Comments on: Alcohols Can Act As Acids Or Bases (And Why It Matters) https://www.masterorganicchemistry.com/2014/10/06/how-to-make-alcohols-more-reactive/ Tue, 21 May 2024 07:49:09 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: Madhav Mittal https://www.masterorganicchemistry.com/2014/10/06/how-to-make-alcohols-more-reactive/#comment-694360 Tue, 21 May 2024 07:49:09 +0000 https://www.masterorganicchemistry.com/?p=8509#comment-694360 Why mostly oxonium ion undergoes SN1 but not SN2?
Should it not be determined by the fact that whether the initial alcohol was primary or secondary or tertiary?

]]> By: Santhosh https://www.masterorganicchemistry.com/2014/10/06/how-to-make-alcohols-more-reactive/#comment-580306 Mon, 18 May 2020 03:03:00 +0000 https://www.masterorganicchemistry.com/?p=8509#comment-580306 Thank you professor. Got it.

]]> By: James Ashenhurst https://www.masterorganicchemistry.com/2014/10/06/how-to-make-alcohols-more-reactive/#comment-580305 Mon, 18 May 2020 02:57:33 +0000 https://www.masterorganicchemistry.com/?p=8509#comment-580305 In reply to Santhosh.

Hydroxyl groups are far more basic than (ordinary) double bonds.

]]> By: Santhosh https://www.masterorganicchemistry.com/2014/10/06/how-to-make-alcohols-more-reactive/#comment-580267 Sat, 16 May 2020 12:52:14 +0000 https://www.masterorganicchemistry.com/?p=8509#comment-580267 If a compound has both double bond and an -OH group, where will it get protonated first?

]]> By: Elizabeth https://www.masterorganicchemistry.com/2014/10/06/how-to-make-alcohols-more-reactive/#comment-504740 Sun, 12 Feb 2017 18:41:57 +0000 https://www.masterorganicchemistry.com/?p=8509#comment-504740 The zoo keepers have actually found a way to get the panda’s to get it on, they play them panda porn.

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