Nov 29, 2021 · By the way, "deprotonation" doesn't necessarily imply just breaking a C–H bond; it really only says that "a proton is lost". In this case, the proton is lost, and a double bond is formed; it's still a …

Dec 17, 2022 · I know deprotonation means the removal of a HX+ H X + from the acid. After googling , I found the deprotonation percentage can be obtained by dividing the HX+ H X + concentration by the …

Mar 28, 2025 · Does this make KOH the limiting reagent? Assuming that for every product molecule that is formed one KOH is lost, but only if the deprotonation is favorable over the catalysis of new …

Sep 9, 2014 · I have been told that the first of the two acids is the stronger acid. According to this person,deprotonation for both occur at the nitrogen.The resulting conjugate bases …

May 11, 2023 · Successive deprotonation - how far can it go? Ask Question Asked 2 years, 7 months ago Modified 1 year, 11 months ago

May 1, 2020 · That deprotonation relies on chelation of the carbonyl oxygen to lithium (via a cyclic transition state*), so goes for the proton nearer to the carbonyl. That would be the "kinetic enolate". * …

Jun 29, 2016 · (1) However, deprotonation implies that protons moves to another acceptor, and in this case it depends entirely on the acceptor. Similarly, in nonwater media dissociation of phenol also …

Feb 28, 2023 · I am attempting to deprotonate the methyl group on 2-methylbenzo[d]thiazol-6-ol (hydroxyl group is protected with a silyl group) in order to attach a phosphate group in the form of …

Feb 26, 2016 · Butyllithium isomers are all stored in alkane solvents. Theoretically, equilibrium should (given enough time) lead to formation of mostly n-hexyllithium in the case of n-BuLi stored in (mostly) …

Jan 17, 2020 · The wikipedia page states clearly that the coloured form of phenolphthalein is the one with two protons removed. What is the evidence that phenolphthalein loses both protons in basic …