The order of stability of the following tautomeric compound is

1. I>II>III              

2. III>II>I

3. II>I>III              

4. II>III>I

Among the following compounds the one that is most reactive towards electrophilic

nitration is

1. benzoic acid

2. nitrobenzene

3. toluene

4. benzene

The correct order of decreasing acid strength of trichloroacetic acid (1), trifluoroacetic

acid (2), acetic acid (3) and formic acid (4) is

1. B>A>D>C        

2. B>D>C>A

3. A>B>C>D        

4. A>C>B>D

Which nomenclature is not according to IUPAC system?

The correct IUPAC name of the compound

 is

1. 3-ethyl-4-ethenylheptane

2. 3-ethyl-4-propylhex-5-ene

3. 3-(1-ethyl propyl) hex-1-ene

4. 4-ethyl-3-propylhex-1-ene

The Lassaigne's extract is boiled with a concentration 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.

Given is cyclohexanol (I), acetic acid (II), 2,4,6-trinitrophenol (III), and phenol (IV).

The order of decreasing acidic character will be

1. III > II > IV > I

2. II>III>I>IV

3. II > III > IV > I

4. III > IV > II > I

which one of the following has the most acidic nature?

1.		2.
3.		4.

The correct order of increasing reactivity of C-X bond towards nucleophile in the following

compounds is

1. I < II < IV < III

2. II < III < I < IV

3. IV < III < I < IV

4. III < II < I < IV

Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

1. CH₃COOCH₃

2. CH₃CONH₂

3. CH₃COOCOCH₃

4. CH₃COCl