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:
(I) 4–Amino–2–methylbut–3–en–2–ol 
(II) 4–Amino–2,2–dimethylbut–3–yn–1–ol

1. NaNO₂/HCl

2. Br₂/H₂O

3. HCl/ZnCl₂ (anhydrous)

4. Cu₂Cl₂ + NH₄OH

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)

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

Product (A) in the below mentioned reaction is:
 

1.

2.

3.

4.

Which of the following compounds is most prone to oxidation?
 

1.	\(\mathrm{CH}_3-\mathrm{CHOH}-\mathrm{CH}_3\)	2.
3.	\(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{O}-\mathrm{CH}_2-\mathrm{CH}_3\)	4.

Product (P) is:

1.		2.
3.		4.