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Alcohols Phenols and Ethers Test - 19

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Alcohols Phenols and Ethers Test - 19
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  • Question 1
    1 / -0

    Assertion : Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.

    Reason : Lewis acid polarises the bromine molecule

    Solution

    Bromination of phenol cannot be carried out in presence of Lewis acid.

  • Question 2
    1 / -0

    Assertion : o-Nitrophenol is less soluble in water than the m- and p-isomers.

    Reason : m- and p- Nitrophenols exist as associated molecules.

    Solution

    Due to intramolecular hydrogen bonding o-Nitrophenol does not form hydrogen bond with water.

  • Question 3
    1 / -0

    Assertion : Ethanol is a weaker acid than phenol.

    Reason : Sodium ethoxide may be prepared by the reaction of ethanol with aqueous NaOH.

    Solution

    Phenoxide ion is stabilized by resonance which is not possible in alkoxide ion.

  • Question 4
    1 / -0

    Assertion : Phenol forms 2, 4, 6 – tribromophenol on treatment with \(Br_2\) in carbon disulphide at 273K.

    Reason : Bromine polarises in carbon disulphide.

    Solution

    Correct assertion: Phenol on treatment with bromine water can form 2,4,6- tribromophenol

    Correct reason: In water, phenol gives phenoxide ions which activate the ring towards electrophilic substitution reaction.

  • Question 5
    1 / -0

    Assertion : Phenols give o- and p-nitrophenol on nitration with conc. \(HNO_3\) and \(H_2SO_4\) mixture.

    Reason : —OH group in phenol is o–, p– directing.

    Solution

    Phenol on treatment with dil. \(HNO_3\) form o-nitrophenol and p-nitrophenol.

  • Question 6
    1 / -0

    When phenol is treated with excess \(Br_2/\)water. It gives 

    Solution

    Phenol on reaction with excess bromine water gives 2,4,6 -tribromophenol.

  • Question 7
    1 / -0

    Ethanol and dimethyl ether form a pair of functional isomers. The boiling point of ethanol is higher than that of dimethyl ether. due to the presence of 

    Solution

    Hydrogen bonding in ethanol.

  • Question 8
    1 / -0

    Which one of the following compounds is resistant to nucleophilic attack by hydroxyl ions?

    Solution

    Diethyl ether is a saturated compound, so it is resistant to nucleophilic attack by a hydroxyl ion (\(OH^- \)).

    Other compounds have unsaturation and the unsaturated 'C' atom bears partial +ve charge, therefore they undergo easy nucleophilic attack by \(OH^- \) ion.

  • Question 9
    1 / -0

    When 3, 3-dimethylbutan-2-ol is heated with conc. \(H_2SO_4\) the major product obtained is: 

    Solution

    When 3, 3-dimethylbutan-2-ol is heated with conc. \(H_2SO_4\) the major product obtained is 2, 3-dimethyl but-2-ene.

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