Answer:

Explanation:
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In this case, since the acid is monoprotic and the KOH has one hydroxyl ion only, we can see that at the equivalence point the moles of both of them are the same:

Thus, since we are given 1.70 g of the acid, we compute the moles of acid that were titrated:

Which equal the moles of KOH. In such a way, since the molarity is defined as moles over liters (M=n/V), the liters are moles over molarity (V=n/M), thus, the resulting volume is:

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Answer:
2.28 × 10^-3 mol/L
Explanation:
The equation for the equilibrium is
CN^- + H2O ⇌ HCN + OH^-
Ka = 4.9 × 10^-10
KaKb = Kw
4.9 × 10^-10 Kb = 1.00 × 10^-14
Kb = (1.00 × 10^-14)/(4.9 × 10^-10) = 2.05 × 10^-5
Now, we can set up an ICE table
CN^- + H2O ⇌ HCN + OH^-
I/(mol/L) 0.255 0 0
C/(mol/L) -x +x +x
E/(mol/L) 0.255 - x x x
Ka = x^2/(0.255 - x) = 2.05 × 10^-5
Check for negligibility
0.255/(2.05 × 10^-5) = 12 000 > 400. ∴ x ≪ 0.255
x^2 = 0.255(2.05 × 10^-5) = 5.20 × 10^-6
x = sqrt(5.20 × 10^-6) = 2.28 × 10^-3
[OH^-] = x mol/L = 2.28 × 10^-3 mol/L
Answer:
Neutrons = ( Atomic mass – Atomic number ) ( A–Z )
Protons and Electrons are equal to the atomic number
For example Neon,
Mass number (A) = 20
Atomic Number (Z) = 10
Number of Protons = 10
Number of Electrons = 10
Number of Neutrons = ( A–Z ) = 10
Electronic distribution :
K= 2
L= 8
Answer
<span>How does adding a non-volatile solute to a pure solvent affect the vapor pressure of the pure solvent?
</span>Answer The third option The solvent's vapor pressure will not be affected.
<span>To make a 2.0 M solution, how many moles of solute must be dissolved in 0.50 liters of solution?
Answer C. 1.0 mole solute.
</span>
Answer:
= 19
ΔG° of the reaction forming glucose 6-phosphate = -7295.06 J
ΔG° of the reaction under cellular conditions = 10817.46 J
Explanation:
Glucose 1-phosphate ⇄ Glucose 6-phosphate
Given that: at equilibrium, 95% glucose 6-phospate is present, that implies that we 5% for glucose 1-phosphate
So, the equilibrium constant
can be calculated as:
![= \frac{[glucose-6-phosphate]}{[glucose-1-[phosphate]}](https://tex.z-dn.net/?f=%3D%20%5Cfrac%7B%5Bglucose-6-phosphate%5D%7D%7B%5Bglucose-1-%5Bphosphate%5D%7D)


= 19
The formula for calculating ΔG° is shown below as:
ΔG° = - RTinK
ΔG° = - (8.314 Jmol⁻¹ k⁻¹ × 298 k × 1n(19))
ΔG° = 7295.05957 J
ΔG°≅ - 7295.06 J
b)
Given that; the concentration for glucose 1-phosphate = 1.090 x 10⁻² M
the concentration of glucose 6-phosphate is 1.395 x 10⁻⁴ M
Equilibrium constant
can be calculated as:
![= \frac{[glucose-6-phosphate]}{[glucose-1-[phosphate]}](https://tex.z-dn.net/?f=%3D%20%5Cfrac%7B%5Bglucose-6-phosphate%5D%7D%7B%5Bglucose-1-%5Bphosphate%5D%7D)

0.01279816514 M
0.0127 M
ΔG° = - RTinK
ΔG° = -(8.314*298*In(0.0127)
ΔG° = 10817.45913 J
ΔG° = 10817.46 J