It should be increasing the rate of the forward reaction will cause a shift to the left because the external stress, which is the increase in rate, will cause the reaction to be unbalanced, and to reach equilibrium it needs to shift to the right.
Answer:
Final pH of the solution: 2.79.
Explanation:
What's in the solution after mixing?
,
where
is the concentration of the solute,
is the number of moles of the solute, and
is the volume of the solution.
.
Acetic (ethanoic) acid:
.
.
Hydrochloric acid HCl:
.
.
HCl is a strong acid. It will completely dissociate in water to produce H⁺. The H⁺ concentration in the solution before acetic acid dissociates shall also be
.
The Ka value of acetic acid is considerably small. Acetic acid is a weak acid and will dissociate only partially when dissolved. Construct a RICE table to predict the portion of acetic acid that will dissociate. Let the change in acetic acid concentration be
.
.
.
.
Rewrite as a quadratic equation and solve for
:

.
The pH of a solution depends on its H⁺ concentration.
At equilibrium
.
.
3.4g AgNO3 x (1 mole AgNO3/169.8732g AgNO3) x (1 mole Ag/1mole AgNO3) x (107.8682g Ag/1 mole Ag) =
<span>2.2 grams Ag </span>
<span>(2 significant figures </span>
Answer:
Because of its weak intermolecular forces.
Explanation:
Hello there!
In this case, according to the given description, it turns out possible for us to recall the chemical structures of both ethanol and dimethyl ether as follows:

Thus, we can see that ethanol have London dispersion forces (C-C bonds), dipole-dipole forces (C-O bonds) and also hydrogen bonds (O-H bonds) which make ethanol a liquid due to the strong hydrogen bonds. On the other hand, we can see that dimethyl ether has just London and dipole forces, which are by far weaker than hydrogen bonding, that makes it unstable when liquid and therefore it tends to vaporize quite readily.
Regards!