5 янв. 2015 г. · Acetone used in SN2 reactions because it is a polar aprotic solvent. Explanation: SN2 reactions prefer polar aprotic solvents.

1 авг. 2020 г. · In acetone and other polar aprotic solvents, the trend in nucleophilicity is the same as the trend in basicity: fluoride is the strongest base ... What is a nucleophile? · Periodic trends in nucleophilicity

25 авг. 2022 г. · Acetone has a carbonyl with a double bonded oxygen meaning that it should be a nucleophile that donates electrons to H+ in water (the electrophile) to form the ... Nucleophile questions : r/chemhelp - Reddit Would acetone with EtSH make it a good enough nucleophile ... Determining SN1/SN2 with water in acetone. - Reddit How is it C for the answer? NaOH and acetone? wouldn't that ... Другие результаты с сайта www.reddit.com

18 дек. 2018 г. · The solvation of sodium halides by acetone leads to a solvent shell that isn't well "fit" for a chloride or bromide anion. How can weaker nucleophiles kick out stronger ones in the ... Predicting order of nucleophilic substitution reactivity Другие результаты с сайта chemistry.stackexchange.com

3 авг. 2015 г. · Ethoxide is a better nucleophile in acetone. Explanation: The solvent affects the nucleophilicity of ethoxide ion.

15 июн. 2023 г. · In acetone, the nucleophilicity order is determined by the relative electron-donating ability of the species. I⁻ is the strongest nucleophile as ...

The more basic the anion, the more likely it is to form stronger interactions with the positive charges of the solvent, decreasing its nucleophilicity.

4 дек. 2012 г. · It's a strong nucleophile due to the negative charge on oxygen, but also a strong base. (For our purposes, anything equally basic to HO(-) or RO ...

Solid-State Reaction Synthesis of Nanoscale Materials: Strategies and Applications ... Acetone as a Nucleophile. Click to copy article linkArticle link ...

The reaction is driven forward because of the lower solubility of the products NaCl and NaBr in acetone even though I- is a weak nucleophile.