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Jun 17, 2020 at 20:47 vote accept Charlie
Jun 15, 2020 at 2:38 history closed Mithoron
Mathew Mahindaratne
Todd Minehardt
Waylander
Tyberius
Duplicate of Ortho-effect in substituted aromatic acids and bases
Jun 14, 2020 at 1:25 answer added anik bhowmick timeline score: 0
Jun 13, 2020 at 20:17 comment added Charlie Yes I looked up IL finar but the book doesn't really explain this matter. I am still confused
Jun 13, 2020 at 15:19 comment added Charlie Please could you provide a complete answer . The reason I am not able to get properly
Jun 13, 2020 at 9:39 comment added ba-13 This kind of sentence is also mentioned in Finar, though not for carboxylic acids(as I have seen), reason was mentioned as steric acceleration as somehow the loss of H+ relieves the molecule of steric strain(I don't know the exact reason that's why I am commenting) and as amines are Lewis bases, steric retardation acts(groups are hindered during their approach).
Jun 13, 2020 at 9:22 comment added Charlie Please check out I have edited my post
Jun 13, 2020 at 9:21 history edited Charlie CC BY-SA 4.0
added 436 characters in body
S Jun 12, 2020 at 23:41 history suggested Blade CC BY-SA 4.0
Quote was lost in the text.
Jun 12, 2020 at 22:33 review Suggested edits
S Jun 12, 2020 at 23:41
Jun 12, 2020 at 22:28 review Close votes
Jun 15, 2020 at 2:38
Jun 12, 2020 at 22:02 review First posts
Jun 12, 2020 at 22:33
Jun 12, 2020 at 22:00 history asked Charlie CC BY-SA 4.0