masterorganicchemistry.com/2013/05/29/alkyne-halogenation-bromination-chlorination/#comment-51792 Sun, 01 Dec 2013 11:44:58 +0000 https://www.masterorganicchemistry.com/?p=7348#comment-51792 “The 3-membered ring intermediate formed has antiaromatic character. That is, there are 4 π electrons constrained in a conjugated ring,” does this mean that one of the two lone pairs of Cl is part of the antiaromatic system?

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