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:
25 mph
Explanation:
So we have to find the unit rate, or you could use the DTS triangle, but both say you have to divide, so our equation is:
176 ÷ 7 = 25.14
But I'm going to round that
So the train is traveling at 25 mph
hope this helps:/
Helium,it has an atomic mass of 4,which means total no. of protons and neutrons,so I think you meant 2 protons and an atomic mass of 4
That depends. there are 2 possible answers.
H
C - C = C - H gives a different answer on the right than on the left.
One the left side, the second Carbon is attached to a double bond and has but one hydrogen attached to it.
The Carbon on the right of the double bond has 2
H
C- C = C - H
H
I'm not sure what you should put. It's one of those things that I would repeat my argument and submit it.
You’ve not put anything below so I’m not sure what the options are but the relative charge of a proton is +1
