5. when a gas expands adiabatically, a) the internal energy of the gas decreases. b) the internal energy of the gas increases. c) there is no work done by the gas.

Answers

Answer 1

When a gas expands adiabatically, the internal energy of the gas decreases. The correct answer is A)

In an adiabatic process, there is no exchange of heat between the system and the surroundings. Therefore, the first law of thermodynamics tells us that any change in the internal energy of the gas is due solely to work done by or on the gas.

When a gas expands adiabatically, it does work on its surroundings by pushing back the external pressure, which results in a decrease in the internal energy of the gas. This is because the work done by the gas causes a decrease in the kinetic energy of the gas molecules, which in turn leads to a decrease in the temperature and internal energy of the gas.

Therefore, option A, "the internal energy of the gas decreases" is the correct answer. Option B is incorrect because the internal energy of the gas actually decreases in an adiabatic expansion. Option C is also incorrect because work is being done by the gas in an adiabatic expansion.

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Related Questions

Calculate the pH of a 0.36 M CH3COONa (sodium acetate) solution. (Ka for acetic acid = 1.8 x 10-5).

Answers

The pH of the 0.36 M CH₃COONa that is sodium acetate solution is 9.2 .

The ka for the acetic acid value = 1.8 × 10⁻⁵

The Sodium acetate that is the conjugate base of the acetic acid. The Sodium acetate called as the weak base.

kb = kw / ka

kb = 10⁻¹⁴ / 1.8 × 10⁻⁵

kb = 5.5 × 10⁻⁸

kb = x² / [B] - x

5.5 × 10⁻⁸ = x² / 0.36 - x

x = 1.5 × 10⁻⁵

The value for the hydrogen ion concentration is :

[H⁺] = 1.5 × 10⁻⁵

The expression for the pOH is as :

pOH = - log (1.5 × 10⁻⁵)

pOH = 4.8

The expression for the pOH is as :

pH = 14 - pOH

pH = 14 - 4.8

pH = 9.2

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To calculate the pH of a 0.36 M CH3COONa solution, you need to consider the hydrolysis of the acetic acid in the solution. The concentration of hydroxide ions can be used to determine the pOH and pH of the solution.

The pH of a 0.36 M CH3COONa (sodium acetate) solution can be calculated by using the ionization constant (Ka) of acetic acid.

The equation for the ionization of acetic acid is: CH3COOH + H2O ⇌ CH3COO- + H3O+

Since sodium acetate is a salt of a weak acid (acetic acid) and a strong base (sodium hydroxide), it undergoes hydrolysis and produces hydroxide ions (OH-) in the solution. The concentration of OH- ions can be used to calculate the pOH and pH of the solution.

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How could you free a protein from a GPI anchor? You may choose more than one answer. O a high salt concentration wash (1 M NaCl) phospholipase C that removes the phosphoalcohol head group detergents to disrupt the membrane a high pH (9.0) bicarbonate wash O glycosylases that degrade the carbohydrate linkages

Answers

To free a protein from a GPI anchor, one could use a combination of detergents to disrupt the membrane, as well as a high pH (9.0) bicarbonate wash.

Phospholipase C can also be used to remove the phosphoalcohol head group, and glycosylases can degrade the carbohydrate linkages. However, a high salt concentration wash (1 M NaCl) is not typically effective for releasing proteins from GPI anchors.

Phospholipase C is an enzyme that cleaves the phosphoalcohol head group from the GPI anchor, releasing the protein from the cell membrane. This method is often used in research labs to free a protein from its GPI anchor.

Detergents are amphipathic molecules that can disrupt cell membranes and solubilize membrane proteins. In the case of a protein with a GPI anchor, detergents can be used to solubilize the membrane and release the protein from the anchor. High salt concentration wash, high pH (9.0) bicarbonate wash, and glycosylases that degrade the carbohydrate linkages are not effective methods to free a protein from a GPI anchor.

Therefore, To free a protein from a GPI anchor use a combination of detergents to disrupt the membrane, as well as a high pH (9.0) bicarbonate wash. Phospholipase C can also be used to remove the phosphoalcohol head group, and glycosylases can degrade the carbohydrate linkages.

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the reaction of 4-pentanoylbiphenyl and hydrazine without potassium hydroxide is a net? a. substitution b. addition c. rearrangement d. elimination

Answers

The reaction of 4-pentanoylbiphenyl and hydrazine without potassium hydroxide is a net addition reaction. The correct option is b.

When 4-pentanoylbiphenyl reacts with hydrazine in the absence of potassium hydroxide, the carbonyl group of the 4-pentanoylbiphenyl undergoes addition reaction with hydrazine to form a hydrazone product. This is an example of a net addition reaction, where two molecules combine to form a single product.

The reaction does not involve the substitution of any functional groups, rearrangement of atoms or elimination of any functional group. The absence of potassium hydroxide in the reaction mixture does not influence the mechanism of the reaction but rather affects the rate of reaction. Potassium hydroxide is often used as a catalyst in the reaction to increase the rate of the reaction. Therefore, the correct option is b.

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Lewis Structures and Formal Charge 1) Three possible Lewis structures for the thiocyanate ion, NCS, are given below: [—c=s] (n=c=s] (n=c-s)" a) Complete each structure by adding the lone pair electrons. b) Determine the formal charges of the atoms in each structure. Formal charge can be used to distinguish between competing structures. In general, the following rules apply: i) The sum of all formal charges in a neutral molecule must be zero. ii) The sum of all formal charges in an ion must equal the charge on the ion. iii) Small or zero formal charges on individual atoms are better than larger ones. iv) When formal charge cannot be avoided on an atom, negative charges are better on more electronegative atoms. c) Decide which Lewis structure is the preferred one and give an explanation below

Answers

The preferred Lewis structure for the thiocyanate ion (NCS-) is [tex][C≡N-S]⁻[/tex].

The Lewis structures and formal charges for the thiocyanate ion[tex](NCS-)[/tex]. Here are the steps:

a) Adding lone pair electrons to each structure:

1. [tex][C≡N-S]⁻: C[/tex] has 2 lone pairs, N has 1 lone pair, and S has 2 lone pairs.
2. [tex][N=C=S]⁻: N[/tex] has 2 lone pairs, C has 3 lone pairs, and S has 2 lone pairs.
3. [tex][N-C≡S]⁻: N[/tex]has 3 lone pairs, C has 2 lone pairs, and S has 1 lone pair.

b) Determining the formal charges:

1. [tex][C≡N-S]⁻: C: 0, N: 0, S: -1[/tex]
2.[tex][N=C=S]⁻: N: -1, C: 0, S: 0[/tex]
3.[tex][N-C≡S]⁻: N: -1, C: 0, S: 0[/tex]

c) Deciding the preferred Lewis structure:

Considering the rules, Structure 1 is preferred because:
i) The sum of all formal charges equals -1, which is the charge on the ion.
ii) It has smaller or zero formal charges on individual atoms.
iii) The negative charge is on the more electronegative atom (Sulfur).

So, the preferred Lewis structure for the thiocyanate ion[tex](NCS-) is [C≡N-S]⁻.[/tex]

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Some chemical reactions proceed by the initial loss or transfer of an electron to a diatomic species. Which of the molecules N2, NO, O2, C2, F2, and CN would you expect to be stabilized by (a) the addition of an election to form AB-, (b) the removal of an electron to form AB + ?

Answers

The stability of diatomic species depends on various factors such as electron affinity and ionization energy. N2- and CN- would be stabilized by the addition of an electron, while F2+ and C2+ would be stabilized by the removal of an electron.

Chemical reactions involve the formation and breaking of bonds between molecules. The stability of a molecule is determined by the number and arrangement of its electrons. Some chemical reactions proceed by the loss or transfer of an electron to a diatomic species. In this context, we can consider the stability of diatomic species N2, NO, O2, C2, F2, and CN.
(a) The addition of an electron to form AB- would stabilize the diatomic species that has a higher electron affinity, i.e., the tendency to attract an electron. Among the given molecules, N2 and CN have the highest electron affinity. Therefore, we can expect N2- and CN- to be more stable.
(b) The removal of an electron to form AB+ would stabilize the diatomic species that has a lower ionization energy, i.e., the energy required to remove an electron. Among the given molecules, F2 and C2 have the lowest ionization energy. Therefore, we can expect F2+ and C2+ to be more stable.

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given the following equation, h2o(g) co(g) → h2(g) co2(g) δg°rxn = -28.6 kj calculate δg°rxn for the following reaction. 4 h2o(g) 4 co(g) → 4 h2(g) 4 co2(g)

Answers

The value of ΔG⁰ for the given reaction is - 114.4kJ.

Gibbs free energy, also known as the Gibbs function, Gibbs energy, or free enthalpy, is a quantity that is used to measure the maximum amount of work done in a thermodynamic system when the temperature and pressure are kept constant.

A compound’s standard energy change of formation is the Gibbs energy change that goes along with the formation of one mole of that same substance from its constituent elements at standard rates

Given,

For the reaction, H₂O + CO = H₂ + CO₂

ΔG⁰ = - 28.6 kJ

For the reaction, 4H₂O + 4CO = 4H₂ + 4CO₂

ΔG⁰ = - 28.6 × 4

= -114.4 kJ

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Estimate the heat capacity for each of the following gases based on their translational and rotational modes: Rn, SO3, O3, HCN .
Options:
R
0.5R
1.5R
2R
2.5R
3R
3.5R

Answers

The heat capacity of Rn is 1.5R, SO3 is 2.5R, and O3 and [tex]HCN[/tex] are 3.5R due to their respective translational and rotational degrees of freedom.

Heat capacity

The heat capacity of a gas depends on the number of degrees of freedom available for energy transfer. For a monatomic gas like [tex]R_n[/tex], there are three translational degrees of freedom, but no rotational degrees of freedom.

For a linear molecule like [tex]SO_3[/tex], there are three translational degrees of freedom and two rotational degrees of freedom. For a nonlinear molecule like [tex]O_3[/tex] or [tex]HCN[/tex], there are three translational degrees of freedom and three rotational degrees of freedom.

The equipartition theorem states that each degree of freedom contributes 1/2kT to the heat capacity, where k is the Boltzmann constant and T is the temperature. Therefore, the heat capacity for each gas can be estimated as:

Rn: 3/2R (only translational degrees of freedom)SO3: 5/2R (3 translational degrees of freedom + 2 rotational degrees of freedom)[tex]O_3[/tex] or [tex]HCN[/tex]: 7/2R (3 translational degrees of freedom + 3 rotational degrees of freedom)

where R is the gas constant.

So the options for the heat capacity of each gas are:

R0.5R1.5R2R2.5R3R3.5

For Rn, the correct option would be R1.5, since the heat capacity only includes translational degrees of freedom.

For [tex]SO_3[/tex], the correct option would be R2.5, since the heat capacity includes both translational and rotational degrees of freedom.

For [tex]O_3[/tex] and [tex]HCN[/tex], the correct option would be R3.5, since the heat capacity includes three rotational degrees of freedom in addition to the three translational degrees of freedom.

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the instability of xenon fluorides is due to its negative enthalpy of formation. true false

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True. The negative enthalpy of formation of xenon fluorides contributes to their instability.


The instability of xenon fluorides is due to its negative enthalpy of formation, indicating that the reaction is exothermic and energy is released when xenon fluorides are formed. This makes them less stable compared to their reactants.

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True. The instability of xenon fluorides is due to its negative enthalpy of formation.

The enthalpy of formation refers to the energy released or absorbed when a compound is formed from its constituent elements. In the case of xenon fluorides, the energy released during the formation of the compound is less than the energy required to break apart the compound, resulting in an overall negative enthalpy of formation. This means that the formation of the compound is thermodynamically unfavorable, and the compound is therefore unstable and prone to decomposition.

Additionally, the electronegativity difference between xenon and fluorine is significant, which contributes to the instability of xenon fluorides. Therefore, xenon fluorides tend to be highly reactive and explosive, making them difficult to handle and store safely.

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give the structure that corresponds to the following molecular formula and h1 nmr spectrum: c5h10 : δ 1.5, s

Answers

The most likely structure for this compound is a branched alkane with a methyl group (CH3) attached to a quaternary carbon

What is NMR spectrum?

The molecular formula C5H10 suggests that the compound has 5 carbon atoms and 10 hydrogen atoms. However, the H1 NMR spectrum you provided only shows a singlet peak at δ 1.5, which indicates that there is only one type of hydrogen in the molecule.

Therefore, the most likely structure for this compound is a branched alkane with a methyl group (CH3) attached to a quaternary carbon (a carbon with four other carbon atoms attached to it). This would give a total of 5 carbon atoms and 10 hydrogen atoms, with only one type of hydrogen atom that would appear as a single peak in the H1 NMR spectrum at around δ 1.5.

One possible structure that fits this description is 2-methyl butane:

  CH3

   |

CH3-C-CH2-CH2-CH3

   |

  CH3

In this structure, the methyl group is attached to a quaternary carbon (the central carbon atom), and all of the carbon atoms are saturated with hydrogen atoms. The H1 NMR spectrum for this compound would show a singlet peak at around δ 1.5 for the nine equivalent hydrogen atoms in the three methyl groups.

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calculate the ph of an aqueous solution, which has an [h3o ] = 1.0x10-11 m.

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The pH of the aqueous solution with an [H3O+] concentration of 1.0x10-11 M is 11.

The pH scale is a logarithmic scale that measures the concentration of hydrogen ions in a solution. A pH of 7 is neutral, while a pH below 7 is acidic and a pH above 7 is basic. The pH can be calculated using the formula pH = -log[H3O+].

In this case, the [H3O+] concentration is 1.0x10-11 M.

To calculate the pH of an aqueous solution with an [H3O+] concentration of 1.0 x 10^-11 M:

The pH is calculated using the formula pH = -log10[H3O+]. In this case, the [H3O+] concentration is 1.0 x 10^-11 M.

By substituting the given concentration into the formula, we get pH = -log10(1.0 x 10^-11). Calculating the logarithm, we find that the pH of the aqueous solution is 11, which is basic.

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Rank the bonds in each set in order of increasing bond length and increasing bond strength: (a) C≡N, C≡O, C≡C; (b) P-I, P-F, P-Br. And Rank the bonds in each set in order of decreasing bond length and decreasing bond strength: (a) Si-F, Si-C, Si-O; (b) N=N, N-N, N≡N.

Answers

Explanation:

There is a well-known relationship between the bond length of a diatomic molecule and the atomic radius of its constituent atoms, known as the covalent radius. Specifically, the covalent radius of an atom is half the bond length between two identical atoms in a diatomic molecule.

Therefore, to determine the atomic radius of chlorine (Cl), we can use the bond length of fluorine (F2) and the fact that the two atoms in F2 are identical.

Since the bond length of F2 is given as 1.28 A, the covalent radius of fluorine is 1.28/2 = 0.64 A.

Since both fluorine and chlorine are halogens, they have similar electronic configurations and form similar covalent bonds. Therefore, we can use the covalent radius of fluorine as an estimate for the covalent radius of chlorine.

Thus, the atomic radius of chlorine is approximately 0.64 A.



Rank the bonds in each set in order of increasing bond length and increasing bond strength: (a) C≡N, C≡O, C≡C; (b) P-I, P-F, P-Br. And Rank the bonds in each set in order of decreasing bond length and decreasing bond strength: (a) Si-F, Si-C, Si-O; (b) N=N, N-N, N≡N

ChatGPT

(a) C≡C < C≡N < C≡O (increasing bond length); C≡O < C≡N < C≡C (increasing bond strength)

Explanation: In a series of molecules with the same central atom, the bond length decreases as the number of bonds between the central atom and the surrounding atoms increases. Therefore, in set (a), the C≡C bond is the shortest, followed by the C≡N bond, and then the C≡O bond. Similarly, the bond strength increases with the number of bonds between the central atom and the surrounding atoms. Therefore, the C≡C bond is the strongest, followed by the C≡N bond, and then the C≡O bond.

(b) P-F < P-Br < P-I (increasing bond length); P-I < P-Br < P-F (increasing bond strength)

Explanation: In a series of molecules with the same surrounding atom, the bond length increases as the central atom gets larger. Therefore, in set (b), the P-I bond is the longest, followed by the P-Br bond, and then the P-F bond. Similarly, the bond strength decreases as the central atom gets larger. Therefore, the P-I bond is the weakest, followed by the P-Br bond, and then the P-F bond.

(c) Si-O < Si-C < Si-F (decreasing bond length); Si-F < Si-C < Si-O (decreasing bond strength)

Explanation: In a series of molecules with the same central atom, the bond length increases as the electronegativity of the surrounding atom increases. Therefore, in set (c), the Si-F bond is the longest, followed by the Si-C bond, and then the Si-O bond. Similarly, the bond strength decreases as the electronegativity of the surrounding atom increases. Therefore, the Si-F bond is the weakest, followed by the Si-C bond, and then the Si-O bond.

(d) N≡N < N-N < N=N (decreasing bond length); N≡N > N-N > N=N (decreasing bond strength)

Explanation: In a series of molecules with the same central atom, the bond length decreases as the number of bonds between the central atom and the surrounding atoms increases. Therefore, in set (d), the N≡N bond is the shortest, followed by the N-N bond, and then the N=N bond. Similarly, the bond strength increases with the number of bonds between the central atom and the surrounding atoms. Therefore, the N≡N bond is the strongest, followed by the N-N bond, and then the N=N bond.

1.(a) In order of increasing bond length: C≡N, C≡C, C≡O and In order of increasing bond strength: C≡O, C≡C, C≡N and (b) In order of increasing bond length: P-F, P-Br, P-I and In order of increasing bond strength: P-I, P-Br, P-F. 2. (a) In order of decreasing bond length: Si-F, Si-O, Si-C and In order of decreasing bond strength: Si-O, Si-C, Si-F and (b) In order of decreasing bond length: N≡N, N=N, N-N and In order of decreasing bond strength: N≡N, N=N, N-N.

1. (a) This is because nitrogen is smaller than carbon, so the triple bond is shorter and stronger. Carbon-oxygen bonds are typically shorter and stronger than carbon-carbon bonds, so C≡O is shorter and stronger than C≡C. In order of increasing bond strength the order is  P-I, P-Br, P-F because oxygen is more electronegative than carbon, so the carbon-oxygen bond is more polar and stronger.

(b) The bond length order is so because fluorine is smaller than bromine or iodine, so the bond is shorter and stronger. and the bond strength order is so because iodine is larger than fluorine or bromine, so the bond is weaker and longer.


2. (a) This is because fluorine is smaller than oxygen, so the bond is shorter and stronger. Oxygen is smaller than carbon, so the bond is shorter and stronger. In order of decreasing bond strength the order is Si-O, Si-C, Si-F because oxygen is more electronegative than carbon, so the carbon-oxygen bond is more polar and stronger. Fluorine is more electronegative than carbon, so the carbon-fluorine bond is more polar and stronger.

(b) The bond length order is so because the triple bond is shorter and stronger than the double bond, which is shorter and stronger than the single bond and the bond strength order is so because the triple bond is stronger than the double bond, which is stronger than the single bond.

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draw the lewis structure. depict the vsepr theory geometry, and indicate the polority of the following molecules clf3, clf4-, clf2 , xef5- if4

Answers

The VSEPR theory geometry for XeF5- would be square pyramidal, with a bond angle of 90 degrees. The molecule is polar due to the asymmetrical distribution of the XeF5- molecule.

To draw the Lewis structure for each molecule, we need to first count the total number of valence electrons in each atom. Chlorine (Cl) has 7 valence electrons and Fluorine (F) has 7 valence electrons, and Xenon (Xe) has 8 valence electrons.
For the molecule ClF3, we have a total of 28 valence electrons. The Lewis structure would look like:

                   Cl
                  /  \
                F    F
                 \   /
                   Cl

The VSEPR theory geometry for ClF3 would be trigonal bipyramidal, with a bond angle of 120 degrees. The molecule is polar due to the asymmetrical distribution of the ClF3 molecule, which results in a dipole moment.
For the ClF4- molecule, we would add an extra electron to the total valence electrons to account for the negative charge, giving us a total of 32 valence electrons. The Lewis structure would look like:

                    Cl
                   / \
                 F   F
                |     |
                 F   F
                   \ /
                    Cl-

The VSEPR theory geometry for ClF4- would be square planar, with a bond angle of 90 degrees. The molecule is nonpolar due to the symmetrical distribution of the ClF4- molecule.
For the ClF2 molecule, we have a total of 20 valence electrons. The Lewis structure would look like:

                   Cl
                   |
                 F    F

The VSEPR theory geometry for ClF2 would be linear, with a bond angle of 180 degrees. The molecule is polar due to the asymmetrical distribution of the ClF2 molecule.
For the XeF5- molecule, we would add an extra electron to the total valence electrons to account for the negative charge, giving us a total of 42 valence electrons. The Lewis structure would look like:

                     F
                    / \
               F - Xe - F
                    \ /
                     F
                      -

The VSEPR theory geometry for XeF5- would be square pyramidal, with a bond angle of 90 degrees. The molecule is polar due to the asymmetrical distribution of the XeF5- molecule.

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the iupac name is: 1‑methylcyclohex‑1‑en‑5‑one 2‑methylcyclohex‑1‑en‑4‑one 5‑methylcyclohex‑4‑en‑1‑one 3‑methylcyclohex‑3‑en‑1‑one

Answers

The IUPAC name given consists of four different compounds: 1-methylcyclohex-1-en-5-one is methyl group, 2-methylcyclohex-1-en-4-one is methyl group, 5-methylcyclohex-4-en-1-one is methyl group, and 3-methylcyclohex-3-en-1-one is methyl group.

In 1-methylcyclohex-1-en-5-one, there is a methyl group at position 1 of the cyclohexene ring, and the ketone functional group is at position 5. Similarly, for 2-methylcyclohex-1-en-4-one, the methyl group is at position 2, and the ketone is at position 4. In 5-methylcyclohex-4-en-1-one, the methyl group is at position 5, and the ketone is at position 1. Finally, in 3-methylcyclohex-3-en-1-one, the methyl group is at position 3, and the ketone is at position 1.

These compounds are all derivatives of cyclohexenone, which is a cyclic ketone with a double bond in its structure. The IUPAC nomenclature system helps in systematically identifying and naming these organic compounds based on their structure. These compounds are examples of structural isomers, as they have the same molecular formula but different arrangements of atoms within their structure. Understanding and applying IUPAC nomenclature is crucial for clear communication among chemists and for the accurate identification of compounds in research and industry, all the compunds mention is methyl group.

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A solution formed from the dissociation of calcium sulfate, caso4. determine the molar solubility of this salt.

Answers

The molar solubility of CaSO4 in the solution is approximately 4.9 × 10⁻³ mol/L.

The dissociation of calcium sulfate, CaSO4, in water results in the formation of calcium ions, Ca2+, and sulfate ions, SO42-. The balanced chemical equation for this dissociation is:

CaSO4(s) ⇌ Ca2+(aq) + SO42-(aq)

To determine the molar solubility of this salt, we need to find the concentration of the ions in the solution at equilibrium. Let's assume that x mol/L of CaSO4 dissociates, which means that the concentration of Ca2+ and SO42- ions in the solution will also be x mol/L.

Using the balanced chemical equation, we can set up an expression for the solubility product, Ksp, which is the product of the concentrations of the ions raised to their stoichiometric coefficients:

Ksp = [Ca2+][SO42-] = x^2

The Ksp for calcium sulfate is 4.93 x 10^-5 at 25°C, so we can solve for x:

4.93 x 10^-5 = x^2

x = 2.22 x 10^-3 mol/L

Therefore, the molar solubility of calcium sulfate is 2.22 x 10^-3 mol/L.
Hi! To determine the molar solubility of calcium sulfate (CaSO4) in a solution, you need to consider its solubility product constant (Ksp). The Ksp value for CaSO4 is 2.4 × 10⁻⁵. When CaSO4 dissociates in water, it forms calcium ions (Ca²⁺) and sulfate ions (SO₄²⁻).

The balanced dissociation equation is:
CaSO4(s) ⇌ Ca²⁺(aq) + SO₄²⁻(aq)

Assuming molar solubility of CaSO4 is 's' mol/L, the concentration of Ca²⁺ and SO₄²⁻ ions in the solution would also be 's' mol/L. The Ksp expression can be written as:

Ksp = [Ca²⁺][SO₄²⁻] = (s)(s) = s²

Now, plug in the Ksp value to solve for 's':

2.4 × 10⁻⁵ = s²
s = √(2.4 × 10⁻⁵) ≈ 4.9 × 10⁻³ mol/L

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thermal energy is added to 160 g of water at the rate of 53 j/s for 2.3 min. How much does the temperature of the water increase?

Answers

The temperature of the water increases by approximately 11.02°C.

To find the temperature increase of the water, we need to use the specific heat formula:

Q = mcΔT

where Q is the thermal energy, m is the mass of water, c is the specific heat capacity of water, and ΔT is the temperature change.

First, let's calculate the total thermal energy (Q) added to the water:

53 J/s * (2.3 min * 60 s/min) = 53 J/s * 138 s

                                              = 7314 J

Next, the mass of the water (m) is given as 160 g, and the specific heat capacity (c) of water is 4.18 J/g°C.

Now, we can plug the values into the formula: 7314 J = (160 g) * (4.18 J/g°C) * ΔT.

Divide both sides by (160 g * 4.18 J/g°C) to find ΔT:

ΔT = 7314 J / (160 g * 4.18 J/g°C)

    ≈ 11.02°C.

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calculate the number of molecules of acetyl-scoa derived from a saturated fatty acid with 22 carbon atoms.

Answers

The number of molecules of acetyl-CoA derived from a saturated fatty acid with 22 carbon atoms is 11.

To calculate this, we need to know that each round of beta-oxidation produces one molecule of acetyl-CoA from a two-carbon unit of the fatty acid chain. In this case, a saturated fatty acid with 22 carbon atoms would go through 11 rounds of beta-oxidation, resulting in the production of 11 molecules of acetyl-CoA.

During beta-oxidation, fatty acids are broken down into two-carbon units that are carried by coenzyme A to the mitochondria, where they are further broken down into acetyl-CoA. The acetyl-CoA then enters the citric acid cycle, which produces energy in the form of ATP. In the case of a saturated fatty acid with 22 carbon atoms, the process of beta-oxidation would produce 11 molecules of acetyl-CoA, which would then enter the citric acid cycle to produce energy for the cell.

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How many grams of sucrose, c12h22o11, a nonvolatile, nonelectrolyte (mw = 342.3 g/mol), must be added to 299.7 grams of water to reduce the vapor pressure to 23.10 mm hg ?

Answers

To solve this problem, we can use Raoult's law, which states that the vapor pressure of a solution is proportional to the mole fraction of the solvent in the solution. In other words, [tex]P_solvent = X_solvent * P°_solvent[/tex]

mass of sucrose comes to be 9.11 g

Since sucrose is a nonvolatile solute, its vapor pressure is negligible and can be assumed to be zero. Therefore, we can use the following equation to calculate the mole fraction of water:[tex]X_water = P_water / P°_water[/tex]

where [tex]P_water[/tex] is the vapor pressure of water in the solution and [tex]P°_water[/tex] is the vapor pressure of pure water. We can rearrange this equation to solve for [tex]P_water[/tex]: [tex]P_water = X_water * P°_water[/tex]

Now we can use the given information to solve for X_water:

[tex]P_water = 23.10 mmHgP°_water = 760 mmHgX_water = P_water / P°_water = 0.0304[/tex]This means that the mole fraction of sucrose in the solution is:

[tex]X_sucrose = 1 - X_water = 0.9696[/tex], To find the mass of sucrose needed, we can use the following equation [tex]mass_sucrose = X_sucrose * mass_solution * (1 / mw_sucrose)[/tex] where mass_solution is the total mass of the solution (water + sucrose) and mw_sucrose is the molar mass of sucrose.

Substituting the given values:  = [tex]0.9696 * (299.7 g + mass_sucrose) * (1 / 342.3 g/mol)[/tex]

Simplifying and solving for mass of sucrose = 9.11 g. Therefore, 9.11 grams of sucrose must be added to 299.7 grams of water to reduce the vapor pressure to 23.10 mmHg.

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What quantity of ethanol is in an 8-ml distillate with a density of 0.812 g/ml?

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To calculate the quantity of ethanol in an 8-ml distillate with a density of 0.812 g/ml, we need to use the formula:
Quantity (in grams) = Density (in g/ml) x Volume (in ml).  There are 3.8976 grams of ethanol in an 8-ml distillate with a density of 0.812 g/ml.


First, we can calculate the mass of the 8-ml distillate by multiplying the volume by the density:
Mass = Density x Volume
Mass = 0.812 g/ml x 8 ml
Mass = 6.496 g
So the total mass of the 8-ml distillate is 6.496 grams.
Next, we need to determine what portion of the mass is ethanol. We can assume that the entire mass of the distillate is due to the combined mass of the ethanol and any other compounds present.
Let's say that the percentage of ethanol in the distillate is x%. This means that the remaining percentage (100 - x) is due to other compounds.
To calculate the mass of ethanol in the distillate, we need to multiply the total mass by the percentage of ethanol:
Mass of ethanol = Total mass x % ethanol
Mass of ethanol = 6.496 g x (x/100)
For example, if the distillate is 60% ethanol, then:
Mass of ethanol = 6.496 g x (60/100)
Mass of ethanol = 3.8976 g
So there are 3.8976 grams of ethanol in an 8-ml distillate with a density of 0.812 g/ml.

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under what conditions is s2p the average of the two sample variances?

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Answer:One way to compare the variability of two populations is to use the pooled variance, which is a weighted average of the two sample variances.

Explanation:The pooled variance is denoted by s2p and it is calculated as follows:

s2p = [(n1 - 1)s12 + (n2 - 1)s22] / (n1 + n2 - 2)

where n1 and n2 are the sample sizes and s12 and s22 are the sample variances. The pooled variance is the average of the two sample variances when the two populations have the same variance and the two sample sizes are equal. In other words, s2p = (s12 + s22) / 2 when σ12 = σ22 and n1 = n2. This is one condition under which s2p is the average of the two sample variances.

how can insulating zro2 be made into an electronic conductor

Answers

Insulating zirconia ( [tex]ZrO_2[/tex]) can be made into an electronic conductor by introducing dopants, which are atoms or molecules that are added to the material to change its properties.

These dopants can create oxygen vacancies in the [tex]ZrO_2[/tex] lattice, which can then act as electron carriers and enable the material to conduct electricity. Some common dopants used for zirconia include yttria (Y2O3), ceria (CeO2), and alumina ([tex]Al_2O_3[/tex]). By carefully controlling the dopant concentration and processing conditions, it is possible to tailor the electronic properties of [tex]ZrO_2[/tex] to meet specific application requirements, such as in fuel cells, sensors, and electronic devices.

In summary, insulating  [tex]ZrO_2[/tex] can be made into an electronic conductor by doping it with impurities like [tex]Y_2O_3[/tex] or CaO, which create oxygen vacancies and ionic conductivity, leading to electronic conductivity in the material.

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Consider the interval 0≤x≤L. What is the second derivative, with respect to x, of the wave function ψn(x) in this interval? Express your answer in terms of n, x, L, and C as needed.d2dx2ψn(x) =

Answers

The second derivative of the wave function ψn(x) in the interval 0≤x≤L is given by the expression:
d2/dx2 ψn(x) = -C (nπ/L)^2 cos(nπx/L).


To find the second derivative of the wave function ψn(x), we need to first know what the wave function represents. In quantum mechanics, the wave function describes the probability amplitude of a particle's position in space. It is a mathematical representation of the wave-like behavior of a particle.
The wave function ψn(x) represents the probability amplitude of a particle in the nth energy state in the interval 0≤x≤L. The second derivative of the wave function with respect to x gives us information about the curvature of the wave.
To find the second derivative, we need to differentiate the wave function twice with respect to x. The first derivative of the wave function ψn(x) is given by:
d/dx ψn(x) = C sin(nπx/L)
Where C is a constant that depends on the normalization of the wave function. The second derivative is given by:
d2/dx2 ψn(x) = -C (nπ/L)^2 cos(nπx/L)
This expression tells us that the second derivative of the wave function is proportional to the negative of the square of the wave number (nπ/L)^2 and the cosine of the position x. This means that the wave function has a maximum curvature at the points where the cosine function equals 1 or -1. These points correspond to the nodes of the wave function.

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what, if any, constraints does a value of m=1 place on the other quantum numbers for an electron in an atom?

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If the any, the constraints have the value of the ml = 1 that place on the  quantum numbers for the electron in the atom is n ≥ 2 and the l ≥ 1.

The electron have the magnetic number of ml = 1, then it will not have the orbital quantum number of the l = 0. The Quantum numbers is that will specify and have properties for the atomic orbitals and will electrons in those orbitals. The electron in the atom or the ion has the four quantum numbers that will describe the state.

The magnetic quantum number is :

ml = 1

ml = -l , -l , +1 ....0.....l, -1, l

l = 0,1,2.....(n-1)

l = 0,1

Therefore, n ≥ 2 and the l ≥ 1.

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complete and balance the following redox reaction in acidic solution h2o2 cr2o7-2

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The balanced redox reaction in an acidic solution involving H2O2 and Cr2O7^-2 is:

Cr2O7^−2(aq) + 8H^+  +  3H2O2(aq)  →   3O2(g) + 2Cr3^+(aq)  +   7H2O

In this reaction, H2O2 acts as the reducing agent, while Cr2O7^-2 acts as the oxidizing agent.

The oxidation number of Chromium changes from +6 to +3, therefore, it gets reduced.

The oxidation number of oxygen changes from -1 to 0, therefore, it gets oxidized.

The addition of 8 H+ ions on the reactant side helps to balance the charges on both sides of the equation and makes the solution acidic.

Finally, the balanced reaction is shown below.

Cr2O7^−2(aq) + 8H^+  +  3H2O2(aq)  →   3O2(g) + 2Cr3^+(aq)  +   7H2O

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Analyte


HCl


Mole of Analyte (HCl)


(Equal to the moles of titrant)





Concentration (M)of analyte (HCl)


Step 1- divide volume dispensed of analyte by 1000 to get L of analyte


Step 2- Divide moles of analyte by liters of analyte to get concentration.






Average concentration(M) of analyte.


Add up the analyte concentrations from the three trials. Divide your answer by 3. Include 3 significant digits in your answer.



Percent error of concentration (M) of analyte.



Actual concentration of HCl = 0. 120 M


Experimental concentration- Use the average you calculated.



Step 1- Subtract experimental value from actual value.


Step 2- Divide answer in Step 1 by actual value.


Step 3- Multiply answer in Step 3 by 100.



Your answer should be expressed as a percentage.

Answers

The average concentration of HCl is calculated by adding up the concentrations from three trials and dividing the sum by 3. The percent error of the experimental concentration is determined by comparing it to the actual concentration and expressing the difference as a percentage.

To calculate the average concentration of HCl, we perform the following steps for three trials:

1. Divide the volume dispensed of HCl by 1000 to convert it to liters.

2. Divide the moles of HCl by the liters of HCl to obtain the concentration in moles per liter (M).

3. Repeat steps 1 and 2 for each trial.

4. Add up the concentrations obtained from the three trials.

5. Divide the sum by 3 to find the average concentration of HCl, rounding the answer to three significant digits.

To calculate the percent error of the experimental concentration compared to the actual concentration, we use the following steps:

1. Subtract the experimental concentration (average concentration calculated) from the actual concentration of HCl (given as 0.120 M).

2. Divide the difference obtained in step 1 by the actual concentration.

3. Multiply the quotient from step 2 by 100 to express the percent error.

The result will provide the percent error of the experimental concentration of HCl compared to the actual concentration.

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A reaction that consumed 3. 50 mol of H2 produced 50. 0 g of H20. What


is the percent yield of the reaction? Round to the nearest tenths place

Answers

To determine the percent yield of the reaction. to compare the actual yield (the amount of product obtained experimentally) to the theoretical yield (the amount of product that would be obtained according to stoichiometry).

Given:

Moles of H2 consumed = 3.50 mol

Mass of H2O produced = 50.0 g

Step 1: Calculate the molar mass of H2O.

The molar mass of H2O is calculated by summing the atomic masses of hydrogen (H) and oxygen (O):

Molar mass of H2O = (2 × atomic mass of H) + atomic mass of O

Molar mass of H2O = (2 × 1.008 g/mol) + 16.00 g/mol

Molar mass of H2O = 18.02 g/mol

Step 2: Calculate the theoretical yield of H2O.

Theoretical yield of H2O = Moles of H2 × (Molar mass of H2O / Moles of H2O per mole of H2)

The balanced equation for the reaction is:

2 H2 + O2 → 2 H2O

From the equation, we can see that 2 moles of H2 produce 2 moles of H2O.

So, Moles of H2O per mole of H2 = 2

Theoretical yield of H2O = 3.50 mol × (18.02 g/mol / 2)

Theoretical yield of H2O = 31.535 g

Step 3: Calculate the percent yield.

Percent yield = (Actual yield / Theoretical yield) × 100

Percent yield = (50.0 g / 31.535 g) × 100

Percent yield ≈ 158.9%

Rounding to the nearest tenths place, the percent yield of the reaction is approximately 158.9%.

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list two groups ( two or more members) of these diatomic molecules with the same number of electrons

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Two groups of diatomic molecules with the same number of electrons are nitrogen (N2) and oxygen (O2), and chlorine (Cl2) and fluorine (F2).

Diatomic molecules are molecules that consist of two atoms of the same element. Nitrogen, oxygen, chlorine, and fluorine are all diatomic molecules, meaning they have two atoms in their structure. Nitrogen and oxygen each have 14 electrons in their outermost electron shell, while chlorine and fluorine each have 14 electrons in their outermost electron shell as well. Therefore, nitrogen and oxygen have the same number of electrons, and chlorine and fluorine have the same number of electrons.

Group 2: Both N2 and O2 molecules have a total of 14 electrons each. N2 has 5 electrons per nitrogen atom, and 2 shared electrons in the triple covalent bond, making a total of 14 electrons for the entire molecule. O2 has 6 electrons per oxygen atom and 2 shared electrons in the double covalent bond, also resulting in a total of 14 electrons for the entire molecule.

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86. What attracts or directs the synthesis enzyme to the template in Translation? a. Start Codon b. 5'-cap c. Primer d. Promoter e. Poly-A Tail
92. Which of the following is the description for Catabolic Reactions? a. the energy of movement b. the breaking down of complex molecules into simpler ones c. energy converted from one form to another d. energy is neither created nor destroyed e. the linking of simple molecules to form complex molecules

Answers

86. The element that attracts or directs the synthesis enzyme to the template in Translation is a. Start Codon. The start codon is a specific sequence of nucleotides that signals the beginning of the translation process. 92. The description for Catabolic Reactions is b. the breaking down of complex molecules into simpler ones. These reactions release energy by breaking down complex molecules and are involved in processes like digestion and cellular respiration.

For the first question (86), the long answer is that the synthesis enzyme is attracted and directed to the template in Translation by the start codon. The start codon, which is usually AUG in eukaryotic cells, signals to the synthesis enzyme that it should begin the process of synthesizing a protein. The start codon is located at the beginning of the messenger RNA (mRNA) sequence, and once the synthesis enzyme recognizes it, it begins to read the codons that follow and assemble the corresponding amino acids to form the protein. For the second question (92), the long answer is that catabolic reactions are the breaking down of complex molecules into simpler ones. These reactions release energy that can be used for cellular processes. Catabolic reactions are the opposite of anabolic reactions, which involve the linking of simple molecules to form complex molecules and require energy input. The energy released from catabolic reactions can be converted from one form to another and used for activities such as movement, transport, and chemical reactions.

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reaction of nickel nitrate hexahydrate with ki and pph3

Answers

Ni(NO3)2·6H2O + 2KI + 3PPh3 → Ni(PPh3)3I2 + 6H2O + 2KNO3

The reaction of nickel nitrate hexahydrate with KI and PPh3 results in the formation of a nickel(II) complex with PPh3 b.

The reaction can be represented by the following balanced equation:

Ni(NO3)2·6H2O + 2KI + 3PPh3 → Ni(PPh3)3I2 + 6H2O + 2KNO3

In this reaction, the KI serves as a source of iodide ions (I-) which react with the nickel(II) ions (Ni2+) from nickel nitrate hexahydrate. The PPh3 (triphenylphosphine) acts as a ligand and coordinates with the nickel(II) ions, forming a coordination complex. The resulting complex is Ni(PPh3)3I2, where three PPh3 ligands are attached to the nickel atom along with two iodide ions. The reaction is typically carried out in a suitable solvent, such as ethanol or acetonitrile.

This reaction is an example of a coordination reaction, where ligands bind to a central metal ion to form a complex. The presence of PPh3 ligands enhances the stability and reactivity of the resulting nickel(II) complex. The reaction conditions and stoichiometry can be adjusted to control the formation and properties of the complex.

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3. What is the ​molar mass​ of baking soda? Show your work.
4. How many ​moles​ of baking soda does the recipe call for? Show your work.
5. What’s the difference between the ​mass​ of baking soda and the ​moles​ of baking soda? Explain

Answers

The molar mass of baking soda (sodium bicarbonate) is approximately 84.01 g/mol. The recipe calls for a certain number of moles of baking soda, which can be calculated using the molar mass and the given mass of baking soda.

To determine the molar mass of baking soda ([tex]NaHCO_{3}[/tex]), we add up the atomic masses of its constituent elements. The atomic mass of sodium (Na) is approximately 22.99 g/mol, hydrogen (H) is 1.01 g/mol, carbon (C) is 12.01 g/mol, and oxygen (O) is 16.00 g/mol. Adding these masses together:

Molar mass of NaHCO_{3} = (22.99 g/mol) + (1.01 g/mol) + (12.01 g/mol) + (3 * 16.00 g/mol) ≈ 84.01 g/mol

To calculate the number of moles of baking soda required by the recipe, we divide the given mass of baking soda by its molar mass. The mass is not provided in the question, so the calculation cannot be performed without additional information.

The difference between the mass of baking soda and the moles of baking soda lies in their units. Mass is measured in grams (g), while moles represent a quantity of particles. The number of moles is obtained by dividing the mass of the substance by its molar mass. Essentially, moles provide a way to count the number of entities (atoms, molecules) in a given sample, whereas mass represents the total amount of matter present.

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How many grams of ammonia are consumed in the reaction of 103.0 g of lead(ii) oxide?

Answers

Approximately 15.7 grams of ammonia are consumed in the reaction of 103.0 g of lead(II) oxide.

To answer this question, we need to first write the balanced chemical equation for the reaction of lead(II) oxide with ammonia:

PbO + 2NH3 → Pb(NH3)2O

From this equation, we can see that 1 mole of lead(II) oxide reacts with 2 moles of ammonia. We can use the molar mass of lead(II) oxide to convert the given mass of 103.0 g into moles:

103.0 g PbO × (1 mole PbO/223.2 g PbO) = 0.462 moles PbO

Since 1 mole of PbO reacts with 2 moles of NH3, we can use stoichiometry to calculate the amount of NH3 consumed in the reaction:

0.462 moles PbO × (2 moles NH3/1 mole PbO) = 0.924 moles NH3

Finally, we can convert moles of NH3 to grams using its molar mass:

0.924 moles NH3 × (17.03 g NH3/1 mole NH3) = 15.62 g NH3

Therefore, 15.62 grams of ammonia are consumed in the reaction of 103.0 grams of lead(II) oxide.
To determine how many grams of ammonia are consumed in the reaction of 103.0 g of lead(II) oxide, we need to use stoichiometry. First, we need a balanced chemical equation for the reaction:

PbO (lead(II) oxide) + 2 NH3 (ammonia) → Pb(NH2)2 (lead(II) amide) + H2O (water)

Now, follow these steps:

1. Calculate the molar mass of lead(II) oxide (PbO): 207.2 g/mol (Pb) + 16.0 g/mol (O) = 223.2 g/mol.
2. Determine the moles of PbO: 103.0 g / 223.2 g/mol ≈ 0.461 mol PbO.
3. Use the stoichiometry from the balanced equation to find the moles of NH3: 0.461 mol PbO × (2 mol NH3 / 1 mol PbO) = 0.922 mol NH3.
4. Calculate the grams of NH3: 0.922 mol NH3 × 17.0 g/mol (NH3) ≈ 15.7 g.

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