Which is the correct statement regarding the relative Rf values of the starting methyl benzoate vs the product, methyl m-nitrobenzoate on a silica gel TLC plate. The product has a higher Rf value on a silica gel TLC plate because it is less polar than the starting methyl benzoate. The product has a lower Rf value on a silica gel TLC plate because it is less polar than the starting methyl benzoate. The product has a higher Rf value on a silica gel TLC plate because it is more polar than the starting methyl benzoate. The product has a lower Rf value on a silica gel TLC plate because it is more polar than the starting methyl benzoate. 1.5 points QUESTION 2 Methyl benzoate is more reactive than benzene in Electrophilic Aromatic Substition [EAS] reactions. True False 1 points QUESTION 3 Methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substition [EAS] reactions. True False

In chromatography, there is a stationary phase and a mobile phase. The ratio of the distance moved by a component and the distance moved by the solvent gives the retention factor (Rf).

Since silica gel is a polar solvent, it will retain the more polar product methyl m-nitrobenzoate compared to the methyl benzoate starting material.

In comparing the electrophillic aromatic substitution of m-nitrobenzoate and methyl benzoate, we must remember that the presence of electron withdrawing groups (such as -NO2 and -CHO) on the aromatic compound deactivates the compound towards electrophillic aromatic substitution hence, methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substition and Methyl benzoate is less reactive than benzene in Electrophilic Aromatic Substition

ABHISHEKPRAKASH2625GO ABHISHEKPRAKASH2625GO · Answer 2

The final result has a higher Rf value because the TLC plate has more polarity than the other compound.

The answer to the following question is as follows:-

False
True

In chromatography, it is a process that is used to separate the different components on the basis of their votality. The ratio of the distance moved by a component and the distance moved by the solvent gives the retention factor (Rf).

In comparing the electrophilic aromatic substitution of m-nitrobenzoate and methyl benzoate, we must remember that the presence of electron-withdrawing groups on the aromatic compound deactivates.

The compound towards electrophilic aromatic substitution hence, methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substitution and Methyl benzoate is less reactive than benzene in Electrophilic Aromatic Substitution.

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