Which of the following sequence of reagents can perform the following conversion:\(\small{\mathrm{CH}_{3}\mathrm{CH}_{2}\mathrm{CH}_{2}\mathrm{OH} \stackrel{?}{\longrightarrow} \mathrm{CH}_{3}\mathrm{CH}_{2}\mathrm{CH}_{2}\mathrm{CH}_{2}\mathrm{NH}_{2}} \)
1. \(SOCl_2 ,KCN , H_2 /Pd \)   
2. \(SOCl_2 ,AgCN , H_2 /Pd \)
3. \(PCl_5 ,AgCN , H_2 /Pd \)
4. Red P/HI
Subtopic:  Amines - Preparation & Properties |
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Find the correct option regarding the reaction


(a) HNO3 acts as an acid.
(b) H2SO4 acts as an acid.
(c) Major product is formed at the ortho, meta.
(d) Major product is formed at para, meta position.

1. a, b, c, d
2. b, d
3. a, c, d
4. c, d
Subtopic:  Amines - Preparation & Properties |
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Among the following, the reaction/s that will not give p-aminoazobenzene is/are:

A. 
B.
C.


1. A only

2. B only

3. C only

4. A and B

   

Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Carbylamine test is used to detect the presence of a primary amino group in an organic compound. Which of the following compound is formed when this test is performed with aniline?

1. 2.
3. 4.
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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The correct statement about the given chemical reaction is :

1. -NH2 group is ortho and para directive, so product (B) is not possible.

2. Reaction is possible and compound (B) will be the major product.

3. The reaction will form sulphonated product instead of nitration.

4. Reaction is possible and compound (A) will be major product. 

Subtopic:  Mechanism |
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In the following reaction, the reason why meta-nitro product also formed is:

1. Low temperature

2. –NH2 group is highly meta-directive

3. Formation of anilinium ion

4. –NO2 substitution always takes place at meta-position

Subtopic:  Mechanism |
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An amine, on reaction with benzene sulphonyl chloride, produces a compound that is insoluble in an alkaline solution. This amine can be prepared by ammonolysis of ethyl chloride. What is the correct structure of this amine?

1.
2. CH3CH2NH2
3. CH3CH2CH2NHCH3
4. CH3CH2CH2NHCH2CH3
Subtopic:  Identification of Primary, Secondary & Tertiary Amines |
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A. Phenyl methanamine
B. N, N-Dimethylaniline
C. N-Methyl aniline
D. Benzenamine

Choose the correct order of basic nature of the above amines.

1. A > C > B > D

2. D > C > B > A

3. D > B > C > A

4. A > B > C > D

Subtopic:  Amines - Preparation & Properties |
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Match Column-I with Column-II 

Column-I Column-II
(a) (i) Wurtz reaction
(b) (ii) Sandmeyer reaction
(c)
\(\small2 \mathrm{CH}_3 \mathrm{CH}_2 \mathrm{Cl}+2 \mathrm{Na} \xrightarrow{\text { Ether }}\\~~~~~~~~ \mathrm{C}_2 \mathrm{H}_5-\mathrm{C}_2 \mathrm{H}_5+2 \mathrm{NaCl}\)
(iii) Fitting reaction
(d)
\(\small2 \mathrm{C}_6 \mathrm{H}_5 \mathrm{Cl}+2 \mathrm{Na} \xrightarrow{\text { Ether }}\\~~~~~~~~~ \mathrm{C}_6 \mathrm{H}_5-\mathrm{C}_6 \mathrm{H}_5+2 \mathrm{NaCl}\)
(iv) Gatterman reaction

Choose the correct answer from the options given below :

Options: (a) (b) (c) (d)
1. (iii) (i) (iv) (ii)
2. (ii) (i) (iv) (iii)
3. (ii) (iv) (i) (iii)
4. (iii) (iv) (i) (ii)
Subtopic:  Diazonium Salts: Preparation, Properties & Uses |
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Which compound among the following undergoes a reaction with CHClin the presence of alcoholic KOH?
1. Thymine and proline
2. Adenine and Iysine
3. Adenine and thymine
4. Adenine and proline
Subtopic:  Cyanides & Isocyanides |
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