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NEET CHEMISTRYAminesMedium

Question

The correct increasing order of basic strength of the given molecules is: (I) (II) (III)

A

III < I < II

B

III < II < I

C

II < I < III

D

II < III < I

Step-by-Step Solution

The basic strength of amines depends on the availability of the lone pair of electrons on the nitrogen atom for donation. Electron-donating groups (EDG) increase the electron density on nitrogen, making the amine more basic. Conversely, electron-withdrawing groups (EWG) decrease the electron density, making the amine less basic. In the standard NEET 2017 question this refers to, the structures are typically (I) Aniline, (II) p-Nitroaniline (which has a strongly electron-withdrawing NO2-NO_2 group), and (III) p-Toluidine (which has an electron-donating CH3-CH_3 group). Therefore, the p-nitroaniline is the least basic, and p-toluidine is the most basic. The correct increasing order is II < I < III.

Exam Context & Concepts Covered

This question aligns with the NEET CHEMISTRY syllabus, specifically targeting concepts from Amines. Mastering this topic is crucial for scoring well in the upcoming medical entrance examinations. Solving conceptually related problems will help you understand the nuances of these concepts and improve your problem-solving speed.

CHEMISTRYAminescorrectincreasingstrengthmolecules

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The products formed when Aniline reacts with $Br_2$ water, and $NaNO_2/HCl$ will be, respectively:

A.p-Bromoaniline; p-Chloroaniline
B.2,4,6-Tribromoaniline; p-Chloroaniline
C.2,4,6-Tribromoaniline; Benzenediazonium chloride
D.p-Bromoaniline; Benzenediazonium chloride
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Aniline gives a set of the following reactions that yielded a coloured product 'Y'. The structure of 'Y' is: (Note: Reaction scheme is missing from the provided text)

A.Option 1
B.Option 2
C.Option 3
D.Option 4
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The structure of C in the below-mentioned reaction is: (Note: Reaction scheme is missing from the provided text)

A.Option 1
B.Option 2
C.Option 3
D.Option 4
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What results from the electrolytic reduction of nitrobenzene in a highly acidic medium?

A.p-Aminophenol
B.Azoxybenzene
C.Azobenzene
D.Aniline
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The reagent required to convert acetamide into methyl amine is:

A.$NaOH/Br_2$
B.Sodalime
C.Hot conc. $H_2SO_4$
D.$PCl_5$
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D is N-methyl aniline in the given below sequence of reaction: $A \xrightarrow{\text{reduction}} B \xrightarrow{CHCl_3/KOH} C \xrightarrow{\text{reduction}} D$. Structure of A can be:

A.Option 1 (Missing)
B.Nitrobenzene
C.CH3NH2
D.Option 4 (Missing)
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Which of the following statements about primary amines is false?

A.Alkyl amines are stronger bases than aryl amines
B.Alkyl amines react with nitrous acid to produce alcohols
C.Aryl amines react with nitrous acid to produce phenols
D.Alkyl amines are stronger bases than ammonia
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What is the correct order of the methyl-substituted amines' basic strength in an aqueous solution?

A.$CH_3NH_2 > (CH_3)_2NH > (CH_3)_3N$
B.$(CH_3)_2NH > CH_3NH_2 > (CH_3)_3N$
C.$(CH_3)_3N > CH_3NH_2 > (CH_3)_2NH$
D.$(CH_3)_2NH > (CH_3)_3N > CH_3NH_2$
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