Answer- A
Explanation- Because you have to look at the symbols and remember which symbol goes with each chemical, if you don't then you could get confused.
I am going to say it is false.
Answer:
33.7
Explanation:
i just know i had a question on it'
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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Answer:
They have similar properties, because they share similar amounts of electrons in their outer shell, valence electrons! This means they will only be able to interact with other elements with those electrons so they often show similar properties.
Explanation:
