Consider the following alcohols,

I.
II.
III.
IV.

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

1.	I < II < III < IV	2.	I > II > III > IV
3.	III  < II < I < IV	4.	II < III < IV < I

The number of  moles of HI consumed by the given compound is:

The strongest acid among the following aromatic compounds is -

The product 'D' in the below mentioned reaction is:
\(CH_3MgBr + \text{cyclopentanone}\ \)
\(\xrightarrow{H_2O}\ A\ \xrightarrow{HBr}\ B\)
\( B\ \xrightarrow{Mg/Ether}\ C \xrightarrow[H_3O^+]{HCHO}\ D\)

1.		2.
3.		4.

An aromatic compound A (C₈H₁₀O) gives the following tests with the given reagents.

The structure of  'A' is:

1.		2.
3.		4.

Compound Y,  C₇H₈O is insoluble in water, dil HCI and aqueous NaHCO₃. It dissolves in dilute NaOH. When Y is treated with bromine water it is converted rapidly into a compound of formula C₇H₅OBr₃.  The structure of Y is:

1.		2.
3.		4.

Compounds I and II can be distinguished by using reagent:

1. NaNO₂/HCl

2. Br₂/H₂O

3. HCl/ZnCl₂ (anhydrous)

4. Cu₂Cl₂ + NH₄OH

The correct order of dehydration of compounds (i), (ii) and (iii) by conc. H₂SO₄ is:

(i)
(ii)
(iii)

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

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

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

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

Ether cannot be produced as a major product by the reaction of- 

1.	CH3CH2Cl + Ag2O(dry)  →
2.	(CH3)3CCl + CH3CH2O-Na+  →
3.
4.

The labeled -O¹⁸ will be:


1. H₂O

2. Methyl benzoate

3. Both 1 and 2

4. Benzoic acid