In the compound given below,

the correct order of acidic nature of the positions (X), (Y) and (Z) is: 

(1) Z>X>Y

(2) X>Y>Z

(3) X>Z>Y

(4) Y>X>Z

Subtopic:  Amines - Preparation & Properties |
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The product obtained on nitration followed by alkaline hydrolysis of acetylated aniline is:

1. o-Nitroacetanilide

2. o- and p-Nitroaniline

3. m-Nitroaniline

4. Acetanilide

Subtopic:  Amines - Preparation & Properties |
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In the chemical reactions,

the compounds 'A' and 'B', respectively, are:

1. Nitrobenzene and chlorobenzene

2. Nitrobenzene and fluorobenzene

3. Phenol and benzene

4. Benzene diazonium chloride and fluorobenzene

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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A reaction that can convert acetamide to methanamine is:

1. Carbylamine reaction

2. Hoffmann bromamide reaction

3. Stephens reaction

4. Gabriels phthalimide synthesis

Subtopic:  Amines - Preparation & Properties | Identification of Primary, Secondary & Tertiary Amines |
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Which one of the following nitro-compounds does not react with nitrous acid?

Subtopic:  Urea & Nitro Compound |
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A given nitrogen-containing aromatic compound a reacts with Sn/HCl, followed by HNO2 to give an unsatable compound B.B, on treament with phenol, forms a beautiful coloured compound C with the molecular formula C12H10N2O. The structure of compound A is

 

Subtopic:  Urea & Nitro Compound |
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The correct statement regarding the basicity of arylamines is

(1) Arylamines are generally more basic than alkylamines because the nitrogen lone-pair electrons are not delocalized by interaction with the aromatic ring p-electron system.

(2) Arylamines are generally more basic than alkylamines because of aryl group.

(3) Arylamines are generally more basic than alkylamines, because the nitrogen atom in arylamines is sp-hybridized

(4) Arylamines are generally less basic than alkylamines because the nitrogen lone-pair electrons are delocalized by interaction with the aromatic ring p-electron system.

Subtopic:  Amines - Preparation & Properties |
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Which of the following will be most stable diazonium salt RN2+X- ?

1. CH3N2+X-

2. C6H5N2+X-

3. CH3CH2N2+X-

4. C6H5CH2N2+X-

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Which of the following is more basic than aniline?

1. Diphenylamine

2. Triphenylamine

3. p-Nitroaniline

4. Benzylamine

Subtopic:  Amines - Preparation & Properties |
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ln the reaction, 

The product is: 

1. 

2. 

3. 

4. 

 

Subtopic:  Amines - Preparation & Properties |
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