(CH₃)₃CCI + (CH₃)₃C${\mathrm{O}}^{-}$ K⁺ → Product

1. S_N Product will be more

2. E₂ Product will be more

3. Both will be the same

4. None of the above

Neopentyl iodide is treated with aq. AgNO₃ solution, a yellow precipitate is formed along with another compound which is

1. (CH₃)₃CCH₂ONO₂

2. 

3. (CH₃)₃CCH₂OH

4. 

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

Consider the following reaction:-

Which response contains all the correct statement about this process?
(1)Dehydration
(2)E₂ mechanism
(3)Carbon skeleton migration
(4)Most stable alkene will form
(5)Single-step reaction

(a)1,3        (b)1,2,3         (c)1,2,5          (d)1,3,4

$\underset{\mathrm{heat}}{\overset{{\mathrm{H}}_3{\mathrm{PO}}_4}{\to }} \mathrm{OH} +$

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