1
NEET 2017
MCQ (Single Correct Answer)
+4
-1
Change Language
Which of the following reactions is appropriate for converting acetamide to methanamine?
A
Hoffmann hypobromamide reaction
B
Stephen's reaction
C
Gabriel phthalimide synthesis
D
Carbylamine reaction
2
NEET 2016 Phase 2
MCQ (Single Correct Answer)
+4
-1
Change Language
Which one of the following nitro-compounds does not react with nitrous acid?
A
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 45 English Option 1
B
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 45 English Option 2
C
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 45 English Option 3
D
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 45 English Option 4
3
NEET 2016 Phase 2
MCQ (Single Correct Answer)
+4
-1
Change Language
A given nitrogen-containing aromatic compound 'A' reacts with Sn/HCl, followed by HNO2 to give instable compound 'B'. 'B', on treatment with phenol, forms a beautiful coloured compound 'C' with the molecular formula C12H10N2O. The structure of compound 'A' is
A
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 44 English Option 1
B
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 44 English Option 2
C
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 44 English Option 3
D
NEET 2016 Phase 2 Chemistry - Organic Compounds Containing Nitrogen Question 44 English Option 4
4
NEET 2016 Phase 1
MCQ (Single Correct Answer)
+4
-1
Change Language
The correct statement regarding the basicity of arylamines is
A
arylamines are generally more basic than alkalmines because of aryl group
B
arylamines are generally more basic than alkylmines, because the nitrogen atom in arylamines is sp-hybridised
C
arylamines are generally less basic than alkylamines because the nitrogen lone-pair electrons are delocalised by interaction with the aromatic ring $$\pi $$-electron system
D
arylamines are generally more basic than alkylamines because the nitrogen lone-pair electrons are not delocalised by interaction with the aromatic ring $$\pi $$-electron system.
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