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Amines Test - 8

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Amines Test - 8
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  • Question 1
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Acylation of amines gives a monosubstituted product whereas alkylation of amines gives poly substituted product.

    Reason (R): Acyl group sterically hinders the approach of further acyl groups.

    Solution

    In alkylation, an amine can react with alkyl halide to form next higher class of amine caused by the presence of electron pair on nitrogen which makes amine to behave as nucleophile and alkyl halide thus undergo nucleophilic substitution reaction. When primary and secondary amines react with acid chlorides, anhydrides and esters to give monosubstituted amides as products. Acylation is carried out in the presence of a base stronger than the amine like pyridine which causes the shift of the equilibrium to the right side.

  • Question 2
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Aromatic 1° amines can be prepared by Gabriel Phthalimide synthesis.

    Reason (R): Aryl halides do not undergo nucleophilic substitution with anion formed by phthalimide.

    Solution

    Aromatic 1° amines cannot be prepared by Gabriel Phthalimide synthesis because aryl halides do not undergo nucleophilic substitution with anion formed by phthalimide.

  • Question 3
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Acetanilide is less basic than aniline.

    Reason (R): Acetylation of aniline results in decrease of electron density on nitrogen.

    Solution

    Acetanilide is less basic than aniline as in amides the carbonyl group (C=O) is a stronger dipole than N-C dipole. Therefore, the ability of N-C group to act as H-bond acceptor (as a base) is restricted in the presence of a C=O dipole.

  • Question 4
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): N, N-Diethylbenzene sulphonamide is insoluble in alkali.

    Reason (R): Sulphonyl group attached to nitrogen atom is strong electron withdrawing group.

    Solution

    N, N-Diethylbenzene sulphonamide is insoluble in alkali because it has no acidic hydrogen. Sulphonyl group attached to nitrogen atom is electron withdrawing group.

  • Question 5
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Nitrating mixture used for carrying out nitration of benzene consists of conc. HNO3+ conc. H2SO4

    Reason : In presence of H2SO4, HNO3 acts as a base and produces NO2+ ions.

  • Question 6
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Acylation of amines gives a monosubstituted product whereas alkylation of amines gives poly-substituted product.

    Reason : Acyl group sterically hinders the approach of further acyl groups

    Solution

    Acylation of amine gives a mososubration product whereas alkyation of amine gives polysubstituted product because acylation in amine takes place at N-atom and alkylation takes place at o and p position.

  • Question 7
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Aniline does not undergo Friedel-Crafts reaction.

    Reason : –NH2 group of aniline reacts with AlCl3 (Lewis acid) to give acid-base reaction.

    Solution

    Aniline does not undergo Friedel craft's reactions because the reagent AlCl3 ​ (the Lewis acid which is used as a catalyst in friedel crafts reaction), being electron deficient acts as a Lewis base. and attacks on the lone pair of nitrogen present in aniline to form an insoluble complex which precipitates out and the reaction does not proceed.

  • Question 8
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Nitration of aniline can be conveniently done by protecting the amino group by acetylation.

    Reason : Acetylation increases the electron-density in the benzene ring.

    Solution

    Acetylation decreases the electron-density in the benzene ring thereby preventing oxidation.

  • Question 9
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Acetanilide is less basic than aniline.

    Reason : Acetylation of aniline results in decrease of electron density on nitrogen.

    Solution

    Acetylation of aniline results in decrease of electron density on nitrogen hence acetanilide is less basic than aniline.

  • Question 10
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Amines are basic in nature.

    Reason : Amines have lone pair of electrons on nitrogen atom.

    Solution

    Amines are basic due to the presence of a lone pair of electrons on nitrogen atom. The lone pair can be easily donated.

  • Question 11
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Only a small amount of HCl is required in the reduction of nitro compounds with iron scrap and HCl in the presence of steam.

    Reason : FeCl2 formed gets hydrolysed to release HCl during the reaction.

    Solution

    Fe + 2HCl → FeCl2 + 2[H]

    Nacent hydrogen is reduced into nitro compounds.

    FeCl2 + H2O(g) → FeO + 2HCl

    Hence, (iv) Both assertion and reason are correct statements and reason is the correct explanation of assertion.

  • Question 12
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Aromatic 1°amines can be prepared by Gabriel phthalimide synthesis.

    Reason : Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.

    Solution

    Aromatic primary amines cannot be prepared by Gabriel phthalimide synthesis because it used for the preparation of aliphatic primary amines. It involves nucleophilic substitution (SN2) of alkyl halides by the anion formed by the phthalimide. But aryl halides do not undergo nucleophilic substitution with the anion formed by the phthalimide.

    Hence, aromatic primary amines cannot be prepared by Gabriel pthalimide synthesis.

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