Subject

Chemistry

Class

NEET Class 12

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 Multiple Choice QuestionsMultiple Choice Questions

11.

The heat is liberated when 1.89 g of benzoic acid is burnt in a bomb calorimeter at 25 °C and it increases the temperature of 18.94 kg of water by 0.632 °C. If the specific heat of water at 25 °C is 0.998 cal/g-deg, then value of the heat of combustion of benzoic acid is

  • 881.1 kcal

  • 981.1 kcal

  • 771.1 kcal

  • 871.2 kcal


12.

Assertion : trans-Pent-2-ene is polar but trans- but-2-ene is non-polar.

Reason : The polarity of cis-isomer is more than trans-isomer, which are either non-polar or less polar.

  • If both assertion and reason are true and reason is the correct explanation of assertion.

  • If both assertion and reason are true but reason is not the correct explanation of assertion.

  • If assertion is true but reason is false.

  • If both assertion and reason are false


13.

Assertion : The number of tetrahedral voids is double the number of octahedral voids.

Reason : The size of the tetrahedral voids is half of that of the octahedral void.

  • If both assertion and reason are true and reason is the correct explanation of assertion.

  • If both assertion and reason are true but reason is not the correct explanation of assertion.

  • If assertion is true but reason is false.

  • If both assertion and reason are false.


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14.

Assertion : The second dissociation constant of fumaric acid is greater than maleic acid.

Reason : Higher the dissociation constant of acid, more is the acidic character.

  • If both assertion and reason are true and reason is the correct explanation of assertion.

  • If both assertion and reason are true but reason is not the correct explanation of assertion

  • If assertion is true but reason is false.

  • If both assertion and reason are false


B.

If both assertion and reason are true but reason is not the correct explanation of assertion

Both fumaric and maleic acids have two ionisable H+ ions i.e., protons. The maleate monoanion shows intramolecular H-bonding, whereas fumarate monoanion shows intermolecular H-bonding. Thus, fumarate monoanion requires more energy to give fumarate dianion. Hence, second dissociation of fumaric acid is more than that ofmaleic acid.


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15.

Assertion : [Fe(CN)6]3- has d2sp3 type hybridisation.

Reason: [Fe(CN)6]3- ion shows magnetic moment corresponding to two unpaired electrons.

  • If both assertion and reason are true and reason is the correct explanation of assertion.

  • If both assertion and reason are true but reason is not the correct explanation of assertion.

  • If assertion is true but reason is false

  • If both assertion and reason are false.


16.

Assertion: Both π(2px) and π*(2px) MO's have one nodal plane.

Reason : All MO's formed by side way overlapping of 2p- orbitals have one nodal plane.

  • If both assertion and reason are true and reason is the correct explanation of assertion.

  • If both assertion and reason are true but reason is not the correct explanation of assertion

  • If assertion is true but reason is false

  • If both assertion and reason are false.


17.

Assertion : Spontaneous process is an irreversible process and may be reversed by some external agency.

Reason : Decrease in enthalpy is a contributory factor for spontaneity.

  • If both assertion and reason are true and reason is the correct explanation of assertion.

  • If both assertion and reason are true but reason is not the correct explanation of assertion.

  • If assertion is true but reason is false

  • If both assertion and reason are false.


18.

H2O is polar, whereas BeF2 is not because

  • electronegativity of F is greaterthan that of O.

  • H2O involves H-bonding, whereas BeF2 is a discrete molecule

  • H2O is angular and BeF2 is linear

  • H2O is linear and BeF2 is angular.


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19.

The correct order of solubility ofthe following compounds in water is

  • Ba(OH)2 < Mg(OH)2

  • BaCO3 > CaCO3

  • Ca(OH)2  Mg(OH)2

  • CaSO4 < MgSO4


20.

(R)-2-Iodobutane is treated with NaI in acetone and allowed to stand for a long time. The product eventually formed is

  • (R)-2-iodobutane

  • (S)-2-iodobutane

  • (±)-2-iodobutane

  • (±)-1, 2-diiodobutane


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