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Alkyl Halides and Amines Mcqs Key
Alkyl Halides and Amines Mcqs Key
CHEMISTRY CLASS 12
A. R– I > R– Br > R– C l B.
> R–
R–FF > R– C l > R– Br C. R–
> R–IC l > R– Br > R– I D. R–
> R–FBr > R– C l > R– F > R–
A. C H3 – C O– C H3 B. C H3 – C H2 – C H O C. C H3 – C H2 – C OOH D. C H3 – C H2 – C H2 – OH
Q. 4 When there is crowding within the substrate molecule, then elimination reaction is favoured over substitution (1)
reaction, because the removal of
Q. 5 All of the following are TRUE about SN 2 reactions EXCEPT they (1)
(1)
A. A B. B C. C D. D
Q. 7 The IUPAC (International Union of Pure and Applied Chemistry) name of the given amine is
(1)
A. C6 H5 − N
+
2
B. C H3 − C H2 − N
+
2
C. C6 H5 − C H2 − N
+
2
D. C H3 − C H2 − C H2 − N
+
2
A. Aryl amines and alkyl amines are equal in basic strength. B. Alkyl amines and ammonia are equal in basic strength.
C. Aryl amines are stronger bases than ammonia. D. Alkyl amines are stronger bases than ammonia.
Q. 12 A nucleophilic substitution reaction is summarized in the form of its rate equation as follows.
(1)
Rate =
−
k[R − X][OH ]
A. E1 mechanism shows second order kinetics. B. The nucleophile attacks and the leaving group leaves at the
same time.
C. The first step is the slow ionisation of the substrate to give a D. The rate of reaction can be expressed as Rate = k[Alkyl
carbocation. halide][Nucleophile].
Q. 14 LiAlH4 , Ether
(1)
C H 3 C ≡ N + 4[H ] −−−−−−−−→