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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In order to solve this question, we must apply the conservation of mass. The total number of nucleons (upper number) and protons (lower number) must be equal before and after the decay. The new nucleon number is
218 - 4
= 214
And new proton number is
84 - 2
= 82
Next, we must identify which element has the proton number 82. That would be lead, Pb.
Therefore, the answer is
5. ²¹⁴Pb₈₂
<h3><u>Answer;</u></h3>
NH3/NH4+
<h3><u>Explanation;</u></h3>
From the equation;
NH3(aq)+HNO3(aq)→NH4+(aq)+NO3−(aq)
NH3 is the base; while NH4+ is the conjugate acid
HNO3 is the acid; while NO3- is the conjugate base
- The conjugate base of a Brønsted-Lowry acid is species that is formed after an acid donates a proton while the conjugate acid of a Brønsted-Lowry base is the species formed after a base accepts a proton.
Hi , the answer is 5.678 x 10^3.
