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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: If you mean table salt i.e. sodium chloride. It is held together by ionic bonds between sodium (Na+) and chloride (Cl-) ions. The sodium ions have a positive charge and the chlorine ions have a negative charge. Since opposite charges attract, they form ionic bonds. Ionic bonds are nothing more than the attraction between positive and negative ions.
Formula of isocyanic acid is HNCO. It colourless, volatile compound. It is poisonous inorganic compound. Melamine is synthesized from urea. The reaction involves two steps. In first step, urea gets converted to isocyanic acid which is an intermediate. In the second step, isocyanic acid gives melamine (molecular formula C₃H₆N₆) and carbon dioxide (CO₂). The balanced chemical reaction involved in second step is given below:
6 HNCO → 1 C₃N₃(NH₂)₃ + 3CO₂
The co-efficient of the reaction are: 6, 1, 3
The correct answer should be B.
The correct answer would be B.
