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How will you carry out the following conversions?

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How will you carry out the following conversions?

Concept: undefined >> undefined
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Match the reactions given in Column I with the statements given in Column II.
| Column I | Column II | ||
| (i) | Ammonolysis | (a) | Amine with lesser number of carbon atoms |
| (ii) | Gabriel phthalimide synthesis | (b) | Detection test for primary amines. |
| (iii) | Hoffmann Bromamide reaction | (c) | Reaction of phthalimide with \[\ce{KOH}\] and \[\ce{R-X}\] |
| (iv) | Carbylamine reaction | (d) | Reaction of alkylhalides with \[\ce{NH3}\] |
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Assertion: Hoffmann’s bromamide reaction is given by primary amines.
Reason: Primary amines are more basic than secondary amines.
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Assertion: Only a small amount of \[\ce{HCl}\] is required in the reduction of nitro compounds with iron scrap and \[\ce{HCl}\] in the presence of steam.
Reason: \[\ce{FeCl2}\] formed gets hydrolysed to release \[\ce{HCl}\] during the reaction.
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Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
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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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Which of the following are characteristics of thermosetting polymers?
(i) Heavily branched cross linked polymers.
(ii) Linear slightly branched long chain molecules.
(iii) Become infusible on moulding so cannot be reused.
(iv) Soften on heating and harden on cooling, can be reused.
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Which of the following polymers are thermoplastic?
(i) Teflon
(ii) Natural rubber
(iii) Neoprene
(iv) Polystyrene
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Which of the following polymers are used as fibre?
(i) Polytetrafluoroethane
(ii) Polychloroprene
(iii) Nylon
(iv) Terylene
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Why are rubbers called elastomers?
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Amongst the following antihistamines, which are antacids?
(i) Ranitidine
(ii) Brompheniramine
(iii) Terfenadine
(iv) Cimetidine
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Both antacids and antiallergic drugs are antihistamines but they cannot replace each other. Explain why?
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