The major end product of the following reaction is

1.
2.
3.
4.

Z

The product of following reacting is

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

The product in the given reaction is

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

Conversion of cyclohexene to cyclohexanol can be conveniently achieved by:

1. NaOH + H₂O

2. Br₂-H₂O

3. Hydroboration, oxidation

4. Hydroboration hydrolysis

Bromination of (E)-2-butenedioic acid gives

(1) (2R, 3S)-2, 3-dibromosuccinic acid

(2) (2R, 3R)-2, 3-dibroniosuccinic acid

(3) a mixture of (2R, 3R) and (2S, 3S)-2, 3-dibromosuccinic acid

(4) (2S, 3S)-2, 3-dibromosuccinic acid

$\stackrel{\mathrm{HBr}}{\to }\left(\mathrm{X}\right) \underset{\mathrm{acetone}}{\overset{\mathrm{NaI}}{\to }}\left(\mathrm{Y}\right) \left(\mathrm{Major}\right)$; Product (Y) is:

(1) cis-2-butene                                 

(2) trans-2-butene

(3) 1-butene                                   

(4) Iso-butene

Which position will be attacked most rapidly by the nitronium ion (-NO₂)⁺ when the compound undergoes nitration with HNO₃/H₂SO₄ :-

1. A

2. B

3. C

4. D

Which of the following substitution of benzene is ortho-para in electrophilic substitution and ortho-para in nucleophilic substitution ?

(1) -NO₂

(2) -NO

(3) -SO₃H

(4) -SO₂Me

Which one of the following undergoes nucleophilic aromatic substitution at the fastest rate?
(1) 

(2) 

(3) 

(4) 

Many organic compounds are prepared by using PCl₅ because:

(1) OH group of alcohol is easily replaced by chlorine atom

(2) chlorines are added to the unsaturated compounds

(3) it removes water from organic compounds

(4) phosphorus atoms are entered in the alcohol