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.
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I don’t know what you mean by classification exactly but it is a redox equation. The reactant side of carbon is losing hydrogen to form carbon dioxide. And oxygen is gaining hydrogen which gives you the water. Redox reactions are also known as combustion reactions.
Answer:
Protons:
- positive
- aka cation
- in the nucleus along with the neutrons
Electrons:
- negative
- aka anion
- situated in the orbital shells/configuration levels (there are many names)
And a water molecule, this is called a dehydration synthesis. when 2 molecule combine, a water molecule leave.
Just like how heat moves from a region of higher
temperature to a region of lower temperature, molecules also tend to move from
a region of higher concentration to a region of lower concentration. This is
called natural diffusion and is naturally happening to reach stability.