<h2>
Emma here<em>
!</em></h2>
Answer:
im pretty sure its decreases going across a row (left to right)
Explanation:
As you move from left to right across a period on the periodic table the size of an atom will decrease
<h3>Hope this helps<em>! </em>Have a nice day<em>!</em></h3>
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.
Learn more about nucleophiles here:-
brainly.com/question/27127109
#SPJ4
Answer:
in some cases this is true a compound is a mixture of elements although it is actualy false the diffrence is actualy baced on what elements it is made of like sulfur Dioxide is when sulfur reacts with the contents of the air when burning and reacting but they arnt always diffrent most caces it is just what element you use.
Explanation: