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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A. actinides do not occur in nature.
Every mole is 22.4 L at STP
Chemical Property
<u>Explanation:</u>
When a substance is changed into another substance, may be due to addition of some other substance or removal of water from that substance.
* its identity changes
*its reactivity changes
*reactivity towards water, air and many other substances will change
*its chemical composition changes
and all these changes occurs due to the chemical properties.
If the physical property changes then there will be change in the state of matter, but its boiling point, melting point , reactivity towards water, air and other substances will not change, and it will not lose its identity.
