(a) Interpretation: Need to explain why the N 2 ( g ) extracted from liquid air do not have the same density as the N 2 ( g ) extracted from its compounds. Concept introduction: In the atmosphere, N 2 ( g ) is mixed with other gases.
(a) Interpretation: Need to explain why the N 2 ( g ) extracted from liquid air do not have the same density as the N 2 ( g ) extracted from its compounds. Concept introduction: In the atmosphere, N 2 ( g ) is mixed with other gases.
Solution Summary: The author explains that N 2 (g) extracted from liquid air does not have the same density as its compounds because it is mixed with noble gas Ar.
Need to explain why the N2(g) extracted from liquid air do not have the same density as the N2(g) extracted from its compounds.
Concept introduction:
In the atmosphere, N2(g) is mixed with other gases.
Interpretation Introduction
(b)
Interpretation:
Need to explain which gas has greater density among N2(g) extracted from liquid air or N2(g) extracted from its compounds.
Concept introduction:
In the atmosphere, N2(g) is mixed with other gases while N2(g) from its compound is pure.
Interpretation Introduction
(c)
Interpretation:
Need to explain the significance of the experiment which Ramsay used to prove the N2(g) extracted from liquid air was itself a mixture of gases.
Concept introduction:
Ramsay’s experiment was very useful in identification of noble gases.
Interpretation Introduction
(d)
Interpretation:
Need to calculate the percent difference in densities at 0.00 C and 1 atm of Rayleigh’s N2(g) extracted from liquid air or N2(g) extracted from its compounds.
Concept introduction:
N2(g) extracted from liquid air do not have the same density as the N2(g) extracted from its compounds because N2(g) extracted from liquid air is mixed with noble gas − Ar.
Predict the major products of the following organic reaction:
O O
+
A
?
Some important notes:
• Draw the major product, or products, of the reaction in the drawing area below.
• If there aren't any products, because no reaction will take place, check the box below the drawing area instead.
• Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are
enantiomers.
Explanation Check
Click and drag to start drawing a structure.
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can someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products
Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided below
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell