Liquid column chromatography on alumina would separate p-nitrotoluene and p-nitroaniline O A. with p-nitroaniline eluted first since the stationary phase has little affinity for polar compounds. O B. with p-nitrotoluene eluted first since the stationary phase absorbs polar compounds strongly. O C. with p-nitrotoluene eluted first since it has a lower boiling point. O D. only slightly since the molecules are nearly the same size. O E. with p-nitroaniline eluted first since equilibria in the moving phase involve ions.

EBK A SMALL SCALE APPROACH TO ORGANIC L
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Chapter36: Grubbs-catalyzed Metathesis Of Eugenol With 1,4-butenediol To Prepare A Natural Product
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Liquid column chromatography on alumina would separate p-nitrotoluene and p-nitroaniline
O A. with p-nitroaniline eluted first since the stationary phase has little affinity for polar compounds.
O B. with p-nitrotoluene eluted first since the stationary phase absorbs polar compounds strongly.
O C. with p-nitrotoluene eluted first since it has a lower boiling point.
O D. only slightly since the molecules are nearly the same size.
O E. with p-nitroaniline eluted first since equilibria in the moving phase involve ions.
Transcribed Image Text:Liquid column chromatography on alumina would separate p-nitrotoluene and p-nitroaniline O A. with p-nitroaniline eluted first since the stationary phase has little affinity for polar compounds. O B. with p-nitrotoluene eluted first since the stationary phase absorbs polar compounds strongly. O C. with p-nitrotoluene eluted first since it has a lower boiling point. O D. only slightly since the molecules are nearly the same size. O E. with p-nitroaniline eluted first since equilibria in the moving phase involve ions.
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