The pH of the solution after adding 28.0 mL of 0.50 M NaOH is approximately 1.85.
The balanced chemical equation for the reaction between HCl and NaOH is:
HCl(aq) + NaOH(aq) → NaCl(aq) + H2O(l)
We can see that the reaction between HCl and NaOH is a neutralization reaction where H+ ions from HCl react with OH- ions from NaOH to form water.
Before the titration, we have a solution of 0.50 M HCl. This means that the concentration of H+ ions in the solution is 0.50 M. When we start adding NaOH, the NaOH reacts with the HCl to form NaCl and water. The H+ ions in the solution are gradually consumed by the NaOH until all of the H+ ions are neutralized. At this point, the solution is neutral with a pH of 7.
To determine the pH after adding 28.0 mL of 0.50 M NaOH, we need to first calculate the moles of HCl present in the solution before the addition of NaOH:
moles of HCl = concentration x volume
moles of HCl = 0.50 M x 0.050 L
moles of HCl = 0.025 mol
We can then calculate the moles of NaOH that have been added to the solution:
moles of NaOH = concentration x volume
moles of NaOH = 0.50 M x 0.028 L
moles of NaOH = 0.014 mol
Since HCl and NaOH react in a 1:1 ratio, we can say that 0.014 mol of H+ ions have been neutralized by the addition of NaOH. This means that the moles of H+ ions remaining in the solution are:
moles of H+ ions remaining = moles of HCl - moles of NaOH
moles of H+ ions remaining = 0.025 mol - 0.014 mol
moles of H+ ions remaining = 0.011 mol
To calculate the pH of the solution, we need to use the equation:
pH = -log[H+]
where [H+] is the concentration of H+ ions in the solution. We can calculate the concentration of H+ ions by dividing the moles of H+ ions remaining by the volume of the solution:
[H+] = moles of H+ ions remaining / volume of solution
[H+] = 0.011 mol / 0.078 L
[H+] = 0.141 M
Finally, we can calculate the pH:
pH = -log[H+]
pH = -log(0.141)
pH = 1.85
Therefore, the pH of the solution after adding 28.0 mL of 0.50 M NaOH is approximately 1.85.
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from a climate perspective, which term applies to carbon dioxide, methane, and nitrous oxide?
From a climate perspective, the term that applies to carbon dioxide, methane, and nitrous oxide is greenhouse gases, option D.
Due to minute concentrations of water vapour (H₂O), carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O) in the atmosphere, the Earth has a natural greenhouse effect. These gases allow solar light to reach the Earth's surface, but they also absorb infrared radiation that the Earth emits, warming the planet's surface. The augmented greenhouse effect must be distinguished from the natural greenhouse effect. The natural greenhouse effect, which is essential to life, is brought on by the levels of greenhouse gases that occur naturally. The Earth's surface would be around 33 °C colder in the absence of the natural greenhouse effect.
The extra radiative forcing brought on by higher greenhouse gas concentrations brought on by human activity is known as the enhanced greenhouse effect. In the lower atmosphere, ozone, carbon dioxide, methane, nitrous oxide, hydrochlorofluorocarbons (HCFCs), and hydrofluorocarbons (HFCs) are the principal greenhouse gases whose concentrations are growing.
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Complete question:
From a climate perspective, what term applies to carbon dioxide, methane, and nitrous oxide.
A. fossil fuels
B. ozone layer
C. inert gases
D. greenhouse gases
p-nitroaniline is less basic than aniline — justify with appropriate drawings.
In summary, the presence of an electron-withdrawing nitro group in p-nitroaniline reduces its basicity compared to aniline by decreasing the availability of the amino group's lone pair of electrons to accept protons. This can be visualized through resonance structures, where the electron density is pulled away from the amino group by the nitro group.
The difference in basicity between p-nitroaniline and aniline can be explained by examining their structures and the effects of the nitro group.
Aniline (C6H5NH2) is an aromatic amine with an amino group (-NH2) attached to a benzene ring. The amino group's lone pair of electrons can accept a proton, making it a basic compound.
On the other hand, p-nitroaniline (C6H4N2O2) has a nitro group (-NO2) attached to the para position of the benzene ring relative to the amino group. The nitro group is electron-withdrawing, which means it pulls electron density away from the amino group through resonance. As a result, the lone pair of electrons on the nitrogen in the amino group becomes less available to accept a proton, making p-nitroaniline less basic than aniline.
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what is e° for the cell mn | mn²⁺(aq) || ag⁺(aq) | ag?
The standard cell potential for the Mn | Mn²⁺(aq) || Ag⁺(aq) | Ag half-cell is 1.98 V.
The standard reduction potential for Mn²⁺/Mn is -1.18 V, and for Ag⁺/Ag is 0.80 V. To calculate the standard cell potential, we use the formula:
E°cell = E°reduction (cathode) - E°reduction (anode)
E°cell = 0.80 V - (-1.18 V)
E°cell = 1.98 V
However, this calculation assumes that the half-reactions are written as reductions. To obtain the standard cell potential for the given oxidation-reduction reaction, we need to reverse the half-reaction for the anode:
Mn → Mn²⁺ + 2e⁻ (reduction)
2Ag⁺ + 2e⁻ → 2Ag (oxidation)
Reversing the oxidation half-reaction changes the sign of its reduction potential. Therefore, the overall cell potential is:
E°cell = E°reduction (cathode) - E°reduction (anode)
E°cell = 0.80 V - (-1.18 V)
E°cell = 1.98 V
So the standard cell potential for the Mn | Mn²⁺(aq) || Ag⁺(aq) | Ag half-cell is 1.98 V.
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What mass of TiCl4 must react with an excess of water to produce 50. 0 g of TiO2 if the reaction has a 78. 9% yield? TiCl4 + 2H20 - TiO2 + 4HCI 93. 9 OOO 63. 48 1195 O 1518 ! Incorrect
Given,TiCl4 + 2H2O → TiO2 + 4HClMolar mass of TiCl4 = 189.6 g/mol. Molar mass of TiO2 = 79.9 g/molNow, the balanced chemical equation is;TiCl4 + 2H2O → TiO2 + 4HClNow, for producing 1 mol of TiO2, 1 mol of TiCl4 is required.
Also, the molar mass of TiO2 is 79.9 g/mol.Moles of TiO2 = Given mass/Molar mass = 50/79.9 = 0.625 molMoles of TiCl4 required = Moles of TiO2 = 0.625 molNow, the percentage yield is given as 78.9%.Therefore,Actual yield = 78.9/100 × Theoretical yield.
Theoretical yield = Moles of TiCl4 × Molar mass of TiCl4 = 0.625 × 189.6 = 118.5 g. Actual yield = 78.9/100 × 118.5 g = 93.48 gTherefore, the mass of TiCl4 required to produce 50.0 g of TiO2 with 78.9% yield is 118.5 g (Theoretical yield) and 93.48 g (Actual yield).
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1. A stock solution has a volume of 57.86 mL and a molarity of 3.35M. If 125mL of water is added to the stock solution what is the new molarity?
2. 22.10mL of 1.20M solution has been added to 100 mL of water. What is the final molarity?
3. A stock solution has a volume of 65.69 mL and a molarity of 3.79M. If 75mL of water is added to the stock solution what is the new molarity?
4. 72.86mL of 0.15M solution has been added to 200 mL of water. What is the final molarity?
I need help with these questions, please
The molarity of the following subquestions are as follows;
The new molarity is 1.06 MThe final molarity is 0.22 MThe new molarity is 1.77 MThe final molarity is 0.0401 MHow to calculate molarity?The molarity of a solution can be calculated using the following expression;
CaVa = CbVb
Where;
Ca and Va = initial concentration and volumeCb and Vb = final concentration and volumeQUESTION 1:
57.86 × 3.35 = 182.86 × Cb
193.831 = 182.86Cb
Cb = 1.06M
QUESTION 2:
22.10 × 1.2 = 122.10 × Cb
26.52 = 122.10Cb
Cb = 0.22 M
QUESTION 3:
65.69 × 3.79 = 140.69 × Cb
248.9651 = 140.69Cb
Cb = 1.77 M
QUESTION 4:
72.86 × 0.15 = 272.86 × Cb
10.929 = 272.86Cb
Cb = 0.0401 M
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which term describes the incomplete breakdown of glucose due the absence of an electron acceptor for the electron transport system?
The term that describes the incomplete breakdown of glucose due to the absence of an electron acceptor for the electron transport system is anaerobic respiration.
Anaerobic respiration occurs when there is no oxygen available to accept electrons from the electron transport chain during cellular respiration. As a result, the electron transport chain cannot function properly, and the cell must rely on an alternate pathway to generate ATP. This alternate pathway involves the use of a different electron acceptor, such as sulfate or nitrate, which are reduced to hydrogen sulfide or nitrogen gas, respectively.
Anaerobic respiration produces less ATP than aerobic respiration because the electron acceptors used are less efficient than oxygen. Additionally, anaerobic respiration produces byproducts such as lactic acid or ethanol, which can be toxic to cells. Therefore, aerobic respiration is the preferred method of energy production for most cells, as it produces more ATP and is less harmful to the cell.
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Suppose you are investigating the reaction: M(s) + 2 HCl(aq) → MCl2(aq) + H2(g). You weigh out a 0.152 gram piece of metal and combine it with 62.1 mL of 1.00 M HCl in a coffee-cup calorimeter. If the molar mass of the metal is 42.26 g/mol, and you measure that the reaction absorbed 154 J of heat, what is the enthalpy of this reaction in kJ per mole of limiting reactant? Enter your answer numerically to three significant figures in units of kJ/molI
The enthalpy of the reaction per mole of metal is -42,778 J/mol/ -42.8 kJ/mol.
First, we need to calculate the number of moles of HCl used in the reaction:
n(HCl) = (1.00 mol/L) x (0.0621 L) = 0.0621 mol
Next, we need to calculate the number of moles of metal used in the reaction:
n(M) = 0.152 g / (42.26 g/mol) = 0.0036 mol
Since the stoichiometric coefficient of HCl in the balanced equation is 2, and the number of moles of HCl is 0.0621 mol, we can see that the limiting reactant is metal. Therefore, we can calculate the enthalpy of the reaction per mole of metal:
ΔHrxn = -q / n(M) = -(154 J) / (0.0036 mol) = -42,778 J/mol
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Write The Net Ionic Equation For The Equilibrium Involving The HSO
the net ionic equation is:
[tex]HSO_{4} + H_{2}O[/tex] ⇌ [tex]H_{3}O+[/tex]
To write the net ionic equation for the equilibrium involving the HSO ion, we need to first write the balanced equation. The HSO ion is the conjugate base of the sulfuric acid, [tex]H_{2} SO_{4}[/tex]. Therefore, the equilibrium we are interested in is:
[tex]HSO_{4} + H_{2}O[/tex] ⇌ H3O+ + [tex]SO_{4}2-[/tex]
To write the net ionic equation, we need to eliminate the spectator ions, which are the [tex]HSO_{4}-[/tex] and [tex]SO_{4}2-[/tex] ions. These ions appear on both sides of the equation and do not participate in the reaction. Therefore, the net ionic equation is:
[tex]HSO_{4} + H_{2}O[/tex] ⇌ [tex]H_{3}O+[/tex]
This equation shows only the ions that are involved in the equilibrium and their changes. The [tex]HSO_{4}-[/tex] ion accepts a proton (H+) from water to form the H3O+ ion, which is the hydronium ion. This reaction can also be described as an acid-base reaction, where the [tex]HSO_{4}-[/tex]ion acts as a base and water acts as an acid. The equilibrium constant for this reaction is known as the acid dissociation constant, Ka, and is equal to 1.2 x [tex]10^{-2}[/tex] for the [tex]HSO_{4}-[/tex] ion.
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What is the predominant form of ethylenediamine at pH 6.441 and pH 9.375? Ethylenediamine has pKb values of 4.072 (pKb1) and 7.152 (pKb2).
Ethylenediamine is a weak base with two pKb values, and it can exist in three different forms: as a fully protonated cation, a partially protonated zwitterion, or a fully deprotonated anion.
To determine the predominant form at a given pH, we need to compare the pH to the pKb values.
At pH 6.441, which is between the two pKb values, ethylenediamine is partially protonated. The dominant species will be the zwitterion, which has a positive charge on one nitrogen and a negative charge on the other nitrogen.
At pH 9.375, which is higher than both pKb values, ethylenediamine is fully deprotonated. The dominant species will be the anion, which has both nitrogens with a negative charge.
Therefore, at pH 6.441, the predominant form of ethylenediamine is the zwitterion, and at pH 9.375, the predominant form is the anion.
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Write an equilibrium expression (Keq) for the reaction.
Hb(CO)4(aq)+4 O2(g)=Hb(O2)4(aq)+4CO(g)
Answer:
Explanation:
The equilibrium expression (Keq) for the given reaction is:
Keq = [Hb(O2)4(aq)][CO(g)]^4 / [Hb(CO)4(aq)][O2(g)]^4
In this expression, the square brackets represent the molar concentrations of the respective species at equilibrium. The coefficients of the species in the balanced equation indicate the stoichiometric relationship between them. The Keq value represents the equilibrium constant, which is a measure of the extent of the reaction at equilibrium.
1. Which of the following reactions best
represents the following particle diagram? (1pt)
a. 2 Na + Cl₂ 2 NaCl
b. Na₂ + 2 cl → Na₂Cl₂
c. Na₂ + Cl₂ → 2 Nacl
d. Na + 2 Cl₂ Nacl
Answer:
a. 2 Na + Cl₂ --> 2 NaCl
Explanation:
a is your answer because Cl is diatomic, there are 2 Na atoms, and the product is 2NaCl.
A chemist fills a reaction vessel with 4. 43 atm methane CH4 gas, 8. 74 atm oxygen O2 gas, 4. 85 atm carbon dioxide CO2 gas, and 2. 72 atm hydrogen H2 gas at a temperature of 25. 0°C. Under these conditions, calculate the reaction free energy ΔG for the following chemical reaction: +CH4gO2g +CO2g2H2g
substance 솨4° (k /mol) ΔGfo (k /mol) So (J/mol-K)
CO2 (g) -393. 5 -394. 4 213. 8
H2 (g) 0 0 130. 7
O2 (g) 0 0 205. 2
CH4 (g) -74. 6 -50. 5 186. 3
The reaction free energy ΔG for the given chemical reaction is 204.2 kJ/mol.
The reaction is:
CH4(g) + O2(g) + CO2(g) → 2H2(g) + 2CO(g)
We can use the standard free energy of formation (ΔGf°) values to calculate the standard free energy change (ΔG°) for the reaction:
ΔG° = ΣnΔGf°(products) - ΣnΔGf°(reactants)
n is the stoichiometric coefficient of each species in the balanced chemical equation.
ΔG° = [2ΔGf°(H2) + 2ΔGf°(CO)] - [ΔGf°(CH4) + ΔGf°(O2) + ΔGf°(CO2)]
ΔG° = [2(0) + 2(-110.5)] - [(-50.5) + 0 + (-394.4)]
ΔG° = -221.8 + 444.9
ΔG° = 223.1 kJ/mol
Now, we need to calculate the reaction free energy ΔG using the reaction quotient Q and the gas constant R:
ΔG = ΔG° + RTlnQ
where T is the temperature in kelvin.
We need to calculate the reaction quotient Q for the given conditions. Since we are given partial pressures, we can use the following expression to calculate Q:
Q = (PH2)^2(PCO)^2 / (PCH4)(PO2)(PCO2)
Substituting the given values, we get:
Q = (2.72 atm)^2(4.85 atm)^2 / (4.43 atm)(8.74 atm)(2.72 atm)
Q = 0.287
Substituting the values in the equation for ΔG, we get:
ΔG = ΔG° + RTlnQ
ΔG = (223.1 kJ/mol) + (8.314 J/mol-K)(298 K)ln(0.287)
ΔG = 223.1 kJ/mol - 18.9 kJ/mol
ΔG = 204.2 kJ/mol
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if we skipped the four washing steps (with water), what major impurity would be in the precipitated crude lidocaine. give the specific name of the one compound. do not explain (3 point).
The major impurity that would be in the precipitated crude lidocaine if the four washing steps (with water) were skipped is diethylamine.
Hope this helps! Have a nice day. :)write chemical equation for third step of a born - haber cycle. express your answer as a chemical equation. identify all of the phases in your answer. ba(g)→ba2 (g) 2e−
The third step in a Born-Haber cycle involves the conversion of a gaseous atom to a gaseous ion.
This step usually involves the loss or gain of one or more electrons, which results in the formation of a cation or an anion, respectively. The energy required to form an ion from a gaseous atom is called the ionization energy, and it is always an endothermic process, meaning that it requires energy input.
The Born-Haber cycle is a way of calculating the enthalpy of formation of ionic compounds from the enthalpies of formation of their constituent elements.
In the third step of the Born-Haber cycle, a gaseous atom of barium (Ba) is converted into a gaseous ion (Ba2+) by losing two electrons (2e-). Therefore, the chemical equation for the third step of the Born-Haber cycle for the formation of barium ion is:
Ba(g) → Ba2+(g) + 2e-
In this equation, Ba is the gaseous atom of barium, Ba2+ is the gaseous ion of barium, and e- represents the two electrons lost by the Ba atom to form the Ba2+ ion. All species in the equation are in the gas phase.
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4. A gas is in a 67°C room with standard pressure. Find the new pressure of
the gas in kPa when the temperature is increased by 30.°C.
The new pressure of the gas, when the temperature is increased by 30°C, is approximately 1.088 kPa.
To find the new pressure of the gas when the temperature is increased by 30°C, we can use the combined gas law, which states that the ratio of pressure to temperature remains constant when the amount of gas and volume are constant. The equation can be expressed as:
(P₁/T₁) = (P₂/T₂)
Where P₁ and T₁ are the initial pressure and temperature respectively, and P₂ and T₂ are the final pressure and temperature respectively.
Given that the gas is in a 67°C room with standard pressure, we can convert the temperatures to Kelvin by adding 273.15 to each value. So, the initial temperature (T₁) is 67 + 273.15 = 340.15 K.
The temperature is increased by 30°C, so the final temperature (T₂) is 67 + 30 + 273.15 = 370.15 K.
Since the pressure is at standard pressure, we can assume it to be 1 atmosphere, which is equivalent to 101.325 kPa.
Using the equation, we can solve for the final pressure (P₂):
(1/340.15 K) = (P₂/370.15 K)
Cross-multiplying, we get:
P₂ = (1/340.15 K) * 370.15 K = 1.088 kPa
Therefore, the new pressure of the gas, when the temperature is increased by 30°C, is approximately 1.088 kPa.
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a 25.0 ml sample of 0.150 m formic acid is titrated with a 0.150 m koh solution. what is the ph at the equivalence point? the ka of formic acid is 1.8 × 10-4.
The pH at the equivalence point of the titration is 12.38.
The balanced chemical equation for the reaction between formic acid (HCOOH) and potassium hydroxide (KOH) is:
HCOOH + KOH → HCOOK + H2O
At the equivalence point, all the formic acid has reacted with the potassium hydroxide, and we are left with a solution containing only the potassium formate (HCOOK) salt. Therefore, the moles of potassium hydroxide added will be equal to the moles of formic acid initially present in the solution:
moles of KOH = 0.150 M x 0.025 L = 0.00375 mol
Since the formic acid is a weak acid, it will not fully dissociate, but will undergo partial neutralization with the strong base potassium hydroxide. The balanced chemical equation for the reaction between formic acid and hydroxide ions is:
HCOOH + OH- → HCOO- + H2O
Using the stoichiometry of the balanced equation, we can calculate the moles of formic acid that react with the hydroxide ions:
moles of HCOOH = 0.00375 mol
moles of OH- = 0.00375 mol
moles of HCOO- formed = 0.00375 mol
The concentration of the formate ion can be calculated as:
[formate ion] = moles of HCOO- / volume of solution at equivalence point
[formate ion] = 0.00375 mol / 0.025 L = 0.15 M
The formate ion will hydrolyze to a small extent, producing hydroxide ions and formic acid:
HCOO- + H2O ⇌ HCOOH + OH-
Using the equilibrium constant expression for this reaction, we can calculate the hydroxide ion concentration:
Kb = ([HCOOH][OH-])/[HCOO-] = 1.8 × 10^-4
[OH-] = sqrt(Kb x [HCOO-] / [HCOOH])
[OH-] = sqrt(1.8 × 10^-4 x 0.15 M / 0.0 M) = 0.024 M
Therefore, the pOH at the equivalence point is:
pOH = -log[OH-] = -log(0.024) = 1.62
Since the solution is neutral at the equivalence point, the pH can be calculated as:
pH = 14.00 - pOH = 12.38
Therefore, the pH at the equivalence point of the titration is 12.38.
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a solution of has a concentration of . this solution was diluted by adding of water. determine the of the new solution:
A 248 mL solution of Ca(OH)₂ having a concentration of 1.31 M. This solution was diluted to 0.631 L. Then, the pOH of the new solution is approximately 0.986.
First, let's calculate the number of moles of Ca(OH)₂ in the original solution;
n = M × V = 1.31 M × 0.248 L = 0.32568 mol
Since the solution was diluted to 0.631 L, the new concentration of Ca(OH)₂ is;
M' = n/V' = 0.32568 mol/0.631 L = 0.516 M
Next, we can use the fact that Ca(OH)₂ completely dissociates in water to find the concentration of hydroxide ions;
[OH⁻] = 2 × [Ca(OH)₂] = 2 × 0.516 M = 1.032 M
Finally, we can use the definition of pOH to find its value;
pOH = -log[OH⁻] = -log(1.032) = 0.986
Therefore, the pOH of the new solution is 0.986.
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--The given question is incomplete, the complete question is
"A 248 mL solution of Ca(OH)₂ has a concentration of 1.31 M. This solution was diluted to 0.631 L. determine the pOH of the new solution."--
predict the products and write the molecular equation when solutions of silver nitrate and sodium carbonate are mixed.
When solutions of silver nitrate and sodium carbonate are mixed, the following reaction takes place: AgNO3 + Na2CO3 → Ag2CO3 + 2NaNO3. The products of this reaction are silver carbonate and sodium nitrate. The molecular equation for this reaction is written as: AgNO3(aq) + Na2CO3(aq) → Ag2CO3(s) + 2NaNO3(aq)
This is a double displacement reaction in which the ions of two compounds switch places to form two new compounds.
Silver carbonate is a white solid that is sparingly soluble in water. It is mainly used in the preparation of other silver compounds and as a catalyst in organic reactions. Sodium nitrate is a white crystalline solid that is commonly used as a fertilizer and in the manufacture of explosives.
In summary, when solutions of silver nitrate and sodium carbonate are mixed, a double displacement reaction occurs, resulting in the formation of silver carbonate and sodium nitrate. The molecular equation for this reaction is AgNO3(aq) + Na2CO3(aq) → Ag2CO3(s) + 2NaNO3(aq).
When solutions of silver nitrate (AgNO3) and sodium carbonate (Na2CO3) are mixed, a double displacement reaction occurs. The products of this reaction are silver carbonate (Ag2CO3) and sodium nitrate (NaNO3). The molecular equation for this reaction is:
2 AgNO3 (aq) + Na2CO3 (aq) → Ag2CO3 (s) + 2 NaNO3 (aq)
In this equation, the silver nitrate and sodium carbonate react to form the solid silver carbonate, which precipitates out of the solution, and the soluble sodium nitrate remains in the solution.
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energy is released from atoms in the form of light when electrons: a) move from high energy levels to low energy levels. b) move in their orbit around the nucleus. c) move from low energy levels to high energy levels. d) are emitted by the atom. e) are absorbed by atoms
Answer:
D
Explanation:
i took chemistry :)
why does chymotrypsin cleave a peptide bond only after amino acids with aromatic or large hydrophobic side chains?
Chymotrypsin is an enzyme that catalyzes the hydrolysis of peptide bonds, breaking them down into smaller peptides and amino acids. Chymotrypsin is specific in its substrate specificity, meaning that it only cleaves peptide bonds in certain types of peptides.
The reason why chymotrypsin cleaves a peptide bond only after amino acids with aromatic or large hydrophobic side chains is due to the unique structure and chemical properties of these amino acids. Therefore, chymotrypsin cleaves a peptide bond only after amino acids with aromatic or large hydrophobic side chains because these amino acids interact with the active site of the enzyme in a way that allows the peptide bond to be cleaved.
Aromatic amino acids, such as tryptophan, tyrosine, and phenylalanine, have a planar, unsaturated ring structure. This ring structure creates a unique interaction with the active site of chymotrypsin, which is composed of a metal ion and several amino acid residues. The aromatic amino acids are able to bind to the active site of chymotrypsin, stabilizing the enzyme-substrate complex and allowing the peptide bond to be cleaved.
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Beside water molecules, what chemical species are present at the greatest concentration when NH3(g) is bubbled into water? Kb for NH3 is 1.8 x 10-5 NH4+ and OH NH3 NH4OH NH2 and H30+
Of the species listed, [tex]NH_4^{+}, OH^-, and H_3O^+[/tex] will be present at the greatest concentrations when [tex]NH_3(g)[/tex] is bubbled into water.
When [tex]NH_3[/tex](g) is bubbled into water, it reacts with water molecules to form ammonium hydroxide ([tex]NH_4OH[/tex]) and hydronium ion [tex](H_3O^+)[/tex], according to the following equation:
[tex]NH_3 + H_2O = NH_4^{+} + OH^-[/tex]
The equilibrium constant for this reaction is the base dissociation constant (Kb) for [tex]NH_3[/tex], which has a value of 1.8 x 10^-5 at 25°C.
At equilibrium, the concentrations of the various species in solution will depend on the concentration of [tex]NH_3[/tex] initially added to the solution, as well as the temperature and pressure of the system. However, in general, at equilibrium, the concentration of [tex]NH_3[/tex] will be significantly lower than the concentrations of [tex]NH_4^+[/tex], [tex]OH^-[/tex], and [tex]H_3O^+[/tex].
The concentration of [tex]NH_4^+[/tex] will be equal to the concentration of [tex]NH_3[/tex] that has reacted with water to form [tex]NH_4OH[/tex]. The concentration of [tex]OH^-[/tex] will be equal to the concentration of [tex]NH_4OH[/tex] that has dissociated into [tex]NH_4^+[/tex] and [tex]OH^-[/tex].
The concentration of [tex]H_3O^+[/tex] will be equal to the concentration of [tex]OH^-[/tex] according to the equilibrium constant expression for water autoionization. The concentration of [tex]NH_2[/tex] is expected to be extremely low because it is an intermediate in the reaction between [tex]NH_3[/tex] and water, and it readily reacts with [tex]H_3O^+[/tex] to form [tex]NH_4^+[/tex].
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a hydrogen tank has a pressure of 101,325 Pa at 30 degrees celcius.At what temperature would its pressure be equal to 1.75 atm?
The temperature at which the pressure will be equal to 1.75 atm, given that the tank has an initial pressure of 101325 Pa is 257.25 degrees celsius
How do i determine the temperature?First, we shall list out the given parameters from the question. This is shown below:
Initial pressure (P₁) = 101325 Pa = 101325 / 101325 = 1 atm Initial temperature (T₁) = 30 degrees Celsius = 30 + 273 = 303 KFinal pressure (P₂) = 1.75 atmFinal temperature (T₂) =?The final temperature can be obtain as follow:
P₁ / T₁ = P₂ / T₂
1 / 303 = 1.75 / T₂
Cross multiply
1 × T₂ = 303 × 1.75
T₂ = 530.25 K
Subtract 273 to obtain answer in degree celsius
T₂ = 530.25 – 273 K
T₂ = 257.25 degrees celsius
Thus, the temperature required is 257.25 degrees celsius
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How much heat (kJ) is required to melt 23.9 g of solid diethyl either (C4H10O) at its melting point. The enthalpy of fusion for diethyl either is 7.27 kJ/mol
The heat required to melt 23.9 g of diethyl ether at its melting point is 2.34 kJ.
To calculate the heat required to melt diethyl ether [tex](C_4H_{10}O)[/tex] at its melting point:
Q = n × ΔHfus
where Q = heat required, n = number of moles of diethyl ether, and ΔHfus = enthalpy of fusion of diethyl ether (in kJ/mol).
First, we need to calculate the number of moles of diethyl ether:
molar mass of [tex]C_4H_{10}O[/tex] = 74.12 g/mol
moles = mass/molar mass = 23.9 g / 74.12 g/mol = 0.322 mol
Next, we can use the given enthalpy of fusion to calculate the heat required:
Q = n × ΔHfus = 0.322 mol × 7.27 kJ/mol = 2.34 kJ
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if 2.10 mol of nitrogen monoxide gas and 2.70 mol of oxygen gas react how many moles of no2 are produced according to the equation?
According to the balanced chemical equation for the reaction between nitrogen monoxide gas and oxygen gas, 2 NO + O2 -> 2 NO2, 2 moles of NO react with 1 mole of O2 to produce 2 moles of NO2. Therefore, the limiting reactant in this scenario is the reactant that is completely consumed first, which is NO.
Since we have 2.10 mol of NO and it reacts with 1.05 mol of O2, we can calculate the number of moles of NO2 produced using the mole ratio of 2:2.10 or 1:1.05. This gives us 2.10 mol of NO2 produced.
To determine the moles of NO2 produced when 2.10 mol of nitrogen monoxide gas and 2.70 mol of oxygen gas react,
we need the balanced chemical equation: 2NO + O2 → 2NO2. Comparing moles of reactants, we have 2.10 mol NO and 2.70 mol O2. Since 2 moles of NO react with 1 mole of O2, we require 1.05 mol O2 (2.10/2) to completely react with 2.10 mol NO. Since we have 2.70 mol O2 available, O2 is in excess and NO is the limiting reactant. Therefore, 2.10 mol NO will produce 2.10 mol NO2 according to the balanced equation.
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which is the weakest acid? group of answer choices so42– h2so4 h2so3 hso3– hso4–
The weakest acid is the one that is least likely to donate a proton (H+ ion) to a base. In general, an acid's strength depends on the stability of its conjugate base. The more stable the conjugate base, the weaker the acid.
Out of the given options, SO42- is the weakest acid because it is the most stable conjugate base. When H2SO4 donates a proton, it forms HSO4-, which is a stronger acid than H2SO4. When HSO4- donates a proton, it forms SO42-, which is a very stable anion due to its complete octet of electrons and its negative charge being spread out over four oxygen atoms.
H2SO4 and H2SO3 are stronger acids than SO42- because their conjugate bases, HSO4- and HSO3-, respectively, are less stable. HSO3- is weaker than H2SO4 because its conjugate base, SO32-, is more stable than HSO4-.
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Consider the reaction: 2brf3(g)br2(g) 3f2(g) using standard thermodynamic data at 298k, calculate the entropy change for the surroundings when 2. 47 moles of brf3(g) react at standard conditions
The entropy change for the surroundings when 2. 47 moles of BrF₃(g) react at standard conditions is -700.38 J/K .
Entropy is the measurement of the amount of thermal energy per unit of temperature in a system that cannot be used for productive labour. Entropy is a measure of a system's molecular disorder or unpredictability since work is produced by organised molecular motion. Entropy theory offers profound understanding of the direction of spontaneous change for many commonplace events. A standout of 19th-century physics is its invention by the German scientist Rudolf Clausius in 1850.
Given the reaction is ,
2 BrF₃ (g) →Br₂ (g) + 3F₂ (g)
∆[tex]H^0_{rxn[/tex] = 208.71235 KJ
= 208.71235 x 10³ J
( As , 1 KJ = 10³ J )
= 208712.35 J
T = 298 K
Now ,∆S⁰ surroundings = - ∆[tex]H^0_{rxn[/tex] / T
∆S⁰ surroundings = - 208712.35 J / 298 K
∆S⁰ surroundings = -208712.35 / 298 J/K
∆S⁰ surroundings = - 700.38 J/K
Therefore , the entropy change for surroundings when 2.47 mol of BrF₃ reacts at Standard condition is - 700.38 J/K .
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how many iron atoms are contained in 354 g of iron? a) 2.62 × 1025 fe atoms b) 2.13 × 1026 fe atoms c) 4.69 × 1024 fe atoms d) 3.82 × 1024 fe atoms e) 9.50 × 1022 fe atoms
Option (d) 3.82 × 10^24 Fe atoms is the closest choice to the calculated value.
To determine the number of iron atoms in 354 g of iron, we need to use Avogadro's number and the molar mass of iron.
The molar mass of iron (Fe) is approximately 55.85 g/mol. We can calculate the number of moles of iron in 354 g by dividing the mass by the molar mass:
Number of moles = 354 g / 55.85 g/mol = 6.33 mol
Next, we use Avogadro's number, which states that there are 6.022 × 10^23 atoms in one mole of any substance. Therefore, the number of iron atoms can be calculated by multiplying the number of moles by Avogadro's number:
Number of iron atoms = 6.33 mol * (6.022 × 10^23 atoms/mol)
Performing the calculation, we find that the number of iron atoms is approximately 3.81 × 10^24 atoms.
Therefore, option (d) 3.82 × 10^24 Fe atoms is the closest choice to the calculated value.
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if a base, such as sodium hydroxide (naoh) were added to milk, would the protein precipitate? why or why not?
If a base like sodium hydroxide (NaOH) is added to milk, the proteins may precipitate.
Milk contains proteins, mainly casein, which exist as micelles in a colloidal suspension.
When sodium hydroxide is added, it increases the pH of the milk. At a higher pH, the casein molecules lose their negative charges, causing them to aggregate and precipitate.
If a base like sodium hydroxide (NaOH) is added to milk, the proteins may precipitate.
This process is known as protein denaturation.
Summary: Adding sodium hydroxide to milk can cause proteins like casein to precipitate due to denaturation at higher pH levels.
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a 0.20 m aqueous solution of propanoic acid, ch3ch2cooh, has a ph of 2.79. calculate the value of ka of propanoic acid
The Ka of propanoic acid is 0.004 M.
Ka (acid dissociation constant) is a measure of the strength of an acid and is defined as the ratio of the dissociation constant of the acid to the concentration of the acid. The dissociation constant of an acid is the equilibrium constant for the dissociation of the acid into its ions in solution.
To calculate the Ka of propanoic acid, we can use the following equation:
Ka = [A-]/[HA]
here A- is the concentration of the conjugate base of the acid, and HA is the concentration of the acid.
Since we are given the Ka value of the propanoic acid in aqueous solution, we can use the Ka value to calculate the concentration of the conjugate base of the acid using the following equation:
[A-] = [HA] * Ka
Using the given value of Ka and the pH of the solution, we can use the following equation to calculate the concentration of the conjugate base of the acid:
[A-] = [HA] * Ka
[A-] = (0.20 M) * (0.20)
[A-] = 0.004 M
Therefore, the Ka of propanoic acid is 0.004 M.
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what is the density (in g/l) of hydrogen gas at 15.0 c and a 1375 psi?
The density of hydrogen gas at 15.0°C and 1375 psi is 0.090 g/L.
To calculate the density of hydrogen gas at 15.0°C and 1375 psi, we can use the ideal gas law:
PV = nRT
Where:
P = Pressure (in atmospheres)
V = Volume (in liters)
n = Number of moles of gas
R = Ideal gas constant (0.0821 L·atm/(mol·K))
T = Temperature (in Kelvin).
First, we need to convert the given pressure from psi to atm:
1375 psi * (1 atm / 14.7 psi) = 93.5 atm
Next, we convert the temperature from Celsius to Kelvin:
15.0°C + 273.15 = 288.15 K
Assuming standard conditions (1 atm and 273.15 K) for molar volume, we can rearrange the ideal gas law equation to solve for density:
density = (P * Molar mass) / (R * T)
The molar mass of hydrogen gas (H₂) is 2.016 g/mol. Substituting the values into the equation:
density = (93.5 atm * 2.016 g/mol) / (0.0821 L·atm/(mol·K) * 288.15 K)
Calculating the density:
density ≈ 0.090 g/L (rounded to three decimal places)
Therefore, the density of hydrogen gas at 15.0°C and 1375 psi is approximately 0.090 g/L.
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