The concentration of
in the stack gas = 12 ppmv
That means 12 L of
is present per ![10^{6} L gas](https://tex.z-dn.net/?f=%2010%5E%7B6%7D%20L%20gas%20)
The given temperature is 273 K (0 C) and pressure is 1 atm. At these conditions, 1 mol of gas would occupy,
![PV = nRT](https://tex.z-dn.net/?f=%20PV%20%3D%20nRT%20)
![(1 atm) (V) = (1 mol)(0.08206\frac{L.atm}{mol.K}) (273 K)](https://tex.z-dn.net/?f=%20%281%20atm%29%20%28V%29%20%3D%20%281%20mol%29%280.08206%5Cfrac%7BL.atm%7D%7Bmol.K%7D%29%20%28273%20K%29%20)
V = 22.4 L
1 mol
occupies 22.4 L
Moles of
= ![12 L *\frac{1 mol}{22.4 L} = 0.5357 mol SO_{2}](https://tex.z-dn.net/?f=%2012%20L%20%2A%5Cfrac%7B1%20mol%7D%7B22.4%20L%7D%20%3D%200.5357%20mol%20SO_%7B2%7D%20%20%20%20)
Mass of
=
=
μg
Converting
:
= ![10^{3} m^{3}](https://tex.z-dn.net/?f=%2010%5E%7B3%7D%20%20%20m%5E%7B3%7D%20%20%20)
Calculating the concentration in μg/
:
![\frac{3.432 * 10^{7} microgram}{10^{3} L} = 3.432 * 10^{4} microgram/m^{3}](https://tex.z-dn.net/?f=%20%5Cfrac%7B3.432%20%2A%2010%5E%7B7%7D%20microgram%7D%7B10%5E%7B3%7D%20L%7D%20%20%20%20%3D%203.432%20%2A%2010%5E%7B4%7D%20%20microgram%2Fm%5E%7B3%7D%20%20)
Answer:
The rate of reaction will maintain constant
Explanation:
Rate of reaction is proportionate to rate constant x [A] ^2 x [B]. This means that the order of reaction with respect to C is 0 as it does not affect the rate of reaction as seen in the rate equation.
Essentially, order of reaction with respect to C is [C] ^0
Hence if [C] triples and becomes [3C]^0, the result will still be 1 as anything to the power of 0 is 1.
Therefore, the answer is that the rate of reaction will remain constant.
Answer:
(a)
(b) ![CO_{2}](https://tex.z-dn.net/?f=CO_%7B2%7D)
Explanation:
The reaction that is carried out by the enzyme catalase produces
The reaction that is carried out by the enzyme catalase produces ![CO_{2}](https://tex.z-dn.net/?f=CO_%7B2%7D)
CPT-I: Carnitine Translocase: CPT-II
- Carnitine palmitoyl transferase II deficiency is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source.
- The disorder presents in one of three clinical forms: lethal neonatal, severe infantile hepatocardiomuscular and myopathic.
What Is Carnitine Palmitoyltransferase II Deficiency?
Carnitine Palmitoyltransferase II (CPT II) deficiency, caused by mutations in the CPT2 gene, is an inherited disease in which the body cannot convert long-chain fatty acids into energy to fuel the body. There are three forms of the disease, and the severity and symptoms vary based on the form. In all three forms, symptoms can be triggered by periods without eating (fasting).
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brainly.com/question/16153580
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