An organic compound A reacts with sodium metal and forms B. On heating with conc. H₂SO₄, A gives diethyl ether. So A and B are:
1. C₃H₇OH and CH₃ONa
2. CH₃OH and CH₃ONa
3. C₄H₉OH and C₄H₉ONa
4. C₂H₅OH and C₂H₅ONa

Which of the following products is not formed upon dehydration of the given compound?

1.		2.
3.		4.

Consider the following alcohols,

I.
II.
III.
IV.

Ease of dehydration of the above alcohols will be in the order of:

Which of the following reagents is most suitable for converting cyclohexanol into cyclohexene?

What is the correct order of dehydration rate for the compounds (i), (ii), and (iii) when treated with concentrated \(\text{H}_2\text{SO}_4\)?

(i)
(ii)
(iii)

1. (i) > (iii) > (ii)                                             

2. (i) > (ii) > (iii)

3. (ii) > (i) > (iii)                                             

4. (ii) > (iii) > (i)

Which of the following reagents causes rapid loss of optical activity in optically active 2-octanol?

The most reactive compound among the following toward electrophilic aromatic substitution reaction is:

1.		2.
3.		4.

The proposed mechanism for hydration of ethene to yield ethanol is as follows:

The wrong step in the above mechanism is: