$$
The ease of dehydrohalogen of alkyl halide with alcoholic KOH is
1. 3º > 2º > 1º
2. 3º < 2º < 1º
3. 3º > 2º < 1º
4. 3º < 2º > 1º

$\underset{∆}{\overset{\mathrm{Zn}}{\to }}$ A$\underset{{\mathrm{NH}}_3/\mathrm{EtOH}}{\overset{\mathrm{Na}}{\to }}$ B

Product 2 is

The increasing order of hydrolysis of the following compounds:

1. (i)<(iii)<(ii)

2. (ii)<(iii)<(i)

3. (ii)<(i)<(iii)

4. (i)<(ii)<(iii)

Read the following road map carefully

(1) Both the ethers obtained by the two routes have opposite but equal optical rotation.

(2) One of the ether is obtained as a racemic mixture.

(3) Step II & III both are SN2 reaction and both have inversion.

(4) Step II has inversion but step III has retention.

$\text{PhOH\hspace{0.17em}}\underset{\text{NaOH}}{\overset{{\text{Me}}_{\text{2}}{\text{SO}}_{\text{4}}}{\to }}\text{\hspace{0.17em}P,}$ P is

(1) Ph–O–SO₂OMe

(2) PhOMe

(3) PhOSO₂OPh

(4) PhMe

Which of the following statement is correct

(1)
(2)
(3)
(4)

Product is

(1) CH₃ – CH₂ – S – CH₂ – CH₂ – OH

(2) CH₃ – CH₂ – O – CH₂ – CH₂ – OH

(3)

(4)

Product, Product is

(1)
(2)
(3)
(4)

In the reaction The product is –

1.
2.
3.
4.

A diol compound with the structure shown below is treated with acid (H⁺) to give product A.


Identify the correct structure of product A.

1.
2.
3.
4.	None of the above .