14 мая 2017 г. · According to EK, ethanol is a better nucleophile because oxygen is more electronegative, making ethanol more basic. ... nucleophile than ethanol ... |
10 февр. 2019 г. · Going off of this remember that the solvent plays a role. So alcohols would be stronger nucleophiles but typically they are in water or a protic ... |
20 апр. 2021 г. · Our textbook says that alkoxides are strong nucleophiles, which makes sense given their charge, but why are alcohols poor nucleophiles? |
27 мар. 2023 г. · Basicity does not always equal nucleophilicity. For example Iodine is less basic than chlorine, but iodine is a a better nucleophile. |
14 мая 2022 г. · An alkoxide anion can and will be a strong nucleophile in many cases so long as there are no acidic protons available to neutralize this effect. |
26 авг. 2021 г. · It can get deprotonated and become quite a strong nucleophile as OH- . ... So the O-H- bond in Ethanol can also break, especially with a strong ... |
29 нояб. 2021 г. · In ethanol, an acid base reaction generates the ethoxide ion. This is even stronger as a base and so elimination is favoured , acting as a base. |
4 февр. 2021 г. · Electronegative atoms tend to have greater electron density, and are therefore nucleophiles. For example, the oxygen in ethanol is a nucleophile ... |
3 мар. 2024 г. · My prof said in class that if the SH deprotonates then it's a good nucleophile, but if that occurs, why wouldn't it apply for the ethanol? |
4 июн. 2018 г. · polar aprotic solvents -> ethanol is a better nucleophile, it is more electronegative, more wiling to react and give away its electron. |
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