The aromatic structure(s) out of given structures is/are-

1.	A, C, D, F & G only	2.	A & D only
3.	A, C, E, F only	4.	All are aromatic

The Huckel's rule-based aromaticity is shown by:

(A)		(B)
(C)		(D)
(E)		(F)

The type of structural isomerism shown by given compounds is-

${\mathrm{CH}}_3-\mathrm{S}-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_3$ and 

The resonance hybrid structure will not exist for- 
a. CH₃OH
b. R - CONH₂
c. CH₃CH = CHCH₂NH₂

Compare the stability of the two resonating structures given below and mark the correct option:

1. (I)  is more stable than (II)

2. (II) is more stable than (I)

3. (I) and (II) both have the same stability 

4. None of the above

0.1688 g organic compound when analyzed by the Dumas method yields 31.7 mL of moist nitrogen measured at 14º C and 758 mm mercury pressure. The % of the nitrogen in the organic compound (Aqueous tension at 14 º C =12 mm) is:

1. 30.9%

2. 10%

3. 40%

4. 21.9 %

0.6 g of an organic compound was Kjeldahlised and NH₃ evolved was absorbed into 50 mL of semi-normal solution of H₂SO₄. The residual acid solution was diluted with distilled water and the volume made up to 150 mL. 20 mL of this diluted solution required 35 mL of N/20 NaOH solution for complete neutralization.

1. 24.2% 

2. 32.4%

3.27.6 %

4. 20.8%

In the Lassaigne’s test for nitrogen in an organic compound, the Prussian blue colour is obtained due to the formation of:

$1.<mspace\; width="1em"></mspace>{\mathrm{Na}}_4\left[\mathrm{Fe}{\left(\mathrm{CN}\right)}_6\right]<mspace\; width="1em"></mspace>$
$2.<mspace\; width="1em"></mspace>{\mathrm{Fe}}_4[\mathrm{Fe}{\left(\mathrm{CN}\right)}_6{]}_3$
$3.<mspace\; width="1em"></mspace>{\mathrm{Fe}}_2\left[\mathrm{Fe}{\left(\mathrm{CN}\right)}_6\right]<mspace\; width="1em"></mspace>$
$4.<mspace\; width="1em"></mspace>{\mathrm{Fe}}_3[\mathrm{Fe}{\left(\mathrm{CN}\right)}_6{]}_4$

The latest technique for isolation, purification and separation of organic compounds is -