In the reaction The product is –

1.
2.
3.
4.

(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

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

(1) cis-2-butene                                 

(2) trans-2-butene

(3) 1-butene                                   

(4) Iso-butene