Comments on: Naming Bicyclic Compounds – Fused, Bridged, and Spiro https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/ Thu, 07 Dec 2023 22:13:57 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: Naming Bicyclic Compounds – Fused, Bridged, and Spiro | Straight A Mindset https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-679053 Thu, 07 Dec 2023 22:13:57 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-679053 […] A Few More Examples Of Bridged Bicyclic Molecules […]

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By: vijaykumar ranade https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-603187 Tue, 06 Jul 2021 04:09:48 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-603187 Monospiro hydrocarbons with two monocyclic rings are numbered consecutively starting in the smaller ring at an atom next to the spiro atom, proceeding around the smaller ring back to the spiro atom and then round the second ring.

Example:

spiro[4.5]decane
not spiro[5.4]decane

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By: T Murgy https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-585556 Fri, 02 Oct 2020 02:32:13 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-585556 Hi, are there any rules on numbering carbon substituents that are not apart of the main ring? For example if there were two methyl groups, each on a different carbon, how do you number each one?

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By: Satyajay Mandal https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-582516 Sun, 26 Jul 2020 05:41:08 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-582516 Hi James
Can you explain to me in details the mystery behind the nomenclature of bicyclic compounds in this site? I would be very glad to hear your reply as I need to send it to someone (@QuestionCookie) on https://chemistry.stackexchange.com as an answer to his/her question on “R/S configuration of bridging carbon in bicyclic system” within 10 hours in order to get a bounty worth +50 reputations from him/her
Thanks
Satyajay Mandal

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By: James Ashenhurst https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-557708 Mon, 08 Jul 2019 18:14:15 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-557708 In reply to hamid.

See the example at the bottom!

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By: hamid https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-556957 Wed, 26 Jun 2019 22:09:12 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-556957 for example, how would i name something like this
6-endo-bromo-8-anti-isobutyl-1,3-exo-dimethylbicyclo[3.2.1]octane
from a configuration diagram

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By: James Ashenhurst https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-553904 Tue, 23 Apr 2019 20:38:01 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-553904 In reply to kawtharbaby.

Glad to hear it. Thank you.

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By: kawtharbaby https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-553522 Sat, 20 Apr 2019 22:32:16 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-553522 ]]> Thanks so much. I find your explanations very useful 🙏

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By: James Ashenhurst https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-547604 Wed, 13 Feb 2019 00:45:23 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-547604 In reply to Najeeb Ullah.

Glad you found it helpful.

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By: James Ashenhurst https://www.masterorganicchemistry.com/2014/08/14/bridged-bicyclic-compounds-and-how-to-name-them/#comment-547603 Wed, 13 Feb 2019 00:45:14 +0000 https://www.masterorganicchemistry.com/?p=8418#comment-547603 In reply to Mrunal.

Not sure I understand the first part of your question. Yes, 2-fluorobicyclo[2.2.2]octane is chiral and will exist as a pair of enantiomers.

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