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Which of the following reactions will yield phenol?
| (i) | ![]() |
| (ii) | ![]() |
| (iii) | ![]() |
| (iv) | ![]() |
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Name the starting material used in the industrial preparation of phenol.
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Which of the following is the correct representation for intermediate of nucleophilic addition reaction to the given carbonyl compound (A):

(i) 
(ii) 
(iii) 
(iv) 
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Write a test to differentiate between pentan-2-one and pentan-3-one.
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Benzaldehyde can be obtained from benzal chloride. Write reactions for obtaining benzalchloride and then benzaldehyde from it.
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Alkenes
and carbonyl compounds
, both contain a π bond but alkenes show electrophilic addition reactions whereas carbonyl compounds show nucleophilic addition reactions. Explain.
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Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?
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Identify the compounds A, B and C in the following reaction.
\[\ce{CH3 - Br ->[Mg/ether] (A) ->[(i) CO][(ii) Water] (B) ->[CH3OH/H+][Δ] (C)}\]
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Which of the following should be most volatile?
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A compound Z with molecular formula \[\ce{C3H9N}\] reacts with \[\ce{C6H5SO2Cl}\] to give a solid, insoluble in alkali. Identify Z.
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Assertion: N-Ethylbenzene sulphonamide is soluble in alkali.
Reason: Hydrogen attached to nitrogen in sulphonamide is strongly acidic.
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Which of the following pairs represents anomers?
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Three structures are given below in which two glucose units are linked. Which of these linkages between glucose units are between C1 and C4 and which linkages are between C1 and C6?
| (I) | ![]() |
| (II) | ![]() |
| (III) | ![]() |
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Why does compound (A) given below not form an oxime?

(A)
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How will you distinguish 1° and 2° hydroxyl groups present in glucose? Explain with reactions.
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Assertion: D (+) – Glucose is dextrorotatory in nature.
Reason: ‘D’ represents its dextrorotatory nature.
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Write the reactions of D-glucose which can’t be explained by its open-chain structure. How can cyclic structure of glucose explain these reactions?
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On the basis of which evidences D-glucose was assigned the following structure?
\[\begin{array}{cc}
\ce{CHO}\\
|\phantom{....}\\
\phantom{..}\ce{(CHOH)4}\\
|\phantom{....}\\
\phantom{..}\ce{CH2OH}
\end{array}\]
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Can nucleic acids, proteins and starch be considered as step growth polymers?
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Which statement about aspirin is not true.
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