True. Coastal regions are affected if it is warm currents over the ocean it make for a higher temperature over the land, if it's a colder current over the ocean it makes for temperatures to drop over land. This happens when the wind blows in from the sea.
Answer:
<u> </u>H2 + <u>2</u><u> </u> Cl2 = <u>2</u><u> </u> HCl2
The two half-reactions are...
Ag→Ag+
and...
NO3→NO
Let's start by balancing the first half-reaction...
Ag→Ag+
The amounts are already balanced; 1:1. The oxygens are balanced. So all that's left is to balance the charge...
Ag→Ag++e−
Now let's do the other equation... Amounts of nitrogen are balanced, so we first need to balance the oxygens...
NO3→NO
4H++NO3→NO+2H2O
Next, we need to balance charge...
4e−+4H++NO3→NO+2H2O
Now let's go ahead and rewrite each half-reaction after being balanced by themselves...
Ag→Ag++e−
4e−+4H++NO3→NO+2H2O
Now we need to multiply by some factor to get the electrons to cancel out. In this case, that factor is 4, which needs to be applied to the top half-reaction...
4(Ag→Ag++e−)=4Ag→4Ag++4e−
Then we combine this half-reaction with the second one above to get...
4Ag+4H++NO3→4Ag++NO+2H2O
Equilibrium occurs when forward and reverse directions of a reversible reaction occur at the same rate so there is no overall change in the amounts of reactants and products.
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
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