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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.
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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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The important thing to note is the reason why electron react is due to the instability of the electrons. All elements wants to aim the electron configuration of the noble gases. This is the most stable form in which each of the orbitals are sufficiently filled. When it comes to bonding, the order of reactivity is: alkynes > alkenes > alkanes. Alkynes are compounds with triple bonds, alkenes with double bonds and alkanes with single bonds. The single bonds are called saturated hydrocarbons. This is because they have reached stability, so it is quite difficult to react this with reducing or oxidizing agents. Alkynes and alkenes are unsaturated hydrocarbons. They readily react with reducing and oxidizing agents so as to become saturated, as well. The underlying principle for this is that single bonds contain sigma bonds which is the head-on overlapping of electrons. These is the strongest type of covalent bond. Double and triple bonds contain pi bonds which is the side overlapping of electrons orbitals. Hence, these electrons would be easily separated making it more reactive especially during protonation.
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Answer:
room temperature
Explanation:
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