A solution of m− chloroaniline, m− chlorophenol and m− chlorobenzoic acid in ethyl acetate was extracted initially with a saturated solution of NaHCO3 to give fraction A . The left over organic phase was extracted with dilute NaOH solution to give fraction B . The final organic layer was labelled as fraction C . Fractions A,B and C, contain respectively:
Held on 7 Jan 2020 · Verified 6 Jul 2026.
m− chlorobenzoic acid, m− chloroaniline and m− chlorophenol
m− chlorobenzoic acid, m− chlorophenol and m− chloroaniline
m− chlorophenol, m− chlorobenzoic acid and m− chloroanilinc
m− chloroaniline, m− chlorobenzoic acid and m− chlorophenol
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Consider the following reaction sequence  Compound $(\mathrm{y})$ develops characteristic colour with neutral $\mathrm{FeCl}_{3}$ solution. Identify the INCORRECT statement from the following for the above sequence.
Given below are two statements: Statement I: Benzene is nitrated to give nitrobenzene, which on further treatment with $\mathrm{CH}_{3} \mathrm{COCl} / \mathrm{AlCl}_{3}$ will give  Statement II: $-\mathrm{NO}_{2}$ group is a $m$-directing, and deactivating group. In the light of the above statements, choose the most appropriate answer from the options given below
Given below are two statements: Statement I: $\left(\mathrm{CH}_{3}\right)_{3} \stackrel{\oplus}{\mathrm{C}}$ is more stable than $\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_{3}$ as nine hyperconjugation interactions are possible in $\left(\mathrm{CH}_{3}\right)_{3} \stackrel{\oplus}{\mathrm{C}}$. Statement II: $\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_{3}$ is less stable than $\left(\mathrm{CH}_{3}\right)_{3} \stackrel{\oplus}{\mathrm{C}}$ as only three hyperconjugation interactions are possible in $\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_{3}$. In the light of the above statements, choose the correct answer from the options given below
Which of the following reactions is an example of Wurtz reaction?
A hydroxy compound $(\mathrm{X})$ with molar mass $122 \mathrm{~g} \mathrm{~mol}^{-1}$ is acetylated with acetic anhydride, using a large excess of the reagent ensuring complete acetylation of all hydroxyl groups. The product obtained has a molar mass of $290 \mathrm{~g} \mathrm{~mol}^{-1}$. The number of hydroxyl groups present in compound (X) is:
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