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Ghella
2 months ago
7

Compounds A and B are colorless gases obtained by combining sulfur with oxygen. Compound A results from combining 6.00 g of sulf

ur with 5.99 g of oxygen, and compound B results from combining 8.60 g of sulfur with 12.88 g of oxygen. Show that the mass ratios in the two compounds are simple multiples of each other.
Chemistry
1 answer:
lorasvet [2.7K]2 months ago
4 0

Answer:

1.5

Explanation:

It is given that:

Compound A and B originate from Sulfur + Oxygen.

Compound A:

6g sulfur + 5.99g Oxygen

Compound B:

8.6g sulfur + 12.88g oxygen

By comparing the ratios:

Compound A:

S: O = 6.00: 5.99

S/0 = 6.0g S / 5.99g O

Compound B:

S: O = 8.60: 12.88

S / O = 8.60g S / 12.88g O

The mass ratio of A and that of B

(6.0g S / 5.99g O) ÷ (8.60g S / 12.88g O)

(6.0 g S / 5.99g O) × (12.88g O / 8.60g S)

(6 × 12.88) / (5.99 × 8.60)

= 77.28 / 51.514

= 1.50017

= 1.5

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Consider the following system at equilibrium:
VMariaS [2998]

Answer:

A - Increase (R), Decrease (P), Decrease(q), Triple both (Q) and (R)

B - Increase(P), Increase(q), Decrease (R)

C - Triple (P) and cut (q) down to a third

Explanation:

According to the principle of Le Chatelier, when a system reaches equilibrium and a change is introduced, the system will respond to counteract that change.

Since P and Q are reactants, raising the amount of either one or both without a proportional rise in R (which is a product) will cause the equilibrium to move towards the right. Similarly, if R decreases while P and Q remain constant, this too will push the equilibrium to the right. Thus, Increase(P), Increase(q), and Decrease(R) will lead to a rightward shift in the equilibrium.

Conversely, raising R without increasing P and Q will draw the equilibrium to the left. Likewise, cutting down P and/or Q without a similar reduction in R will shift the equilibrium leftward. Therefore, Increase(R), Decrease(P), Decrease(q), and triple both (Q) and (R) will shift the equilibrium to the left.

If there are equivalent changes in P and Q, with R remaining unchanged, then the equilibrium remains stationary. So, tripling (P) while reducing (q) to one third will not alter the equilibrium.

6 0
2 months ago
66.667 mL of 3.000 M H2SO4 (aq) solution was neutralized by the stoichiometric amount of 4.000 M Al(OH)3 solution in a coffee cu
eduard [2782]

Answer:

\large \boxed{\Delta_{\textbf{r}}H =\text{-4600 J$\cdot$ mol}^{-1}}

Explanation:

This scenario is unrealistic since Al(OH)₃ is not soluble in water.

The question consists of two parts:

A. Stoichiometry — where we determine volumes, masses, and moles for the products

B. Calorimetry — where we assess the enthalpy of the reaction.

A. Stoichiometry

1. Determine the volume of Al(OH)₃

(a) The balanced chemical equation:

                 2Al(OH)₃ + 3H₂SO₄ ⟶ Al₂(SO₄)₃ + 6H₂O

M/V:            66.667

c/mol·L⁻¹:   4.000       3.000

(b) Moles of H₂SO₄

\rm \text{66.667 mL H$_{2}$}SO_{4} \times \dfrac{\text{3.000 mmol H$_{2}$SO}_{4}}{\text{1 mL H$_{2}$SO}_{4}} = \text{200.00 mmol H$_{2}$SO}_{4}

(c) Moles of Al(OH)₃

The molar ratio stands at 2 mmol Al(OH)₃: 3 mmol H₂SO₄

\text{Moles of Al(OH)}_{3} = \text{200.00 mmol of H$_{2}$SO}_{4} \times \dfrac{\text{2 mmol Al(OH)}_{3}}{\text{3 mmol H$_{2}$SO}_{4}}\\\\= \text{133.33 mmol Al(OH)}_{3}

(d) Volume of Al(OH)₃

\text{Moles of Al(OH)}_{3} = \text{200.00 mmol of H$_{2}$SO}_{4} \times \dfrac{\text{1 mL Al(OH)}_{3}}{\text{4 mmol H$_{2}$SO}_{4}} = \text{50.000 mL Al(OH)}_{3}

B. Calorimetry

This reaction has two energy exchanges.

q₁ = heat from the reaction

q₂ = heat used to heat the calorimeter

 q₁ + q₂ = 0

nΔH + mCΔT = 0

Data:

Moles of Al₂(SO₄)₃ = 0.066 667 mol

C = 1.10 J°C⁻¹g⁻¹

T_initial = 22.3 °C

T_final = 24.7 °C

Calculations

(a) Mass of solution

Assume solutions are as dense as water (though not realistic).

Mass of sulfuric acid solution            =   66.667 g 

Mass of aluminium hydroxide solution =  50.000    

                                             TOTAL =  116.667 g

(b) ΔT

ΔT = T_final - T_initial = 24.7 °C - 22.3 °C = 2.4°C

(c) ΔH

\begin{array}{ccccl}n\Delta H & +& mC \Delta T& = &0\\\text{0.066 667 mol }\times \Delta H& + & \text{116.667 g} \times 1.10 \text{ J$^{\circ}$C$^{-1}$g$^{-1}$} \times 2.4 \, ^{\circ}\text{C} & = & 0\\0.066667 \Delta H \text{ mol} & + & \text{310 J} & = & 0\\&&0.066667 \Delta H \text{ mol} & = & \text{-310 J} & & \\\end{array}\\

\begin{array}{ccccl}& &\Delta H & = & \dfrac{\text{-310 J}}{\text{0.066667 mol}}\\\\& &\Delta H & = & \textbf{-4600 kJ/mol}\\\end{array}\\\large \boxed{\mathbf{\Delta_{\textbf{r}}H} =\textbf{-4600 J$\cdot$ mol}^{\mathbf{-1}}}

This result appears nonsensical, but it is derived from your given figures.

6 0
2 months ago
Freon-11, CCl3F has been commonly used in air conditioners. It has a molar mass of 137.35 g/mol and its enthalpy of vaporization
alisha [2963]

Answer:

180.56 kilojoules of heat energy is extracted when 1.00 kg of freon-11 evaporates.

Explanation:

The molar mass of freon-11 is 137.35 g/mol

The enthalpy of vaporization for freon-11 is 24.8 kJ/mol at its normal boiling point of 24°C. Given that,\Delta H_{vap}=24.8 kJ/mol

Mass of freon-11 evaporated = 1.00 kg = 1000 g

Moles of freon-11 evaporated can be calculated as

\frac{1000 g}{137.35 g/mol}=7.2807 mol

The energy removed in the form of heat when 1.00 kg of freon-11 vaporizes is:

7.28067 mol\times \Delta H_{vap}=7.2807 mol\times 24.8 kJ/mol

=180.56 kJ

0 0
1 month ago
Write a balanced equation for the reaction of NaCH3COO (also written as NaC2H3O2) and HCl.
lorasvet [2795]
The balanced equation is:

NaCH₃COO + HCl → NaCl + HCH₃COO

Make 
4 0
3 months ago
Read 2 more answers
Find the age t of a sample, if the total mass of carbon in the sample is mc, the activity of the sample is a, the current ratio
Alekssandra [3086]
N₀ signifies the quantity of C-14 atoms per kg of carbon in the original sample at time = 0 seconds, when the carbon composition matched that in today’s atmosphere. As time progresses to ts, the number of C-14 atoms per kg declines to N, due to radioactive decay. λ indicates the decay constant.
Hence, we have N = N₀e - λt, which is the equation for radioactive decay. Rearranging gives us N₀/N = e λt, or In(N₀/N) = - λt, which becomes equation 1.
The sample contains mc kg of carbon, leading to an activity measured as A/mc decay per kg. The variable r represents the initial mass of C-14 in the sample at t=0 relative to the total mass of carbon which is calculated as [(total number of C-14 atoms at t = 0) × ma] / total mass of carbon. Thus, N₀ equates to r/ma, which becomes equation 2.
The activity of the radioactive element is directly related to the atom count at the moment. The activity equation A = dN/dt = λ(N) indicates that: A = λ₁(N × mc). Rearranging provides N = A / (λmc), represented in equation 3.
By integrating equations 2 and 3, we can solve for t yielding
t = (1/λ) In(rλmc/m₀A).

6 0
2 months ago
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