On hydrolysis of a ''compound'', two compounds are obtained. One of which one treatment with sodium nitrite and hydrochloric acid gives a product which does not respond to iodoform test. The second one reduces Tollens reagent and Fehling's solution. The ''compound'' is
A
CH3CH2CH2NC
B
CH3CH2CH2CN
C
CH3CH2CH2ON $$=$$ O
D
CH3CH2CH2CON(CH3)2
2
NEET 2013
MCQ (Single Correct Answer)
+4
-1
Nitrobenzene on reaction with conc. HNO3/H2SO4 at 80$$-$$100oC forms which one of the following products?
A
1, 4-Dinitrobenzene
B
1, 2, 4 - Trinitrobenzene
C
1, 2-Dinitrobenzene
D
1, 3-Dinitrobenzene
3
NEET 2013
MCQ (Single Correct Answer)
+4
-1
In the reaction
A is
A
H3PO2 and H2O
B
H+/H2O
C
HgSO4/H2SO4
D
Cu2Cl2
4
AIPMT 2012 Mains
MCQ (Single Correct Answer)
+4
-1
An organic compound (C3H9N) (A), when treated with nitrous acid, gave an alcohol and N2 gas was evolved. (A) on warming with CHCl3 and caustic potash gave (C) which on reduction gave isopropylmethylamine. Predict the structure of (A)
