A solution of water (Kf=1.86 ∘C/m) and glucose freezes at − 1.95 ∘C. What is the molal concentration of glucose in this solution? Assume that the freezing point of pure water is 0.00 ∘C.Express your answer to three significant figures and include the appropriate units.

The concentration in ppm of a pollutant that has been measured at 425 mg per 170 kg of sample is 2500 ppm.

To calculate the concentration in parts per million (ppm) of a pollutant that has been measured at 425 mg per 170 kg of the sample, we need to convert the mass of the pollutant to a concentration in ppm.

First, we need to convert the mass from milligrams to kilograms:
425 mg = 0.425 kg

Next, we can use the formula for concentration in ppm:
Concentration (ppm) = (mass of pollutant/mass of sample) x 10^6

Plugging in the values we have:
Concentration (ppm) = (0.425 kg / 170 kg) x 10^6
Concentration (ppm) = 2500 ppm

Therefore, the concentration of the pollutant is 2500 ppm.

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Answer:

Explanation:

The ideal gas law is given by:

PV = nRT

where P is the pressure, V is the volume, n is the number of moles of gas, R is the universal gas constant, and T is the temperature.

Rearranging the equation to solve for n, we get:

n = PV / RT

where:

P = 120 kPa

V = 32.4 L

R = 8.31 J/mol·K (universal gas constant)

T = 25°C + 273.15 = 298.15 K (temperature in kelvins)

Substituting the values:

n = (120 kPa * 32.4 L) / (8.31 J/mol·K * 298.15 K)

n = 1.34 mol (rounded to two significant figures)

Therefore, there are approximately 1.34 moles of He gas present in the given conditions.

The solubility product constant (Ksp) for barium phosphate ([tex]Ba_{3} (PO_{4} )2^{2}[/tex]) can be determined from the molar solubility using the following equation:

the solubility product constant for barium phosphate is 1.09×[tex]10^{-41}[/tex].

[tex]Ksp = [Ba^{2+} } ][PO42-]^2[/tex]

where [[tex]Ba^{2+}[/tex]] and [[tex]PO_{4}^{2-}[/tex]] are the molar concentrations of barium ions and phosphate ions, respectively, at equilibrium.

Since the stoichiometry of the compound is 1:2 (one barium ion combines with two phosphate ions), we can assume that [[tex]Ba^{2+}[/tex]] = x and

[[tex]PO_{4}^{2-}[/tex]] = 2x. Therefore,

[tex]Ksp = x(2x)^2 = 4x^3[/tex]

The molar solubility of barium phosphate is given as 6.61×[tex]10^{-7}[/tex] M, which represents the value of x. Substituting this value into the equation for Ksp, we get:

Ksp = [tex]4(6.61×10-7)^3[/tex] = 1.09×[tex]10^{-41}[/tex]

Therefore, the solubility product constant for barium phosphate is

1.09×[tex]10^{-41}[/tex].

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Rounding to two decimal places, the mass percent of hydrogen in NaHCO3 is 1.19%.

To determine the mass percent of H in sodium bicarbonate (NaHCO3), we need to first calculate the molar mass of NaHCO3.

NaHCO3 molar mass = (1 x Na) + (1 x H) + (1 x C) + (3 x O)
= 23 + 1 + 12 + 48
= 84 g/mol

Next, we need to calculate the molar mass of H in NaHCO3.

H molar mass = 1 g/mol

To calculate the mass percent of H in NaHCO3, we use the following formula:

Mass percent of H = (mass of H / total mass of NaHCO3) x 100

The mass of H in NaHCO3 can be calculated by multiplying the number of H atoms by the molar mass of H:

Mass of H = 1 x 1 g/mol = 1 g/mol

The total mass of NaHCO3 is 84 g/mol, as calculated earlier.

Now we can substitute the values in the formula:

Mass percent of H = (1 g/mol / 84 g/mol) x 100
= 1.19%

Therefore, the mass percent of H in NaHCO3 is 1.19%, rounded to two decimal places.

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10.8 grams of Ag2CO3 will precipitate when excess Na2CO3 solution is added to 75.0 mL of 0.520 M AgNO3 solution.

The balanced equation shows that 1 mole of AgNO3 reacts with 1 mole of Na2CO3 to form 1 mole of Ag2CO3. The given volume and concentration of AgNO3 can be used to calculate the number of moles of AgNO3:

75.0 mL x (1 L / 1000 mL) x 0.520 mol/L = 0.0390 mol AgNO3

Since the reaction goes to completion, the number of moles of Ag2CO3 formed will be equal to the number of moles of AgNO3 present:

0.0390 mol Ag2CO3

To convert moles to grams, we need to multiply by the molar mass of Ag2CO3:

0.0390 mol x 275.75 g/mol = 10.8 g Ag2CO3

Therefore, 10.8 grams of Ag2CO3 will precipitate.

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Dipole-dipole forces and dispersion forces are the intermolecular forces present in HBr. Because bromine has a higher electronegativity than hydrogen, HBr is a polar molecule.

London dispersion forces (LDF), dipole-dipole interactions, and hydrogen bonds are the three different intermolecular forces. All substances at least have LDF, but molecules can have any combination of these three types of intermolecular interactions.

Water (H2O), hydrogen chloride (HCl), and hydrogen fluoride (HF) are all examples of dipole-dipole forces. Hydrogen chloride, or HCl Permanent dipole HCl. In contrast to the hydrogen atom, which has a partially positive charge, the chlorine atom has a partially negative charge.

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No, the proposed Lewis structure for BeH2 (H---Be----H) is not reasonable. The reason is that the total number of valence electrons is not correctly distributed.

In a reasonable Lewis structure, each atom should achieve a stable electron configuration by sharing or transferring valence electrons. Beryllium (Be) has 2 valence electrons, and each hydrogen atom (H) has 1 valence electron. Therefore, BeH2 has a total of 4 valence electrons.

A reasonable Lewis structure for BeH2 would be:

H-Be-H

In this structure, beryllium shares its 2 valence electrons with the 2 hydrogen atoms. Each hydrogen atom achieves a stable electron configuration with 2 electrons, and beryllium also achieves a stable electron configuration with 4 electrons.

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All of the following contain [tex]sp^2[/tex] hybridized atoms in their functional group except: an anhydride. The correct answer is option (D)

An anhydride is formed by the dehydration of two carboxylic acid molecules. Each carboxylic acid molecule contains an [tex]sp^2[/tex] hybridized carbonyl carbon atom, but the anhydride molecule formed by their reaction has two carbonyl groups that are each [tex]sp^3[/tex] hybridized.
Therefore, an anhydride does not contain [tex]sp^2[/tex] hybridized atoms in its functional group.

The term "[tex]sp^2[/tex] hybridization" refers to the hybridization of atomic orbitals of an atom in a molecule. In [tex]sp^2[/tex] hybridization, the s orbital and two p orbitals of an atom combine to form three hybrid orbitals that have a trigonal planar arrangement. These hybrid orbitals form sigma bonds with other atoms in the molecule, while the unhybridized p orbitals can form pi bonds.

In organic chemistry, several functional groups contain [tex]sp^2[/tex] hybridized atoms. These include carboxylic acids, nitriles, aldehydes, and anhydrides. However, the question asks which of these functional groups does not contain [tex]sp^2[/tex] hybridized atoms.

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The pH when 3.9 g of sodium acetate, NaC₂H₃O₂, is dissolved in 300.0 mL of water is 3.94.

To find the pH when 3.9 g of sodium acetate, NaC₂H₃O₂, is dissolved in 300.0 mL of water, we need to first find the concentration of the acetate ion, C₂H₃O₂⁻.

First, find the moles of sodium acetate.
molar mass of NaC₂H₃O₂ = 82.03 g/mol

moles of NaC₂H₃O₂ = 3.9 g / 82.03 g/mol

= 0.0475 mol

Find the concentration of acetate ion.

volume of solution = 300.0 mL = 0.3 L

concentration of acetate ion = moles of NaC₂H₃O₂ / volume of solution

= 0.0475 mol / 0.3 L

= 0.158 M

Use the Ka of acetic acid, NaC₂H₃O₂, to find the pH.

Ka = 1.8×10⁻⁵

pKa = -log(Ka) = -log(1.8×10⁻⁵) = 4.74 (rounded to 2 decimal places)

pH = pKa + log([C₂H₃O₂⁻]/[NaC₂H₃O₂])

= 4.74 + log(0.158/1)

= 4.74 + (-0.80)

= 3.94 (rounded to 2 decimal places)

Therefore, the pH when 3.9 g of sodium acetate is dissolved in 300.0 mL of water is approximately 3.94.

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A diprotic acid has two acidic hydrogen atoms, meaning it can donate two protons. The pKa values given tell us the strength of each acidic hydrogen atom.

The pH of a 0.10 M solution of this diprotic acid that has been one quarter neutralized means that 25% of the acid has been converted to its conjugate base. This means that one of the two acidic hydrogen atoms has been neutralized, leaving only one left to donate.

We can use the Henderson-Hasselbalch equation to solve for the pH:

pH = pKa2 + log([A-]/[HA])

We know pKa2 is 6.50 and that one quarter of the acid has been neutralized, which means that [A-]/[HA] is 0.25. We can solve for [HA] by subtracting 0.25 from 1 and multiplying by the initial concentration of 0.10 M:

[HA] = (1-0.25) x 0.10 M = 0.075 M

Now we can plug in the values and solve for pH:

pH = 6.50 + log(0.25/0.075) = 5.41

Therefore, the pH of a 0.10 M solution of this diprotic acid that has been one quarter neutralized is 5.41.

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103,000lbs/day of alum need (Al₂(SO₄)³·14 H₂O) are required for a 45 MGD water treatment plant that requires an optimum dosage of 25 ppm Al³⁺ for coagulation.

If the optimum dosage for coagulation is 25 ppm Al³⁺ and the water treatment plant has a flow rate of 45 MGD (million gallons per day), we can calculate the amount of alum required per day as follows:
25 ppm Al³⁺ x 45 MGD = 1,125 pounds of Al₂(SO₄)³·14 H₂O per day
However, the molecular weight of Al₂(SO₄)³·14 H₂O is 594.1 g/mol, which means that 1 mole of Al₂(SO₄)³·14 H₂O weighs 594.1 grams. Therefore, we need to convert pounds to grams by multiplying by a conversion factor of 453.592 grams per pound:
1,125 pounds/day x 453.592 grams/pound = 510,837 grams/day
Finally, we can convert grams to pounds per day by dividing by 453.592 grams per pound:
510,837 grams/day ÷ 453.592 grams/pound = 1,126.4 pounds/day (rounded to the nearest tenth)
Therefore, approximately 1,126.4 pounds per day of alum (Al₂(SO₄)³·14 H₂O) are required for a 45 MGD water treatment plant that requires an optimum dosage of 25 ppm Al³⁺ for coagulation. Rounded to the nearest thousandth, this is approximately 103,000 pounds per day.

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According to the VSEPR theory, each carbon atom in cubane should have a tetrahedral shape around it. The bond angle associated with this shape is 109.5 degrees. If we assume an ideal cubic shape for cubane, the actual bond angles around each carbon would be 90 degrees.

C)The ideal cubic shape would require all bond angles to be 90 degrees, but the tetrahedral shape around each carbon atom means that some of the bond angles are 109.5 degrees. This creates a strain in the molecule, making it unstable.

1. According to the VSEPR theory, what should be the shape around each carbon atom? What shape is associated with this bond angle?

Answer: In cubane, each carbon atom is bonded to one hydrogen atom and three other carbon atoms. According to the VSEPR theory, the electron groups around each carbon atom will arrange themselves to minimize electron repulsion. With four electron groups (one hydrogen and three carbons), the shape around each carbon atom should be tetrahedral. The bond angle associated with a tetrahedral shape is 109.5 degrees.

2. If you assume an ideal cubic shape, what are the actual bond angles around each carbon?

Answer: In an ideal cubic shape, the bond angles between the carbon atoms are equal to the angles between the edges of a cube. These angles can be calculated using the dot product between two adjacent edge vectors, which yields a bond angle of 90 degrees around each carbon atom.

3. Explain how your answers to questions 2a and 2b suggest why this molecule is so unstable.

Answer: The instability of cubane can be attributed to the difference between the ideal tetrahedral bond angle (109.5 degrees) predicted by VSEPR theory and the actual bond angle in the cubic shape (90 degrees). The smaller bond angle in cubane creates significant strain and repulsion between the electron groups around each carbon atom. This strain makes the molecule highly unstable and prone to explosive reactions, as demonstrated by the incidents mentioned in your question.

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Astatine, radon, lead, and bismuth is the increasing order of atomic radius.

Due to the inclusion of a second electron shell and electron shielding, atomic size grows as you descend a column. As you move right across a row, the size of the atoms gets smaller due to more protons.

The atomic numbers of the chemical elements are organised in ascending order. Periods are horizontal rows, while groups are vertical columns. Chemical characteristics of elements belonging to the same group are comparable. This is due to the fact that they both have the same valency and amount of outside electrons.

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The ratio of the square roots of their molar masses is approximately 0.66. This means that NH3 molecules effuse about 1.5 times faster than CO molecules.

According to Graham's Law of Effusion, the rate of effusion of a gas is inversely proportional to the square root of its molar mass. The molar mass of NH3 is approximately 17 g/mol, while the molar mass of CO is approximately 28 g/mol. Therefore, the ratio of the square roots of their molar masses is approximately 0.66. This means that NH3 molecules effuse about 1.5 times faster than CO molecules.
Ammonia (NH3) molecules effuse faster than carbon monoxide (CO) molecules due to their lower molecular mass. To determine the rate, we can use Graham's Law of Effusion:
Rate₁ / Rate₂ = √(M₂ / M₁)
In this case, Rate₁ refers to the effusion rate of NH3, and Rate₂ refers to the effusion rate of CO. M₁ and M₂ are their respective molecular masses.
The molecular mass of NH3 is 14 (nitrogen) + 3(1) (hydrogen) = 17 g/mol, and the molecular mass of CO is 12 (carbon) + 16 (oxygen) = 28 g/mol.
Plugging these values into the equation:
Rate_NH3 / Rate_CO = √(28 / 17)
Rate_NH3 / Rate_CO ≈ 1.63
This means that ammonia (NH3) molecules effuse approximately 1.63 times faster than carbon monoxide (CO) molecules.

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We must apply the Nernst equation, which connects a battery's voltage to the concentration of the ions participating in the process, to answer this problem. The Nernst equation reads as follows: E = E° - (RT/nF)ln(Q)

Car battery voltage can vary from 12.6 to 14.4, as we can see when we check more closely. The car battery's voltage will be 12.6 volts when the engine is off and fully charged. As "resting voltage," this is understood.

Part A: The appropriate half-reactions are:  Mg → Mg2+ + 2e- (oxidation)

Cu₂₊ + 2e- → Cu (reduction)

The standard electrode potentials are: E°(Mg2+/Mg) = -2.37 V,

E°(Cu₂+/Cu) = +0.34 V

The reaction quotient at equilibrium is:

Q = [Mg₂₊]/[Cu₂₊] = (1.0×10⁻⁴)/(1.4) = 7.14×10⁻⁵

With these values entered into the Nernst equation, we obtain:

E = 0.34 - (8.31×298)/(2×96485)ln(7.14×10⁻⁵) - (-2.37)

E = 1.10 V

As a result, the battery's initial voltage is 1.10 V.

Part B: We must use the equation to get the battery's voltage after supplying 4.7 A for 8.0 hours.

E = E° - (RT/nF)ln(Q) - (IΔt/nF)

We must first determine how many moles of electrons were exchanged during the reaction:

n = 2 (from the balanced equation)

At the new concentration, the reaction quotient is:

Q' = ([Mg₂₊] - Δ[Mg₂₊])/([Cu₂₊] + Δ[Cu₂₊])

= (1.0×10⁻⁴ - 2nMg)/(1.4 + 2nCu)

= (1.0×10⁻⁴ - 2(4.7)(8×3600))/(1.4 + 2(4.7)(8×3600))

= 3.64×10⁻⁵

where Δ[Mg₂₊] = 2nMg and Δ[Cu₂₊] = -2nCu.

With these values entered into the Nernst equation, we obtain:

E = 0.34 - (8.31×298)/(2×96485)ln(3.64×10⁻⁵) - (-2.37) - (4.7×8×3600)/(2×96485)

E = 1.07 V

As a result, the battery's voltage is 1.07 V after providing 4.7 A for 8.0 hours.

Part C: When [Mg₂₊] = 0, the reaction will come to an end. We may use the following equation to determine how long it will take for this to occur:

Q = [Mg₂₊]

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The total number of products, including stereoisomers, formed in this reaction would be 2 products (from the addition of bromine at either the 2-position or the 4-position) multiplied by 4 stereoisomers for each product, resulting in a total of 8 products, including stereoisomers.

When (R)-2,4-dimethylhex-2-ene is treated with HBr in the presence of peroxides, it undergoes a radical bromination reaction, resulting in the addition of a bromine atom to one of the carbon atoms in the double bond. The addition can occur at either the 2-position or the 4-position of the double bond, resulting in two possible products.

Additionally, since the molecule has two chiral centers, there are four possible stereoisomers for each product, depending on the configuration of the bromine atom and the two methyl groups attached to the stereocenters.

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To make a 0.6 mL of a 1 M solution of sodium borohydride, you will need to follow these steps:

Determine the amount of sodium borohydride required:

The formula weight of sodium borohydride is 37.83 g/mol. To make a 1 M solution, you need 1 mole of sodium borohydride per liter of solution. Since you are making only 0.6 mL of solution, you need to calculate how much of sodium borohydride is required.

1 M = 1 mol/L

Therefore, 1 mole of sodium borohydride is required to make a 1 M solution in 1 liter of solution.

To make 0.6 mL of a 1 M solution, you need to calculate the amount of sodium borohydride required as follows:

1 M = 1 mol/L = 37.83 g/L

0.6 mL = 0.0006 L

Therefore, the amount of sodium borohydride required is:

0.6 mL x 37.83 g/L = 0.022698 g

Dissolve sodium borohydride in a small amount of solvent:

Sodium borohydride is a highly reactive compound and can react violently with water. Therefore, it is recommended to dissolve it in a suitable solvent. One commonly used solvent is tetrahydrofuran (THF). Add the calculated amount of sodium borohydride to a small amount of THF and stir gently until it dissolves.

Dilute to the final volume:

Add THF to make up the final volume of 0.6 mL. Mix well.

Note: Always handle sodium borohydride with caution and use appropriate safety equipment as it is a strong reducing agent and can react violently with water or other incompatible materials.

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The formed carbonic acid, [tex]H_{2} CO_{3}[/tex] decomposes in to other water & carbon dioxide gas. [tex]NiCO_{3}[/tex](s) + 2 HCl(aq) + [tex]H_{2} CO_{3}[/tex](aq) = [tex]NiCl_{2}[/tex](aq) + [tex]H_{2} CO_{3}[/tex](aq).

What effect does carbonic acid have on the body?

Carbonic acid is necessary for carbon dioxide transport in the blood. Because the partial pressure of carbon dioxide in the tissues is greater than the partial pressure of blood running through the tissues, it enters the blood.

What beverages contain carbonic acid?

Carbonic acid is formed from the carbon dioxide that dissolves, which is found in virtually all soft drinks. To make soft drinks full of flavor, carbonic acid is added. So when vial is opened, its pressure drops and indeed the carbon dioxide dissolves into water and carbon dioxide, causing it to fizz.

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Every element in the question can be classified as a metal, nonmetal, or a metalloid:
- F (Fluorine): Nonmetal
- Te (Tellurium): Metalloid
- Mg (Magnesium): Metal
- Co (Cobalt): Metal
- He (Helium): Nonmetal
- Ga (Gallium): Metal

The elements were classified as above because:

1. F (Fluorine): Fluorine is a nonmetal. It belongs to Group 17 (Halogens) of the periodic table.
2. Te (Tellurium): Tellurium is a metalloid. It is found in Group 16 (Chalcogens) and is located along the metal-nonmetal dividing line in the periodic table.
3. Mg (Magnesium): Magnesium is a metal. It is an alkaline earth metal found in Group 2 of the periodic table.
4. Co (Cobalt): Cobalt is a metal. It is a transition metal located in Group 9 of the periodic table.
5. He (Helium): Helium is a nonmetal. It is a noble gas, found in Group 18 of the periodic table.
6. Ga (Gallium): Gallium is a metal. It is located in Group 13 of the periodic table.

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The solubility of Ag₃PO₄ (silver phosphate) in water is approximately 6.4 x 10⁻⁴ g/L.

To calculate the solubility of Ag₃PO₄ in water, we first need to understand its dissociation in water: Ag₃PO₄(s) ↔ 3Ag⁺(aq) + PO₄³⁻(aq). Let the solubility be represented by 's'. This means that for every mole of Ag₃PO₄ dissolved, 3 moles of Ag+ and 1 mole of PO₄³⁻ are formed.

The equilibrium constant for the reaction, Ksp, is given by the expression: Ksp = [Ag⁺]³[PO₄³⁻]. Since 3 moles of Ag+ are produced per mole of Ag₃PO₄, [Ag+] = 3s, and [PO₄³⁻] = s. So, Ksp = (3s)³(s).

The Ksp for Ag₃PO₄ is 2.8 x 10⁻¹⁸. Solving for 's' (solubility in mol/L), we get s ≈ 1.2 x 10⁻⁵ mol/L. To convert this to g/L, multiply by the molar mass of Ag₃PO₄ (418.58 g/mol): (1.2 x 10⁻⁵ mol/L) x (418.58 g/mol) ≈ 6.4 x 10⁻⁴g/L.

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The order of solubility in water for the compounds is: c. monoacylglycerol > b. diacylglycerol > a. triacylglycerol. Monoacylglycerol is the most soluble, followed by diacylglycerol, and then triacylglycerol.

The solubility of these acylglycerols in water is determined by their polar and nonpolar regions. Each of the compounds contains palmitic acid, which is a long hydrophobic hydrocarbon chain. However, they also have hydrophilic regions due to the presence of glycerol and ester linkages.

Monoacylglycerol has the highest solubility because it has one palmitic acid chain and more hydrophilic regions, making it more compatible with water. Diacylglycerol, having two palmitic acid chains, has a higher hydrophobic character but still maintains some solubility due to its hydrophilic regions.

Triacylglycerol, with three palmitic acid chains, has the least solubility because its nonpolar regions dominate, making it more hydrophobic and less likely to dissolve in water.

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The balanced equation for the formation of one mole of NO2(g) from its elements in their standard states is:

N2(g) + 2O2(g) → 2NO2(g)

To balance the equation, we first need to ensure that the number of atoms of each element is the same on both sides of the equation. There are two nitrogen atoms and four oxygen atoms on the right-hand side, so we need to balance the equation by multiplying N2(g) by 1 and O2(g) by 2:

This equation shows that one mole of NO2 gas can be formed from one mole of N2 gas and two moles of O2 gas. All of the species in the equation are in the gas phase. The formation of NO2 is an exothermic reaction, meaning that it releases energy as heat. The balanced equation is an important tool for understanding the stoichiometry of chemical reactions and can be used to determine the amount of reactants or products needed or produced in a reaction.

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Barium hydroxide (Ba(OH)₂) is a base that disassociates wholly in water to form Ba²⁺ and OH⁻ ions.

Ba(OH)₂(s) → Ba²⁺(aq) + 2OH⁻(aq)

To find the pH, pOH, [H⁺], and [OH⁻] of the resulting solution, we need to first find the concentration of hydroxide ions ([OH⁻]) in the solution, which can be calculated using the stoichiometry of the reaction and the molarity of the solution:

moles of Ba(OH)₂ = mass / molar mass

moles of Ba(OH)₂ = 7.6 g / (137.33 g/mol + 2(16.00 g/mol))

moles of Ba(OH)₂ = 0.0321 mol

molarity of Ba(OH)₂ solution = moles / volume

molarity of Ba(OH)₂ solution = 0.0321 mol / 3 L

molarity of Ba(OH)₂ solution = 0.0107 M

Since each molecule of Ba(OH)₂ produces two hydroxide ions when it dissociates, the concentration of hydroxide ions in the solution is twice the molarity of the Ba(OH)₂ solution:

[OH⁻] = 2 × 0.0107 M

[OH⁻] = 0.0214 M

We can now use the concentration of hydroxide ions to find the pOH:

pOH = -㏒[OH⁻]

pOH = -㏒(0.0214)

pOH = 1.67

The pH of the solution can be found using the equation:

pH + pOH = 14

pH = 14 - pOH

pH = 14 - 1.67

pH = 12.33

Finally, we can use the equation:

pH = -㏒[H⁺]

to find the concentration of hydrogen ions in the solution:

[H+] = 10^(-pH)

[H+] = 10 ^ -12.33

[H+] = 4.47 × 10⁻¹³ M

So the pH of the solution is 12.33, the pOH is 1.67, the [H⁺] is 4.47 × 10⁻¹³M, and the [OH⁻] is 0.0214 M.

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For a first-order reaction, the rate law is denoted as: Rate = k[A]; here k is known as the rate constant and [A] is called as the concentration of the reactant.

For a first-order reaction, the concentration of the reactant decreases exponentially with time:

[A] = [A]₀[tex]e^{-kt}[/tex]

where [A]₀ is the initial concentration of the reactant at t = 0.

The half-life ([tex]t_{1/2}[/tex]) of a first-order reaction is the time it takes for the concentration of the reactant to decrease to half its initial value. Therefore, at t = [tex]t_{1/2}[/tex], [A] = [A]₀/2.

Substituting [A] = [A]₀/2 and t =  [tex]t_{1/2}[/tex], into the equation for a first-order reaction gives:

[A]₀/2 = [A]₀[tex]e^{-k*t_{1/2} }[/tex]

Simplifying the above equation, we get:

1/2 = [tex]e^{-k*t_{1/2} }[/tex]

The next step is taking the natural logarithm (㏑):

㏑(1/2) = -k* [tex]t_{1/2}[/tex]

Simplifying further, we get:

[tex]t_{1/2}[/tex] = (㏑2)/k

Therefore, the expression that relates the rate constant to the half-life  for a first-order reaction is:

k = (㏑ 2)/ [tex]t_{1/2}[/tex]

This equation shows that the rate constant is inversely proportional to the half-life of the reaction, meaning that a shorter half-life corresponds to a faster rate of reaction (larger value of k).

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The right response is 8900 kg. Density is measured in kilogrammes per cubic metres (SI), grammes per millilitres, or grammes per cubic centimetres. Newton units of force. Copper has a density of 8.83 g cm 3 in C.G.S. Copper has a density of 8.96 g/cm³.  

1.074g/mL * 1kg/1000g * 1mL/1cm³ * [100cm/1m].

= 1074 kg/m³.

Here, you'll employ two conversion factors, one of which will let you move from grammes to kilogrammes. Each atom of copper contains one conduction electron. It has an atomic mass of 63.54 g/mol and a density of 8.89 g/m3. It has a density that is 8.4 times greater than that of water. force has a density of 1 gm/cc, while copper has a density of 8.4 gm/cc. Therefore, copper has a relative density of 8.4.

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a. Glcα(1 → 4)Glc: reducing sugar

b. Glc α (1 → 1)Glc α Glcα(1 → 1)Glcα: nonreducing sugar

c. Glc α (1 → 2)Fruc β Glcα(1 → 2)Frucβ: reducing sugar

d. Glc β (1 → 6)GlcGlcβ(1 → 6)Glc: reducing sugar

e. Gal β (1 → 4)GlcGalβ(1 → 4)Glc: reducing sugar

A. Glcα(1 → 4)Glc: This disaccharide has a free anomeric carbon on each glucose molecule, so it is a reducing sugar.

B. Glc α (1 → 1)Glc α Glcα(1 → 1)Glcα: In this case, both anomeric carbons are involved in the glycosidic bond, making this a nonreducing sugar.

C. Glc α (1 → 2)Fruc β Glcα(1 → 2)Frucβ: This disaccharide has one free anomeric carbon on the glucose molecule, making it a reducing sugar.

D. Glc β (1 → 6)GlcGlcβ(1 → 6)Glc: Similar to A, this disaccharide has a free anomeric carbon on each glucose molecule, making it a reducing sugar.

E. Gal β (1 → 4)GlcGalβ(1 → 4)Glc: This disaccharide has free anomeric carbons on both the galactose and glucose molecules, making it a reducing sugar.

In summary, disaccharides A, C, D, and E are reducing sugars, while disaccharide B is a nonreducing sugar based on their reaction with Fehling's solution.

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The molar solubility of barium fluoride (BaF2) in a liquid or solution can be calculated using the Ksp value. So, the molar solubility of barium fluoride in the liquid or solution is approximately 1.83×10^-2 M.

The equation for the Ksp of BaF2
Ksp = [Ba2+][F-]^2
where [Ba2+] is the molar concentration of Ba2+ ions and [F-] is the molar concentration of F- ions in the solution.
To calculate the molar solubility of BaF2 in a liquid or solution, we need to determine the maximum concentration of Ba2+ and F- ions that can exist in equilibrium with solid BaF2 at a given temperature. This maximum concentration is the molar solubility of BaF2 in that liquid or solution.
For example, let's calculate the molar solubility of BaF2 in pure water at room temperature (25°C). From the K s p equation, we know that:
K s p = 2.45×10−5 = [Ba2+][F-]^2
Assuming that the initial concentration of Ba2+ and F- ions in pure water is zero, we can let x be the molar solubility BaF2. Then, we have:
Ksp = [Ba2+][F-]^2 = (x)(2x)^2 = 4x^3
Solving for x, we get:
x = (Ksp/4)^(1/3) = (2.45×10−5/4)^(1/3) = 0.0089 M
Therefore, the molar solubility of BaF2 in pure water at room temperature is 0.0089 M.

We can similarly calculate the molar solubility of BaF2 in other liquids or solutions by using the same method and plugging in the appropriate Ksp value.
To calculate the molar solubility of barium fluoride in a liquid or solution, you'll need to use the Ksp (solubility product constant) value provided (2.45×10^-5). Here's a step-by-step explanation:
1. Write the balanced dissociation equation for barium fluoride:
  BaF2(s) ↔ Ba^2+(aq) + 2F^-(aq)
2. Set up the solubility equilibrium expression using Ksp:
  Ksp = [Ba^2+][F^-]^2
3. Define the molar solubility (x) of barium fluoride in the liquid or solution:
  [Ba^2+] = x, [F^-] = 2x
4. Substitute the molar solubility values into the Ksp expression:
  2.45×10^-5 = (x)(2x)^2
5. Solve for x (molar solubility):
  2.45×10^-5 = 4x^3
  x^3 = (2.45×10^-5)/4
  x^3 = 6.125×10^-6
  x = (6.125×10^-6)^(1/3)
  x ≈ 1.83×10^-2 M
So, the molar solubility of barium fluoride in the liquid or solution is approximately 1.83×10^-2 M.

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The volume of an ideal gas at 6.97 atm and 493 K when 89.5 mol is present is 519.46 L.

The equation of state for a fictitious perfect gas is known as the ideal gas law, sometimes known as the generic gas equation. It is a good estimate of how many gases behave under various circumstances.

Using the ideal gas law equation, we can calculate the volume of the gas:

PV = nRT

where P = 6.97 atm, n = 89.5 mol, R = 0.082057 L⋅atm mol⋅K, and T = 493 K.

Substituting these values into the equation, we get:

V = (nRT) / P
V = (89.5 mol) x (0.082057 L⋅atmmol⋅K) x (493 K) / 6.97 atm
V = 519.46 L

Therefore, the volume of the gas is 519.46 L.

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Answer:

The atomic number  of Au is 79.

Therefore, its configuration is:

1s²2s²2p⁶3s²3p⁶3d¹⁰4s²4p⁶4d1

¹⁰5s²5p⁶4f¹⁴5d¹⁰6s¹ or [Xe]4f¹⁴5d¹⁰6s¹

AgI(s) dissolution has an equilibrium constant of 0.436.

The cell's half-reactions are as follows:

[tex]Ag+(aq) + e- = Ag(s) (reduction)Ag+(aq) + I-(aq) = AgI(s). (oxidation)[/tex]

The two half-reactions can be added to produce the total reaction:

[tex]2Ag+(aq) + I- = Ag(s) + AgI(s).(aq)[/tex]

The reaction's typical potential is:

[tex]E° is equal to E°(cathode) - E°(anode) = 0 - (+0.9509 V) = -0.9509 V.[/tex]

The equilibrium constant for the reaction and the standard potential are related by the Nernst equation:

[tex]E = (RT/nF) ln - E°(Q)[/tex]

where: E = the cell potential under abnormal circumstances

R = 8.314 J/mol K, the gas constant.

Temperature is T. (in Kelvin)

n is the number of electron moles transported in the equation for balancing.

96485 C/mol is the Faraday constant, or F.

Reaction quotient is Q.

The reaction quotient Q and the equilibrium constant K are equal at equilibrium:

[tex]Q is equal to [Ag+]2[I-]/[AgI] = K.[/tex]

The standard potential and the reaction quotient can be used to calculate the cell potential under non-standard conditions:

[tex]E = (RT/nF) ln - E°(K)[/tex]

Changing the values:

E = 0.9509 V - 8.314 J/mol K (298 K)/(2 mol96485 C/mol) ln(K)

Simplifying:

ln(K) is equal to (2,96485 C/mol/8,314 J/mol K)(-E + E°) = -0.8265 V.

The exponential of both sides is as follows:

[tex]K = e^(-0.8265) = 0.436[/tex]

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AgI(s) dissolution has an equilibrium constant of 0.436.

The cell's half-reactions are as follows:

[tex]Ag+(aq) + e- = Ag(s) (reduction)Ag+(aq) + I-(aq) = AgI(s). (oxidation)[/tex]

The two half-reactions can be added to produce the total reaction:

[tex]2Ag+(aq) + I- = Ag(s) + AgI(s).(aq)[/tex]

The reaction's typical potential is:

[tex]E° is equal to E°(cathode) - E°(anode) = 0 - (+0.9509 V) = -0.9509 V.[/tex]

The equilibrium constant for the reaction and the standard potential are related by the Nernst equation:

[tex]E = (RT/nF) ln - E°(Q)[/tex]

where: E = the cell potential under abnormal circumstances

R = 8.314 J/mol K, the gas constant.

Temperature is T. (in Kelvin)

n is the number of electron moles transported in the equation for balancing.

96485 C/mol is the Faraday constant, or F.

Reaction quotient is Q.

The reaction quotient Q and the equilibrium constant K are equal at equilibrium:

[tex]Q is equal to [Ag+]2[I-]/[AgI] = K.[/tex]

The standard potential and the reaction quotient can be used to calculate the cell potential under non-standard conditions:

[tex]E = (RT/nF) ln - E°(K)[/tex]

Changing the values:

E = 0.9509 V - 8.314 J/mol K (298 K)/(2 mol96485 C/mol) ln(K)

Simplifying:

ln(K) is equal to (2,96485 C/mol/8,314 J/mol K)(-E + E°) = -0.8265 V.

The exponential of both sides is as follows:

[tex]K = e^(-0.8265) = 0.436[/tex]

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