The major product in the acid catalysed dehydration of
would be
1. 
2. 
3. 
4. 
Which of the following reactions will give 2° chiral alcohol as one or more of major organic products?
| (1) | |
| (2) | |
| (3) | |
| (4) | None |
The major product of the following reaction sequence will be

| 1. | |
| 2. | |
| 3. | |
| 4. |
In the following reactions X, Y and Z are respectively :
| X | Y | Z | |
| (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:
(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
W. Product W is:
1. 
2. 
3. 
4. 
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)
Product (x) will be:
(a)
(b)
(c)
(d)