Comments on: Homotopic, Enantiotopic, Diastereotopic

By: James Ashenhurst

James Ashenhurst — Tue, 23 Sep 2025 00:15:33 +0000

In reply to George Metanis. Thank you. Looking into this.

By: George Metanis

George Metanis — Mon, 22 Sep 2025 20:11:17 +0000

Whenever i tap into this specific page it kicks my account out for some odd reason making me unable to check the quiz.

By: Abu

Abu — Mon, 27 Jan 2025 04:30:22 +0000

Enantiotopic and disteriotopic atom and face

By: Vanessa

Vanessa — Sun, 15 Oct 2023 20:16:20 +0000

This was so brief, simple, and understanding

By: frank bubinza

frank bubinza — Wed, 28 Jun 2023 07:34:24 +0000

the article is straight forward, thanks a lot I’ve benefited

By: James Ashenhurst

James Ashenhurst — Tue, 16 Feb 2021 19:10:31 +0000

In reply to Peter. Certainly. To take a simple example, (R,S)-1,2-cyclohexane diol. Every methylene (i.e. CH2) carbon in that molecule bears a pair of diastereotopic protons.

By: Peter

Peter — Mon, 15 Feb 2021 15:43:36 +0000

For meso compounds, can they still have diastereotopic protons?

By: James Ashenhurst

James Ashenhurst — Fri, 16 Oct 2020 17:51:30 +0000

In reply to George. Fixed. Thank you George!

By: Rose

Rose — Sun, 10 May 2020 19:25:41 +0000

It’s really helpful, clearly described..I want some examples on diastereotpic faces of alkenes with symmetry and addition criterion

By: James Ashenhurst

James Ashenhurst — Tue, 10 Mar 2020 21:15:26 +0000

Yes – thank you, and you are right, it does refer to an earlier version!