2 нояб. 2018 г. · A base/nucleophile as weak as ethanol can substitute or eliminate because the carbocation is an incredibly reactive species. Without the ...

12 февр. 2018 г. · Which is stronger nucleophile, chloride or amine? Well, how do you compare nucleophilicity? It's ...

25 июн. 2017 г. · A base/nucleophile as weak as ethanol can substitute or eliminate because the carbocation is an incredibly reactive species. Without the ...

25 сент. 2020 г. · For the legitimate reason, C2 2 H5 5 O− − is a stronger nucleophile because the C2 2 H5 5 ethyl group is an electron donating group, ...

3 нояб. 2016 г. · CH3O- is a better nucleophile than OH-, because the negative charge density on O in CH3O- is more due to +I effect of CH3 group.

4 июн. 2022 г. · The logic to my ranking is thus: small, and negatively charged are almost always great nucleophiles, the smaller the better.

31 окт. 2016 г. · Here, alcohol is weak nucleophile can't readily attack carbonyl carbon. *Acid is activated by acid protonation which gives a resonance ...

7 мая 2021 г. · Alcoholic KOH dissociates in water to give RO- ions which is a strong base and abstracts hydrogen giving rise to elimination reaction. Whereas, ...

29 июн. 2018 г. · Yes, phenol is more stable than aliphatic alcohol due to the delocalization of the lone pair present on the oxygen atom with the π π bond of the ...

27 мая 2020 г. · Comparing CN- and C2H5O- in terms of their ability to function as nucleophile, CN- appears to be a stronger nucleophile than C2H5O-. The reason ...