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: 4-allylanisole
Explanation: The doublets behind the 7 ppm belongs to the
para-substituted benzene ring. The three single-proton multi-plets around 5−6 ppm predicts that there has to be a single subsituted alkene group
A single plus a doublet around 3-4 ppm belongs to CH3 and CH2 Groups as they could be attached to the subsituted alkene group.
Moreover the interpretation of the NMR that there is no peak with a higher intensity for >180 ppm represents an absence of Carbonyl group.
The Predicted Number is attached from a chemical database along with their peaks information
Explanation:
Let us assume that the value of
= 
Also at 1500 K,
= 

Relation between
and
is as follows.

Putting the given values into the above formula as follows.



Also, 
or, 
= 
= 
Thus, we can conclude that the value of
is
.
The homologous structures and the analogous structures of different species.
1) Adding salt on the roads in the winter time,
2) Adding salt to the ice bath when making ice cream.
3) Mixing 2 substances when making coolant for a car.