The IUPAC name of the given compound is:
 
  

1. Ethanoic propanoic anhydride

2. Propanoic ethanoic anhydride

3. 1-Ethanoyloxypropanone

4. 3-Ethanoyloxypropan-3-one

The IUPAC name of  the given-below compound is:

1. Butane-2,3-dial

2. Butane-1,3-dione

3. Butane-2,3-dione

4. 1, 2-Dimethylethanedione

The IUPAC name of        ​    is:

(1) propene-1, 3-dial 

(2) Propene-1, 3-dicarbaldehyde

(3) Pent-3-ene-1, 5-dial

(4) Pent-2-ene-1, 5-dial

\(CH_3-CH-CH_2-O-C_2H_5\\ ~~~~~~~~~~~~~~|\\ ~~~~~~~~~~~~~OH\)    

1. 1-Ethoxypropan-2-ol

2. 3-Ethoxypropan-2-ol

3. 1-Ethoxy-2-hydroxypropane

4. None of these

The IUPAC name of  is:

1. 2, 6-Dimethylhepta-2, 5-dienoic acid

2. 3, 7-Dimethylhepta-2, 5-dienoic acid

3. 1-Hydroxy-2, 6-dimethylhepta-2, 5-dienone

4. None of the above

The silver sulphate solution is used to separate:

1. nitrate and bromide

2. nitrate and chlorate

3. bromide and iodide

4. nitrate and nitrite

The most stable carbocation among the following is:

1.		2.
3.		4.

The electromeric effect in organic compounds is a

1. Temporary effect

2. Permanent effect

3. Electromeric effect is only observed in inorganic molecules

4. None of the above

The stability of 2,3-dimethyl but-2-ene is more than 2-butene. This can be explained in terms of:

1. resonance

2. hyperconjugation

3. electromeric effect

4. inductive effect

(CH₃)₄N⁺ is neither an electrophile, nor a nucleophile because it:

1. does not have electron pair for donation as well as cannot attract electron pair

2. neither has electron pair available for donation nor can accommodate electron since all shells of N are fully occupied.

3. can act as Lewis acid and base

4. none of the above