Your balanced equation for this reaction is:
HCOOH (aq) + H2O (aq) → HCOO- (aq) + H3O+ (aq)
So from the reaction, we can see when formic acid dissolved in water so H3O+ ions will be formed.
and we can see that it is a balanced equation as:
we have H atoms = 4 on both sides of the reaction
and C atoms = 1 atom on both sides of the reaction
and O atoms = 3 atoms on both sides of the reaction
So it is our final balanced equation of the reaction.
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:-
brainly.com/question/27127109
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Answer:
Keeps tides on the shore and away from the city
Explanation
Sorry I don’t get the question Buh I’m sure you’ll get it eventually
