Lassaigne's extract is boiled with conc. HNO3 while testing for halogens. By doing so, it:

1. Helps in the precipitation of AgCl

2. Increases the solubility product of AgCl

3. Increases the concentration of NO3- ions

4. Decomposes Na2S and NaCN, if formed.

Subtopic:  Qualitative Analysis of Organic Compounds |
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In Duma's method of estimation of nitrogen 0.35 g of an organic compound gave 55 ml of nitrogen collected at 300 K temperature and 715 mm pressure. The percentage composition of nitrogen in the compound would be

(Aqueous tension at 300 K-15 mm)

1. 16.45

2. 17.45

3. 14.45

4. 15.45

Subtopic:  Quantitative Analysis of Organic Compounds |
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In pyrrole

the electron density is maximum on

1. 2 and 3         2. 3 and 4

3. 2 and 4         4. 2 and 5

Subtopic:  Electron Displacement Effects |
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Hydrogen cyanide and hydrogen isocyanide are:

1. Tautomers

2. Positional isomers

3. Metamers

4. Chain isomers

Subtopic:  Structural Isomers |

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The number of different amines corresponding to the formula C3H9N is:

1. 2

2. 3

3. 4

4. 5

Subtopic:  Structural Isomers |
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The number of optical isomers of pent-3-en-2-ol is:

1. 2             

2. 4

3. 8             

4. 16

Subtopic:  Stereo Isomers |
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Buta-1,3-diene and But-2-yne are:

1. Position isomers

2. Functional isomers

3. Chain isomers

4. Tautomers

Subtopic:  Structural Isomers |
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Sulphur trioxide is:

1. An electrophile             

2. A nucleophile

3. A homolytic agent         

4. A base

Subtopic:  Nucleophile & Electrophile |
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(CH3)4N+ is neither an electrophile nor a nucleophile because of it:

1.  Does not have an electron pair for donation and it also cannot attract an electron pair.
2. Neither has an electron pair available for donation nor can accommodate electrons since all shells of N are fully occupied.
3. Can act as Lewis acid and base.
4. None of the above.

Subtopic:  Nucleophile & Electrophile |
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The stability of 2,3-dimethylbut-2-ene is more than 2-butene. This can be explained in terms of:

1. Resonance

2. Hyperconjugation

3. Electromeric effect

4. Inductive effect

Subtopic:  Electron Displacement Effects |
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