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svp [43]
3 years ago
12

2) 2KClO3 --> 2KCl + 3O2

Chemistry
1 answer:
aleksandrvk [35]3 years ago
8 0

2 \text{ KClO}_3 \to 2 \text{ KCl}+3\text{ O}_2

a)

2 \text{ mols of KClO}_3 \equiv 3  \text{ mols of O}_2

19 \text{ mols of KClO}_3 \equiv 3\cdot 9,5  \text{ mols of O}_2

\boxed{19 \text{ mols of KClO}_3 \equiv 28,5  \text{ mols of O}_2}

b)

2 \text{ mols of KClO}_3 \equiv 2  \text{ mols of KCl}

62 \text{ mol of KClO}_3 \equiv 62  \text{ mol of KCl}

Using the atomic mass given in the periodic table:

62\cdot(39+35,5+16\cdot3) \text{ g of KClO}_3 \equiv 62  \text{ mol of KCl}

62\cdot122,5 \text{ g of KClO}_3 \equiv 62  \text{ mol of KCl}

7595 \text{ g of KClO}_3 \equiv 62  \text{ mol of KCl}

\boxed{7,595 \text{ kg of KClO}_3 \equiv 62  \text{ mol of KCl}}

c)

2 \text{ KCl}+3\text{ O}_2\to 2 \text{ KClO}_3

3 \text{ mols of O}_2 \equiv 2 \text{ mols of KCl}

Using the atomic mass given in the periodic table:

3\cdot(2\cdot 16) \text{ g of O}_2 \equiv 2\cdot(39+35,5)  \text{ g of KCl}

96\text{ g of O}_2 \equiv 149\text{ g of KCl}

\dfrac{39}{149}\cdot 96\text{ g of O}_2 \equiv \dfrac{39}{149}\cdot 149\text{ g of KCl}

\boxed{25,13\text{ g of O}_2 \equiv 39\text{ g of KCl}}

This result is an aproximation.

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8 0
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Calculate the equilibrium constant k for the isomerization of glucose-1-phosphate to fructose-6-phosphate at 298 k. express your
k0ka [10]
We cannot solve this problem without using empirical data. These reactions have already been experimented by scientists. The standard Gibb's free energy, ΔG°, (occurring in standard temperature of 298 Kelvin) are already reported in various literature. These are the known ΔG° for the appropriate reactions.

<span>glucose-1-phosphate⟶glucose-6-phosphate          ΔG∘=−7.28 kJ/mol
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Therefore, the reaction is a two-step process wherein glucose-6-phosphate is the intermediate product.

glucose-1-phosphate⟶glucose-6-phosphate⟶fructose-6-phosphate 

In this case, you simply add the ΔG°. However, since we need the reverse of the second reaction to end up with the terminal product, fructose-6-phosphate, you'll have to take the opposite sign of ΔG°.

ΔG°,total = −7.28 kJ/mol  + 1.67 kJ/mol = -5.61 kJ/mol

Then, the equation to relate ΔG° to the equilibrium constant K is

ΔG° = -RTlnK, where R is the gas constant equal to 0.008317 kJ/mol-K.
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6 0
3 years ago
Read 2 more answers
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goldenfox [79]

Answer:

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3. True

4. True

5. False

Explanation:

1. Hypochlorous acid (HOCl)  is a weak acid that forms when chlorine dissolves in water, and is partially dissociated, forming hypochlorite. HOCl is considered a strong oxidizing agent responsible for the killing action of germs in chlorine solutions.

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3/4 . Methylene chloride is an organochloride compound with the formula CH2Cl2. It is  a colorless, volatile liquid with a moderately sweet aroma is widely used as a solvent. It is normally stable, non-flammable and non-explosive when mixed with air at temperatures below 100 °C, but its vapor is flammable only when present in relatively high concentrations of about 14% to 22% in air. Research shows that it is very much possibly carcinogenic, and it has been linked to cancer of the lungs, liver, pancreas, breast cancer and salivary gland cancer in laboratory animals.

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6 0
3 years ago
The composition of a liquid-phase reaction 2A - B was monitored spectrophotometrically. The following data was obtained: t/min 0
o-na [289]

Answer:

1) The order of the reaction is of FIRST ORDER

2)   Rate constant k = 5.667 × 10 ⁻⁴

Explanation:

From the given information:

The composition of a liquid-phase reaction 2A - B was monitored spectrophotometrically.

liquid-phase reaction 2A - B signifies that the reaction is of FIRST ORDER where the rate of this reaction is directly proportional to the concentration of A.

The following data was obtained:

t/min                    0         10         20          30             40          ∞

conc B/(mol/L)    0       0.089    0.153     0.200       0.230    0.312

For  a first order reaction:

K = \dfrac{1}{t} \ In ( \dfrac{C_{\infty} - C_o}{C_{\infty} - C_t})

where :

K = proportionality  constant or the rate constant for the specific reaction rate

t = time of reaction

C_o = initial concentration at time t

C _{\infty} = final concentration at time t

C_t = concentration at time t

To start with the value of t when t = 10 mins

K_1 = \dfrac{1}{10} \ In ( \dfrac{0.312 - 0}{0.312 - 0.089})

K_1 = \dfrac{1}{10} \ In ( \dfrac{0.312 }{0.223})

K_1 =0.03358 \  min^{-1}

K_1 \simeq 0.034 \  min^{-1}

When t = 20

K_2= \dfrac{1}{20} \ In ( \dfrac{0.312 - 0}{0.312 - 0.153})

K_2= 0.05 \times  \ In ( 1.9623)

K_2=0.03371 \ min^{-1}

K_2 \simeq 0.034 \ min^{-1}

When t = 30

K_3= \dfrac{1}{30} \ In ( \dfrac{0.312 - 0}{0.312 - 0.200})

K_3= 0.0333 \times  \ In ( \dfrac{0.312}{0.112})

K_3= 0.0333 \times  \ 1.0245

K_3 = 0.03412 \ min^{-1}

K_3 = 0.034 \ min^{-1}

When t = 40

K_4= \dfrac{1}{40} \ In ( \dfrac{0.312 - 0}{0.312 - 0.230})

K_4=0.025 \times  \ In ( \dfrac{0.312}{0.082})

K_4=0.025 \times  \ In ( 3.8048)

K_4=0.03340 \ min^{-1}

We can see that at the different time rates, the rate constant of k_1, k_2, k_3, and k_4 all have similar constant values

As such :

Rate constant k = 0.034 min⁻¹

Converting it to seconds ; we have :

60 seconds = 1 min

∴

0.034 min⁻¹ =(0.034/60) seconds

= 5.667 × 10 ⁻⁴ seconds

Rate constant k = 5.667 × 10 ⁻⁴

4 0
3 years ago
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