
In Dumas method for the estimation of nitrogen in an organic compound, nitrogen is determined in the form of:
A) Gaseous nitrogen.
B) Sodium Cyanide.
C) Ammonium sulphate.
D) Gaseous ammonia.
Answer
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Hint:We must remember that the Dumas’ method is a method used for quantitative nitrogen content. The product of this method is a mixture of gases from which a diatomic gas is isolated which has atomic number seven and is present in abundant amounts in the earth’s atmosphere.
Complete step by step answer: Now we can discuss Duma's method and how it works.
Dumas' method:
In Dumas method, a known mass of the compound is heated with cupric oxide in an environment of . The carbon and hydrogen within the compound are oxidized to and water respectively, while nitrogen is about free. The oxides of nitrogen produced are reduced to nitrogen by heated copper gauze. The gaseous mixture consisting of , and is collected over a solution of potash. Except nitrogen all the gases are absorbed by the solution. The quantity of gas (nitrogen) collected is measured.
Therefore, the option A is correct.
Note: Now we discuss the advantages and limitations of Dumas method.
The Dumas method has the benefits of being easy to use and fully automatable. It has been developed into a considerably faster method than the Kjeldahl method, and may take a couple of minutes per measurement, as compared to the hour or more for Kjeldahl. It also doesn't make use of toxic chemicals or catalysts. Also, like Kjeldahl, it doesn't provide a measure of true protein, because it registers non-protein nitrogen, and different correction factors are needed for various proteins because they need different amino alkanoic acid sequences.
Complete step by step answer: Now we can discuss Duma's method and how it works.
Dumas' method:
In Dumas method, a known mass of the compound is heated with cupric oxide in an environment of
Therefore, the option A is correct.
Note: Now we discuss the advantages and limitations of Dumas method.
The Dumas method has the benefits of being easy to use and fully automatable. It has been developed into a considerably faster method than the Kjeldahl method, and may take a couple of minutes per measurement, as compared to the hour or more for Kjeldahl. It also doesn't make use of toxic chemicals or catalysts. Also, like Kjeldahl, it doesn't provide a measure of true protein, because it registers non-protein nitrogen, and different correction factors are needed for various proteins because they need different amino alkanoic acid sequences.
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