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NEET CHEMISTRYAminesMedium

Question

The final product C, obtained in this reaction, would be: [Reaction Scheme Missing]

A

Option 1 (Missing)

B

Option 2 (Missing)

C

Option 3 (Missing)

D

Option 4 (Missing)

Step-by-Step Solution

The specific chemical reaction scheme (showing the starting material, intermediate steps A and B, and reagents) is missing from the provided text. In the context of the Class 12 NCERT Chemistry curriculum for Amines and typical AIPMT/NEET questions, these sequences usually involve multi-step conversions such as the Hoffmann bromamide degradation (converting an amide to an amine with one less carbon), reduction of nitriles/isocyanides, or the diazotisation of aniline followed by coupling or substitution. Without the reaction pathway, the exact structure of product 'C' cannot be determined.

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.

CHEMISTRYAminesproductobtainedreactionreactionscheme

More Amines Questions

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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
MediumSolve

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
MediumSolve

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
MediumSolve

What results from the electrolytic reduction of nitrobenzene in a highly acidic medium?

A.p-Aminophenol
B.Azoxybenzene
C.Azobenzene
D.Aniline
MediumSolve

The reagent required to convert acetamide into methyl amine is:

A.$NaOH/Br_2$
B.Sodalime
C.Hot conc. $H_2SO_4$
D.$PCl_5$
EasySolve

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)
MediumSolve

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
MediumSolve

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.$(CH_3)_2NH > (CH_3)_3N > CH_3NH_2$
MediumSolve

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