Answer:
Explanation:
For the growth and flourishing of animals Aromatic amino acids are very important, but because of lack of shikimate these amino acids are not synthesized in animals pathway.But this pathway is found in both plants and micro organisms and they have the ability to produce these amino acids as well as some secondary metabolites required in animals.
There are different role played by this pathway in organisms such as;
1) It serve as a source of Tryptophan and phenylalanie which are important aromatic amino acid.
2)Neuroactive substances such as serotonin,epinephrine are biosynthesized as result of the product from the pathway.
3)Alkaloids that's found in plants as well as antibiotics possessed by microbes, which are essential therapeutical in animals are secondary metabolites that is biosynthesized as a result of the activities of this product of this pathway.
4)Shikimate is useful in the synthesizing of 6-Fluoroshikimic acid.
5) The shikimate pathway is important for the synthesis of a plethora of aromatic compounds in both plants and bacteria as well as fungi.
Answer:
Outside air
Nose
Lungs
Bloodstream
Cell
Explanation:
We breathe in oxygen from the outside air in through our nose and it travels to our lungs. Inside our lungs, we have Avioli's that diffuse oxygen into our bloodstream and the bloodstream helps the oxygen travel into our cells.
Hope this helps :)
We can use a variety of formulas to determine our answers here.
Our formula for pOH is -log(mol), and we can plug it in as -log(0.010). Take note that OH- is a base, not an acid.
So, the pOH of OH- is 2.
To find pH we can set up this simple equation:
pH + pOH = 14
All we need to do is subtract 2 from 14, therefore the pH is 12.
This makes sense since acids range in the pH of 1-6, and we are dealing with a base. Hope I could help!
Describe the process by which Ag+ ions are precipitated out of solution. 4. In your testing, several precipitates are formed, and then dissolved as complexes.
Answer:
The structure with the ring flipped is the most stable
Explanation:
We have the trans 1,2 - dimethylcyclohexane. With the wedge/dash structure we could not figure is this form is stable (If we do a comparison with the cis structure). But when we do a chair structure and ring flipped structure, this is easier to look.
The picture attached shows the structures, they are labeled as 1, 2 and 3, according to this problem.
In the chair structure, according to the picture below, you can see that both methyls are heading in the axial positions of the ring (One facing upward and the other downward). This is pretty stable, however, when the methyls are in those positions, the methyl position 1, can undergoes an 1,3 diaxial interactions with the hydrogens atoms (They are not drawn, but still are there), so this interaction makes this structure a little less stable that it can be.
On the other side, the ring flipped structure, we can see that both methyls are in the equatorials positions of the ring, and in these positions, it can avoid the 1,4 diaxial interactions with the hydrogens atoms, making this structure the most stable structure.
Hope this helps
