I think your answer is D. However I’m not 100% sure.
Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive. Since soft nucleophiles are less strongly solvated than hard nucleophiles, these solvents boost the relative reactivity of soft anions.
<h3>
Ethanol is either a nucleophile or a base.</h3>
The ethanol is a base Because carbocation is an extremely reactive species, a base or nucleophile as weak as ethanol can replace or remove it. SN1 and E1 would not be conceivable without the carbocation or a strong departing group.
<h3>How do solvents impact anionic nucleophile's reactivity?</h3>
In polar aprotic solvents, nucleophilic substitution reactions of anionic nucleophiles often proceed more quickly. The normal relative reactivity order in such solvents (like DMSO)is Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive.
Learn more about nucleophiles here:-
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None since CO3 does not exist.
<h2>Answer:</h2>
Rutherford's models
<h2>Explanations:</h2><h2>What is the electron cloud model?</h2>
There are known as the region where electrons are found especially in the nucleus.
According to the five basic atomic models which have contributed to the structure of the atom itself, the Rutherford's models of the atom include a structure that is mostly made of empty space compared to thomson that proposed the plum pudding model of the atom
