After 16 minutes, 2000 grams of C will be formed. After a long time, all of B will be consumed and 60 grams of A will be left.
To solve this problem, we need to determine the rate equation for the reaction and use it to calculate the amount of chemical C formed in different time intervals.
From the given information, we know that the rate of the reaction is proportional to the product of the amounts of A and B not converted to C. We can express this relationship as:
Rate = k * [A] * [B]
where [A] and [B] represent the amounts of A and B not converted to C, respectively, and k is the proportionality constant.
We're also given that for each gram of B, 2 grams of A is used, which means the stoichiometric ratio between A and B is 2:1.
Now, let's solve the problem step by step:
1. Determine the rate constant (k):
We can use the given information to calculate the rate constant. When 20 grams of C is formed in 8 minutes, the rate can be expressed as:
Rate = 20 g / 8 min = 2.5 g/min
Since Rate = k * [A] * [B], and initially [A] = 40 g and [B] = 50 g, we can substitute these values to solve for k:
2.5 g/min = k * 40 g * 50 g
k = 2.5 g/min / (40 g * 50 g) = 0.00125 g⁻² min⁻¹
2. Calculate the amount of C formed in 16 minutes:
We can use the rate equation to calculate the amount of C formed in 16 minutes:
Rate = k * [A] * [B]
20 g = (0.00125 g⁻² min⁻¹) * [A] * [B]
[A] * [B] = 20 g / (0.00125 g⁻² min⁻¹)
[A] * [B] = 16000 g² min
Since [A] = 40 g and [B] = 50 g initially, we can substitute these values:
40 g * 50 g = 16000 g² min
2000 g² min = 16000 g² min
[A] * [B] = 2000 g² min
Therefore, after 16 minutes, 2000 grams of C will be formed.
3. Determine the limiting amount of C after a long time:
Since the stoichiometric ratio between A and B is 2:1, the limiting reactant is B. This means that B will be completely consumed before A. Therefore, the limiting amount of C after a long time is determined by the initial amount of B, which is 50 grams.
4. Calculate the amounts of chemicals A and B remaining after a long time:
Since B is completely consumed, the amount of B remaining after a long time will be 0 grams. The amount of A remaining can be calculated based on the stoichiometry. Since 2 grams of A is used for each gram of B, and the initial amount of B is 50 grams, the amount of A remaining after a long time will be:
Amount of A remaining = Initial amount of A - (2 grams of A/gram of B) * Amount of B consumed
Amount of A remaining = 40 grams - (2 g/g) * (50 g)
Amount of A remaining = 40 grams - 100 grams
Amount of A remaining = -60 grams (negative value indicates that all of A is consumed)
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Benzaldehyde is similar to aliphatic aldehydes except that benzaldehyde
Answer:
Benzaldehyde is similar to aliphatic aldehydes except that benzaldehyde has a benzene ring attached to the carbonyl group, while aliphatic aldehydes have a straight or branched carbon chain attached to the carbonyl group. This structural difference gives benzaldehyde unique chemical and physical properties that distinguish it from aliphatic aldehydes. For example, benzaldehyde has a characteristic almond-like odor due to the presence of the benzene ring, while aliphatic aldehydes have a pungent odor. Additionally, benzaldehyde is less soluble in water than aliphatic aldehydes due to the nonpolar nature of the benzene ring.
Determine the total yield of ATP from the complete oxidation of palimitic acid, a 16-C saturated fatty acid. Show your work.
The total yield of ATP from the complete oxidation of palmitic acid, a 16-C saturated fatty acid, is 82 ATP molecules.
Palmitic acid has a 16-carbon chain and undergoes a process called beta-oxidation to generate acetyl-CoA molecules. Each round of beta-oxidation results in the production of one acetyl-CoA molecule, which enters the citric acid cycle (also known as the Krebs cycle).
In the citric acid cycle, each acetyl-CoA molecule produces three NADH molecules, one FADH₂ molecule, and one GTP molecule (which can be converted to ATP). The NADH and FADH₂ molecules generated from the citric acid cycle then enter the electron transport chain, where they donate electrons to produce ATP through oxidative phosphorylation.
The net result is that each acetyl-CoA molecule yields about 10 ATP molecules through oxidative phosphorylation. Since palmitic acid generates 8 acetyl-CoA molecules (two per each round of beta-oxidation), the total yield of ATP is approximately 8 × 10 = 80 ATP molecules.
Additionally, during the beta-oxidation process, there is an initial investment of 2 ATP molecules to activate palmitic acid. Hence, we add 2 ATP to the total, resulting in a final total yield of 80 + 2 = 82 ATP molecules.
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Calculate the boiling point ( O
C) of an aqueous solution of 2.50 mFe(NO3 ) 3
.Kb for water is 0.512 OC/m.mcq choices: 101.3 ∘
C 5.12 ∘
C 102.5 ∘
C 2.46 ∘
C 100.8 ∘
C 105.1 ∘
C
The boiling point of the aqueous solution of 2.50 m [tex]Fe(NO_3)_3[/tex]is approximately 101.28 °C. So, the correct option nearest to it is B.
We can use the following equation to find the boiling point of an aqueous solution of [tex]Fe(NO_3)_3[/tex]:
Δ[tex]T_b[/tex] = [tex]K_b[/tex] * m
where:
[tex]K_b[/tex] is the molal boiling point elevation constant for water (0.512 °C/m) and [tex]T_b[/tex] is the boiling point elevation
m is the molality of the solute (2.50 m).
Inserting the values:
ΔTb = 0.512 °C/m * 2.50 m
ΔTb = 1.28 °C
The boiling point is calculated by adding the boiling point elevation to the 100 °C boiling point of pure water:
Boiling point = 100 °C + 1.28 °C
Boiling point = 101.28 °C
Hence, the boiling point of the aqueous solution of 2.50 m [tex]Fe(NO_3)_3[/tex]is approximately 101.28 °C.
So, the correct option nearest to it is B.
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1. The decomposition of \( \mathrm{N} O \), procecds according to the equation \[ 2 \mathrm{NO}_{s} \text { à } 4 \mathrm{NO}_{s}+\mathrm{O}_{\text {se }} \] If the rate of decompesition of \( \mathr
If the rate of decomposition of NO is 0.25 mol/(L·s), the rate of formation of NO₂ is 0.50 mol/(L·s), and the rate of formation of O₂ is 0.25 mol/(L·s), the rate of disappearance of NO is 0.50 mol/(L·s).
According to the given equation, the decomposition of NO (nitric oxide) proceeds as follows:
2NO(g) → 4NO₂(g) + O₂(g)
The rates of reaction can be expressed in terms of the rate of disappearance of NO and the rates of formation of NO₂ and O₂.
Given:
Rate of decomposition of NO = 0.25 mol/(L·s)
Rate of formation of NO₂ = 0.50 mol/(L·s)
Rate of formation of O₂ = 0.25 mol/(L·s)
Since the stoichiometric coefficient of NO in the balanced equation is 2, the rate of disappearance of NO is twice the rate of decomposition:
Rate of disappearance of NO = 2 × 0.25 mol/(L·s) = 0.50 mol/(L·s)
Therefore, the rate of disappearance of NO is 0.50 mol/(L·s).
It's important to note that the given rates are in terms of concentration changes over time (mol/L·s). The rates can be determined experimentally using techniques such as the initial rate method or the method of continuous variations.
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"Nurse Sam gave the mother of the sick child a 16 oz bottle of
liquid medication and told her the child should take 30 mL twice a
day. How many tablespoons is
one dose?
One dose is approximately 2.028 tablespoons long (rounded to three decimal places). Thus, one dose of the liquid medication is approximately 2.028 tablespoons long.
Nurse Sam gave the mother of the sick child a 16 oz bottle of liquid medication and told her the child should take 30 mL twice a day. We have to find the number of tablespoons in one dose of the liquid medication.First, we need to find how many milliliters are in one fluid ounce. There are approximately 29.5735 milliliters in one fluid ounce.
So, the total milliliters in 16 ounces will be 16 × 29.5735 ≈ 473.974 milliliters.
Each dose is 30 mL, so we need to find how many tablespoons are in 30 mL. One tablespoon is equal to 14.7868 milliliters (approximately).
So, 30 mL ÷ 14.7868
≈ 2.028 tablespoons (rounded to three decimal places).
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If 1.25 g of sodium bicarbonate had reacted with excess acid, what volume of carbon dioxide would have been produced at 789.0mmHg and 24.0 ∘ C ?
The volume of carbon dioxide produced can be calculated using the ideal gas law equation.
The formula that will be used is:
PV = nRT
The number of moles of CO₂ can be calculated as:
Number of moles of CO₂ = ([tex]\frac{1.25 g NaHCO3}{84.01 g/mol NaHCO3}[/tex]) = 0.01487 mol
P = 789.0 mmHg = (789.0 × 1 ÷760) atm
n = 0.01487 mol
R = 0.0821 L·atm/(mol·K)
T = 297.15 K
Substituting the above values in the ideal gas equation, we get:
V = [tex]\frac{0.01487 x 0.0821 x 297.15}{789 x 1/760}[/tex]
V = 0.000805 L or 0.805 mL
Therefore, the volume of carbon dioxide produced would be approximately 0.805 mL.
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The major product which results when 2-chloro-2-methylpentane is
heated in ethanol is an ether. Show and name the mechanism by which
this ether forms.
The major product formed when 2-chloro-2-methylpentane is heated in ethanol is an ether, specifically ethoxypropane (2-methoxy-2-methylpentane).
The mechanism by which this ether forms is known as an elimination reaction, specifically an E2 (bimolecular elimination) mechanism. Here is a step-by-step explanation of the mechanism:
1. In the presence of heat, the strong base ethanol (CH₃CH₂O⁻) abstracts a proton (H⁺) from the beta carbon adjacent to the chlorine atom in 2-chloro-2-methylpentane.
2. The resulting carbanion (CH₃CH₂CH(CH₃)CH₂⁻) undergoes a concerted elimination reaction, where the C-Cl bond breaks and a new C-C double bond forms. Simultaneously, the leaving group (chloride ion) leaves.
3. The intermediate formed is an alkene (2-methylpent-2-ene), which is then attacked by ethanol, acting as a nucleophile, to form the ether product (2-methoxy-2-methylpentane or ethoxypropane).
This E2 mechanism proceeds via a one-step concerted process, where both the proton abstraction and bond formation occur simultaneously
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If 8.2mol of hydrogen is produced, how many moles of hydrofluoric acid (HF) reacted? (Round to the nearest tenth)[tex]Si + 4HF -\ \textgreater \ 2H2 + SiF4[/tex]
Answer:
18.53
Explanation:
just finished and passed
how does the melting point range and the melting temperature enable you to judge the relative purity of the crude and pure product? (hint: there are two correct answers and both need to be selected to receive credit) group of answer choices larger range and lower temperature indicates a less pure product larger range and lower temperature indicates a more pure product narrow range and higher temperature indicates a less pure product narrow range and higher temperature indicates a more pure product
The correct answers are:
Narrow range and higher temperature indicate a more pure product.
Larger range and lower temperature indicate a less pure product.
There are two things to take into account when determining the relative purity of a chemical based on its melting point: the range and the temperature at which the compound melts.
Because impurities frequently disturb the molecules' normal structure, a wider range of melting temperatures suggests a less pure product. A smaller range signifies that the compound is more pure because it is made up of a single, clearly defined ingredient.
A more pure compound also has a higher melting point. A compound's melting point can be lowered, and its melting range can be expanded, by impurities. Because the compound needs more energy to overcome the intermolecular interactions and change from solid to liquid, a higher melting temperature denotes a higher level of purity.
In contrast, a wider range and lower melting point signify a less pure product because impurities or other compounds can cause the normal lattice structure to be disrupted and reduce the melting point.
Therefore, both a narrow range and higher temperature indicate a more pure product, while a larger range and lower temperature indicate a less pure product.
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Identify the important (diagnostic) peaks from the IR spectrum. List the cm −1
and the bond that corresponds to each peak below. Be sure to also add labels to your IR spectrum (write the corresponding bond type next to each peak on the IR spectrum itself). If any important peaks are absent, note that. 3. Identify the functional group(s) present in your molecule. 4. From the mass spectrum, identify the m/z value for the parent ion and base peak(s). Be sure to label these on your MS. Parention Base peak(s) 5. Using information from the IR and MS, determine the molecular formula and calculate the degree of unsaturation. Be sure to show your work. 6. From the "CNMR spectrum, list each carbon resonance with its chemical shift, possible hybridization, and number of attached hydrogens. 7. From the 'H NMR, list each proton resonance with its chemical shift and integration. 8. On the basis of your analysis above, propose a structure that fits all the data. Be sure the structure you propose fits your IR,MS, ' H and 13
C NMR data. 9. Attach copies of your labeled spectra to this sheet. For IR, label all important stretches with the appropriate bond. For MS, label the parent ion and base peak and draw the structure of the fragment for the base peak and any other significant peaks. For 1
H and 13
CNMR, draw the structure of the molecule and indicate which C or H gives rise to each peak. Unknown H411 Unknown H411 Unknown H411 Unknown H411 Unknown C311 1 Unknown M211 Unknown M211 Unknown R160
In order to identify the important (diagnostic) peaks from the IR spectrum, list the cm −1 and the bond that corresponds to each peak below, the IR spectrum should be consulted.
The major important peaks from the IR spectrum of the given molecule are listed below: The important (diagnostic) peaks from the IR spectrum are given below:Functional groups present in the given molecule: The presence of ester group can be confirmed by observing the absorption band in the range of 1700–1750 cm−1 and 1050–1150 cm−1. The presence of aromatic rings can be confirmed by observing the absorption band in the range of 1600–1400 cm−1. Thus, the functional groups present in the given molecule are ester and aromatic rings.The molecular formula of the given molecule can be determined from the molecular ion peak (M+) of the mass spectrum. The molecular ion peak (M+) is observed at m/z = 164. The molecular weight of the molecule can be calculated by adding the masses of the individual atoms in the molecule.
Molecular weight = 12 + 9 + 6 + 12 + 1 + 1 + 1 + 16 + 16 + 14 + 14 = 100 u
The molecular formula of the given molecule can be calculated by dividing the molecular weight of the molecule by the mass of the empirical formula. The empirical formula of the molecule can be determined by dividing the percentages of each element by its atomic mass. From the given data, the empirical formula is C4H5O2.Calculation of degree of unsaturation:Degree of unsaturation = (2n + 2 - X - H) / 2where n is the number of carbons, X is the number of halogens, and H is the number of hydrogens.The degree of unsaturation for the given molecule can be calculated as follows:Degree of unsaturation = (2 x 4 + 2 - 5 - 2) / 2= 1. The degree of unsaturation is 1, which indicates the presence of one ring or one pi bond.
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The molal freezing point depression constant =Kf·7.23°C·kgmol−1 for a certain substance X. When 10.g of urea NH22CO are dissolved in 350.g of X, the solution freezes at −12.0°C. Calculate the freezing point of pure X.
The freezing point of pure substance X is approximately -7.6°C.
To calculate the freezing point of pure X, we can use the formula for freezing point depression: ΔT = Kf * m
where ΔT is the change in freezing point, Kf is the molal freezing point depression constant, and m is the molality of the solution.
Given:
Kf = 7.23°C·kgmol⁻¹
m = mass of solute / mass of solvent = 10.g / 350.g = 0.0286 mol/kg
We can rearrange the formula to solve for ΔT:
ΔT = Kf * m
Substituting the given values:
ΔT = 7.23°C·kgmol⁻¹ * 0.0286 mol/kg
ΔT ≈ 0.207 K
The solution freezes at -12.0°C, so the freezing point of pure X can be found by subtracting the depression from the freezing point of the solution: Freezing point of pure X = -12.0°C + 0.207 K ≈ -7.6°C
Therefore, the freezing point of pure substance X is approximately -7.6°C.
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If (S)-glyceraldehyde has a specific rotation of −8,7 ∘
, what is the specific rotation of (R)-glyceraldehyde? Select one: a. cannot be determined from the information given b. 0 0
c. −8.7 0
d. +8.7 ∘
The specific rotation of (R)-glyceraldehyde cannot be determined from the information given (option a).
The specific rotation of an optically active compound depends on its molecular structure and the direction in which it rotates plane-polarized light. The specific rotation values for different enantiomers (mirror-image isomers) of a compound are typically different.
In this case, we are given the specific rotation of (S)-glyceraldehyde as -8.7°. However, this information does not provide any direct information about the specific rotation of (R)-glyceraldehyde. The specific rotation of (R)-glyceraldehyde could be positive, negative, or even zero, depending on its molecular structure and its interaction with polarized light.
Therefore, based on the information given, we cannot determine the specific rotation of (R)-glyceraldehyde, and the correct answer is option a: cannot be determined from the information given.
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5. describe a difference between observations of testing phosphate ion in whole milk and skim milk. determine if there is a difference in the amount of phosphorous between whole and skim milk. explain.
We would anticipate finding a higher concentration of calcium in whole milk than in skim milk. Whole milk and skim milk phosphate ion testing observations would not significantly differ from one other. There can be a little, but insignificant, difference in phosphorus content between whole and skim milk and dairy milk.
Testing for calcium ions in whole milk and skim milk yields different results: You would anticipate finding a higher concentration of calcium in whole milk than in skim milk. Higher fat content in whole milk includes fat-soluble vitamins like vitamin D. Calcium from the food is more easily absorbed when vitamin D is present. As a result, vitamin D has been added to whole milk, which helps the body absorb and retain calcium. As a result, whole milk often contains more calcium than skim milk.
Difference between whole milk and skim milk phosphate ion testing observations: Whole milk and skim milk phosphate ion testing observations would not significantly differ from one another. Since phosphate ions are a naturally occurring component of milk and are necessary for a number of biological functions, they can be found in both whole milk and skim milk. When milk is processed to create skim milk, the fat content is removed while the majority of the other ingredients, including phosphorus, are kept. As a result, there wouldn't be much of a difference in the concentration of phosphate ions between whole milk and skim milk.
Difference in phosphorus content between whole and skim milk: There can be a little, but insignificant, difference in phosphorus content between whole and skim milk. The quantity of phosphorus, an important mineral contained in milk, remains largely constant throughout all varieties of milk. Due to the removal of the fat part, skim milk, which has had its fat content reduced, may have a somewhat lower concentration of phosphorus than whole milk. This change, however small, is unlikely to have a substantial effect on the dairy milk's overall phosphorus level.
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--The question is incomplete, the complete question is:
"Describe a difference between observations of testing calcium ion in whole milk and skim milk. Determine if there is a difference in the amount of calcium between whole and skim milk. Explain. 5. Describe a difference between observations of testing phosphate ion in whole milk and skim milk. Determine if there is a difference in the amount of phosphorus between whole and skim milk. Explain."--
Draw the major organic product(s) of the following reaction. CH3CH₂-CEC-H ▾ -85 NaNH, / NH3(I) . You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the dr right corner. Separate multiple products using the + sign from the drop-down menu **** H₂C H3C 000 F n [References] CH-CH₂CH₂-Br
The final structure of the product is as follows:
H₂C
H3C
CH₃CH₂-C≡CH
The given reaction is a deprotonation reaction. The compound, CH3CH2-C≡C-H, is treated with sodium amide in liquid ammonia, resulting in the formation of an alkyne. The mechanism of the reaction is given below:
CH3CH2-C≡C-H + NaNH2 (Liquid ammonia) → CH3CH2-C≡C^-Na^+ + NH3
The alkynide ion formed then reacts with the solvent, liquid ammonia, and gives an alkyne as the final product. The equation for the reaction is given below:
CH3CH2-C≡C^-Na^+ + NH3 → CH3CH2-C≡CH + Na^+NH2
Therefore, the major organic product obtained from the given reaction is propyne. The final structure of the product is shown below:
H₂C
H3C
CH₃CH₂-C≡CH
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A. Nuclear Equations Complete the nuclear equations by filling in the correct symbols: 31e+ 96 404 + AI + on + Mo Na + He B. Radiation Measurement 1. Time (min) 1 Counts 34 38 1 34 2. Average background count. Total counts 3 counts/min (cpm) C. Radiation Levels from Radioactive Sources 1. Radiation Source 2. Counts/min 3. Average Back- (cpm) ground (cpm) - 35 mineral 1 615 Mineral 2 3293 Smoke detector 489 Plate Radio Source 6719 7349 Questions and Problems Q1 Which item was the most radioactive? -35 -35 -35 -35 4. Radiation from Source (cpm)
The radiation levels from different radioactive sources are listed, and it is determined that the Plate Radio Source was the most radioactive. The radiation from this source was measured at 6719 counts per minute (cpm)
The answer for the following Nuclear equation, radiation level and count, and radioactivity is as follows:
A. Nuclear Equations:
31e+ + 96 404AI → 96 41Mo + 0n + 2He
235U + 1n → 93 36Kr + 140 56Ba + 3 1n
B. Radiation Measurement:
Time (min) Counts
1 34
2 38
Average background count: 3 counts/min (cpm)
Total counts: 34 + 38 = 72
C. Radiation Levels from Radioactive Sources:
Radiation Source 2. Counts/min 3. Average Background (cpm)
-35 mineral 1 615
Mineral 2 3293 489
Smoke detector 489 489
Plate Radio Source 6719 7349
Q1. Which item was the most radioactive?
The Plate Radio Source was the most radioactive with a count of 6719 counts/min (cpm).
Q4. Radiation from Source (cpm):
The radiation from the Plate Radio Source was 6719 cpm.
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You want a buffer solution, and you choose the following acid and conjugate base: carbonic acid and sodlum hydrogen carbonate. \( K_{L} a=4.3 \) times \( 10^{\wedge}\{-7) \) for carbonic acid. The ini
The exact concentrations required for the buffer solution, we need additional information such as the desired pH range and the total volume of the buffer solution.
The initial step in preparing a buffer solution using carbonic acid ([tex]H_2CO_3[/tex]) and sodium hydrogen carbonate ([tex]NaHCO_3[/tex]) is to calculate the required ratio between the acid and its conjugate base.
To achieve an effective buffer, you typically want the ratio of the concentrations of the acid and the conjugate base to be close to 1.
To determine the appropriate concentrations, you can start by writing the dissociation reactions for carbonic acid and sodium hydrogen carbonate:
Carbonic acid dissociation:
[tex]\ce{H2CO3 \rightleftharpoons H+ + HCO3-}[/tex]
Sodium hydrogen carbonate dissociation:
[tex]\ce{NaHCO3 \rightleftharpoons Na+ + HCO3-}[/tex]
Given the acid dissociation constant (Ka) for carbonic acid as
[tex]Ka = 4.3 * 10^{-7}[/tex],
we can set up an equation to calculate the concentration ratio between [tex]HCO_3^-[/tex] and [tex]H_2CO_3[/tex]:
Ka =[tex][H^+][HCO_3^-] / [H_2CO_3][/tex]
Since the concentration of [tex]H_2CO_3[/tex] is unknown, we need to express it in terms of the concentration of [tex]HCO_3^-[/tex] using the Henderson-Hasselbalch equation:
[tex]pH = pKa + \log\left(\frac{{[HCO_3^-]}}{{[H_2CO_3]}}\right)[/tex]
In this case, the pKa is equal to the negative logarithm of the Ka value:
[tex]pKa = -\log_{10}(Ka) = -\log_{10}(4.3 \times 10^{-7})[/tex]
Once you know the pH and the pKa, you can calculate the ratio [[tex]HCO_3^-[/tex]] / [[tex]H_2CO_3[/tex]]. However, for a buffer solution, you need the ratio of the concentrations of [tex]H_2CO_3[/tex] and [tex]NaHCO_3[/tex] to be close to 1.
To proceed further and determine the exact concentrations required for the buffer solution, we need additional information such as the desired pH range and the total volume of the buffer solution. Please provide more details to continue the calculation.
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Which climatic zone is very dry for nearly the entire year?
arid
temperate continental
tropical wet
Mediterranean
Answer:
Arid
Explanation:
What is in the structure of myoglobin that reacts with potassium ferricyanide(III) to cause the color change? What are the purplish-red and the brown forms of myoglobin? Since myoglobin has oxygen binding property, can these the purplish-red and the brown forms of myoglobin still bind oxygen?
The structure of myoglobin consists of a protein chain folded into a compact three-dimensional structure. Within the protein structure, there is a heme group, which is a prosthetic group that contains an iron atom coordinated to a porphyrin ring. The iron atom in the heme group is responsible for the oxygen-binding capability of myoglobin.
When myoglobin reacts with potassium ferricyanide(III) (K₃Fe(CN)₆), it undergoes a chemical reaction known as oxidation. During this process, the iron atom in the heme group can be oxidized from the ferrous (Fe²⁺) state to the ferric (Fe³⁺) state. This oxidation results in a change in the electronic structure and color of the heme group, leading to the observed color change.
The purplish-red form of myoglobin is associated with the reduced state, where the iron atom is in the ferrous (Fe²⁺) state. In this state, myoglobin can readily bind oxygen, allowing for oxygen transport and storage in tissues. The binding of oxygen to myoglobin in its purplish-red form results in the formation of oxy-myoglobin, which has a bright red color.
On the other hand, the brown form of myoglobin is associated with the oxidized state, where the iron atom is in the ferric (Fe³⁺ state. In this state, myoglobin has a diminished ability to bind oxygen. The brown color observed in oxidized myoglobin is due to changes in the electronic structure of the heme group.
Therefore, the purplish-red form of myoglobin (reduced state) can bind oxygen, while the brown form of myoglobin (oxidized state) has a reduced oxygen-binding capability. The color change associated with the oxidation of myoglobin reflects the alteration in the electronic properties of the heme group, influencing its oxygen-binding capacity.
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which is williamson ether synthesis
2. \( \mathrm{H}_{3} \mathrm{O}^{+} \)
The given reactant, \( \mathrm{H}_3\mathrm{O}^+ \), is not commonly used in the Williamson ether synthesis.
The Williamson ether synthesis is a chemical reaction that involves the formation of an ether compound by the reaction of an alkoxide ion with a primary alkyl halide or a sulfonate ester.
In the context of the given reactant, \( \mathrm{H}_3\mathrm{O}^+ \) is a strong acid, specifically a hydronium ion. However, it is not commonly used as a reagent in the Williamson ether synthesis.
The typical nucleophile employed in this reaction is an alkoxide ion, such as sodium or potassium alkoxide. The alkoxide attacks the primary alkyl halide or sulfonate ester, displacing the halide or leaving group and forming the desired ether product.
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F. Solubility versus temperature; saturated and unsaturated
solutions
Label 4 weighing boats or papers as follows and weigh the
stated amounts onto each one:
a- 1.0g
NaCl
Solubility vs temperature:
Solubility refers to the quantity of solute that can dissolve in a given amount of solvent at a certain temperature. It's crucial to know the solubility of a substance because it helps determine the appropriate amount of substance to use to form a solution.
For some solutes, their solubility varies directly with temperature, i.e., solubility increases with temperature. Examples of such substances include sugar and sodium chloride. Therefore, increasing the temperature of the solution leads to an increase in solubility, while decreasing temperature results in a decrease in solubility.
Conversely, other substances such as Ca(OH)2 show an inverse relationship between solubility and temperature.
Saturated and unsaturated solutions:
A saturated solution refers to a solution that has dissolved as much solute as possible at a particular temperature and pressure. Therefore, adding more solute to a saturated solution results in the formation of undissolved solids.
On the other hand, an unsaturated solution is one that still has the capacity to dissolve more solute.
Experiment:
The experiment requires four weighing boats or papers, which should be labeled as follows:
1.0g NaCl
To carry out the experiment:
Take four weighing boats or papers.
Weigh 1.0g of NaCl onto each boat or paper.
Then, add the salt samples into different volumetric flasks containing different volumes of water.
Determine which flasks have saturated and unsaturated solutions by observing whether the salt completely dissolves or leaves some undissolved solid.
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What is the hydronium ion concentration in an aqueous nitric acid solution with a pH of 1.430 ? [H 3
O +
]= What is the pH of an aqueous solution of 1.40×10 −2
M hydrochloric acid?
The hydronium ion concentration in the nitric acid solution is [H3O+] = 4.48 × 10^−2 M.
The pH of the hydrochloric acid solution is pH = 1.85.
1. To find the hydronium ion concentration in the nitric acid solution with a pH of 1.430, we can use the equation pH = -log[H3O+]. Rearranging the equation, we have [H3O+] = 10^(-pH). Plugging in the given pH value:
[H3O+] = 10^(-1.430) = 4.48 × 10^(-2) M
Therefore, the hydronium ion concentration in the nitric acid solution is [H3O+] = 4.48 × 10^(-2) M.
2. The pH of an aqueous solution can be calculated using the equation pH = -log[H3O+]. In the case of hydrochloric acid (HCl), it is a strong acid, meaning it completely ionizes in water to produce H3O+ ions. Therefore, the concentration of H3O+ is equal to the concentration of HCl.
Given that the concentration of hydrochloric acid is 1.40 × 10^(-2) M, we can directly use this value to calculate the pH:
pH = -log(1.40 × 10^(-2)) = 1.85
Therefore, the pH of the hydrochloric acid solution is pH = 1.85.
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1.
What is the pH of 0.0100 M solution of phthalic acid (H2P)
2.If 25.0 mL of 0.20 M NaOH is added to 20.0 mL of 0.25 M
boric acid (HaBO3).
what is the pH of the resultant solution?H3BO3, Ka1= 6.4 ×
Boric acid ([tex]H3BO3[/tex]) is a weak acid, and the pH of the resultant solution is determined by the acid's dissociation in water. H3BO3 has two dissociation constants: [tex]Ka1=6.4 × 10-10 andKa2=5.8 × 10-14[/tex].
We must first determine the degree of dissociation (α) of the acid before calculating the pH of the solution, given that the acid is a weak acid. [tex]α=√(K_a/[H_3BO_3])At 25°C, [H3BO3] = 0.1 mol/Lα=√((6.4×10^-10)/(0.1))=2.02×10^-5.[/tex]
The [H3O+] of the resulting solution can now be determined from the equation: [tex]Ka=[H_3O^+]^2/[H_3BO_3]Ka1=(H_3O^+)2/[H3BO3]H3BO3 = 0.1 mol/L, Ka1 = 6.4 x 10^-10.[/tex]
Therefore,[tex][H3O+]2 = 0.1 x 6.4 x 10^-10[/tex]. Hence, [tex][H3O+] = 8.0 x 10^-6 M.[/tex]The pH of the resulting solution can be calculated using the following equation: [tex]pH = -log[H3O+].[/tex] Therefore, [tex]pH = -log(8.0 x 10^-6) = 5.10.[/tex]Thus, the pH of the resulting solution is 5.10.
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Suppose you had some water drops on the sides of the cuvet when you measured the absorbance of unknown solution. How would your calculated empirical formula of the unknown hydrate solution be different? Justify your answer. (Hint: Beer's Law).
Presence of water drops on the cuvet during absorbance measurement can lead to inaccurate readings, affecting the calculated empirical formula.
If there were water drops on the sides of the cuvet when measuring the absorbance of the unknown solution, it would affect the accuracy of the absorbance reading and, consequently, the calculated empirical formula of the unknown hydrate solution.
Beer's Law states that the absorbance of a solution is directly proportional to the concentration of the absorbing species and the path length of the light through the solution. However, in this case, the water drops on the sides of the cuvet would introduce additional water molecules into the light path, effectively increasing the path length. This would lead to an overestimation of the absorbance reading.
Since the empirical formula calculation is based on the absorbance values, an overestimation of absorbance would result in an erroneously higher concentration of the absorbing species. As a result, the calculated empirical formula of the unknown hydrate solution would also be skewed, potentially leading to an incorrect determination of the ratio of hydrate to anhydrous compound.
To ensure accurate results, it is crucial to remove any water drops or moisture from the cuvet before measuring the absorbance.
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Write the cell notation for an electrochemical cell consisting of an anode where Pb (s) is oxidized to Pb2+ (aq) and a cathode where H+ (aq) is reduced to H2 (g) at a platinum electrode . Assume all aqueous solutions have a concentration of 1 mol/L and gases have a pressure of 1 bar.
The cell notation for an electrochemical cell is a shorthand representation that describes the components and their arrangement in the cell. It consists of several components arranged in a specific order. The cell notation for the electrochemical cell described can be written as follows:
Anode: Pb (s) | Pb2+ (aq) || Cathode: H+ (aq) | Pt (s), H2 (g)
Let's break down the cell notation step by step:
1. The anode is where the oxidation half-reaction occurs. In this case, Pb (s) is oxidized to Pb2+ (aq). The solid lead (Pb) is written on the left side of the vertical line (|), representing the anode.
2. The vertical lines (||) separate the anode and cathode compartments of the cell.
3. The cathode is where the reduction half-reaction takes place. Here, H+ (aq) is reduced to H2 (g). The platinum (Pt) electrode is written on the right side of the vertical line (|), representing the cathode. The hydrogen gas (H2) is written beside the platinum electrode.
4. The cell notation also includes the states of the reactants and products. In this case, (s) represents a solid, (aq) represents an aqueous solution, and (g) represents a gas.
5. Additionally, the concentration of the aqueous solutions is specified to be 1 mol/L, and the pressure of the gas is 1 bar. This information is not included in the cell notation but is important to note.
Therefore, the cell notation for the electrochemical cell is:
Anode: Pb (s) | Pb2+ (aq) || Cathode: H+ (aq) | Pt (s), H2 (g)
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3. If the K a
for the weak acid, HA, is 2.40×10 −6
, what is the pH of 0.0750M solution of HA? Answer: 5. If the acid dissociation constant for formic acid, HCOOH, is 1.74×10 −4
, what is the molar concentration of formate, HCOO −
, in a solution containing 150.0μMH +
and 35.0μM formic acid? Answer: 6. Determine the concentration ratio of acetate to acetic acid when the pH of the acetic acid plus acetate solution is 5.45 and the K a
of acetic acid is 1.81×10 −5
.
The concentration ratio of acetate (C2H3O2-) to acetic acid (CH3COOH) is approximately equal to the antilog of [tex](5.45 - log(1.81×10^-5)).[/tex]
3. To find the pH of a weak acid solution, we can use the formula pH = -log[H+], where [H+] is the concentration of hydrogen ions. In this case, the weak acid is HA with a concentration of 0.0750M.
Since HA is a weak acid, it partially dissociates in water to produce hydrogen ions (H+) and the conjugate base (A-). The balanced chemical equation for this dissociation is HA ⇌ H+ + A-.
The equilibrium constant expression for this dissociation can be written as Ka = [H+][A-]/[HA].
Given that the Ka for HA is 2.40×10⁻⁶, we can assume that the concentration of [H+] formed from the dissociation of HA is negligible compared to the initial concentration of HA.
So, we can approximate [H+] as x (the concentration of H+ ions) and [A-] as x (the concentration of A- ions). Since [HA] = 0.0750 M, the concentration of HA will be 0.0750 - x.
Now, we can substitute these values into the equilibrium constant expression and solve for x:
2.40×10⁻⁶ = x * x / (0.0750 - x)
Simplifying the equation, we get:
2.40×10⁻⁶ = x² / (0.0750 - x)
Next, we can assume that x is very small compared to 0.0750. This allows us to simplify the equation further:
2.40×10⁻⁶ = x² / 0.0750
Cross multiplying, we get:
2.40×10⁻⁶ * 0.0750 = x²
x^2 = 1.8×10^-7
Taking the square root of both sides, we find:
x = 1.34×10⁻⁴
Therefore, the concentration of H+ ions in the solution is 1.34×10⁻⁴ M.
Now, we can calculate the pH using the formula pH = -log[H+]:
pH = -log(1.34×10⁻⁴)
pH = 3.87
So, the pH of the 0.0750 M solution of HA is approximately 3.87.
5. To find the molar concentration of formate ions (HCOO-) in a solution containing H+ and formic acid (HCOOH), we can use the acid dissociation constant (Ka) for formic acid.
The balanced chemical equation for the dissociation of formic acid is HCOOH ⇌ H+ + HCOO-.
The equilibrium constant expression for this dissociation can be written as Ka = [H+][HCOO-]/[HCOOH].
Given that the Ka for formic acid is 1.74×10⁻⁴, we can assume that the concentration of [HCOO-] formed from the dissociation of HCOOH is negligible compared to the initial concentration of HCOOH.
Let's assume the concentration of H+ ions is x and the concentration of HCOO- ions is x. Since the initial concentration of formic acid (HCOOH) is 35.0μM, its concentration will be 35.0 - x.
Now, we can substitute these values into the equilibrium constant expression and solve for x:
1.74×10⁻⁴ = x * x / (35.0 - x)
Simplifying the equation, we get:
1.74×10⁻⁶ = x² / (35.0 - x)
Next, we can assume that x is very small compared to 35.0. This allows us to simplify the equation further:
[tex]1.74×10^-4 = x^2 / 35.0[/tex]
Cross multiplying, we get:
[tex]1.74×10^-4 * 35.0 = x^2[/tex]
[tex]x^2 = 6.09×10^-6[/tex]
Taking the square root of both sides, we find:
x = 7.80×10⁻⁴
Therefore, the molar concentration of formate ions (HCOO-) in the solution is approximately 7.80×10^-4 M.
6. To determine the concentration ratio of acetate (C2H3O2-) to acetic acid (CH3COOH) in a solution with a given pH and the Ka of acetic acid, we need to consider the Henderson-Hasselbalch equation.
The Henderson-Hasselbalch equation is given by the formula: pH = pKa + log([C2H3O2-]/[CH3COOH])
Given that the pH is 5.45 and the pKa for acetic acid is -log(Ka) = -log(1.81×10^-5), we can substitute these values into the equation:
[tex]5.45 = -log(1.81×10^-5) + log([C2H3O2-]/[CH3COOH])[/tex]
Let's assume the concentration of acetate ions (C2H3O2-) is x and the concentration of acetic acid (CH3COOH) is y.
Therefore, the concentration ratio [C2H3O2-]/[CH3COOH] can be written as x/y.
Using logarithmic properties, we can simplify further:
[tex]5.45 + log(y) = -log(1.81×10^-5) + log(x)[/tex]
Rearranging the equation, we get:
[tex]log(x) - log(y) = 5.45 - log(1.81×10^-5)[/tex]
Taking the antilog of both sides, we find:
x/y = antilog(5.45 - log(1.81×10^-5))[tex]x/y = antilog(5.45 - log(1.81×10^-5))[/tex]
Therefore, the concentration ratio of acetate (C2H3O2-) to acetic acid (CH3COOH) is approximately equal to the antilog of
[tex](5.45 - log(1.81×10^-5)).[/tex]
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Calculating the pH at equivalence of a titration
A chemist titrates 50.0 mL of a 0.8279 M dimethylamine ((CH), NH) solution with 0.1635 M HCl solution at 25 °C. Calculate the pH at equivalence. The pK, of dimethylamine is 3.27. Round your answer to
The pH at equivalence of the titration is approximately 3.27.
To calculate the pH at equivalence, we need to determine the number of moles of HCl that react with the dimethylamine solution. At the equivalence point, the moles of HCl added are stoichiometrically equal to the moles of dimethylamine in the solution.
Given:
Volume of dimethylamine solution = 50.0 mL = 0.0500 L
Molarity of dimethylamine solution = 0.8279 M
Molarity of HCl solution = 0.1635 M
pKₐ of dimethylamine = 3.27
First, we need to calculate the moles of dimethylamine in the solution:
moles of dimethylamine = (Molarity of dimethylamine) * (Volume of dimethylamine solution)
moles of dimethylamine = (0.8279 M) * (0.0500 L)
Since the stoichiometry of the reaction between HCl and dimethylamine is 1:1, the moles of HCl required for complete neutralization are equal to the moles of dimethylamine.
Next, we calculate the concentration of HCl at the equivalence point:
concentration of HCl = (moles of dimethylamine) / (Volume of dimethylamine solution)
concentration of HCl = (0.8279 M) * (0.0500 L) / (0.0500 L)
concentration of HCl = 0.8279 M
Now, we can use the Henderson-Hasselbalch equation to calculate the pH at equivalence:
pH = pKₐ + log10(concentration of salt / concentration of acid)
Since we are at the equivalence point, the concentration of salt (dimethylammonium chloride) is equal to the concentration of acid (HCl), which is 0.8279 M.
pH = 3.27 + log10(0.8279 M / 0.8279 M)
pH = 3.27 + log10(1)
pH = 3.27 + 0
pH = 3.27
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Determine the number of IR-active CO stretching modes for Mn(CO)5Cl. This molecule has a C4v point group, as shown below. Structure of Mn(CO)5Cl Taking only the C-O stretching modes for Mn(CO)5 Cl (only the vectors between the C and O atoms): (1) Using these vectors and their variations to create the reducible representation. E 2C4 C2 2σv 2σd Γ Answer Answer Answer Answer Answer (2) By comparing the reducible representation so created and the irreducible representation gave in the character table, break up this reducible representation to the component irreducible representation even without calculations. Γ = Answer Answer + Answer +Answer (3) Examining the C4h character Table, it is found that Mn(CO)5 has Answer IR active bands and Answer Raman active bands in the region of C-O strecth absorption.
The reducible representation for Mn(CO)5Cl is Γ = A1 + B1 + B2 + 2E, and it has two IR-active bands and one Raman-active band in the C-O stretch absorption region.
The number of IR-active CO stretching modes for Mn(CO)5Cl can be determined by analyzing its point group symmetry, which is C4v.
(1) To create the reducible representation, we consider the vectors between the C and O atoms.
We have two C-O stretching vectors. Using the operations of the C4v point group (E: identity, 2C4: rotation by 90 degrees, C2: rotation by 180 degrees, 2σv: reflection in vertical planes, 2σd: reflection in diagonal planes), we can determine how these vectors transform under each operation:
E: The vectors remain unchanged.
2C4: The vectors remain unchanged.
C2: The vectors change sign.
2σv: The vectors change sign.
2σd: The vectors remain unchanged.
Therefore, the reducible representation is: Γ = 2A1 + B1 + B2 + E
(2) By comparing the reducible representation to the irreducible representations given in the character table of the C4v point group, we can break down the reducible representation into its component irreducible representations. Based on the character table, we can see that:
A1 appears once.
B1 appears once.
B2 appears once.
E appears twice.
Therefore, the reducible representation breaks down as follows:
Γ = A1 + B1 + B2 + 2E
(3) Examining the C4h character table, we find that Mn(CO)5 has two IR-active bands and one Raman-active band in the region of C-O stretch absorption.
In conclusion, the reducible representation for Mn(CO)5Cl is Γ = A1 + B1 + B2 + 2E, and it has two IR-active bands and one Raman-active band in the C-O stretch absorption region.
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What mass of water in grams contains 1.3 g of Ca? (1.3 g of Ca is the recommended daily allowance of calcium for 19 - to 24−year−olds) Express your answer in grams to two significant figures. X Incorrect; Try Again; 5 attempts remaining
The mass of water in grams that contains 1.3 g of Ca is 2.3 g (to two significant figures).
The formula to find out the mass of water that contains 1.3 g of Ca is explained below:1.3 g of Ca is the recommended daily allowance of calcium for 19 - to 24−year−olds. The molar mass of Ca is 40.08 g/mol.Therefore, the number of moles of Ca in 1.3 g of Ca can be found as:Number of moles of Ca = (1.3 g) / (40.08 g/mol)
= 0.0324 mol As Ca has a charge of +2, we have to multiply the number of moles of Ca with 2 to find the number of moles of Ca ions.
Number of moles of Ca2+ ions = 0.0324 mol × 2
= 0.0648 mol Now, we need to find out the mass of water that contains 0.0648 mol of Ca2+ ions. For every Ca2+ ion, we need two H2O molecules to keep the ion hydrated. Therefore, Number of moles of H2O = 0.0648 mol × 2
= 0.1296 mol The molar mass of water is 18.02 g/mol. Thus, the mass of water that contains 0.1296 mol of H2O can be calculated as: Mass of water = (0.1296 mol) × (18.02 g/mol)
= 2.337 g ≈ 2.3 g Therefore, the mass of water in grams that contains 1.3 g of Ca is 2.3 g (to two significant figures).
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Using tramadol as an example, explain the significance on CYP2D6 genotype on drug effects. (6 marks) This question will be graded as comprehensive/concise(6), most points made (4), surface level answe
Tramadol is an opioid drug used to treat moderate to severe pain. It is an example of a drug whose effects can be influenced by CYP2D6 genotype.
CYP2D6 is an enzyme that is involved in the metabolism of many drugs, including tramadol. The activity of this enzyme varies between individuals, depending on their genotype. Individuals with different genotypes may metabolize tramadol differently, leading to differences in drug effects.
The CYP2D6 gene has multiple variants, which can be classified into different genotype groups based on their function. The most common CYP2D6 genotypes are:
Poor metabolizers (PMs): Individuals with two non-functional alleles for CYP2D6 are classified as PMs. They have a significantly reduced ability to metabolize tramadol, which can lead to higher levels of the drug in their body and an increased risk of side effects.
Intermediate metabolizers (IMs): Individuals with one functional and one non-functional allele for CYP2D6 are classified as IMs. They have a reduced ability to metabolize tramadol compared to individuals with two functional alleles, which can lead to a higher risk of side effects.
Normal metabolizers (NMs): Individuals with two functional alleles for CYP2D6 are classified as NMs. They have a normal ability to metabolize tramadol.
Extensive metabolizers (EMs): Individuals with more than two functional alleles for CYP2D6 are classified as EMs. They have an increased ability to metabolize tramadol, which can lead to lower levels of the drug in their body and a reduced risk of side effects.
Overall, the CYP2D6 genotype can influence the metabolism and effects of tramadol. Individuals with different genotypes may require different doses of tramadol or may experience different side effects.
It is important for healthcare professionals to be aware of an individual's CYP2D6 genotype when prescribing tramadol.
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The analysis of a chemical used in photographic developing fluid indicates a chemical composition of 65.45% C, 5.45% H, and 29.09% O. The molar mass is found to be 110.0 g/mol. Determine the molecular formula. [Atomic masses: H = 1, C = 12, O=16]. O A. C6H₂O₂ B. C6H4O2 O C. C4H601 O D. C6H6O1 O E. C4H6Oz
The molecular formula: C3H3O x 2= C6H6O. The correct option is D.
The empirical formula of a substance represents the simplest whole-number ratio of the different atoms that exist in one molecule of the compound. The molecular formula, on the other hand, gives the exact number of different atoms present in a single molecule of the substance. The given chemical has 65.45% of Carbon, 5.45% Hydrogen, and 29.09% Oxygen in its chemical composition. Molecular mass of chemical= 110 g/mol Therefore, we can assume the following proportions for the chemical: Carbon = 65.45 / 12
= 5.45416Hydrogen
= 5.45 / 1
= 5.45Oxygen
= 29.09 / 16
= 1.81806 To convert these proportions to their simple whole-number ratios, we can divide them all by the smallest proportion, which is 1.81806 (that for Oxygen) Carbon
= 5.45416 / 1.81806
= 3Hydrogen
= 5.45 / 1.81806
= 3Oxygen
= 1.81806 / 1.81806
= 1.
Thus, the empirical formula for the given chemical is C3H3O.Substituting the respective atomic masses: H = 3 x 1
= 3C
= 3 x 12
= 36O
= 1 x 16
= 16 Total molecular weight of empirical formula
= 55 g/mol Since we are looking for the molecular formula, we need to find a factor that when multiplied by the empirical formula will give the molecular formula's molecular weight. The required factor is: Molecular weight of the chemical / Molecular weight of empirical formula= 110 / 55
= 2 Thus, multiplying the empirical formula by this factor, we get the molecular formula: C3H3O x 2
= C6H6O.The correct answer is option D. C6H6O1.
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