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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Step 
<u>find the mass of a single washer</u>
Divide the total mass by the number of washers


Step 
<u>Convert kg to mg</u>
we know that

so

therefore
<u>the answer is</u>

The focal length, like you said it's the distance between the FOCAL point and the mirror.
Hope this helps.... :)
Explanation:
When a metal replaces another metal in solution, we say such a reaction has undergone a single displacement reaction.
In such a reaction, metal higher up in the activity series replaces another one due to their position.
To known the metal or metals that will replace the given copper, we need to reference the activity series of metals.
Every metal higher than copper in the series will displace copper from the solution.
So, there metals are: potassium, sodium, lithium, barium, strontium etc.