What is the correct order of the methyl-substituted amines' basic strength in an aqueous solution?

1. CH3NH> (CH3)2NH > (CH3)3N

2. (CH3)2NH > CH3NH2 > (CH3)3N

3. (CH3)3N > CH3NH2 > (CH3)2NH

4. (CH3)3N > CH3NH2 > (CH3)2NH

Subtopic:  Amines - Preparation & Properties |
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Which of the following compounds has a higher basic character than aniline?

1. Diphenylamine

2. Triphenylamine

3. p-nitroaniline

4. Benzylamine

Subtopic:  Amines - Preparation & Properties |
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In a set of reactions propanoic acid yielded a compound D

CH3CH2COOHSOCl2BNH3CBr2KOHD 
The structure of D would be :

1. CH3CH2CH2NH2

2. CH3CH2CONH2

3. CH3CH2NHCH3

4. CH3CH2NH2

Subtopic:  Amines - Preparation & Properties |
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Which one of the following on reduction with lithium aluminium hydride yield a secondary amine?

1. Nitroethane

2. Methylisocyanide

3. Acetamide

4. Methyl cyanide

Subtopic:  Identification of Primary, Secondary & Tertiary Amines | Cyanides & Isocyanides |
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 The structure of C in the below mentioned reaction is 

1. 
2.
3.
4.
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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What is the product formed in the below reaction?
  \(+ NaNO_2 + HCl \longrightarrow Product\)

1.  2.
3. 4.
Subtopic:  Amines - Preparation & Properties |
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Which of the following is incorrect regarding the primary amine?

1. Alkyl amines are stronger bases than aryl amines
2. Alkyl amines react with nitrous acid to produce alcohols
3. Aryl amines react with nitrous acid to produce phenols
4. Alkyl amines are stronger bases than ammonia
Subtopic:  Amines - Preparation & Properties |
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The reagent that is used to convert acetamide into methyl amine is:

1. NaOH-Br2

2. Soda lime

3. Hot conc. H2SO4

4. PCl5

Subtopic:  Amines - Preparation & Properties | Mechanism |
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Aniline gives a set of the following reactions that yielded a colored product 'Y'.
    

The structure of 'Y' is -

1.
2.
3.
4.
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Nitrobenzene on reaction with conc. HNO3 /H2SO4 at 80 – 100 ºC forms:

1. 1,3– Dinitrobenzene

2. 1,4–Dinitrobenzene

3. 1,2,4–Trinitrobenzene

4. 1,2–Dinitrobenzene

Subtopic:  Urea & Nitro Compound |
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