How many moles exist in 390 g of silver nitrate ?

4.37 grams of O₂ will be left over after the reaction is complete.

The balanced chemical equation for the reaction is:

4NO₂ + O₂→ 2N₂O₅

From the equation, we can see that 4 moles of NO and 1 mole of O₂ react to form 2 moles of N₂O₅.

To find the amount of each reactant and product in the reaction, we need to first calculate the number of moles of each substance. We can use the molecular weight of each substance to convert the given mass into moles.

The molecular weights of the substances are:

NO₂ = 46.0055 g/mol

O₂ = 31.9988 g/mol

N₂O₅ = 108.0104 g/mol

Number of moles of NO₂ = 5.31 g / 46.0055 g/mol = 0.1156 mol

Number of moles of O₂ = 5.31 g / 31.9988 g/mol = 0.1659 mol

According to the balanced chemical equation, 4 moles of NO₂ react with 1 mole of O₂ to produce 2 moles of N₂O₅.

Therefore, the limiting reactant is NO₂ because there are only 0.1156 mol of it available, while there are 0.1659 mol of O₂ available. This means that all of the NO₂ will be used up, and there will be some excess O₂ left over.

To calculate the amount of N₂O₅ produced, we can use the mole ratio from the balanced chemical equation:

4 mol NO₂ : 1 mol O₂ : 2 mol N₂O₅

Since we know that 0.1156 mol of NO₂ will be used up, we can use the mole ratio to calculate the amount of N₂O₅

produced:

0.1156 mol NO₂ x (2 mol N₂O₅ / 4 mol NO₂) = 0.0578 mol N₂O₅

To find the mass of N₂O₅ produced, we can use the molecular weight:

0.0578 mol N₂O₅ x 108.0104 g/mol = 6.24 g N₂O5

Therefore, 6.24 grams of N₂O₅ will be produced, and there will be some excess O₂ left over. To calculate the amount of O₂ left over, we can use the mole ratio from the balanced chemical equation:

4 mol NO2 : 1 mol O₂ : 2 mol N₂O₅

Since we know that 0.1156 mol of NO₂ will be used up, we can use the mole ratio to calculate the amount of O₂  required:

0.1156 mol NO₂ x (1 mol O₂ / 4 mol NO₂) = 0.0289 mol O₂

Therefore, the amount of O₂ left over is:

0.1659 mol O₂ - 0.0289 mol O₂ = 0.1370 mol O₂

To find the mass of O₂ left over, we can use the molecular weight:

0.1370 mol O₂ x 31.9988 g/mol = 4.37 g O₂

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The mass of hydrofluoric acid contained in the sample is approximately 0.1876 g.

To find the mass of hydrofluoric acid (HF) in the sample, follow these steps:

1. Write the balanced chemical equation for the reaction:
 [tex]HF + NaOH → NaF + H2O[/tex]

2. Determine the moles of sodium hydroxide (NaOH) used in the titration:
  [tex]Moles of NaOH = Volume (L) × Molarity[/tex]
 [tex]Moles of NaOH = 25.21 mL × (1 L/1000 mL) × 0.372 M[/tex]
 [tex]Moles of NaOH = 0.00937692 mol[/tex]

3. Determine the moles of hydrofluoric acid (HF) using the stoichiometry from the balanced equation:
  [tex]Moles of HF = Moles of NaOH (1 mol HF / 1 mol NaOH)[/tex]
 [tex]Moles of HF = 0.00937692 mol[/tex]

4. Determine the molar mass of hydrofluoric acid (HF):
  [tex]Molar mass of HF = 1(1.01 g/mol H) + 1(19.00 g/mol F) = 20.01 g/mol[/tex]

5. Calculate the mass of hydrofluoric acid (HF) in the sample:
  Mass of HF = Moles of HF × Molar mass of HF
 [tex]Mass of HF = 0.00937692 mol × 20.01 g/mol[/tex]
  [tex]Mass of HF = 0.1876 g[/tex]

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The potential impact of a growing bison population on soil and plant functionalities is uncertain. Bison & elk have a lot in common physically and physiologically, therefore there might be competition over food system between two varieties.

There is little functional redundancy in keystone species. This indicates that no other organism would've been able to replace the species' ecological roles when it were to vanish from ecosystem. The environment would've been forced to undergo a significant transformation, allowing for the influx of new, potentially exotic species.

Predators have a significant impact on an environment. They influence the makeup of ecosystems by releasing pollen and nutrients from foraging. Also, they influence lower organisms in the food chain by regulating the dispersion, abundance, or variability of the prey, a phenomenon called as trophic cascades.

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A pressure of 1.20 atm, a volume of 31.0 litres, and a temperature of 87.0So, you have approximately 58.2 grams of carbon dioxide gas.

To find the number of grams of carbon dioxide (CO₂) in this situation, follow these steps:
1. Convert the temperature from Celsius to Kelvin by adding 273.15.
  T(K) = 87.0°C + 273.15 = 360.15 K
2. Use the ideal gas law formula, which is PV = nRT, where P is pressure, V is volume, n is the number of moles, R is the ideal gas constant, and T is temperature.
3. Rearrange the formula to solve for n (number of moles): n = PV / RT
4. Plug in the values:
  P = 1.20 atm
  V = 31.0 L
  R = 0.0821 L·atm/mol·K (the ideal gas constant)
  T = 360.15 K
  n = (1.20 atm * 31.0 L) / (0.0821 L·atm/mol·K * 360.15 K)
5. Calculate the number of moles:
  n ≈ 1.322 moles of CO₂
6. Find the molar mass of CO₂:
  Molar mass of CO₂ = (1 * 12.01 g/mol) + (2 * 16.00 g/mol) = 44.01 g/mol
7. Multiply the number of moles by the molar mass to find the mass of CO₂:
  Mass = n * molar mass
  Mass ≈ 1.322 moles * 44.01 g/mol
8. Calculate the mass of CO₂:
  Mass ≈ 58.2 grams

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The poor specificity of the sulfur reduction test is responsible for not being able to differentiate between H ₂S produced by anaerobic respiration and H ₂S  produced by putrefaction.

What is the sulfur reduction test, The sulfur reduction test is a biochemical test that helps to determine the ability of an organism to reduce sulfur and produce H ₂S (hydrogen sulfide). The test is carried out by inoculating a sulfur-containing medium with the test organism and observing whether the medium changes colour due to the production of H ₂S.

Why is the sulfur reduction test not able to differentiate between H ₂S produced by anaerobic respiration and H ₂S produced by putrefaction, The sulfur reduction test is not able to differentiate between H ₂S produced by anaerobic respiration and H ₂S produced by putrefaction due to the poor specificity of the test.

This means that the test is not able to distinguish between the different sources of H ₂S production and can only detect the presence or absence of H ₂S without providing information on its source.

Therefore, the test has poor specificity but not poor sensitivity since it is able to detect the presence of H ₂S, but cannot distinguish between its different sources.

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[tex]M_{2} V_{2}[/tex] The volume of water needed to create a 0.330 M [tex]H_{2} SO_{4}[/tex] solution from a 1.00 M solution is 91.36 mL.

To calculate the volume of water needed to create a 0.330 M [tex]H_{2} SO_{4}[/tex] solution from a 1.00 M solution, we can use the dilution formula:

[tex]M_{1} V_{1}[/tex] = [tex]M_{2} V_{2}[/tex]

where [tex]M_{1}[/tex] is the initial concentration (1.00 M), [tex]V_{1}[/tex] is the initial volume (45.0 mL), [tex]M_{2}[/tex] is the final concentration (0.330 M), and [tex]V_{2}[/tex] is the final volume.

1.00 M × 45.0 mL = 0.330 M × [tex]V_{2}[/tex]

Solve for [tex]V_{2}[/tex]:

[tex]V_{2}[/tex] = (1.00 M × 45.0 mL) / 0.330 M
[tex]V_{2}[/tex] = 136.36 mL

Now, subtract the initial volume from the final volume to find the volume of water that needs to be added:

136.36 mL - 45.0 mL = 91.36 mL

Therefore, you must add 91.36 mL of water to the 45.0 mL of 1.00 M H2SO4 solution to create a 0.330 M [tex]H_{2} SO_{4}[/tex] solution.

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The equation for the acid dissociation constant (K₂) of carbonic acid (H₂CO₃) is:  K₂ = [HCO₂⁻][H₂O⁺] / [H₂CO₃][H₂O]

Where:

[HCO₂⁻] represents the concentration of bicarbonate ion in solution

[H₂O⁺] represents the concentration of hydronium ion in solution

[H₂CO₃] represents the concentration of carbonic acid in solution

[H₂O] represents the concentration of water in solution

The equation shows the ratio of the concentration of the products (bicarbonate ion and hydronium ion) to the concentration of the reactant (carbonic acid) and the concentration of water.

What is an acid dissociation?

Acid dissociation, also known as acid ionization, refers to the process by which an acid breaks down or ionizes into its constituent ions when it is dissolved in water. This process involves the transfer of a proton (H⁺ ion) from the acid molecule to a water molecule, forming a hydronium ion (H₃O⁺) and the conjugate base of the acid.

The general chemical equation for acid dissociation can be written as:

HA(aq) + H2O(l) ⇌ H3O⁺(aq) + A⁻(aq)

where HA represents the acid molecule, H₂O represents a water molecule, H₃O⁺ represents the hydronium ion, and A⁻ represents the conjugate base of the acid.

The extent of acid dissociation is quantified by the acid dissociation constant (Ka), which is a measure of the tendency of an acid to donate a proton. The larger the value of Ka, the stronger the acid, and the more likely it is to dissociate in water. Ka is defined as the ratio of the concentrations of the products (H₃O⁺ and A⁻ ions) to the concentration of the acid molecule (HA) at equilibrium:

Ka = [H3O⁺][A⁻] / [HA]

Acid dissociation plays an important role in many chemical and biological processes, including the regulation of pH in biological systems and the corrosion of metals.

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Complete question is: The equation for the acid dissociation constant (K₂) of carbonic acid (H₂CO₃) is:  K₂ = [HCO₂⁻][H₂O⁺] / [H₂CO₃][H₂O].

The pH of a 0.10M [tex]C_{6} H_{5} O_{}[/tex] solution is 11.50 which is calculated using the expression of pOH.

[tex]K_{b}[/tex] = [tex]K_{w} / K_{a}[/tex]

    = [tex]1 * 10 ^{-14}[/tex] / [tex]1. 0 * 10 ^{-10}[/tex]

    = [tex]1.0 * 10^{-4}[/tex]

pH is defined as the quantitative measure of the acidity or basicity of aqueous or of other liquid solutions. pH is called as the potential of hydrogen ions where pOH is called as the potential of hydroxide ions.  pH scale is known as a scale which is used to determine the solution's hydrogen ion (H+) concentration. The term pH and pOH that denote the negative log of the concentration of the hydrogen ion or hydroxide ions. High pH indicates that a solution is basic while high pOH means that a solution is acidic.

We know that the expression for pOH is,

pOH = -Log [tex]\sqrt{K_{b} C}[/tex]

Putting all the values in the expression of pOH we get,

pH = 11.50

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The correct question is,

The Ka of C6H5OH is 1.0×10−10 .What is the pH of a 0.10 M C 6H 5O-solution?

We can use the ideal gas law, that relates the pressure, volume, temperature, and number of moles of a gas and results in 15.5 g of argon gas at a pressure of 1.27 atm and temperature of 361 K occupies volume of 10.8 L.

PV = nRT  where:

P = pressure of the gas in atmospheres (atm)

V = volume of the gas in liters (L)

n = number of moles of the gas

R = ideal gas constant, 0.08206 L.atm/(mol.K)

T = temperature of the gas in Kelvin (K)

First, we need to calculate the number of moles of argon gas present in 15.5 g. We can use the molar mass of argon, which is 39.95 g/mol:

n = m/M = 15.5 g / 39.95 g/mol = 0.388 mol

Next, we can rearrange the ideal gas law to solve for V:

V = nRT/P

Plugging in the given values:

V = (0.388 mol)(0.08206 L.atm/(mol.K))(361 K)/(1.27 atm)

Solving this expression yields:

V = 10.8 L

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To find the molar mass of the gas, we can use the ideal gas law:

PV = nRT

where P is the pressure in Pa, V is the volume in m^3, n is the number of moles of gas, R is the ideal gas constant (8.31 J/(mol·K)), and T is the temperature in K.

First, we need to convert the given values to the appropriate units:

12.0 g -> 0.0120 kg

2.8 dm^3 -> 0.0028 m^3

27°C -> 300 K (adding 273 to convert from Celsius to Kelvin)

100 kPa -> 100,000 Pa

Now we can rearrange the ideal gas law to solve for n:

n = PV/RT

n = (100,000 Pa) x (0.0028 m^3) / [(8.31 J/(mol·K)) x (300 K)]

n = 0.001214 mol

Finally, we can calculate the molar mass (M) using the formula:

M = m/n

where m is the mass of the gas (in grams). Since we have the mass in kilograms, we need to multiply by 1000 to convert to grams:

M = (0.0120 kg x 1000 g/kg) / 0.001214 mol

M = 9906.2 g/mol

Therefore, the molar mass of the gas is approximately 9906 g/mol.

Precipitation-hardened alloys are suitable primarily for low-temperature applications due to a combination of factors that limit their performance at high temperatures they are  recrystallization resumes, there is no dispersion strengthening, there is no dispersion strengthening.

In summary, precipitation-hardened alloys are more suitable for low-temperature applications because high temperatures lead to recrystallization, weakening of precipitates, and reduced dispersion strengthening, all of which negatively impact the strength and performance of the alloy.

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why are most precipitation-hardened alloys suitable only for low-temperature applications? (select all that apply.)

At high temperatures, recrystallization resumes.

At high temperatures,  the alloy becomes bake-hardened.

At high temperatures, the precipitates lose their strength.

At high temperatures, the alloy becomes more brittle.

At high temperatures, there is no dispersion strengthening.

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If the urea hydrolysis test with Providencia stuartii took 48 hours to turn pink, it would not necessarily be a false result. The test is considered positive when the color turns pink, indicating urease production.

A false positive result would occur if the color changed to pink, but the organism does not actually produce urease. A false negative result would occur if the color did not change, but the organism does produce urease. In this scenario, since the color eventually turned pink, it indicates a positive result for urease production.

Reasons for a slower reaction might include:
1. Lower bacterial concentration in the sample, leading to a slower enzymatic reaction.
2. Variability in the urea hydrolysis rate among different strains of Providencia stuartii.
3. Environmental factors, such as temperature or pH, affecting the speed of the enzymatic reaction.

In summary, the 48-hour reaction time for the urea hydrolysis test with Providencia stuartii is not necessarily a false result, as it indicates urease production. The slower reaction could be due to various factors, such as bacterial concentration, strain variability, or environmental conditions.

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Answer:

A

Explanation:

In order for a titration to be effective, the reaction must produce a precipitate. The correct answer is option B, "reaction must produce a precipitate."

For a titration to be effective, the reaction must be stoichiometric, quantitative, and rapid. A stoichiometric reaction is one in which the amount of reactants is proportional to the amount of products.

A quantitative reaction is one in which all the reactants are consumed, leaving no excess. A rapid reaction is one that occurs quickly and does not take a long time to complete.

However, a reaction producing a precipitate is not necessary for the titration to be effective. Hence option B is correct.

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we need to add 13.65 g of benzoic acid to 5.0 L of 0.050 M sodium benzoate solution to prepare a benzoic acid/benzoate buffer with a pH of 4.25.

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

4.25 = 4.2 + log([A-]/[HA])

log([A-]/[HA]) = 0.05

[A-]/[HA] = 1.13

Next, we need to calculate the concentration of benzoic acid required to achieve the desired [A-]/[HA] ratio:

[A-] + [HA] = 0.05 M

[A-]/[HA] = 1.13

[HA] = 0.05 / (1 + 1.13) = 0.0224 M

[A-] = 0.05 - 0.0224 = 0.0276 M

Finally, we can calculate the mass of benzoic acid required to prepare the buffer:

mass = molarity x volume x formula weight

mass = 0.0224 M x 5.0 L x 122.12 g/mol

mass = 13.65 g

Benzoic acid is a colorless crystalline solid with the chemical formula C7H6O2. It is a weak organic acid and is naturally found in many fruits and berries, such as cranberries, prunes, and plums. The acid has a distinct, somewhat pleasant odor and is commonly used as a food preservative due to its antimicrobial properties. It is also used in the production of various other chemicals, such as benzoyl chloride and benzyl benzoate, and is a key component in the synthesis of drugs, such as benzylpenicillin.

In terms of its chemical properties, benzoic acid is slightly soluble in water but highly soluble in organic solvents such as ethanol and diethyl ether. It has a relatively low melting point of 122.4 °C and a boiling point of 249.2 °C. The acid is often synthesized from toluene or benzene and is a valuable intermediate in many industrial processes.

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Calcium carbonate (CaCO3) reacts with hydrochloric acid (HCl)  according to the following balanced chemical equation. Therefore, 400 mg of Tums (containing 40.0% CaCO3 by mass) can neutralize 31.98 mL of 0.100 M HCl.

CaCO3(s) + 2 HCl(aq) → CaCl2(aq) + CO2(g) + H2O(l)

From this equation, we can see that one mole of CaCO3 reacts with two moles of HCl. Therefore, we need to calculate the number of moles of CaCO3 in 400 mg of Tums:

mass of CaCO3 = 0.4 g × 0.4 = 0.16 g

number of moles of CaCO3 = mass / molar mass = 0.16 g / 100.09 g/mol = 0.001599 mol

To neutralize this amount of CaCO3, we will need twice as many moles of HCl,  or

number of moles of HCl = 2 × 0.001599 mol = 0.003198 mol

Now, we can use the concentration of the hydrochloric acid solution (0.100 M) and the number of moles of HCl to calculate the volume of HCl required to neutralize the CaCO3:

number of moles of HCl = concentration × volume

volume = number of moles of HCl / concentration = 0.003198 mol / 0.100 mol/L = 0.03198 L

Finally, we can convert the volume to milliliters:

0.03198 L × 1000 mL/L = 31.98 mL

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Answer: No, Calcium sulfate (CaSO4) is insoluble in water because water dipole strength is too weak to separate the anions and cations of the CaSO4 as both Ca 2+ and SO4 2- ions are big and bigger anion stabilizes bigger cation strongly which makes lattice energy high.

Explanation: Hope this helps!!

The energy that would be released for the formation of 25 moles of liquid water is 6130kJ.

Given the number of moles of liquid water = 25

Let the energy released = E

The formation of 25 moles of liquid water requires the input of energy and results in the release of energy.

This can be calculated as follows:

Energy required for formation of 25 moles of liquid water:

[tex]H_2 + 1/2O_2 -- > H_2O(l)[/tex]

[tex]H_2O (l) -- > H_2O(g)[/tex]

The enthalpy of formation of H2 = 0kJmol

The enthalpy of formation of O2 = 0kJmol

The enthalpy of formation of liquid H2O = -286kJ/mol

The enthalpy of sublimation of liquid H2O to gaseous H2O = 40.8kJ

The enthalpy of formation of gaseous H2O = -286kJ/mol + 40.8kJ = -245.2kJ/mol

For 25 moles the energy released = 25 * 245.2kJ = 6130kJ

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CaO(s) + CO2(g) → CaCO3(s) Above 1200 K, however, the opposite process takes place: calcium carbonate breaks down into calcium oxide and releases carbon dioxide.

When heated, a compound will split into two or more components, which may be elements or other compounds. As a result, when calcium carbonate is heated, calcium oxide and carbon dioxide are produced.

Lime, a crucial component in the production of steel, glass, and paper, and carbon dioxide are produced when calcium carbonate breaks down. Calcium carbonate is utilised in industrial settings to neutralize acidic situations in both soil and water due to its antacid qualities.

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Question:

Calcium carbonate is heated name the;  reactant and the state:  product and the state:  word equation:  balanced formula:  type of reaction:

Answer:

When endothermic reaction takes place, the system gains heat from the surroundings and so the temperature of the surroundings decreases ie. it gets colder

Explanation:

A chemical reaction is exothermic if heat is released by the system into the surroundings.

STUDY WELL!

the new temperature is 393.75 K.

_______________________________________________________

To solve this problem, we can use the combined gas law, which relates the pressure, volume, and temperature of a gas:

P₁V₁/T₁ = P₂V₂/T₂

where P is the pressure, V is the volume, and T is the temperature.

We are given that the pressure and amount of gas remain constant, so we can simplify the equation to:

V₁/T₁ = V₂/T₂

Substituting the given values, we get:

2.00 L / 315 K = 2.50 L / T₂

Solving for T₂, we get:

T₂ = (2.50 L * 315 K) / 2.00 L = 393.75 K

Therefore, the new temperature is 393.75 K.

The new temperature of the gas is approximately 393.75 K when the volume is changed to 2.50 L.

To find the new temperature of the gas, we can use Charles's Law, which states that the initial volume (V₁) divided by the initial temperature (T₁) is equal to the final volume (V₂) divided by the final temperature (T₂), as long as the pressure and amount of gas remain constant. The formula for Charles's Law is:
[tex]\frac{V_1}{T_1} = \frac{V_2}{T_2}[/tex]
Given the initial volume (V₁) = 2.00 L and the initial temperature (T₁) = 315 K, we want to find the new temperature (T₂) when the volume is changed to 2.50 L (V₂).
First, plug in the known values into the formula:
[tex]\frac{(2.00 )}{(315)} = \frac{(2.50)}{(T_2)}[/tex]
Next, cross-multiply to solve for T₂:
[tex](2.00 ) * (T_2) = (2.50) * (315)[/tex]
Now, divide both sides by 2.00 L to isolate T₂:
[tex]T_2 = \frac{(2.50  * 315 )}{(2.00 )}[/tex]
Finally, perform the calculation to find the new temperature:
[tex]T_2 = \frac{787.5}{2}[/tex]
T₂ ≈ 393.75 K

So, the new temperature of the gas is approximately 393.75 K when the volume is changed to 2.50 L.

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To calculate (a) the (molar) Gibbs energy of mixing and (b) the (molar) entropy of mixing when the two major components of air (nitrogen and oxygen) are mixed to form air, the mole fractions of N2 and O2 are needed.

Given that mole fractions of N2 and O2 are 0.78 and 0.22, respectively. The formula for calculating Gibbs energy of mixing and entropy of mixing is as follows.∆Gmix=∆Hmix−T∆SmixΔ G mix = Δ H mix - T Δ S mixΔSmix=−RΣxi ln xiΔ S mix = - RΣ x i ln x iWhere,ΔHmix = Enthalpy of mixing of the two gasesΔGmix = Gibbs energy of mixing of the two gasesΔSmix = Entropy of mixing of the two gasesT = TemperatureR = Gas constantxi = Mole fraction of gas i.

(a) The Gibbs energy of mixing is given as,∆Gmix=∆Hmix−T∆Smix=0.2095 kJ/mol(b) The entropy of mixing is given as,ΔSmix=−RΣxi ln xi=-0.193 J/K mol The value of Gibbs energy of mixing is positive indicating that the mixing process is not spontaneous. However, the value of entropy of mixing is negative indicating that the mixing process is spontaneous.

Therefore the giving process is spontaneous.

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The effect of raising the pH value of the solution from pH 4.0 to pH 9.0 on the reaction rate catalyzed by an enzyme with an optimum pH of 7.0 is to increase the reaction.

The pH value is a measure of acidic/basic solution. Characteristic of pH

Enzyme is affected by pH changes. The rate of the enzymatic reaction depends on the pH of the medium.

1) Every enzyme has an optimal pH value at which the rate of enzymatic reaction is maximized.

2) At higher or lower pH, the rate of enzymatic reaction decreases.

3) The optimum pH for most enzymes is in the pH 5 to pH 9 range.

4) With a few exceptions, the pH of pepsin is very acidic and the pH of arginase is very alkaline. Now, the pH of the solution rises from pH 4.0 to pH 9.

0 is the optimal pH of the enzyme 7. Therefore, the reaction rate increases.

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⁣[tex]5.6 \times 10^1^7[/tex] atoms of phosphorus is equal to [tex]9.32 \times 10^-7[/tex] moles.

Either a positively charged electron or a large number of negatively charged electrons surround the central nucleus of an atom. The positively charged nucleus is made up of two comparatively large particles called protons and neutrons.

As many atoms, molecules, or ions (referred to as entities) are present in one mole of substance as there are in  [tex]12[/tex] grammes of carbon-[tex]12[/tex], it is known as a mole. It is about equal to the Avogadro's number [tex]6.022 \times 10^23[/tex]  , which is entities per mole.

We must divide this amount by Avogadro's number to get the number of moles in  [tex]5.6 \times 10^1^7[/tex] atoms of phosphorus:

Number of moles =[tex](5.6 \times 10^17 atoms) / (6.022 \times 10^23 atoms/mol)[/tex]

Number of moles = [tex]9.32 \times 10^-7[/tex]mol

Therefore, ⁣[tex]5.6 \times 10^1^7[/tex] atoms of phosphorus is equal to [tex]9.32 \times 10^-7[/tex] moles.

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Approximately 29.5 g of NaCN is required to make 14.7 L of HCN at STP.

To solve this problem, we will use the ideal gas law to calculate the number of moles of HCN produced and then use stoichiometry to determine the mass of NaCN required.

First, we need to determine the number of moles of HCN produced using the ideal gas law:

[tex]PV = nRT[/tex]

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

At STP (standard temperature and pressure), P = 1 atm and T = 273 K. The volume of HCN produced is given as 14.7 L.

Plugging these values into the ideal gas law, we get:

[tex]n = PV/RT = (1 atm) *(14.7 L)/(0.0821 L atm/mol K * 273 K) = 0.603 mol[/tex]

So, 0.603 mol of HCN is produced.

Now we can use stoichiometry to determine the mass of NaCN required. From the balanced chemical equation:

NaCN + HCl → NaCl + HCN

we can see that 1 mole of NaCN produces 1 mole of HCN.

Therefore, the mass of NaCN required can be calculated as:

mass of NaCN = number of moles of NaCN x molar mass of NaCN

The molar mass of NaCN is 49.01 g/mol.

So, the mass of NaCN required is:

mass of [tex]NaCN = 0.603 mol * 49.01 g/mol = 29.5 g[/tex]

Therefore, approximately 29.5 g of NaCN is required to make 14.7 L of HCN at STP.

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The theoretical dependence between capacitive reactance and frequency. Capacitive reactance (Xc) is the opposition offered by a capacitor to the flow of alternating current (AC) due to its capacitance.

The relationship between capacitive reactance and frequency is inverse and proportional. Mathematically, it is given by the following formula:

Xc = 1 / (2 * π * f * C)

where Xc is the capacitive reactance in ohms, f is the frequency of the AC signal in hertz (Hz), and C is the capacitance of the capacitor in farads (F).

As per this formula, capacitive reactance (Xc) is inversely proportional to the frequency (f) of the AC signal. In other words, as the frequency increases, the capacitive reactance decreases, and as the frequency decreases, the capacitive reactance increases.

This means that a capacitor will act more like a short circuit (i.e. offer less opposition to the flow of current) at higher frequencies and more like an open circuit (i.e. offer more opposition to the flow of current) at lower frequencies.

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There were 0.01 moles of HCl present in the 10.0 mL sample.

The balanced chemical equation for the reaction between HCl and Ba(OH)2 is:

2HCl + Ba(OH)2 -> 2H2O + BaCl2

From the equation, we can see that two moles of HCl are required to react with one mole of Ba(OH)2.

To find the number of moles of HCl in the sample, we need to first calculate the number of moles of Ba(OH)2 that reacted with the HCl.

The number of moles of Ba(OH)2 is given by:

moles of Ba(OH)2 = concentration x volume (in liters)

moles of Ba(OH)2 = 0.4 mol/L x (12.5/1000) L

moles of Ba(OH)2 = 0.005 mol

Since two moles of HCl react with one mole of Ba(OH)2, the number of moles of HCl is:

moles of HCl = 2 x 0.005 mol

moles of HCl = 0.01 mol

Therefore, there were 0.01 moles of HCl present in the 10.0 mL sample.

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Answer:

When methane (CH4) and methanol (CH3OH) are burned, they react with oxygen (O2) to form carbon dioxide (CO2) and water (H2O). The balanced chemical equations for the combustion of methane and methanol are:

CH4 + 2O2 → CO2 + 2H2O

CH3OH + 1.5O2 → CO2 + 2H2O

The amount of energy released during combustion depends on the amount of reactants consumed, and can be calculated using the standard enthalpy of formation of the products and reactants. The standard enthalpy of formation is the amount of energy released or absorbed when one mole of a compound is formed from its constituent elements in their standard states at a specified temperature and pressure.

Using the standard enthalpy of formation values from a chemistry data book, we can calculate the energy released by each experiment:

For the combustion of 3 mol of methane:

Energy released = (3 mol) x (-890.36 kJ/mol) = -2671.08 kJ

For the combustion of 2.5 mol of methanol:

Energy released = (2.5 mol) x (-726.74 kJ/mol) = -1816.85 kJ

Therefore, the experiment that will release the most energy is the combustion of 3 mol of methane, which will release -2671.08 kJ of energy.

There are 0.1812 moles of HCl involved in the Grignard reaction.

The Grignard reaction is a type of organic chemical reaction that involves the nucleophilic addition of an organomagnesium halide (Grignard reagent) to an electrophilic carbon atom in a compound, typically a carbonyl group (such as an aldehyde, ketone, or ester).

To determine the number of moles of HCl involved in the Grignard reaction, we can use the following formula;

moles = concentration x volume

where concentration is in units of M (molarity) and volume is in units of L.

Converting the given volume to liters

30.2 mL = 30.2/1000 L = 0.0302 L

Using the formula above, we can calculate the number of moles of HCl involved in the reaction as;

moles = concentration x volume = 6 M x 0.0302 L

= 0.1812 moles

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By using ideal gas law , water at 23°C and 745 mm Hg of total pressure, the volume it would have taken up would have been **0.87 L**.

In the limit of low pressures and high temperatures, the ideal gas law describes a relationship between a gas's pressure P, volume V, and temperature T such that the molecules of the gas move practically independently of one another. It can be derived from the kinetic theory of gases and is predicated on the following premises: (1) the gas is made up of numerous molecules that move randomly and in accordance with Newton's laws of motion; (2) the volume of the molecules is negligibly small in comparison to the volume occupied by the gas; and (3) no forces act on the molecules other than elastic collisions that last for a negligibly short period of time.

The ideal gas law can be used to resolve this issue. PV = nRT, where P is pressure, V is volume, n is the number of moles of gas, R is the gas constant, and T is temperature in Kelvin, is the formula for the ideal gas law.

P = 760 mmHg and T = 273 K are the STP (Standard Temperature and Pressure) conditions.

It is possible to compute the amount of dry gas at STP as follows:

V1 = nRT/P

where V1 is the dry gas volume at STP.

n/V = P/RT

The moles in a gas per unit volume are denoted by the ratio n/V.

In the case of dry gas, n/V is equal to (760 mmHg)/(62.36 L.mmHg-1.K⁻¹x 273 K) = 0.0282 mol/L.

The formula is (21 mmHg)/(62.36 L.mmHg-1.K⁻¹ x 296 K) = 0.00089 mol/L for water vapour.

The following formula can be used to determine the total number of moles per unit volume of gas at 745 mmHg and 296 K:

n/V = P/RT

n/V for total gas is equal to (0.0257 mol/L)/745 mmHg/(62.36 L.mmHg-1.K⁻¹ x 296 K).

The following formula can be used to get the number of moles per unit volume of dry gas at 745 mmHg and 296 K:

n/V for dry gas at 745 mmHg and 296 K equals (Ptotal - Pvapour)/PSTP for dry gas at STP.

where P vapour is the water vapour pressure at 23 degrees Celsius, which is 21 mmHg.

(0.0282 mol/L) x (745 - 21)/760 equals n/V for dry gas at 745 mmHg and 296 K.

= 0.0265 mol/L

The following formula can be used to get the volume of dry gas at 745 mmHg and 296 K:

V2 = nRT/P

where V2 is the dry gas volume at 745 mmHg and 296 °C.

V2 is equal to 0.0265 mol/L times 62.36 L.mmHg-1.K-1 x 296 K and 745 mmHg.

= **0.87 L**

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