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Amines Test - 48

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Amines Test - 48
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  • Question 1
    1 / -0
    By the presence of a halogen atom in the ring, basic properties of aniline is 
    Solution
    By the presence of a halogen atom in the ring, basic properties of aniline is increased because it is more electronegative so donation of electron will be easy, so basicity increases.

    hence A is correct
  • Question 2
    1 / -0
    Which of the following is most basic
    Solution
    In general, methylamine $$CH_3NH_2$$) is a stronger base than ammonia (NH3) and dimethylamine $$((CH_3)_2NH$$ is a stronger base than methylamine. However, in water, triethylamine $$((CH_3CH_2)_3N)$$ which should be even stronger based on stronger inductive effect, is a weaker base than dimethylamine or methylamine.

    Hence B is correct
  • Question 3
    1 / -0
    Which one of the following is not a base
    Solution
    substance that accepts and H+ from water is considered a base Both $$NH_3$$ and H2O are amphoteric 
  • Question 4
    1 / -0
    Which of the following amines would undergoes diazotisation
    Solution
    Only primary aromatic amines can undergo diazotization.
  • Question 5
    1 / -0
    If methyl is alkyl group, then which order of basicity is correct
    Solution
    Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of the basicity of aliphatic amines should be primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like $$CH_3$$  group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than  methyl    group, there will be steric hindrance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from -$$CH_3$$ ​   to$$C_2H_5$$    results in change of the order of basic strength. Thus, there is a subtle interplay of the inductive effect, solvation effect and steric hinderance of the alkyl group which decides the basic strength of alkyl amines in the aqueous state.
  • Question 6
    1 / -0
    Which one less of alkaline
    Solution
    NO2 is electron withdrawing group so the stability is decreasing
    Hence A is correct answer
  • Question 7
    1 / -0
    The decreasing order of the  basic character of the three amines and ammonia is 
    Solution
    Electron donors are bases. Electron withdrawing groups (eg, benzyl) decrease the basicity of amines and  Electron donating groups (eg, alkyl) increase the acidity of amines. 
    so The correct order of basicity of amines in
    $$ C_{2}H_{5}NH_{2}> CH_{3}NH_{2}> NH_{3}> C_{6}H_{5}NH_{2} $$ 
    Hence B is correct answer
  • Question 8
    1 / -0
    Among the following compounds nitrobenzene , benzene, aniline and phenol, the strongest basic behaviuor  in acid medium is exhibited by :
    Solution
    Because the N atom in aniline has a lone pair to donate and also due to +I effect of -$$ NH_{2} $$ group
  • Question 9
    1 / -0
    Among the following the weakest base is 
    Solution
    $$CH_3CONH_2>CH_3CH_2NH_2>C_6H_5CH_2NH_2>C_6H_5CH_2NHCH_3$$

    So the weekest base is B
  • Question 10
    1 / -0
    Arrange the following in increasing order of basicity 
    $$ CH_{3}NH_{2},(CH_{3})_{2}NH,C_{6}H_{5}NH_{2},(CH_{3})_{3}N $$
    Solution
    The correct order is 
    $$ (CH_{3})_{3}N> (CH_{3})_{2}NH> CH_{3}NH_{2}> C_{6}H_{5}NH_{2} $$
    Hence B is correct order
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