Table 19.3 Elution sequence for compounds Hydrocarbons Fastest (will elute with nonpolar solvent) Olefins Ethers Halocarbons Aromatics Ketones Order of elution Aldehydes Esters Alcohols Amines Acids, strong bases Slowest (need a polar solvent)

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Consider a sample that is a mixture composed of biphenyl, benzoic acid, and benzyl alcohol. The sample is spotted on a TLC plate and developed in a dichloromethane– cyclohexane solvent mixture. Predict the relative Rf values for the three components in the sample. Hint: See Table .

Table 19.3 Elution sequence for compounds
Hydrocarbons
Fastest (will elute with nonpolar solvent)
Olefins
Ethers
Halocarbons
Aromatics
Ketones
Order of elution
Aldehydes
Esters
Alcohols
Amines
Acids, strong bases
Slowest (need a polar solvent)
Transcribed Image Text:Table 19.3 Elution sequence for compounds Hydrocarbons Fastest (will elute with nonpolar solvent) Olefins Ethers Halocarbons Aromatics Ketones Order of elution Aldehydes Esters Alcohols Amines Acids, strong bases Slowest (need a polar solvent)
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Consider a sample that is a mixture composed of biphenyl, benzoic acid, and benzyl alcohol. The sample is spotted on a TLC plate and developed in a dichloromethane-cyclohexane solvent mixture.

The relative Rf values for the three components in the sample have to be predicted.

The formula for the calculating relative Rf value has to be given below,

Rf = Distance travelled by the compoundDistance travelled by the solvent

 

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