I believe it would be c: 3 because you can have the numbers -1,0,1.
The first dissociation for H2X:
H2X +H2O ↔ HX + H3O
initial 0.15 0 0
change -X +X +X
at equlibrium 0.15-X X X
because Ka1 is small we can assume neglect x in H2X concentration
Ka1 = [HX][H3O]/[H2X]
4.5x10^-6 =( X )(X) / (0.15)
X = √(4.5x10^-6*0.15)
∴X = 8.2 x 10-4 m
∴[HX] & [H3O] = 8.2x10^-4
the second dissociation of H2X
HX + H2O↔ X^2 + H3O
8.2x10^-4 Y 8.2x10^-4
Ka2 for Hx = 1.2x10^-11
Ka2 = [X2][H3O]/[HX]
1.2x10^-11= y (8.2x10^-4)*(8.2x10^-4)
∴y = 1.78x10^-5
∴[X^2] = 1.78x10^-5 m
The name of the positively charged nonmetal ion is changed to end in –ide, is not true of binary compounds.
Hope this help!
Answer:
The molarity of urea in this solution is 6.39 M.
Explanation:
Molarity (M) is <em>the number of moles of solute in 1 L of solution</em>; that is
To calculate the molality, we need to know the number of moles of urea and the volume of solution in liters. We assume 100 grams of solution.
Our first step is to calculate the moles of urea in 100 grams of the solution,
using the molar mass a conversion factor. The total moles of 100g of a 37.2 percent by mass solution is
60.06 g/mol ÷ 37.2 g = 0.619 mol
Now we need to calculate the volume of 100 grams of solution, and we use density as a conversion factor.
1.032 g/mL ÷ 100 g = 96.9 mL
This solution contains 0.619 moles of urea in 96.9 mL of solution. To express it in molarity, we need to calculate the moles present in 1000 mL (1 L) of the solution.
0.619 mol/96.9 mL × 1000 mL= 6.39 M
Therefore, the molarity of the solution is 6.39 M.
P1v1/t1 = p2t2/t2
p is constant
v1=600, t1 =20c=293K
v2=?, t2=60c=333K
temperature must be in Kelvin
do the math