Answer:
The rule is especially applicable to carbon, nitrogen, oxygen, and the halogens, but also to metals such as sodium or magnesium. ... All four of these electrons are counted in both the carbon octet and the oxygen octet, so that both atoms are considered to obey the octet rule.
1-H NMR spectroscopy tool will be used for distinguishing a sample of 1,2,2-tribromopropane from 1,1,2-tribromopropane.
The preferred method for determining or validating the structure of organic molecules or those containing protons is H NMR. When compared to other nuclei, a solution-state proton spectrum may be obtained relatively quickly, and it contains a wealth of knowledge regarding a compound's structure.
It can be calculated by simply counting the number of unique hydrogens on one side of the symmetry plane will give you the count of signals individual molecules emit in a 1H NMR spectrum.
Therefore, 1-H NMR spectroscopy tool will be used for distinguishing a sample of 1,2,2-tribromopropane from 1,1,2-tribromopropane.
To know more about 1-H NMR spectroscopy
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Answer:
6.68 X 10^-11
Explanation:
From the second Ka, you can calculate pKa = -log (Ka2) = 6.187
The pH at the second equivalence point (8.181) will be the average of pKa2 and pKa3. So,
8.181 = (6.187 + pKa3) / 2
Solving gives pKa3 = 10.175, and Ka3 = 10^-pKa3 = 6.68 X 10^-11
I think it's 2:1 or 2:1:4. I mostly think it's 2:1 though. (:
