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Amines Test - 12

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Amines Test - 12
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  • Question 1
    1 / -0
    The strongest base in aqueous solution among the following amines is:
    Solution

  • Question 2
    1 / -0
    Diphenyl hydrazine is same as :
    Solution
    Diphenyl hydrazine is same as hydrazobenzene.
    Two phenyl groups are attached to two nitrogen atoms of hydrazine.

  • Question 3
    1 / -0
    Which of the following is a secondary amine?
    Solution
    $$C_{6}H_{5}NHCH_{3}$$  contains 2 alkyl group attached to the nitrogen atom
    So, it is a secondary amine

  • Question 4
    1 / -0
    Out of the following compounds, which is the most basic in aqueous solution?
    Solution
    $$(CH_{3})_{2}NH$$ is the most basic compound out of the compounds given.

    The explanation is as follows :
    It is more basic than $$CH_{3}NH_{2}$$ because of one more methyl group that increases basicity by $$+I$$ effect.

    But a number of factors count into basicity.
    One of the important ones being the solvation effect.

    In $$N(CH_{3})_{3}$$, due to excess steric hinderance, the solvation of the resulting ion is reduced. So, the conjugate acid is not much stabilized. So, it is less basic.

    Option B is correct.
  • Question 5
    1 / -0
    $$o-Br-{ C }_{ 6 }{ H }_{ 4}-{ NH }_{ 2 }$$ is :
    Solution
    Since a benzenoid ring is attached directly to the nitrogen atom, it is an aromatic amine.
    Also, only 1 hydrogen of ammonia is replaced by alkyl group and there are 2 hydrogens intact. So, it is a $$1^0$$ amine.

    Hence, option $$B$$ is correct.

  • Question 6
    1 / -0
    Which of the following is a secondary amine?
    Solution
    Dimethylamine is $$(CH_{3})_{2}NH$$
    So clearly, 2 alkyl groups are attached to the nitrogen atom.
    So, it is a secondary amine
  • Question 7
    1 / -0
    The correct order of basic strength is:
    Solution
    To determine the order of basicity of amines, we have to check for the availability of lone pair, means how easily the lone pair on the nitrogen atom is available for the attack of an electrophile.
    A) $$NH_3$$:- it has lone pair which is available on it.
    B) $$CH_3NH_2$$:- there is positive inductive effect of methyl group, so electron density on nitrogen is more than that of $$NH_3$$.
    C) $$C_6H_5NH_2$$:- the lone pair of nitrogen is taking part in resonance with benzene ring, so it is least available to the attack of an electrophile compared to others.
    So, the order is $${ CH }_{ 3 }{ NH }_{ 2 }>{ NH }_{ 3 }>{ C }_{ 6 }{ H }_{ 5 }{ NH }_{ 2 }$$.
  • Question 8
    1 / -0
    The total number of $$\sigma$$ and $$\pi$$ bonds present in azobenzene are:
    Solution
    A single bond contains 1 $$\sigma$$-bond and a double bond contains one $$\sigma$$ and one $$\pi$$-bond. 

    Azobenzene contains 25 $$\sigma$$ bonds and 7 $$\pi$$ bonds.

    Hence, the correct option is 'B'

  • Question 9
    1 / -0
    Gabriel phthalimide reaction is used for the preparation of: 
    Solution
    Gabriel phthalimide reaction is used for the preparation of primary aliphatic amines.
    In presence of $$NaOH$$ or $$KOH$$, phthalimide reacts with primary aliphatic alkyl halide to form primary aliphatic amine.
    Here, $$-X$$ group is replaced with $$-NH_2$$ group. The side product is phthalic acid.
  • Question 10
    1 / -0
    Which of the following is a $${ 1 }^o$$ amine? 
    Solution
    In a one degree amine, only one hydrogen atom of $$NH_3$$ is replaced by alkyl group.

    So, A is correct because one of the hydrogens has been replaced by $$(CH_{3})_{3}C-$$ group.

    General formula for primary amine is $$RNH_2$$

    Note that the kind of alkyl group does not matter in deciding the type of amine, what matters is the number of hydrogen replaced.

    Option A is correct.
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