In Duma's method for estimation of nitrogen, 0.25 g of an organic compound gave 40 mL of nitrogen collected at 300 K temperature and 725 mm pressure. If the aqueous tension at 300 K is 25 mm, the percentage of nitrogen in the compound is:

1.	17.36	2.	18.20
3.	16.76	4.	15.76

Hyperconjugation occurs among the following compounds:

The enolic form of ethyl acetoacetate is given below-

 

The number of σ and π bonds in the enolic form are respectively:

1. 18 sigma bonds and 2 pi-bonds
2. 16 sigma bonds and 1 pi-bond
3. 9 sigma bonds and 2 pi-bonds
4. 9 sigma bonds and 1 pi-bond

In Kjeldahl’s method for estimation of nitrogen present in the soil sample, ammonia evolved from 0.75g of sample neutralized 10ml of 1M H₂SO₄. The percentage of nitrogen in the soil is:

Which structure corresponds to the IUPAC name 3-Ethyl-2-hydroxy-4-methylhex-3-en-5-ynoic acid?

1.		2.
3.		4.

The correct order of increasing bond length of  C-H, C-O, C-C and C=C is:

1.  $\mathrm{C}-\mathrm{C}<\mathrm{C}=\mathrm{C}<\mathrm{C}-\mathrm{O}<\mathrm{C}-\mathrm{H}$

2.  $\mathrm{C}-\mathrm{O}<\mathrm{C}-\mathrm{H}<\mathrm{C}-\mathrm{C}<\mathrm{C}=\mathrm{C}$

3.  $\mathrm{C}-\mathrm{H}<\mathrm{C}-\mathrm{O}<\mathrm{C}-\mathrm{C}<\mathrm{C}=\mathrm{C}$

4.  $\mathrm{C}-\mathrm{H}<\mathrm{C}=\mathrm{C}<\mathrm{C}-\mathrm{O}<\mathrm{C}-\mathrm{C}$

In Duma’s method of estimation of nitrogen 0.35 of an organic compound gave 55 mL of nitrogen collected at 300 K temperature and 715 mm pressure. The percentage composition of nitrogen in the compound would be:
(Aqueous tension at 300K= 15 mm)

The Lassaigne’s extract is boiled with conc. ${\mathrm{HNO}}_3$ while testing for halogens, because it:

1. Helps in the precipitation of $\mathrm{AgCl}$
2. Increases the solubility product of $\mathrm{AgCl}$
3. Increases the concentration of ${\mathrm{NO}}_3^{-}$ ions
4. Decomposes ${\mathrm{Na}}_2\mathrm{S}$ and $\mathrm{NaCN}$, if formed

The IUPAC name of the compound having the formula CH≡C–CH=CH₂ is:

1. 3-butene-1-yne

2. 1-butyn-3-ene

3. but-1-yne-3-ene

4. 1-butene-3-yne