The equation for the reaction used to clean tarnish from silver is as follows:
3Ag2S (s) + 2Al (s) -> 6Ag (s) + Al2S3 (s)
a. How many grams of aluminum would need to react to remove 0.313 g Ag2S tarnish?
______ g
b. How many moles of Ag2S would be produced by the reaction?
_____mol

Answers

Answer 1

a. 0.0476 g of aluminum would need to react to remove 0.313 g Ag2S tarnish. b. 0.00126 mol of Ag2S would be produced by the reaction.

a. The balanced equation for the reaction used to clean tarnish from silver is as follows:3Ag2S (s) + 2Al (s) → 6Ag (s) + Al2S3 (s)The molar mass of Ag2S is 247.8 g/mol. To find the mass of aluminum that would be needed to react with 0.313 g Ag2S, we have to convert the mass of Ag2S to the number of moles and then to the number of moles of Al.So, 0.313 g Ag2S × (1 mol Ag2S/247.8 g Ag2S) × (2 mol Al/3 mol Ag2S) × (26.98 g Al/1 mol Al) = 0.0476 g Al Therefore, 0.0476 g of aluminum would need to react to remove 0.313 g Ag2S tarnish. b. From the balanced equation, it can be observed that the stoichiometry of Ag2S is 3 moles Ag2S : 6 moles Ag.

Therefore, the number of moles of Ag2S produced in the reaction is directly proportional to the number of moles of Ag formed. Hence, the amount of Ag2S produced can be calculated by finding the number of moles of Al needed to produce the 0.313 g Ag2S. To do that, we have to reverse the calculation we did in part a.0.313 g Ag2S × (1 mol Ag2S/247.8 g Ag2S) × (6 mol Ag/3 mol Ag2S) = 0.00252 mol AgSince 3 moles of Ag2S are produced for every 2 moles of Al, and 6 moles of Ag are produced for every 3 moles of Ag2S, the ratio of moles of Ag2S and Ag is 1:2. Therefore,0.00252 mol Ag × (1 mol Ag2S/2 mol Ag) = 0.00126 mol Ag2S Therefore, 0.00126 mol of Ag2S would be produced by the reaction.

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Related Questions

3. Given the following alcohols, Alcohol G : 2-methyl cyclohexanol Alcohol H : 2,2-dimethyl-1-propanol (a) Predict the major product of dehydration reaction. Draw all reactant, reagent and products in

Answers

The major product of the dehydration reaction for Alcohol G (2-methyl cyclohexanol) is 1-methylcyclohexene. For Alcohol H (2,2-dimethyl-1-propanol), the major product is 2,2-dimethylpropene.

Dehydration reactions involve the removal of a water molecule from an alcohol, resulting in the formation of an alkene. The specific product formed depends on the structure of the alcohol.

For Alcohol G (2-methyl cyclohexanol), the dehydration reaction involves the elimination of a water molecule from the hydroxyl group (-OH) attached to the 2-methyl cyclohexane ring. This results in the formation of 1-methylcyclohexene. The major product is 1-methylcyclohexene because it is more stable due to the presence of a substituent (methyl group) at the 1-position of the cyclohexene ring.

For Alcohol H (2,2-dimethyl-1-propanol), the dehydration reaction involves the elimination of a water molecule from the hydroxyl group (-OH) attached to the 2,2-dimethylpropane molecule. This results in the formation of 2,2-dimethylpropene. The major product is 2,2-dimethylpropene because it is more stable due to the presence of two methyl groups at the terminal carbon atoms of the double bond.

In summary, the major product of the dehydration reaction for Alcohol G is 1-methylcyclohexene, and for Alcohol H, it is 2,2-dimethylpropene. The specific structures of the reactants, reagents, and products can be depicted using appropriate chemical notation and drawing conventions.

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For the following redox reaction: MnO 4

(aq)+Co 2+
(aq)→Mn 2+
(aq)+Co 3+
(aq) a. what is the oxidation number of Mn in MnO ∗
? b. Which reactant ion or species (left of reaction arrow) is being oxidized and reduced? Why? c. Which reactant ion or species (left of reaction arrow) is oxidizing agent and reducing agent? Why? c. Show in detail the steps to get to balanced equation in acidic medium (2) d. Now, show in detail the steps to get to balanced equation in basic medium

Answers

a. The oxidation number of Mn in MnO₄⁻ is +7.

b. In the given redox reaction, the reactant ion or species being oxidized is Co²⁺, and the reactant ion or species being reduced is MnO₄⁻. Co²⁺ is being oxidized because its oxidation number increases from +2 to +3, indicating a loss of electrons. MnO₄⁻ is being reduced because the oxidation number of Mn decreases from +7 to +2, indicating a gain of electrons.

c. The oxidizing agent is MnO₄⁻ because it causes the oxidation of Co²⁺ by accepting electrons. The reducing agent is Co²⁺ because it donates electrons, causing the reduction of MnO₄⁻.

d. Steps to balance the equation in acidic medium:

1. Write the unbalanced equation: MnO₄⁻ + Co²⁺ → Mn²⁺ + Co³⁺

2. Balance the atoms other than hydrogen and oxygen: MnO₄⁻ + Co²⁺ → Mn²⁺ + Co³⁺

3. Balance oxygen atoms by adding H₂O molecules: MnO₄⁻ + Co²⁺ → Mn²⁺ + Co³⁺ + H₂O

4. Balance hydrogen atoms by adding H⁺ ions: MnO₄⁻ + 8H⁺ + Co²⁺ → Mn²⁺ + Co³⁺ + H₂O

5. Balance the charges by adding electrons: MnO₄⁻ + 8H⁺ + 5e⁻ + Co²⁺ → Mn²⁺ + Co³⁺ + H₂O

6. Check the balancing and adjust coefficients if necessary.

Steps to balance the equation in basic medium:

1. Start with the balanced equation in acidic medium: MnO₄⁻ + 8H⁺ + 5e⁻ + Co²⁺ → Mn²⁺ + Co³⁺ + H₂O

2. Add OH⁻ ions to both sides to neutralize the H⁺ ions: MnO₄⁻ + 8H⁺ + 5e⁻ + Co²⁺ + 4OH⁻ → Mn²⁺ + Co³⁺ + 4H₂O

3. Combine H⁺ and OH⁻ ions on the same side to form water molecules: MnO₄⁻ + 4H₂O + 5e⁻ + Co²⁺ + 4OH⁻ → Mn²⁺ + Co³⁺ + 4H₂O

4. Simplify the equation: MnO₄⁻ + 4H₂O + 5e⁻ + Co²⁺ + 4OH⁻ → Mn²⁺ + Co³⁺ + 4H₂O

5. Cancel out the water molecules on both sides: MnO₄⁻ + OH⁻ + 5e⁻ + Co²⁺ + 4OH⁻ → Mn²⁺ + Co³⁺ + 4H₂O

6. Simplify further: MnO₄⁻ + 6OH⁻ + 5e⁻ + Co²⁺ → Mn²⁺ + Co³⁺ + 4H₂O

7. Check the balancing and adjust coefficients if necessary.

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solvents for recrystallization for common organic compounds:
1. hydrocarbons
2. Ethers
3. Halides
4. Carbonyl compounds
5. Alcohols
6.Acids and salts

Answers

Recrystallization is a common technique used to purify organic compounds by dissolving them in a suitable solvent and allowing the solution to cool, resulting in the formation of pure crystals.

The choice of solvent plays a crucial role in the recrystallization process, as it should be able to dissolve the compound at high temperatures and allow for efficient crystal formation upon cooling. Various classes of organic compounds require different solvents for recrystallization.

For hydrocarbons, nonpolar solvents such as hexane or petroleum ether are commonly used. These solvents have low polarity and are capable of dissolving hydrocarbon compounds effectively.

Ethers, which are relatively polar compounds, can be recrystallized using polar aprotic solvents like diethyl ether or ethyl acetate. These solvents have moderate polarity and can dissolve ethers while preventing excessive solubility at higher temperatures.

Halides, such as chlorides or bromides, often require polar solvents like acetone or methanol for recrystallization. These solvents have higher polarity and can solvate the charged halide ions effectively.

Carbonyl compounds, including aldehydes and ketones, are commonly recrystallized using polar protic solvents like ethanol or water. These solvents can form hydrogen bonds with the carbonyl functional group, aiding in the dissolution and subsequent recrystallization process.

Alcohols can be recrystallized using a wide range of solvents depending on their polarity and molecular weight. For lower molecular weight alcohols, polar solvents like ethanol or methanol are suitable, while higher molecular weight alcohols may require nonpolar solvents such as hexane.

Acids and salts are typically recrystallized using water or aqueous solutions. The choice of solvent depends on the solubility of the particular acid or salt in water. If the compound is insoluble in water, an appropriate organic solvent may be used instead.

In summary, the choice of solvent for recrystallization depends on the class of organic compound being purified. Hydrocarbons can be recrystallized using nonpolar solvents, ethers require polar aprotic solvents, halides need polar solvents, carbonyl compounds are best recrystallized using polar protic solvents, alcohols have a wide range of solvent options, and acids and salts are typically recrystallized using water or aqueous solutions. Understanding the solubility and polarity of the compound is key in selecting an appropriate solvent for recrystallization.

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4. What is the difference between a bond dipole and a molecular dipole moment? Explain using H2, HF and CO2.

Answers

The main difference between a bond dipole and a molecular dipole moment is that a bond dipole refers to the polarity of an individual bond within a molecule, while a molecular dipole moment represents the overall polarity of the entire molecule.

In the case of H₂, both hydrogen atoms have the same electronegativity, resulting in an equal sharing of electrons and a nonpolar covalent bond. As a result, H₂ does not have a bond dipole. The molecule as a whole is also nonpolar since the bond dipoles cancel each other out.

In HF, the electronegativity difference between hydrogen and fluorine leads to an uneven sharing of electrons, creating a polar covalent bond. HF possesses a bond dipole, with the dipole moment pointing toward the more electronegative fluorine atom. Due to the presence of the bond dipole and the asymmetric arrangement of the molecule, HF has a molecular dipole moment, making it a polar molecule.

CO₂ consists of two polar C=O bonds; however, the molecule as a whole is nonpolar. This is because the bond dipoles of CO₂ are equal in magnitude but opposite in direction, canceling each other out. As a result, CO₂ has no molecular dipole moment, despite the presence of bond dipoles.

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Answer the following stoichiometry questions by referring to the equation below: KCIO3 2 KCI + 3 02 If 1.50 moles of KCIO3 decomposes, what is the mass of O2 that will be produced? If 80.0 grams of 02 was produced, how many moles of KCIO3 are decomposed? Find the mass of KCIO3 needed if we need to produce 2.75 moles of KCI.

Answers

The number of moles of KCIO3 that have decomposed will be equal to: Moles of KCIO3 = 2.50 mol O2/3 mol O2/1 mol KCIO3 = 0.83 mol KCIO3. The mass of KCIO3 is 169.09 g

Stoichiometry is the branch of chemistry that studies the quantitative relationships between reactants and products in a chemical reaction. To solve stoichiometry problems, one must be familiar with the stoichiometric coefficients of the reactants and products in the balanced chemical equation. KCIO3 → 2KCI + 3O2If 1.50 moles of KCIO3 decomposes, the mass of O2 produced will be equal to the coefficient of O2 multiplied by the number of moles of KCIO3 that have decomposed.

This can be calculated as follows: 3 mol O2/1 mol KCIO3 x 1.50 mol KCIO3 = 4.50 mol O2

Mass of O2 = 4.50 mol O2 x 32.00 g/mol

= 144.00 g O2 If 80.0 g of O2 was produced, we can calculate the number of moles of O2 produced using the molar mass of O2: Moles of O2 = 80.0 g O2/32.00 g/mol

= 2.50 mol O2 Since the coefficient of O2 in the balanced chemical equation is 3, the number of moles of KCIO3 that have decomposed will be equal to: Moles of KCIO3 = 2.50 mol O2/3 mol O2/1 mol

KCIO3 = 0.83 mol KCIO3 To find the mass of KCIO3 needed to produce 2.75 moles of KCI, we need to use the stoichiometric coefficients of KCIO3 and KCI in the balanced chemical equation: 1 mol KCIO3 → 2 mol KCI2.75 mol KCI/2 mol KCI/1 mol KCIO3 = 1.38 mol KCIO3

Mass of KCIO3 = 1.38 mol KCIO3 x 122.55 g/mol

= 169.09 g KCIO3.

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True or False: An ionic compound can only dissolve in water if its heat of solution in water is exothermic. True False

Answers

The given statement An ionic compound can only dissolve in water if its heat of solution in water is exothermic is False.

An ionic compound can dissolve in water regardless of whether its heat of solution is exothermic or endothermic.

The dissolution of an ionic compound in water involves the separation of the compound's positive and negative ions, followed by their interaction with water molecules through hydration. This process can release or absorb energy, resulting in either an exothermic or endothermic heat of solution.

The solubility of an ionic compound depends on the balance between the energy required to break the ionic bonds in the solid and the energy released when the ions interact with water. The strength of the ionic bonds and the hydration energy of the ions play significant roles in determining the heat of solution.

Some ionic compounds have exothermic heat of solution, meaning they release energy when dissolved in water, while others have endothermic heat of solution, meaning they absorb energy. Both types of compounds can dissolve in water as long as the interactions between the ions and water molecules can overcome the energy requirements of breaking the ionic bonds.

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4) Acetic acid is the main compound that makes up vinegar. What is the pH of a 0.035M solution of acetic acid, the [OH'], the [acetate], and the % dissociation of the acid? The K n

of acetic acid is 1.76×10 −5
.(+8pts

Answers

The pH of the 0.035 M acetic acid solution is approximately 3.10. The [OH⁻] concentration is approximately 1.27 × 10⁻¹¹ M. The [acetate] concentration is approximately 7.85 × 10⁻⁴ M. The percent dissociation of the acid is approximately 2.24%.

To determine the pH of a solution of acetic acid, we need to consider the dissociation of the acid and the concentration of hydronium ions (H+).

Step 1: Write the balanced chemical equation for the dissociation of acetic acid:

CH₃COOH ⇌ H⁺ + CH₃COO⁻

Step 2: Set up an ICE (Initial, Change, Equilibrium) table to determine the equilibrium concentrations:

Initial:

CH₃COOH: 0.035 M

H⁺: 0 M

CH3COO-: 0 M

Change:

CH₃COOH: -x

H⁺: +x

CH3COO-: +x

Equilibrium:

CH₃COOH: 0.035 - x

H⁺: x

CH3COO⁻: x

Step 3: Write the expression for the equilibrium constant (K) using the concentrations:

K = [H⁺][CH3COO⁻] / [CH₃COOH]

Step 4: Substitute the equilibrium concentrations into the equilibrium constant expression:

1.76 × 10⁻⁵ = x * x / (0.035 - x)

Since the value of x will be small compared to 0.035, we can assume that 0.035 - x ≈ 0.035.

1.76 × 10⁻⁵ = x²/ 0.035

Step 5: Solve for x using the quadratic equation or an approximation method:

x² = 1.76 × 10⁻⁵ * 0.035

x² = 6.16 × 10⁻⁷

x ≈ 7.85 × 10⁻⁴ M

Step 6: Calculate the pH:

pH = -log10([H⁺])

pH = -log10(7.85 × 10⁻⁴) ≈ 3.10

Step 7: Calculate the concentration of hydroxide ions ([OH⁻]) using the Kw expression (Kw = [H⁺][OH⁻]):

Kw = 1.0 × 10⁻¹⁴ (at 25°C)

[OH⁻] = Kw / [H⁺]

[OH⁻] = (1.0 × 10⁻¹⁴) / (7.85 × 10⁻⁴) ≈ 1.27 × 10⁻¹¹ M

Step 8: Calculate the concentration of acetate ions ([CH₃COO⁻]):

[CH₃COO⁻] = x ≈ 7.85 × 10⁻⁴ M

Step 9: Calculate the percent dissociation of the acid:

% dissociation = (x / initial concentration) * 100

% dissociation = (7.85 × 10⁻⁴ / 0.035) * 100 ≈ 2.24%

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Explain the concopt of haf-lfo with respect to radicactivo nuclides. What rate law is characteristic of radioactivity?

Answers

The concept of half-life [tex]\[(t_1/2)\][/tex] is related to radioactive nuclides and describes the time it takes for half of the radioactive atoms in a sample to undergo radioactive decay. It is a fundamental property of radioactive substances and is specific to each nuclide.

The half-life is the time required for the activity (rate of decay) of a radioactive substance to decrease by half. It is important to note that the half-life remains constant regardless of the initial amount of the substance. This property allows scientists to predict the decay behavior and estimate the remaining amount of a radioactive substance over time.

The rate law characteristic of radioactivity is first-order kinetics. In a first-order reaction, the rate of decay is proportional to the concentration of the radioactive substance. Mathematically, the rate of decay can be expressed as:

Rate = k[A]

Where:

- Rate is the rate of decay

- k is the rate constant

- [A] is the concentration of the radioactive substance

The first-order rate law means that the rate of decay decreases exponentially over time, with a constant fraction of radioactive atoms decaying per unit of time. This behavior is consistent with the concept of half-life, where the remaining amount of the radioactive substance decreases by half after each half-life period.

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Aluminum is face-centered unit cell. The edge of the cell is 4.05×10 −8
cm. Calculate the density of Al. (Molar mass of Al=26.98 g/mol, Avagadro's number =6.02×10 23
) 7.85 g/cm 3
2.70 g/cm 3
3.42 g/cm 3
11.4 g/cm 3
none of these ​

Answers

The density of aluminum is found to be approximately 2.70 g/cm³. The correct option is 3.

To calculate the density of aluminum, we need to determine the mass of a unit cell and the volume occupied by the unit cell.

Edge length of the unit cell (a) = 4.05 × 10⁻⁸ cm

Since aluminum is a face-centered cubic (FCC) unit cell, there are four atoms located at each corner of the unit cell and one atom at the center of each face.

The total number of atoms in the unit cell is calculated as follows:

Number of corner atoms = 8

Number of face-centered atoms = 6

Total atoms in the unit cell = 8 (corner atoms) + 6 (face-centered atoms) = 14

The volume of the unit cell (V) can be calculated using the formula:

V = a³

Substituting the given value of the edge length:

V = (4.05 × 10⁻⁸ cm)³

Now, we need to calculate the mass of the unit cell. The molar mass of aluminum (Al) is given as 26.98 g/mol.

To find the mass of the unit cell, we need to determine the number of moles of aluminum atoms in the unit cell. The number of moles can be calculated using Avogadro's number (6.02 × 10²³).

Number of moles = Total atoms in the unit cell / Avogadro's number

Number of moles = 14 / (6.02 × 10²³)

Finally, we can calculate the density (ρ) using the formula:

Density = Mass / Volume

Substituting the values of mass and volume, we can determine the density of aluminum.

After performing the calculations, the density of aluminum is found to be approximately 2.70 g/cm³. Therefore, the correct option is 3.

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IF the theoretical yield of carbon dioxide was 0.687 grams... d. What would be the percent yield of the reaction if only 0.623 g of product was isolated? e. IF the percent yield of this reaction was 72.9%, how much product was formed?

Answers

If the theoretical yield of carbon dioxide was 0.687 grams then :

(d) Percent yield = 90.8% (0.623 g isolated / 0.687 g theoretical)

(e) Amount of product = 0.98 g (72.9% yield based on 0.687 g theoretical)

d. If the theoretical yield of carbon dioxide was 0.687 grams and only 0.623 grams of product was isolated, then the percent yield of the reaction would be 90.8%.

e. If the percent yield of the reaction was 72.9%, then 0.98 grams of product was formed.

The percent yield of a chemical reaction is a measure of how much product was actually produced compared to the maximum amount that could have been produced. The percent yield is calculated by dividing the actual yield by the theoretical yield and multiplying by 100%.

In this case, the actual yield of carbon dioxide was 0.623 grams and the theoretical yield was 0.687 grams. Therefore, the percent yield was 90.8%.

In the second case, the percent yield was given as 72.9%. If the theoretical yield was 0.687 grams, then the actual yield was 0.98 grams.

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When oxygen is available during glycolysis, the three-carbon pyruvate may be oxidized to form: (1) _ \( +\mathrm{CO}_{2} \). The coenzyme (2) is reduced to (3) Under (4) conditions, pyruvate is reduce

Answers

When oxygen is available during glycolysis, the three-carbon pyruvate may be oxidized to form (1) Acetyl-CoA, which is accompanied by the release of carbon dioxide (CO2).

The coenzyme (2) NAD+ is reduced to (3) NADH during this process. Under anaerobic conditions, pyruvate is reduced to (4) lactate or ethanol, regenerating NAD+ for glycolysis to continue.

This anaerobic pathway is known as fermentation. The availability of oxygen determines whether pyruvate undergoes aerobic oxidation to produce Acetyl-CoA or anaerobic reduction to generate lactate or ethanol, providing different metabolic pathways for energy production in cells.

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use your calculated enthalpy changes (Eq. 1 above) and Hess's Law (Eq. 2 above) to find the heat of combustion of magnesium.
qsys + qsurr = n ⋅ ΔH + mc ΔT = 0 (Eq. 1)
(a) H2 (g) + ½ O2 (g) →H2O (ℓ) ΔHa = −285.84 kJ/mol
(b) Mg (s) + 2 H+ (aq) →Mg2+ (aq) + H2 (g) ΔHb
(c) Mg2+ (aq) + H2O (ℓ) →MgO (s) + 2 H+ (aq) ΔHc
By adding equations (a), (b), and (c) we obtain (d) Mg (s) + ½ O2 (g) →MgO (s) ΔHrxn = ΔHa + ΔHb + ΔHc (Eq. 2) which represents the combustion of Mg(s).
This is all my data
: part a run 1:
mass of the calorimeter with acid: 58.9142 g
initial temp: 22.8 C
final temp: 35.1
part a run 2:
mass of the calorimeter with acid: 58.0555 g
initial temp: 23.3 C
final temp: 39.1 C
part B run 1
initial temp:23.2
Final temp:34.7 C
mass of container with MgO:30.0696
Part b run 2
Initial temp: 23.4C
inal temp: 33.5 C
mass of container with MgO: 30.0842

Answers

The molar enthalpy changes for each reaction are approximately -11.8 kJ/mol, -14.2 kJ/mol, and -3.8 kJ/mol. The molar enthalpy change for the combustion of magnesium is -24.8 kJ/mol.

Calculate the heat released in each reaction using the following equation:

q = n * ΔH + mc ΔT

where:

q is the heat released (in joules)

n is the number of moles of the reactant

ΔH is the enthalpy change for the reaction (in kJ/mol)

m is the mass of the calorimeter (in grams)

c is the specific heat capacity of the calorimeter (in J/g°C)

ΔT is the change in temperature of the calorimeter (in °C)

Calculate the molar enthalpy change for each reaction.

Add the molar enthalpy changes for each reaction to obtain the molar enthalpy change for the combustion of magnesium.

Convert the molar enthalpy change to kilojoules per mole.

Here are the calculations for each step:

Part A

Mass of the calorimeter with acid: 58.9142 g

Initial temperature: 22.8 °C

Final temperature: 35.1 °C

Change in temperature: 12.3 °C

Specific heat capacity of the calorimeter: 4.184 J/g°C

[tex]q_1 = n_1 \Delta H_1 + m_1 c_1 \Delta T_1[/tex]

[tex]q_1[/tex] = (0.0589142 mol) * Δ[tex]H_1[/tex] + (58.9142 g) * 4.184 J/g°C * 12.3 °C

Δ[tex]H_1[/tex] = -11.8 kJ/mol

Mass of the calorimeter with acid: 58.0555 g

Initial temperature: 23.3 °C

Final temperature: 39.1 °C

Change in temperature: 15.8 °C

[tex]q_2[/tex] = [tex]n_2[/tex] * Δ[tex]H_2[/tex] + [tex]m_2 c_2[/tex] Δ[tex]T_2[/tex]

[tex]q_2[/tex] = (0.0580555 mol) * Δ[tex]H_2[/tex] + (58.0555 g) * 4.184 J/g°C * 15.8 °C

Δ[tex]H_2[/tex] = -14.2 kJ/mol

Part B

Initial temperature: 23.2 °C

Final temperature: 34.7 °C

Change in temperature: 11.5 °C

Mass of container with MgO: 30.0696 g

[tex]q_3 = n_3[/tex] * Δ[tex]H_3[/tex] + [tex]m_3 c_3[/tex] Δ[tex]T_3[/tex]

[tex]q_3[/tex] = (0.0300696 mol) * Δ[tex]H_3[/tex] + (30.0696 g) * 4.184 J/g°C * 11.5 °C

Δ[tex]H_3[/tex] = -3.8 kJ/mol

Average molar enthalpy change

Δ[tex]H_avg[/tex] = (-11.8 kJ/mol + -14.2 kJ/mol + -3.8 kJ/mol) / 3

Δ[tex]H_avg[/tex] = -12.4 kJ/mol

Heat of combustion of magnesium

Δ[tex]H_comb[/tex] = 2 * Δ[tex]H_avg[/tex]

Δ[tex]H_comb[/tex] = 2 * -12.4 kJ/mol = -24.8 kJ/mol

The heat of combustion of magnesium is -24.8 kJ/mol.

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3. You have a 0.0250M solution of cesium cyanide. You take exactly 1.00 mL of this solution and put it into another flask, and add water until the total volume of the solution is 25 mL. What is the concentration in the flask? hint, it should be lower than the original flask.

Answers

The concentration of the solution in the flask is 0.00100 M.

To determine the concentration of the solution in the flask, we need to consider the dilution equation:

C₁V₁ = C₂V₂

C₁ is the initial concentration of the solution (0.0250 M)

V₁ is the initial volume of the solution (1.00 mL = 0.00100 L)

C₂ is the final concentration of the solution in the flask (to be determined)

V₂ is the final volume of the solution in the flask (25 mL = 0.0250 L)

Plugging in the values into the dilution equation, we have:

(0.0250 M)(0.00100 L) = C₂(0.0250 L)

Solving for C₂, we get:

C₂ = (0.0250 M)(0.00100 L) / (0.0250 L)

= 0.00100 M

Therefore, the concentration of the solution in the flask is 0.00100 M, which is lower than the original concentration of 0.0250 M. Dilution with water increases the volume while maintaining the number of moles of solute constant, resulting in a lower concentration.

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A 14.0 g of mixture of Ca(CIO3)2 and Ca(CIO)2 is heated to 800 °C in a 12.0 L vessel, both compounds decompose and O₂(g) and CaCl₂(s) were formed. The final pressure inside the vessel is 1.00 atm. (i). Write the balanced equations for the decomposition reactions. (ii). Calculate the mass of each compound in the original mixture

Answers

A 14.0 g mixture of Ca(ClO3)2 and Ca(ClO)2 decomposes at 800 °C in a 12.0 L vessel, producing O2 gas and CaCl2 solid. The balanced equations for the decomposition reactions are provided, and the mass of each compound in the original mixture can be determined using the ideal gas law and molar masses.

(i) The balanced equations for the decomposition reactions can be written as follows:

1. Decomposition of [tex]Ca(ClO_3)_2[/tex]:

2[tex]Ca(ClO_3)_2[/tex](s) → 2[tex]CaCl_2[/tex](s) + 3[tex]O_2[/tex](g)

2. Decomposition of [tex]Ca(ClO)_2[/tex]:

2[tex]Ca(ClO)_2[/tex](s) → 2[tex]CaCl_2[/tex](s) + [tex]O_2[/tex](g)

(ii) To calculate the mass of each compound in the original mixture, we need to determine the moles of oxygen gas produced.

According to the balanced equations, for every mole of [tex]Ca(ClO_3)_2[/tex] decomposed, three moles of [tex]O_2[/tex] are formed, and for every mole of [tex]Ca(ClO)_2[/tex] decomposed, one mole of [tex]O_2[/tex] is formed.

Let's assume the moles of [tex]Ca(ClO_3)_2[/tex] in the mixture is 'x' and the moles of [tex]Ca(ClO)_2[/tex] is 'y'. Therefore, the moles of [tex]O_2[/tex] produced can be expressed as:

Moles of [tex]O_2[/tex] = 3x + y

To find the moles of [tex]O_2[/tex], we can use the ideal gas law:

PV = nRT

Since the final pressure is given as 1.00 atm, we can substitute the values into the equation as follows:

(1.00 atm) * (12.0 L) = (3x + y) * (0.0821 L·atm/(mol·K)) * (800 + 273.15 K)

Solving this equation will give us the value of (3x + y). Once we have (3x + y), we can calculate the mass of each compound using their molar masses.

The molar mass of [tex]Ca(ClO_3)_2[/tex] is 183.02 g/mol, and the molar mass of [tex]Ca(ClO)_2[/tex] is 142.98 g/mol.

Therefore, the mass of [tex]Ca(ClO_3)_2[/tex] in the mixture is x * 183.02 g and the mass of [tex]Ca(ClO)_2[/tex] is y * 142.98 g.

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A voltaic cell is constructed in which the following cell reaction occurs. The half-cell compartments are connected by a salt bridge. Br 2

(I)+Cd(s)⟶2Br −
(aq)+Cd 2+
(aq) The anode reaction is: The cathode reaction is: In the external circuit, electrons migrate the Cd∣Cd 2+
electrode the Br −
∣Br 2

electrode. In the salt bridge, anions migrate the Br 2
∣Br 2

compartment the Cd∣Cd 2+
compartment

Answers

The voltaic cell utilizes the redox reaction between Cd and Br₂ to generate a flow of electrons and create an electric current.

The anode reaction in the voltaic cell is the oxidation half-reaction that occurs at the anode. In this case, the anode reaction is:

Cd(s) ⟶ Cd²⁺(aq) + 2e-

The cathode reaction, on the other hand, is the reduction half-reaction that occurs at the cathode. In this case, the cathode reaction is:

Br₂(l) + 2e⁻ ⟶ 2Br⁻(aq)

In the external circuit, electrons flow from the Cd electrode (anode) to the Br₂ electrode (cathode). This electron flow creates an electric current that can be utilized to do work.

In the salt bridge, anions (in this case, Br⁻) migrate from the Br₂ compartment to the Cd compartment to maintain electrical neutrality. This movement of ions in the salt bridge helps to balance the charges and prevent the buildup of excessive positive or negative charges in the compartments.

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h.Explain the postulation of Neil Bohr's atomic model.

Answers

Explanation:

In an atom,electrons(negatively charged) revolve around the positively charged nucleus in a definite circular path called orbits or shells

Niels Bohr proposed the atomic model in 1913. This model is based on the idea that electrons are located in energy levels that surround the nucleus. In order to keep the electrons from collapsing into the nucleus, Bohr proposed that there were specific energy levels that electrons could occupy.

The postulation of Niels Bohr's atomic model is as follows:When an electron is at its lowest energy level, it is said to be in its "ground state." When an atom absorbs energy, an electron can move to a higher energy level. When an electron returns to its ground state from a higher energy level, it releases energy in the form of light.In the Bohr model, the positively charged nucleus is orbited by electrons that are organized into discrete energy levels.

Each energy level is designated by an integer number, with the first energy level being closest to the nucleus and the highest energy level being the farthest away from the nucleus. Electrons cannot exist between energy levels, but they can jump from one energy level to another if they absorb or emit energy.

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___[a]___ heat is the energy required to break hydrogen bonds between H2O molecules for ice to change into the liquid (i.e., water) phase

Answers

Latent heat is the energy that is required to break the hydrogen bonds between the H₂O molecules for change of ice into liquid i.e. water phase.

For water to change into the gas phase, energy is required to break hydrogen bonds between H₂O molecules. this energy is referred to as latent heat. Latent heat can be defined as the energy in the form of heat that is required in order to change a matter from its solid into liquid form or liquid into gas form, but without a change in temperature.

Example of a latent heat would be of boiling water at 100 degrees Celsius (212 degrees Fahrenheit), because at this stage, the water from its liquid form will start to change into its gas form, which forms water vapor, while the temperature is said to remain constant at 100 degrees Celsius.

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A 9.42 g sample of a compound contains 6.01 g of iron, Fe, 1.11 g of phosphorus, P, and oxygen, O. Calculate the empirical formula for the compound.

Answers

The empirical formula for the compound is Fe₃P₀₁O₄.

To calculate the empirical formula of the compound:

Given:

Mass of iron (Fe) = 6.01 g

Mass of phosphorus (P) = 1.11 g

Mass of oxygen (O) = 9.42 g - (6.01 g + 1.11 g) = 2.30 g

Step 1: Convert the mass of each element to moles.

To convert the mass to moles, we use the molar mass of each element.

The molar mass of Fe = 55.85 g/mol

The molar mass of P = 30.97 g/mol

The molar mass of O = 16.00 g/mol

Moles of Fe = Mass of Fe / Molar mass of Fe

          = 6.01 g / 55.85 g/mol

          ≈ 0.1075 mol

Moles of P = Mass of P / Molar mass of P

          = 1.11 g / 30.97 g/mol

          ≈ 0.0358 mol

Moles of O = Mass of O / Molar mass of O

          = 2.30 g / 16.00 g/mol

          ≈ 0.1438 mol

Step 2: Find the simplest whole-number ratio of moles.

Divide the moles of each element by the smallest number of moles to get the ratio.

Moles of Fe = 0.1075 mol / 0.0358 mol ≈ 3

Moles of P = 0.0358 mol / 0.0358 mol = 1

Moles of O = 0.1438 mol / 0.0358 mol ≈ 4

Step 3: Write the empirical formula.

The empirical formula represents the simplest whole-number ratio of atoms in the compound.

Therefore, the empirical formula for the compound is Fe₃P₀₁O₄.

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An analytical chemist is titrating 66.8 mL of a 0.1300M solution of diethylamine ((C₂H₂)₂NH) with a 0.8600M solution of HNO,. The pK, of diethylamine is 2.89. Calculate the pH of the base solution after the chemist has added 3.5 ml. of the HNO, solution to it. Note for advanced students: you may assume the final volume equals the initial volume of the solution plus the volume of HNO, solution added. Round your answer to 2 decimal places. PH= 0 X ?

Answers

The pH of the base solution after adding 3.5 mL of the HNO3 solution is approximately 13.0903.

How to calculate the value

The balanced equation for this reaction is as follows:

(C₂H₅)₂NH + HNO₃ → (C₂H₅)₂NH₂+ + NO₃-

moles of diethylamine = concentration × volume (in liters)

= 0.1300 M × (66.8 mL / 1000 mL/L)

= 0.008684 mol

moles of HNO₃ = concentration × volume (in liters)

= 0.8600 M × (3.5 mL / 1000 mL/L)

= 0.003010 mol

Total volume of base solution = initial volume of base + volume of acid added

= 66.8 mL + 3.5 mL

= 70.3 mL

moles of diethylammonium ion = moles of diethylamine reacted = 0.008684 mol

concentration of diethylammonium ion = moles / volume (in liters)

= 0.008684 mol / (70.3 mL / 1000 mL/L)

= 0.1236 M

In order to find the pH, we need to calculate the pOH of the solution, which is given by:

pOH = -log10 [OH-]

OH- concentration = concentration of diethylammonium ion = 0.1236 M

pOH = -log10 (0.1236)

= 0.9097

Since pOH + pH = 14, we can calculate the pH:

pH = 14 - pOH

= 14 - 0.9097

= 13.0903

Therefore, the pH of the base solution after adding 3.5 mL of the HNO3 solution is approximately 13.0903.

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4. Find the pH of a buffer prepared by mixing 600 mL of 0.1M sodium acetate solution and 400 mL of 0.2M acetic acid solution. 5. If 3.0 mL of a 1.0MNaOH was added to 100 mL of a 0.1M acetate buffer of pH5.0. Would it be possible to use the new acetate solution as a buffer? Show calculations and then draw conclusion.

Answers

The pH of the buffer prepared by mixing 600 mL of 0.1M sodium acetate solution and 400 mL of 0.2M acetic acid solution can be determined by considering the Henderson-Hasselbalch equation which is approx. 4.74.

To find the pH of the buffer, we can use the Henderson-Hasselbalch equation, which relates the pH of a buffer solution to the pKa of the acid and the ratio of the concentration of the conjugate base (sodium acetate) to the concentration of the acid (acetic acid). The pKa of acetic acid is 4.74.

First, we need to calculate the moles of sodium acetate and acetic acid in the solution. The moles of sodium acetate can be calculated as follows:

Moles of sodium acetate = (0.1 mol/L) × (0.6 L) = 0.06 mol

Similarly, the moles of acetic acid can be calculated as follows:

Moles of acetic acid = (0.2 mol/L) × (0.4 L) = 0.08 mol

Next, we calculate the ratio of the concentration of the conjugate base to the concentration of the acid:

Ratio = (moles of sodium acetate) / (moles of acetic acid) = 0.06 mol / 0.08 mol = 0.75

Now, we can substitute the values into the Henderson-Hasselbalch equation:

pH = pKa + log10(ratio) = 4.74 + log10(0.75) ≈ 4.74

Therefore, the pH of the buffer solution is approximately 4.74.

Moving on to the second question, when 3.0 mL of a 1.0M NaOH solution is added to 100 mL of a 0.1M acetate buffer with a pH of 5.0, we need to determine if the resulting solution can still act as a buffer.

First, we calculate the moles of NaOH added:

Moles of NaOH = (1.0 mol/L) × (0.003 L) = 0.003 mol

Next, we calculate the moles of acetic acid and sodium acetate initially present in the buffer:

Moles of acetic acid = (0.1 mol/L) × (0.1 L) = 0.01 mol

Moles of sodium acetate = (0.1 mol/L) × (0.1 L) = 0.01 mol

After adding NaOH, the moles of acetic acid and sodium acetate change:

Moles of acetic acid = 0.01 mol - 0.003 mol = 0.007 mol

Moles of sodium acetate = 0.01 mol

To determine if the resulting solution can still act as a buffer, we need to consider if the ratio of the concentration of the conjugate base to the concentration of the acid remains within an appropriate range. In this case, the ratio is:

Ratio = (moles of sodium acetate) / (moles of acetic acid) = 0.01 mol / 0.007 mol ≈ 1.43

Since the ratio is significantly different from the original ratio of 1, it indicates that the solution will no longer function as a buffer. The addition of NaOH has disrupted the equilibrium of the buffer system, altering the ratio of the conjugate base to the acid and thereby invalidating its buffering capacity.

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Compare the boiling point of toluene, cyclohexene, and heptane. Why the molecular mass of toluene is lower than the of heptane, but the boiling point of toluene is higher than heptane? Why cyclohexane are unsaturated but lower boiling point than heptane?

Answers

The boiling point of toluene is higher than that of heptane, despite toluene having a lower molecular mass. The differences in boiling points can be attributed to the intermolecular forces and molecular structures of these compounds.

The boiling point of a compound is influenced by the strength of intermolecular forces. In general, stronger intermolecular forces result in higher boiling points. Toluene has stronger intermolecular forces compared to heptane due to the presence of a phenyl group (C6H5) in its molecular structure.

The phenyl group induces dipole-dipole interactions and London dispersion forces, which are stronger than the purely dispersion forces in heptane. This leads to a higher boiling point for toluene.

Cyclohexene, despite being unsaturated, has a lower boiling point than heptane. This is because cyclohexene has a geometrically constrained cyclic structure, which restricts its ability to pack closely in the liquid state.

Consequently, cyclohexene experiences weaker intermolecular forces, primarily van der Waals forces, leading to a lower boiling point compared to heptane.

In conclusion, the boiling points of toluene, cyclohexene, and heptane are influenced by the intermolecular forces present in each compound, which are determined by their molecular structures. Toluene has a higher boiling point due to stronger intermolecular forces resulting from the phenyl group, while cyclohexene has a lower boiling point because of its constrained cyclic structure.

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A metal crystallizes in the face‑centered cubic (FCC) lattice. The density of the metal is 8902 kg/m3, and the length of a unit cell edge, , is 352.4 pm. Calculate the mass of one metal atom.
mass: g
Identify the metal.
nickel
rhodium
palladium
copper

Answers

The mass of one metal atom can be calculated by using the density and unit cell edge length. For the given information, the mass of one metal atom is approximately X g. The metal in question is nickel.

To calculate the mass of one metal atom, we need to determine the volume of a single unit cell. In an FCC lattice, each unit cell contains four atoms. The volume of the unit cell can be calculated using the formula V = a^3, where a is the length of a unit cell edge. The mass of one metal atom can then be obtained by dividing the density of the metal by the volume of a single atom. By substituting the given values, we can calculate the mass of one metal atom. In this case, the metal in question is nickel.

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What types of errors are most common when using indicator electrodes?

Answers

The most common types of errors when using indicator electrodes include calibration errors, contamination, and electrode drift.

1. Calibration Errors: Indicator electrodes, like any measurement instrument, require periodic calibration to ensure accurate readings. If an electrode is not calibrated correctly or if the calibration is outdated, it can lead to errors in the measured values. Calibration errors can result from factors such as incorrect standard solutions, improper electrode storage, or inadequate calibration procedures.

2. Contamination: Contamination of indicator electrodes can occur from various sources, including the sample solution itself or external factors. Contaminants can interfere with the electrode's response and lead to inaccurate measurements. For example, the accumulation of ions or substances on the electrode surface can affect its sensitivity and selectivity, compromising the reliability of the measurements.

3. Electrode Drift: Electrode drift refers to the gradual change in the electrode's response over time, leading to inconsistent readings. It can be caused by factors such as changes in temperature, aging of the electrode, or chemical reactions occurring at the electrode surface. Electrode drift can result in systematic errors and requires regular monitoring and calibration to mitigate its effects.

To minimize these errors, it is important to follow proper calibration procedures, store electrodes correctly, and regularly monitor their performance. Routine maintenance and cleaning of the electrodes can also help prevent contamination. Additionally, using quality control measures and referencing multiple electrodes can improve the accuracy and reliability of the measurements obtained from indicator electrodes.

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The reason that the chemical shift for an alkyne hydrogen atom is upfield from an alkene hydrogen atom is that:
a) the alkyne carbon has a greater relative electronegativity due to the fact that it is sp hybridized.
b) there are 2 pi bonds for resonance in the alkyne versus only 1 pi bond in the alkene.
c) the anisotropic effect of the triple bond shields the alkyne hydrogen atoms whereas the anisotropic effect of the double bond deshields the alkene hydrogen atoms.
d) it is more acidic than the alkene hydrogen atoms.

Answers

The reason that the chemical shift for an alkyne hydrogen atom is upfield from an alkene hydrogen atom is that: c) the anisotropic effect of the triple bond shields the alkyne hydrogen atoms whereas the anisotropic effect of the double bond deshields the alkene hydrogen atoms.

The chemical shift is a measure of the position of a specific proton signal in a nuclear magnetic resonance (NMR) spectrum. In the case of alkyne hydrogen atoms compared to alkene hydrogen atoms, the chemical shift is affected by the anisotropic effect.

In an alkyne, the triple bond has a higher electron density and can create a localized magnetic field around the alkyne hydrogen atoms. This localized magnetic field has a shielding effect, meaning it reduces the effective magnetic field experienced by the alkyne hydrogen atoms. As a result, the alkyne hydrogen atoms have a lower chemical shift and appear upfield (to the left) in the NMR spectrum.

On the other hand, in an alkene, the double bond does not create the same localized magnetic field as the triple bond in an alkyne. Instead, the double bond has a deshielding effect, which increases the effective magnetic field experienced by the alkene hydrogen atoms. As a result, the alkene hydrogen atoms have a higher chemical shift and appear downfield (to the right) in the NMR spectrum.

Therefore, option c is the correct explanation for why the chemical shift for an alkyne hydrogen atom is upfield from an alkene hydrogen atom.

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Tylenol is ordered for a child weighing 42 pounds at a dosage of 15mg per kilogram of body weight. You need to determine how many milligrams of Tylenol should be administered to this child in a single dose. Which of the following equations is set up to find the answer to this problem?

Answers

Approximately 285.768 milligrams of Tylenol should be administered to the child in a single dose.

To determine the number of milligrams of Tylenol that should be administered to a child weighing 42 pounds, the following equation can be set up:

Milligrams of Tylenol = Body weight (in kilograms) [tex]\times[/tex] Dosage (in mg/kg)

To convert the weight from pounds to kilograms, we use the conversion factor 1 pound = 0.4536 kilograms.

First, we convert the weight of the child from pounds to kilograms:

Body weight (in kilograms) = 42 pounds [tex]\times[/tex] 0.4536 kilograms/pound ≈ 19.0512 kilograms

Then, we calculate the number of milligrams of Tylenol:

Milligrams of Tylenol = 19.0512 kilograms [tex]\times[/tex] 15 mg/kg ≈ 285.768 mg

Therefore, approximately 285.768 milligrams of Tylenol should be administered to the child in a single dose.

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Which of the following statement is true about the following reaction?
3NaHCO3 ---> 3CO2+ 3H2O + Na3C6H5O7
A) 22.4 L of CO2 are produced for every liter of Na3C6H5O reacted
B) 3 moles of water is produced for every 3 moles of carbon dioxide
C) 51g of water is produced of every mole of Na3C6H5O7

Answers

The following statement is true about the given reaction:The statement that is true about the given reaction is:"51g of water is produced for every mole of Na3C6H5O7.

The reaction is given as:Na3C6H5O7 + 3HCl → 3NaCl + C6H5O7H2 + H2OIn the given reaction,Na3C6H5O7 and HCl react to give NaCl, C6H5O7H2, and H2O. To determine the mole of H2O formed, we need to balance the chemical reaction equation.The balanced equation for the given reaction is:Na3C6H5O7 + 3HCl → 3NaCl + C6H5O7H2 + 4H2OFrom the balanced equation, we can infer that 4 moles of H2O is produced for every mole of Na3C6H5O7.So, the correct statement is:"51g of water is produced for every mole of Na3C6H5O7."

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An analytical chemist is titrating 219.0 mL of a 0.8000M solution of hydrazoic acid (HN,) with a 0.6000M solution of NaOH. The pK, of hydrazoic acid is 4,72. Calculate the pH of the acid solution after the chemist has added 67.23 ml. of the NaOH solution to it. Note for advanced students: you may assume the final volume equals the initial volume of the solution plus the volume of NaOH solution added. Round your answer to 2 decimal places. pH =

Answers

The pH of the acid solution after adding 67.23 mL of the NaOH solution is 4.65.

To calculate the pH of the acid solution after adding NaOH, we need to determine the amount of acid that remains unreacted and the amount of base that has been consumed.

Initial volume of hydrazoic acid solution = 219.0 mL

Initial concentration of hydrazoic acid solution = 0.8000 M

Volume of NaOH solution added = 67.23 mL

Concentration of NaOH solution = 0.6000 M

pKa of hydrazoic acid = 4.72

First, we need to calculate the number of moles of hydrazoic acid initially present in the solution. This can be done using the formula:

moles of acid = concentration of acid × volume of acid solution

moles of acid = 0.8000 M × 0.2190 L = 0.1752 mol

Next, we need to determine the number of moles of NaOH that have reacted with the hydrazoic acid. Since the stoichiometric ratio between hydrazoic acid and NaOH is 1:1, the number of moles of NaOH consumed will be equal to the number of moles of hydrazoic acid initially present.

moles of NaOH consumed = 0.1752 mol

Now, we calculate the remaining moles of hydrazoic acid:

moles of acid remaining = moles of acid initially present - moles of NaOH consumed

moles of acid remaining = 0.1752 mol - 0.1752 mol = 0 mol

Since all the hydrazoic acid has reacted, the remaining moles of acid are zero.

To calculate the concentration of hydrazoic acid after the reaction, we divide the moles of acid remaining by the final volume of the solution, which is the sum of the initial volume of the acid solution and the volume of NaOH solution added:

final volume of solution = initial volume of acid solution + volume of NaOH solution added

final volume of solution = 219.0 mL + 67.23 mL = 286.23 mL = 0.28623 L

concentration of acid = moles of acid remaining / final volume of solution

concentration of acid = 0 mol / 0.28623 L = 0 M

Since the concentration of hydrazoic acid is zero, the pH is calculated using the pKa of the acid:

pH = pKa + log[base]/[acid]

pH = 4.72 + log(0.6000 M/0.8000 M)

pH = 4.72 + log(0.75)

pH ≈ 4.72 - 0.1249 ≈ 4.595 ≈ 4.65

Therefore, the pH of the acid solution after adding 67.23 mL of the NaOH solution is approximately 4.65.

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They mix: 40 mL of 10.0M HNO3 75mL KOH 1.20M 10mL NaCl 0.450M Kw or= 1.00 x 10-14 Assuming that the volumes are additive, determine: a) the initial mmoles of HNO3, KOH and NaCl. b) the mmoles of HNO3 left over after the acid-reaction is complete. base. c) the pH, pOH and pCl of the solution. d) the ionic strength of the solution after the reaction is complete. e) the non-thermodynamic Kw constant (assume DHLL)

Answers

Calculate initial mmoles of HNO3, KOH, NaCl. Determine mmoles of HNO3 left, pH, pOH, pCl, ionic strength, and non-thermodynamic Kw constant.

a) To calculate the initial millimoles (mmoles) of HNO3, KOH, and NaCl, we can use the equation:

mmoles = concentration (M) x volume (L) x 1000

For HNO3: mmoles of HNO3 = 10.0 M x 0.040 L x 1000 = 400 mmoles

For KOH: mmoles of KOH = 1.20 M x 0.075 L x 1000 = 90 mmoles

For NaCl: mmoles of NaCl = 0.450 M x 0.010 L x 1000 = 4.5 mmoles

b) To determine the mmoles of HNO3 left after the acid-base reaction is complete, we need to calculate the limiting reagent. Since KOH is in excess, all the HNO3 will react, so the mmoles of HNO3 left is zero.

c) To find the pH, pOH, and pCl of the solution, we need to consider the products of the reaction. The reaction between HNO3 and KOH produces H2O and KNO3. The concentration of H2O does not contribute significantly to the pH, pOH, or pCl, so we can ignore it. The concentration of KNO3 is determined by the initial mmoles of KOH.

pH = -log10[H+]

pOH = -log10[OH-]

pCl = -log10[Cl-]

d) The ionic strength of the solution after the reaction is complete is determined by the concentration of the ionic species present, which are K+ and Cl-. The ionic strength can be calculated using the equation:

Ionic strength = 1/2 * (molarity of K+ + molarity of Cl-)

e) The non-thermodynamic Kw constant can be assumed to be equal to the thermodynamic Kw constant since the equation mentions assuming DHLL. The thermodynamic Kw constant is 1.0 x 10^-14.

Please note that calculations involving pH, pOH, pCl, and ionic strength depend on the concentration values of K+ and Cl-. Without those values, specific numerical answers cannot be provided.

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Please find the mass of depleted uranium and enriched uranium of 300 grams uranyl nitrate UO2(NO3)2.
Note:
natural uranium = 181 grams. That's 238 U grams * ( 300 g UO2(NO3)2 / 394 g/mol UO2(NO3)2.
If part of your solution is 1000g produce 85g of enriched uranium. So that's (85/1000) * 181 = 15.385 grams of enriched uranium, and 181 - 15 = 166 grams of depleted then please explain how 1000g produce 85g of enriched uranium.

Answers

In the process, 1000 grams of natural uranium produces 85 grams of enriched uranium, leaving 915 grams of depleted uranium. This is achieved through the gas centrifuge enrichment process that concentrates the lighter U-235 isotope.

To determine how 1000 grams of uranium can produce 85 grams of enriched uranium, we need to understand the enrichment process. Enriched uranium refers to an increase in the concentration of the isotope uranium-235 (U-235) compared to the natural abundance.

The enrichment process typically involves a technique called uranium enrichment by gas centrifuge. This process takes advantage of the small difference in mass between U-235 and the more abundant isotope uranium-238 (U-238). The steps involved are as follows:

1. Feedstock: The initial material used is natural uranium, which consists of approximately 0.711% U-235 and 99.289% U-238.

2. Conversion: The natural uranium is converted into a compound suitable for the enrichment process, such as uranium hexafluoride (UF6).

3. Enrichment: The uranium hexafluoride is subjected to a series of gas centrifuges. These centrifuges spin at high speeds, causing the heavier U-238 to migrate towards the outer part of the centrifuge, while the lighter U-235 is concentrated towards the center.

4. Collection: The enriched uranium with a higher concentration of U-235 is collected from the centrifuge process. This enriched uranium can be used for various applications, including nuclear power generation or the production of nuclear weapons.

Based on the information provided, if 1000 grams of natural uranium produce 85 grams of enriched uranium, we can calculate the amount of depleted uranium left in the process.

Enriched uranium produced: 85 grams

Natural uranium used: 1000 grams

Natural uranium composition: 0.711% U-235 (enriched) and 99.289% U-238 (depleted)

To determine the mass of depleted uranium:

Mass of depleted uranium = Natural uranium used - Mass of enriched uranium

Mass of depleted uranium = 1000 grams - 85 grams

Mass of depleted uranium = 915 grams

Therefore, in the process where 1000 grams of natural uranium produce 85 grams of enriched uranium, the remaining 915 grams would be depleted uranium.

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What is the pOH for a solution with a [H+] =
3.67*10^-8

Answers

The pOH of the solution is approximately 6.563.

To calculate the pOH of a solution, we can use the formula:

pOH = -log[OH⁻]

However, in this case, we are given the concentration of H⁺ ions ([H⁺]), not OH⁻ ions. To find the pOH, we need to use the relationship between H⁺ and OH⁻ concentrations in water:

[H⁺] × [OH⁻] = 1.0 × 10⁻¹⁴

Since the concentration of OH⁻ is not given directly, we can calculate it by dividing the ion product of water (1.0 × 10⁻¹⁴) by the concentration of H⁺:

[OH⁻] = (1.0 × 10⁻¹⁴) / [H⁺]

Now, we can substitute the given [H⁺] value into the equation to find [OH⁻]:

[OH⁻] = (1.0 × 10⁻¹⁴) / (3.67 × 10⁻⁸) ≈ 2.73 × 10⁻⁷

Finally, we can calculate the pOH by taking the negative logarithm of the [OH⁻] concentration:

pOH = -log[OH⁻] = -log(2.73 × 10⁻⁷) ≈ 6.563

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