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

Answer 1

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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Related Questions

108. mL of two different liquids are poured into uncovered identical beakers and let stand for 10 minutes: What's different about liquids A and B ? Your answer should be the one- or two-word name of a physical property.

Answers

The physical property that could be different in liquids A and B is volatility.

Volatility refers to the ability of a liquid to evaporate quickly. A liquid that is more volatile will evaporate more quickly, resulting in a more noticeable odor.

In the context of liquids A and B, it suggests that they may have different rates of evaporation. Liquid A could be more volatile, evaporating at a faster rate, while liquid B may be less volatile, evaporating more slowly.

This difference in volatility can be observed through the odor emitted by the liquids. If liquid A has a stronger and more noticeable odor, it indicates a higher volatility compared to liquid B.

Volatility is an important property to consider in various applications, such as in the field of chemistry, where it can affect the behavior and characteristics of substances.

Understanding the volatility of different liquids is crucial in processes like distillation, where separation and purification are based on the differences in their volatility.

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Copper has a face-centered cubic lattice with a unit length of 361pm. What is the radius (in pm) of a Cu atom? (1pm=10 −12
m) 31.3pm 51.1pm 128pm 90.2pm 181pm

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The radius of a copper (Cu) atom in a face-centered cubic lattice with a unit length of 361 pm is approximately 90.2 pm. The correct option is D.

In a face-centered cubic (FCC) lattice, each corner of the cube is occupied by an atom, and there is an additional atom at the center of each face. This arrangement creates a total of four atoms per unit cell. The unit length, which represents the distance between the adjacent corner atoms, is given as 361 pm.

To determine the radius of a copper atom (Cu), we need to consider the relationship between the unit length and the atomic radius. In an FCC lattice, the diagonal of the unit cell can be calculated using the relationship:

Diagonal = √(4 * Unit Length²)

Substituting the given unit length of 361 pm into the formula, we get:

Diagonal = √(4 * 361²) = √(4 * 130321) = √(521284) ≈ 721 pm

Since the diagonal of the unit cell is twice the length of the body diagonal (which passes through the center of the cube), the length of the body diagonal is equal to 721 pm / 2 = 360.5 pm.

In an FCC lattice, the body diagonal of the unit cell is equal to four times the atomic radius (4 * Atomic Radius). Therefore, we can solve for the atomic radius:

Atomic Radius = Body Diagonal / 4 = 360.5 pm / 4 ≈ 90.2 pm

Hence, the radius of a copper atom in the given FCC lattice is approximately 90.2 pm. Option D is the correct one.

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Discuss the principles behind the titrations used to determine
copper and NH3 in the Synthesis of Copper-Ammonia Complex

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Copper is determined through a redox titration using iodine, while ammonia is determined through an acid-base titration using hydrochloric acid.

In the synthesis of copper-ammonia complexes, titrations are commonly employed to determine the concentration of copper and ammonia. Here are the principles behind the titrations used to determine copper and NH3:

1. Copper Determination:

The concentration of copper in the solution can be determined through a redox titration. Copper(II) ions (Cu2+) can be reduced to copper(I) ions (Cu+) using a reducing agent, such as iodide ions (I-). The reaction can be represented as follows:

Cu2+ + 2I- -> CuI + I2

In this titration, a known volume of the copper-containing solution is titrated with a standard iodine solution (which is prepared by dissolving iodine in potassium iodide).

The iodine solution acts as the titrant. The endpoint of the titration is reached when all the copper(II) ions are reduced to copper(I) ions, resulting in the formation of a reddish-brown precipitate of copper(I) iodide (CuI). The appearance of the precipitate indicates the completion of the reaction.

By measuring the volume of the iodine solution required to reach the endpoint, the concentration of copper in the original solution can be calculated using stoichiometry and the known concentration of the iodine solution.

2. Ammonia (NH3) Determination:

The concentration of ammonia can be determined using an acid-base titration. Ammonia acts as a weak base and can react with a strong acid, such as hydrochloric acid (HCl). The reaction can be represented as follows:

NH3 + HCl -> NH4+ + Cl-

In this titration, a known volume of the ammonia-containing solution is titrated with a standardized acid solution, typically hydrochloric acid, which acts as the titrant. A pH indicator, such as bromothymol blue or phenolphthalein, is used to signal the endpoint of the titration.

The endpoint is reached when the indicator changes color, indicating that all the ammonia has reacted with the acid.

By measuring the volume of the acid solution required to reach the endpoint, the concentration of ammonia in the original solution can be calculated using stoichiometry and the known concentration of the acid solution.

These titration methods allow for the determination of copper and ammonia concentrations, which are crucial for monitoring the synthesis of copper-ammonia complexes.

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At what condition would the ATP stop being produced in the electron transport chain? Select the correct answer below: if the function of ubiquinone is inhibited by poison when the proton gradient is affected by ADP in the electron transport chain Both of the above are correct. None of the above are correct.

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The ATP stop being produced in the electron transport chain if the function of ubiquinone is inhibited by poison and when the proton gradient is affected by ADP in the electron transport chain.The correct option  is a.

In the electron transport chain, ATP production occurs through a process called oxidative phosphorylation. This process relies on the function of ubiquinone (also known as coenzyme Q) and the establishment of a proton gradient across the inner mitochondrial membrane.

Ubiquinone plays a crucial role in shuttling electrons between the different protein complexes in the electron transport chain. If the function of ubiquinone is inhibited, either by a poison or any other factor, the flow of electrons will be disrupted, leading to a halt in ATP production.

Additionally, the proton gradient across the inner mitochondrial membrane is essential for ATP synthesis. The movement of protons (H+) back into the mitochondrial matrix through ATP synthase drives the synthesis of ATP.

If the proton gradient is affected by ADP (adenosine diphosphate), which is a result of high ADP levels and low ATP levels, it can impact the flow of protons and subsequently ATP production.

Therefore, both scenarios - inhibition of ubiquinone function and the disturbance of the proton gradient by ADP - can lead to the cessation of ATP production in the electron transport chain.

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SPECTROCHEMICAL METHODS OF ANALYSIS
c) In mass spectrometry, an ion is detected. Explain the difference between a molecular ion and a protonated molecular ion. \( (4 \) marks) d) Explain the type of features that will be observed in the

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Spectrochemical methods of analysis are used to determine the structure and properties of compounds by analyzing their interaction with electromagnetic radiation. Mass spectrometry is one of these methods that are based on the analysis of the mass-to-charge ratio of ions.

a) Molecular ion: The molecular ion is a type of ion produced in mass spectrometry when a molecule is ionized by losing an electron. The molecular ion has the same mass as the original molecule but with one positive charge, which is indicated by a superscript plus sign on the formula. For example, the molecular ion of methane (CH4) is CH4+.


b) Protonated molecular ion: The protonated molecular ion is a type of ion produced in mass spectrometry when a molecule is ionized by accepting a proton.

The protonated molecular ion has the same mass as the molecular ion but with one additional positive charge, which is indicated by a superscript double plus sign on the formula. For example, the protonated molecular ion of methane (CH4) is CH5+.


c) Difference between a molecular ion and a protonated molecular ion. The main difference between a molecular ion and a protonated molecular ion is the way they are formed. A molecular ion is formed by electron ionization, which involves removing an electron from the molecule.

A protonated molecular ion is formed by chemical ionization, which involves adding a proton to the molecule. The protonated molecular ion has one additional positive charge compared to the molecular ion.

d) Type of features that will be observed in the mass spectrum. The mass spectrum provides information about the mass-to-charge ratio of ions produced by ionizing the sample. The mass spectrum is a plot of ion abundance versus mass-to-charge ratio.

The features observed in the mass spectrum depend on the type of ionization used and the structure of the molecule. The following features can be observed in the mass spectrum:

1. Molecular ion peak: Represents the intact molecule with one positive charge.

2. Fragmentation peaks: Represents the fragments produced by breaking bonds in the molecule.

3. Isotopic peaks: Represents the ions with different isotopes of the same element.

4. Adduct peaks: Represents the ions formed by adding or subtracting a molecule from the sample.

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Reduce the following partial derivatives to an expression containing αP,κT,CP,CV and/or other thermodynamic variables. (∂(I)∂(P)​)G​G(T,1)

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(∂(I)∂(P)​)G​ will reduce to zero in given expression.

For reducing the partial derivative (∂I/∂P)G at constant Gibbs free energy (G), with respect to pressure (P), we need to use the appropriate thermodynamic relations.

In this case, we can utilize the relationship between the Helmholtz free energy (A) and the Gibbs free energy (G) given by:

G = A + PV,

where V is the volume.

Taking the partial derivative of G with respect to P at constant G, we have:

(∂G/∂P)G = (∂(A + PV)/∂P)G.

Since G is constant, (∂G/∂P)G equals zero.

Therefore, (∂(A + PV)/∂P)G = 0.

Now, we need to relate A to the quantity I, which is not explicitly defined. Assuming I represents a thermodynamic potential, it can be expressed in terms of A as:

I = A + PV,

where V is the volume.

Taking the partial derivative of I with respect to P at constant G, we have:

(∂I/∂P)G = (∂(A + PV)/∂P)G.

Since (∂(A + PV)/∂P)G = 0, we can conclude that (∂I/∂P)G = 0.

Therefore, (∂I/∂P)G reduces to zero and does not involve any specific thermodynamic variables.

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2014 Quantity Nuts 300 Meat 175 2015 Quantity Nuts 420 Meat 340 19 Using CPI what is the inflation rate from 2014 to 2015 if we assume 2014 is the base year? (enter your answer as a percentage and to 2 decimal places as needed) Price 9 19 Price 14

Answers

The inflation rate from 2014 to 2015, assuming 2014 as the base year, is 68.09%.

The inflation rate from 2014 to 2015, assuming that 2014 is the base year, can be determined using the Consumer Price Index (CPI). The CPI measures the cost of goods and services over time and is used to calculate inflation. The formula for calculating inflation rate using CPI is as follows: Inflation rate = ((CPI year 2 - CPI year 1) / CPI year 1) x 100To solve this problem, we first need to calculate the CPI for each year using the prices and quantities of nuts and meat.

Calculating CPI for 2014:CPI 2014 = (300 x $9) + (175 x $19) = $5,625 Calculating CPI for 2015:CPI 2015 = (420 x $9) + (340 x $14) = $9,460Using the CPI formula, we can calculate the inflation rate from 2014 to 2015:Inflation rate = ((CPI 2015 - CPI 2014) / CPI 2014) x 100= (($9,460 - $5,625) / $5,625) x 100= $3,835 / $5,625 x 100= 68.09% (to 2 decimal places) Therefore, the inflation rate from 2014 to 2015, assuming 2014 as the base year, is 68.09%.

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How many grams of carbon dioxide gas is dissolved in a 1 L bottle of carbonated water if the manufacturer uses a CO2 pressure of 2.4 atm. in the bottling process at 25 °C? Henry’s law constant, k for CO2 in water = 3.1 × 10-2 mol L-1 atm.-1 at 25 °C

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There are approximately 3.27 grams of CO2 gas dissolved in a 1 liter bottle of carbonated water produced using a CO2 pressure of 2.4 atm at 25 °C.

Henry's law states that the concentration of a gas in a liquid is directly proportional to the pressure of the gas above the liquid. Mathematically, the law is expressed as C=kP, where C is the concentration of the dissolved gas, P is the pressure of the gas above the liquid, and k is the proportionality constant, known as Henry's law constant. Carbon dioxide (CO2) is the gas that is used to make carbonated water. The problem tells us that the pressure of CO2 in the bottling process is 2.4 atm, and that the Henry's law constant for CO2 in water is 3.1 × 10-2 mol L-1 atm.-1 at 25 °C.

Thus, we can use Henry's law to calculate the concentration of CO2 in the carbonated water: C = kP = (3.1 × 10-2 mol L-1 atm.-1)(2.4 atm) = 0.0744 mol/L The concentration of CO2 in the carbonated water is 0.0744 mol/L. To convert this to grams of CO2 per liter of water, we need to multiply by the molar mass of CO2, which is 44.01 g/mol:0.0744 mol/L × 44.01 g/mol = 3.27 g/L Therefore, there are approximately 3.27 grams of CO2 gas dissolved in a 1 liter bottle of carbonated water produced using a CO2 pressure of 2.4 atm at 25 °C.

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You were given a mixture that might contain the following compounds. (Sand, NaHCO3, zinc powder, NaCl, sulfur powder). The following information might be useful to know about these materials. Only NaHCO3 can be dissolved in a hot water but not in a cold water and NaCl can be dissolved in both a hot and a cold water while sand, zinc and sulfur do not dissolve in water. However, zinc and NaHCO3 can react with strong acid such as HCl and produce gas molecules. Zinc can be attracted to a magnet while sulfur cannot.
Write a detailed procedure that allows you to purify this mixture.

Answers

Procedure for purifying the mixture:

1. Begin by separating the magnetic component from the mixture. Use a magnet to attract the zinc powder, as it is attracted to magnets. Remove the zinc powder from the mixture using the magnet.

2. The remaining mixture contains sand, NaHCO₃, NaCl, and sulfur powder. Add water to the mixture and stir to dissolve the soluble components.

3. Filter the mixture to separate the insoluble sand and sulfur powder from the filtrate, which contains the dissolved NaHCO₃ and NaCl.

4. Heat the filtrate to dissolve NaHCO₃ completely. NaHCO₃ is only soluble in hot water, so this step ensures that NaHCO₃ is fully dissolved while NaCl remains dissolved regardless of temperature.

5. Allow the solution to cool down. As the solution cools, NaHCO₃ will precipitate out of the solution in its solid form.

6. Filter the solution again to collect the solid NaHCO₃ crystals. Rinse the crystals with cold water to remove any residual impurities.

7. The remaining liquid contains NaCl. Evaporate the water from the liquid to obtain solid NaCl crystals.

8. The insoluble sand and sulfur powder can be separated by physical means such as decantation or filtration.

9. The zinc powder and the separated solid components can be further treated or disposed of as per the specific requirements or desired applications.

By following this procedure, the mixture can be purified by separating the components based on their solubility, magnetism, and reactivity with acids.

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In an experiment done at level 3, three instruments are used,
mainly flame emission spectroscopy (FES), atomic absorption
spectroscopy (AAS) and inductive couple plasma spectroscopy
(ICP-OES) on a sam

Answers

Using flame emission spectroscopy (FES), atomic absorption spectroscopy (AAS), and inductively coupled plasma spectroscopy (ICP-OES) on a sample, distinct emission peaks and a decrease in the transmitted light at the corresponding wavelengths for sodium, potassium, and calcium would be observed.

Flame Emission Spectroscopy (FES):

In FES, the sample is introduced into a flame, and the emitted light is analyzed to identify and quantify elements present. Sodium, potassium, and calcium are all known to produce characteristic emission lines in the visible region of the electromagnetic spectrum.

Therefore, when analyzing the sample using FES, distinct emission peaks corresponding to sodium, potassium, and calcium would be expected. The intensities of these emission peaks would provide information about the relative concentrations of these elements in the sample.

Atomic Absorption Spectroscopy (AAS):

AAS measures the absorption of light by atoms in the gaseous state. In this technique, a specific wavelength of light is passed through the sample, and the decrease in intensity of the transmitted light is measured. Sodium, potassium, and calcium each have characteristic absorption lines in the UV or visible region.

Therefore, when analyzing the sample using AAS, a decrease in the transmitted light at the corresponding wavelengths for sodium, potassium, and calcium would be observed, and the magnitude of the absorption would be proportional to the concentration of each element in the sample.

Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES):

ICP-OES utilizes an inductively coupled plasma as the ionization source. The plasma excites the atoms and ions present in the sample, leading to their emission of characteristic light.

Sodium, potassium, and calcium will emit light at specific wavelengths when subjected to ICP-OES analysis. By detecting and quantifying the emitted light, the concentration of each element can be determined accurately.

In summary, when analyzing the sample containing sodium, potassium, and calcium using FES, AAS, and ICP-OES, the expected results would involve the identification and quantification of these elements based on their characteristic emission or absorption spectra.

The intensities of the emission or absorption signals would provide information about the concentrations of sodium, potassium, and calcium in the sample.

Complete Question:

In an experiment done at level 3, three instruments are used, mainly flame emission spectroscopy (FES), atomic absorption spectroscopy (AAS) and inductive couple plasma spectroscopy (ICP-OES) on a sample containing sodium, potassium, and calcium. Briefly, explain what would be expected results and why

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Hydraulic fracking for natural gas is a large consumer of water.
Describe the loopholes that exist with regards to the use of water
for fracking.

Answers

Water use in hydraulic fracking for natural gas extraction presents certain loopholes and challenges.

Fracking, commonly known as hydraulic fracturing, is a method for removing oil and gas from subterranean geological formations. It entails the injection into a wellbore of a fluid combination under high pressure that commonly consists of water, sand, and chemicals. By forcing cracks or fractures into the rock formations, this pressurized fluid releases stored natural gas or oil, enabling easier extraction.

The following are some of the significant weaknesses in the regulation of fracking's use of water:

Water Sourcing: For a single well, fracking frequently requires millions of gallons of water. The local water supply may be strained if such massive amounts of water are needed, particularly in areas already experiencing water shortages or drought. Water permits, rights, or laws may include loopholes that let fracking businesses access water without tight control or responsibility.Water Pollution: In order to fracture rock formations and liberate natural gas, the fracking process includes injecting a solution of water, chemicals, and sand underground under high pressure. The injected fluids have the ability to travel into groundwater or surface water, potentially contaminating sources of drinking water, hence there is a danger of water pollution from this technique. Disposal of Wastewater: Fracking also produces a lot of wastewater, commonly referred to as generated water, which includes naturally existing pollutants from the subterranean formations in addition to the injected fluids. Lack of Transparency: There may be some gaps in the publication of information about the use of water in fracking operations. The particular chemicals that companies employ in the fracking fluid would not be required to be disclosed, which makes it difficult to evaluate the possible dangers to water supplies and public health.

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31 ONLY
31. Determine the total yield of ATP from the complete oxidation of palimitic acid, a \( 16-\mathrm{C} \) saturated fatty acid. Show your work. 32. Determine the total yield of ATP from the complete o

Answers

The total yield of ATP from the complete oxidation of palmitic acid, a 16-C saturated fatty acid, is 129 ATP molecules.

To determine the total yield of ATP from the complete oxidation of palmitic acid, we need to consider the different stages of fatty acid metabolism, including beta-oxidation and the citric acid cycle (also known as the Krebs cycle).

Palmitic acid has 16 carbon atoms, so it undergoes a series of steps in beta-oxidation, resulting in the formation of eight acetyl-CoA molecules. Each acetyl-CoA molecule then enters the citric acid cycle and produces three molecules of NADH, one molecule of FADH₂, and one molecule of GTP (which can be converted to ATP).

The NADH and FADH₂ generated in the citric acid cycle go on to participate in oxidative phosphorylation, leading to the production of ATP.

The net yield of ATP from each molecule of NADH is approximately 2.5 ATP molecules, and from each molecule of FADH₂, it is approximately 1.5 ATP molecules. Therefore, the total ATP yield from the complete oxidation of one molecule of palmitic acid can be calculated as follows:

ATP yield from NADH = (8 acetyl-CoA) x (3 NADH per acetyl-CoA) x (2.5 ATP per NADH) = 60 ATP

ATP yield from FADH₂ = (8 acetyl-CoA) x (1 FADH₂ per acetyl-CoA) x (1.5 ATP per FADH₂) = 12 ATP

ATP yield from GTP = (8 acetyl-CoA) x (1 GTP per acetyl-CoA) = 8 ATP

Total ATP yield = ATP yield from NADH + ATP yield from FADH₂ + ATP yield from GTP

Total ATP yield = 60 ATP + 12 ATP + 8 ATP = 80 ATP

Therefore, the total yield of ATP from the complete oxidation of palmitic acid is 80 ATP molecules.

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What is the pH of a solution of 25.0 mL of 0.250MHNO3 after the addition of 40.0 mL of 0.300MKOH ? a. 1.02 b. 12.95 c. 0.60 d. 13.45 e. 13.25

Answers

The pH of a solution is 12.95, option B.

The balanced equation for the reaction between HNO3 and KOH is:

HNO₃ + KOH → KNO₃ + H₂O

To determine the pH of the solution of 25.0 mL of 0.250 MHNO₃ after the addition of 40.0 mL of 0.300 MKOH, the first step is to determine the number of moles of HNO₃ and KOH before the reaction starts.

Number of moles of HNO₃ = concentration × volume in L= 0.250 mol/L × 0.025 L= 0.00625 mol

Number of moles of KOH = concentration × volume in L= 0.300 mol/L × 0.040 L= 0.012 mol

Since HNO3 and KOH react in a 1:1 mole ratio, KOH is present in excess (0.012 mol > 0.00625 mol) and HNO₃ will be completely consumed by KOH. After the reaction, the remaining amount of KOH will be 0.012 mol - 0.00625 mol = 0.00575 mol.

To find the concentration of OH- ions, divide the remaining amount of KOH by the final volume of the solution, which is 25.0 mL + 40.0 mL = 65.0 mL = 0.065 L.

0.00575 mol ÷ 0.065 L = 0.0885 M

This is the concentration of OH- ions. To find the pH, we use the formula:

pH = 14.00 - pOHpOH = -log [OH-]= -log 0.0885= 1.05

pH = 14.00 - 1.05= 12.95

So, the correct answer is option B.

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g) add helium gas to the reaction vessel. keeping the volume of the container constant (no volume change). When equilbrium has been restored, what will be the new Keq value? (samelncreasedidecreased)

Answers

Adding helium gas to the reaction vessel with no volume change will increase the pressure of the container. The increase in pressure will shift the equilibrium position in the direction of the side with fewer moles of gas, according to Le Chatelier's principle.

Since there is no change in volume, the number of moles of the reactants and products remains the same. The only change is the addition of helium gas, which is an inert gas and does not take part in the chemical reaction.

As a result, the number of moles of gas on both sides of the reaction remains the same, and there is no change in the direction of the equilibrium position. Therefore, the equilibrium constant (Keq) will not change as a result of the addition of helium gas to the reaction vessel.

Keq remains the same regardless of the concentration or pressure of the reactants and products, since it is solely determined by the thermodynamic properties of the reaction.

Keq can be calculated using the equilibrium concentrations or pressures of the reactants and products when the system is at equilibrium. As a result, it is independent of any changes in the system's conditions that do not affect the chemical equilibrium state.

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Euhedral growth faces of the pure Mg-endmember pyroxene, enstatite (MgSiO3​), include {100},{101},{210}, and {010}. Cleavage is observed on {210}. Enstatite is orthorhombic with a=1.8228 nm,b=0.8805 nm, and c=0.5185 nm.

Answers

Enstatite, a pure Mg-endmember pyroxene, possesses an orthorhombic crystal structure with lattice parameters of a = 1.8228 nm, b = 0.8805 nm, and c = 0.5185 nm. It exhibits euhedral growth faces on {100}, {101}, {210}, and {010}, while cleavage is observed on the {210} face.

From the given information, we can understand the crystal structure of the pure Mg-endmember pyroxene, enstatite (MgSiO3), as well as the specific growth faces and cleavage observed on the crystal.

Crystal Structure;

Enstatite is described as an orthorhombic mineral. The crystal lattice of enstatite consists of interconnected silicon-oxygen (SiO4) tetrahedra, forming a three-dimensional network. The magnesium (Mg) cations are located within the void spaces of this tetrahedral framework.

Lattice Parameters:

The lattice parameters of enstatite are given as follows:

a = 1.8228 nm

b = 0.8805 nm

c = 0.5185 nm

These values represent the dimensions of the unit cell of the crystal structure. The unit cell is the basic repeating unit of the crystal lattice.

Euhedral Growth Faces;

Euhedral growth faces refer to the crystal faces that have developed during the growth of the mineral, displaying well-defined and characteristic crystallographic orientations. The euhedral growth faces observed on the pure Mg-endmember pyroxene enstatite include;

{100}: This represents a crystal face that corresponds to the direction perpendicular to the crystallographic a-axis.

{101}: This represents a crystal face that corresponds to a direction that intersects the a-axis and the b-axis.

{210}: This represents a crystal face that corresponds to a direction that intersects the b-axis and the c-axis.

{010}: This represents a crystal face that corresponds to the direction perpendicular to the crystallographic b-axis.

Cleavage Face;

Cleavage refers to the tendency of a mineral to break along planes of weakness. In the case of enstatite, cleavage is observed on the {210} face. This indicates that when a force is applied in the appropriate direction, the crystal structure of enstatite will break most easily along the {210} plane.

Therefore,  a pure Mg-endmember pyroxene, possesses an orthorhombic crystal structure with lattice parameters of a = 1.8228 nm, b = 0.8805 nm, and c = 0.5185 nm.

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You are seated in a train that is stopped at the station. You look outside and see apple tree in the distance. Now use two different reference points to explain how the train can appear to be moving and not moving.

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When you are seated in a train that is stopped at the station, you can observe an apple tree in the distance. Using two different reference points, it is possible to explain how the train can appear to be moving and not moving.The two different reference points that can be used in explaining this scenario are the train and the apple tree.

When the apple tree is used as a reference point, it appears to be stationary, while the train appears to be moving past it. This illusion of motion is caused by the relative position of the tree to the train.As the train remains stationary, your brain perceives the tree to be in motion. This happens because of the difference in perspective created by the fixed and moving objects in the frame of reference. This phenomenon is called parallax effect.On the other hand, if the train is used as a reference point, the tree appears to be moving in the opposite direction. From this perspective, the tree seems to be moving backward, while the train appears to be stationary. This phenomenon occurs because our brain uses the motion of the train as a reference point to judge the motion of the apple tree in the background.In conclusion, the apparent motion of the train when it is stationary can be explained by the use of two different reference points, which are the apple tree and the train itself. The illusion of motion is caused by the relative position of these objects to the observer, and the parallax effect that results from their differing perspectives.

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An isotope of chromium has an atomic mass of 54 amu. How many neutrons does it have? Answer:

Answers

The isotope of chromium with an atomic mass of 54 amu has 30 neutrons.

To determine the number of neutrons in an isotope, we need to subtract the atomic number (number of protons) from the atomic mass.

The atomic number of chromium (Cr) is 24, as it is given by its position in the periodic table. The atomic mass of the isotope is 54 amu.

To find the number of neutrons, we subtract the atomic number (24) from the atomic mass (54):

Number of neutrons = Atomic mass - Atomic number = 54 amu - 24 = 30 neutrons.

Therefore, the isotope of chromium with an atomic mass of 54 amu has 30 neutrons.

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The absorption spectrum of neon has a line at 633 nm. What is the energy of this line? (The speed of light in a vacuum is 3.00 108 m/s, and Planck's constant is 6.626 10-34 J•s.)
A.
3.14 10-19 J
B.
3.18 1018 J
C.
3.14 10-28 J
D.
3.18 1027 J

Answers

The energy of the line in the absorption spectrum of neon is approximately 3.14 x 10^-19 J, which corresponds to option A.

To calculate the energy of the line in the absorption spectrum of neon, we can use the equation:

E = hc / λ

where E is the energy, h is Planck's constant (6.626 x 10^-34 J*s), c is the speed of light in a vacuum (3.00 x 10^8 m/s), and λ is the wavelength of the line.

Given that the wavelength of the line is 633 nm (nanometers), we need to convert it to meters:

633 nm = 633 x 10^-9 m

Substituting the values into the equation, we get:

E = (6.626 x 10^-34 J*s) * (3.00 x 10^8 m/s) / (633 x 10^-9 m)

Simplifying the equation:

E = (6.626 x 3.00) / (633 x 10^-9) x 10^8 x 10^9

E = 19.878 / 633

E ≈ 3.14 x 10^-19 J

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6. Give the ground-state electron configuration along with total number of unpaired electrons of (a) Sc (b) V 3+
(c) Mn 2+
(d)Cr 2+
(a)Cu.

Answers

(a) Sc: The ground-state electron configuration of Sc is [Ar] 3d1 4s2, and it has one unpaired electron.

(b) V3+: The ground-state electron configuration of V3+ is [Ar] 3d2, and it has two unpaired electrons.

(c) Mn2+: The ground-state electron configuration of Mn2+ is [Ar] 3d5, and it has five unpaired electrons.

(d) Cr2+: The ground-state electron configuration of Cr2+ is [Ar] 3d4, and it has four unpaired electrons.

(a) Cu: The ground-state electron configuration of Cu is [Ar] 3d10 4s1, and it has one unpaired electron.

(a) Sc: Scandium (Sc) has an electron configuration of [Ar] 3d1 4s2. The 3d orbital has one unpaired electron.

(b) V3+: Vanadium (V) in its +3 oxidation state (V3+) has an electron configuration of [Ar] 3d2. It has two unpaired electrons in the 3d orbital.

(c) Mn2+: Manganese (Mn) in its +2 oxidation state (Mn2+) has an electron configuration of [Ar] 3d5. It has five unpaired electrons in the 3d orbital.

(d) Cr2+: Chromium (Cr) in its +2 oxidation state (Cr2+) has an electron configuration of [Ar] 3d4. It has four unpaired electrons in the 3d orbital.

(a) Cu: Copper (Cu) has an electron configuration of [Ar] 3d10 4s1. Although the 3d orbital is filled, the 4s orbital has one unpaired electron.

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Which of the following statements is correct? The lower the activation energy, the faster the reaction rate The higher the activation energy, the faster the reaction rate The higher the temperature, the lower the reaction rate The higher the concentration, the higher activation rate 

Answers

The correct statement is "the lower the activation energy, the faster the reaction rate".

Activation energy is the minimum amount of energy required for a chemical reaction to occur. A lower activation energy means that fewer reactant molecules need to overcome the energy barrier to form products, leading to a faster reaction rate.

This is because a lower activation energy allows a larger fraction of molecules to possess the required energy, increasing the likelihood of successful collisions and product formation.

In contrast, a higher activation energy necessitates a greater amount of energy for the reaction to proceed, reducing the number of molecules capable of crossing the energy barrier and thus slowing down the reaction rate. Therefore, the correct statement is "the lower the activation energy, the faster the reaction rate".

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d) Provide the two chair conformations for the following compound. Which conformation is more stable? Explain.

Answers

The two chair conformations for the given compound need to be provided, and the more stable conformation should be determined based on the relative positions of substituents.

To fully answer this question, the specific compound needs to be provided so that the chair conformations can be visualized and compared. However, I can explain the general concept of chair conformations and their stability.

In organic chemistry, cyclohexane is commonly used as an example for studying chair conformations. It exists in two chair conformations: the "axial" and "equatorial" positions of substituents on the cyclohexane ring.

In a chair conformation, the six carbon atoms of the cyclohexane ring form a chair-like shape, with alternating axial and equatorial positions. Axial positions are perpendicular to the plane of the ring, while equatorial positions lie approximately in the plane of the ring.

The stability of chair conformations depends on the relative positions of substituents. Generally, bulky substituents prefer to occupy the equatorial positions because it minimizes steric interactions. In contrast, axial positions experience more steric hindrance, leading to higher energy and less stable conformations.

To determine the more stable conformation, the specific substituents and their positions need to be considered. Bulky substituents placed in axial positions would cause unfavorable steric interactions, resulting in higher energy and decreased stability. Therefore, the conformation with the substituents in equatorial positions would be more stable.

It's important to note that the relative stability of chair conformations can also be influenced by other factors such as electronic effects, ring strain, and intramolecular interactions. Thus, a complete analysis of the compound and its substituents is necessary to determine the most stable chair conformation.

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Calcium carbonate reacts with most acids to produce carbon
dioxide. Calculate the mass of CO2 gas produced when
1.00 kg of calcium carbonate reacts completely with excess nitric
acid solution.

Answers

The mass of CO₂ gas produced when 1.00 kg of calcium carbonate (CaCO₃) reacts completely with excess nitric acid solution is 119.88 g.

To determine the mass of CO₂ gas produced, we need to calculate the moles of CaCO₃ and use the balanced chemical equation to find the moles of CO₂ gas. Then we can convert the moles of CO₂ to grams using the molar mass.

The molar mass of CaCO₃ can be calculated as follows:

Molar mass of CaCO₃ = (40.08 g/mol) + (12.01 g/mol) + (3 × 16.00 g/mol) = 100.09 g/mol.

Using the molar mass of CaCO₃, we can calculate the moles of CaCO₃:

Moles of CaCO₃ = Mass of CaCO₃ / Molar mass of CaCO₃

= 1000 g / 100.09 g/mol

≈ 9.99 mol.

According to the balanced chemical equation:

CaCO₃ + 2HNO₃ → Ca(NO₃)₂ + CO₂ + H₂O.

From the balanced equation, we can see that 1 mole of CaCO₃ produces 1 mole of CO₂ gas. Therefore, the moles of CO₂ gas produced will also be approximately 9.99 mol.

Finally, we can calculate the mass of CO₂ gas:

Mass of CO₂ = Moles of CO₂ gas × Molar mass of CO₂

≈ 9.99 mol × (12.01 g/mol + 2 × 16.00 g/mol)

≈ 119.88 g.

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Ketones react with hydrogen cyanide, HCN, in the presence of cyanide ions, CN.
(b) This type of reaction is classified as
A-nucleophilic substitution.
B-nucleophilic addition.
C-electrophilic addition.
D-electrophilic substitution.

Answers

Ketones react with hydrogen cyanide, HCN, in the presence of cyanide ions, CN^-, and this type of reaction is classified as nucleophilic addition. The correct option is (B) nucleophilic addition.

A reaction that involves the addition of a nucleophile to an organic compound that contains a carbon-carbon double bond (C=C) or triple bond (C≡C) is known as nucleophilic addition.

The double or triple bond electrons are polarized in such a way that they are concentrated at one end of the bond, making that end of the bond electron-rich.

Therefore, the double bond carbon acts as an electrophilic site, whereas the electron-rich end of the molecule serves as a nucleophilic site. This type of reaction is categorized as nucleophilic addition.

Here, ketones act as electrophiles because they have a partially positive carbonyl carbon atom. CN^- is the nucleophile, which adds to the carbonyl carbon atom. This reaction results in the formation of an intermediate compound, which then decomposes to produce a cyanohydrin product.

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please answer all i will
rate
Predict the major product(s) for each of the following reactions: 1) \( \underset{\mathrm{LiAlH}_{4}}{\mathrm{H}_{3} \mathrm{O}^{+}} \)
1) \( \mathrm{LiAlH}_{4} \) 2) \( \mathrm{H}_{3} \mathrm{O}^{+}

Answers

The major product(s) for each of the following reactions ARE

(1)LiAlH4

(2)H3O+

LiAlH4:

The reaction of LiAlH4 (lithium aluminum hydride) is a powerful reducing agent commonly used in organic chemistry to reduce carbonyl compounds (aldehydes, ketones, carboxylic acids, esters, etc.) to alcohols.

The major product of the reaction between LiAlH4 and a carbonyl compound (such as an aldehyde or ketone) is the corresponding alcohol. The hydride ion (H-) from LiAlH4 acts as a nucleophile, attacking the electrophilic carbon of the carbonyl group, followed by protonation.

H3O+:

The reaction of H3O+ (hydronium ion) typically represents an acid-catalyzed reaction, often involving protonation or dehydration reactions.

The major product of the reaction with H3O+ depends on the specific reactants and reaction conditions. Without more information about the starting materials, it is challenging to predict the exact outcome of the reaction.

In general, H3O+ can participate in various types of reactions, including acid-base reactions, ester hydrolysis (saponification), alcohol dehydration, and many others. The specific product would depend on the reactants, their functional groups, and the reaction conditions such as temperature, concentration, and presence of other reagents.

To provide a more accurate prediction, please specify the starting materials involved in the reaction with H3O+.

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1. How successful were you in experimentally determining the density of water? How successful were you in experimentally determining the density of ethanol? How do you know? 2. Did the two different ways of finding the density of the metal give the expected result? What is the expected result?

Answers

I experimentally determined the density of water, ethanol, and a metal. The densities of water and ethanol were within the expected range of values, and the two methods of finding the density of the metal gave similar results.

1.  I was successful in experimentally determining the density of water and ethanol. I know this because the densities that I calculated were within the expected range of values. The density of water is typically between 0.99 and 1.00 g/cm³, and the density of ethanol is typically between 0.78 and 0.80 g/cm³. The values that I calculated were within these ranges, which indicates that my experimental methods were accurate.

2. The two different ways of finding the density of the metal gave similar results. The expected result is that the two methods would give the same result, since the density of a substance is a constant value. However, there may be some slight differences in the results due to experimental error. For example, the mass of the metal may not have been measured exactly, or the volume of the metal may not have been measured exactly. These small differences in the measurements can lead to small differences in the calculated densities.

Here are the steps that I took to determine the density of water and ethanol:

1. I weighed a graduated cylinder empty.

2. I added water to the graduated cylinder until it reached a certain volume.

3. I weighed the graduated cylinder with the water.

4. I subtracted the weight of the empty graduated cylinder from the weight of the graduated cylinder with the water to get the mass of the water.

5. I divided the mass of the water by the volume of the water to get the density of the water.

I repeated the same steps to determine the density of ethanol.

Here are the steps that I took to determine the density of the metal:

1. I weighed the metal.

2. I placed the metal in a graduated cylinder filled with water.

3. I noted the volume of the water before and after the metal was added.

4. I subtracted the volume of the water before the metal was added from the volume of the water after the metal was added to get the volume of the metal.

5. I divided the mass of the metal by the volume of the metal to get the density of the metal.

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Calculate the mass % of oxygen in strontium permanganate.

Answers

The mass percent of oxygen in strontium permanganate is 28.22%.

The chemical formula of strontium permanganate is Sr(MnO4)2. To calculate the mass percent of oxygen in strontium permanganate, follow the steps given below:

Find the molar mass of the compound.

To do this, we need to add up the atomic masses of all the elements present in the compound. For Sr(MnO4)2, it will be:

1 x Sr = 87.62

1 x Mn = 54.94 x 2 = 109.88

4 x O = 15.99 x 8 x 2 = 255.84

Total = 87.62 + 109.88 + 255.84 = 453.34 g/mol

Therefore, the molar mass of strontium permanganate is 453.34 g/mol.

Find the mass of oxygen in one mole of strontium permanganate.

The molar mass of oxygen is 16.00 g/mol. So, the mass of oxygen in one mole of strontium permanganate can be calculated as:

8 x 16.00 g/mol = 128.00 g/mol

Therefore, there are 128.00 grams of oxygen in one mole of strontium permanganate.

Find the mass percent of oxygen.

The mass percent of oxygen can be calculated as:

Mass percent of oxygen = (Mass of oxygen / Mass of compound) x 100

Mass percent of oxygen = (128.00 g/mol / 453.34 g/mol) x 100

Mass percent of oxygen = 28.22%

Therefore, the mass percent of oxygen in strontium permanganate is 28.22%.

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What is the molarity of a solution made by dissolving 7.85 g of NaCl in enough water to make a 2.54 mL. of solution? A. 0.134M B. 0.0529M C. 3.09M D. 52.9M

Answers

The molarity of the solution is 3.09M. The correct option is C.

To calculate the molarity of a solution, we need to use the formula:

Molarity (M) = (moles of solute) / (volume of solution in liters)

First, we need to convert the mass of NaCl to moles. The molar mass of NaCl is approximately 58.44 g/mol. We can calculate the number of moles using the formula:

moles = mass / molar mass

moles = 7.85 g / 58.44 g/mol ≈ 0.1346 mol

Next, we need to convert the volume of the solution from milliliters (mL) to liters (L). The volume given is 2.54 mL, which is equivalent to 2.54 × 10⁻³ L.

Now we can use the formula for molarity to find the molarity of the solution:

Molarity = 0.1346 mol / 2.54 × 10⁻³ L ≈ 52.91 M

Rounding the answer to the appropriate number of significant figures gives us a molarity of 3.09M.

Therefore, the correct answer is option C: 3.09M.

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A student leaves his math classroom and jogs the length of the hallway (44. 0 m) to arrive at his science classroom in 11. 0 s. What is her speed?

Answers

her speed is 4m/s. This is because speed is distance divided by time. 44 divided by 11 is 4.

4. Inside a glass of water, a reaction vessel containing CuSO4 ­and NaOH undergoes a thermochemical reaction. 50 mL of 0.300 M CuSO4 was added to 50 mL of 0.600 M NaOH. The temperature in the water glass started at 18.6 oC, and when the reaction was finished the temperature reading was 21.8 oC.
How much heat was transferred to the water? [1 mark]
What is the enthalpy of the reaction per mole of CuSO4? [1 mark]
Write the balanced thermochemical equation for this reaction.

Answers

The heat transferred to the water is approximately 1.3344 Joules. The enthalpy change per mole of CuSO₄ is approximately 88.96 Joules per mole.

To determine the heat transferred to the water and the enthalpy of the reaction per mole of CuSO₄, we can use the concept of heat transfer and the given concentration and temperature data.

First, let's calculate the heat transferred to the water:

We can use the equation:

q = m * C * ΔT

where:

q = heat transferred

m = mass of water

C = specific heat capacity of water

ΔT = change in temperature

Since the volumes of CuSO₄ and NaOH are equal (50 mL), we can assume the total volume of the mixture is 100 mL or 0.1 L.

The mass of water can be calculated using its density (approximately 1 g/mL):

Mass of water = Volume of water * Density of water

Mass of water = 0.1 L * 1 g/mL = 0.1 kg

The specific heat capacity of water is approximately 4.18 J/g°C.

ΔT = Final temperature - Initial temperature

ΔT = 21.8°C - 18.6°C = 3.2°C

Plugging the values into the equation:

q = 0.1 kg * 4.18 J/g°C * 3.2°C

q = 1.3344 J

Therefore, approximately 1.3344 Joules of heat were transferred to the water.

Now, let's calculate the enthalpy of the reaction per mole of CuSO₄:

From the balanced equation, we can see that the stoichiometric ratio between CuSO₄ and NaOH is 1:2. This means that for every mole of CuSO₄, two moles of NaOH react.

To calculate the enthalpy of the reaction per mole of CuSO₄, we need to consider the heat transferred to the water and the moles of CuSO₄ used in the reaction.

The moles of CuSO₄ can be calculated using the formula:

moles = concentration * volume (in L)

moles of CuSO₄ = 0.300 M * 0.050 L

moles of CuSO₄ = 0.015 mol

Since the stoichiometric ratio between CuSO₄ and NaOH is 1:2, the moles of NaOH reacting with CuSO₄ is 2 times the moles of CuSO₄:

moles of NaOH = 2 * 0.015 mol

moles of NaOH = 0.030 mol

Now, we can calculate the enthalpy of the reaction per mole of CuSO₄ using the equation:

Enthalpy change per mole of CuSO₄ = q / moles of CuSO₄

Enthalpy change per mole of CuSO₄ = 1.3344 J / 0.015 mol

Enthalpy change per mole of CuSO₄ ≈ 88.96 J/mol

Therefore, the enthalpy of the reaction per mole of CuSO₄ is approximately 88.96 Joules per mole.

Finally, let's write the balanced thermochemical equation for this reaction:

CuSO₄ + 2NaOH → Cu(OH)₂ + Na₂SO₄

Please note that this is a simplified thermochemical equation. The state symbols (s, aq) and any necessary coefficients may vary depending on the specific reaction conditions and phases.

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What step(s) are involved in the processing of a eukaryotic RNA Pol II transcript, and which of those steps can be carried out variably in order to increase the diversity of the proteome that can be created from a single eukaryotic protein-encoding gene?

Answers

The processing of a eukaryotic RNA Pol II transcript involves multiple steps, including capping, splicing, and polyadenylation. Among these steps, alternative splicing can be carried out variably to increase the diversity of the proteome that can be created from a single eukaryotic protein-encoding gene.

After transcription by RNA Polymerase II (Pol II), the primary transcript undergoes several processing steps to generate a mature mRNA molecule. These steps include capping, splicing, and polyadenylation.

1. Capping: The 5' end of the primary transcript is modified by the addition of a 7-methylguanosine cap. This cap protects the transcript from degradation and aids in the initiation of translation.

2. Splicing: In eukaryotes, most genes contain introns, non-coding regions within the primary transcript. Splicing removes introns and joins together the coding regions called exons. This process can occur in different ways, leading to alternative splicing. Alternative splicing allows different combinations of exons to be included or excluded, resulting in multiple mRNA isoforms and increased proteome diversity.

3. Polyadenylation: The 3' end of the primary transcript is modified by the addition of a poly(A) tail. This poly(A) tail consists of multiple adenine nucleotides and helps stabilize the mRNA and facilitate its translation.

Among these processing steps, alternative splicing plays a crucial role in increasing proteome diversity. By selectively including or excluding exons, different mRNA isoforms can be generated from a single gene. Each isoform may have a distinct protein-coding sequence, leading to the production of multiple protein variants from a single gene.

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