The main reason for larger number of oxidation states exhibited b

Subject

Chemistry

Class

NEET Class 12

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 Multiple Choice QuestionsMultiple Choice Questions

31.

The correct order of acid strength is

  • HClO < HClO2 < HClO3 < HClO4

  • HClO4 < HClO < HClO2 < HClO3

  • HClO2 < HClO3 < HClO4 < HClO

  • HClO4 < HClO3 < HClO2 < HClO


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32.

The main reason for larger number of oxidation states exhibited by the actinides than the corresponding lanthanides, is

  • lesser energy difference between 5f and 6d orbitals than between 4f and 5d orbitals

  • larger atomic size of actinides than the lanthanide

  • more energy difference between 5f and 6d orbitals than between 4f and 5d orbitals

  • greater reactive nature of the actinides than the lanthanides


A.

lesser energy difference between 5f and 6d orbitals than between 4f and 5d orbitals

The main reason for larger number of oxidation states exhibited by actinides than corresponding lanthanides is lesser energy difference between 5f and 6d orbitals than between 4f and 5d-orbitals.


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33.

Aniline in a set of reactions yielded a product D

The structure of the product D would be

  • C6H5CH2NH2

  • C6H5NHCH2CH3

  • C6H5NHOH

  • C6H5CH2OH


34.

In a set of reactions, acetic acid yielded a product D.

CH3COOH SOCl2  A anhyd. AlCl3Benzene B HCN C HOH  D

The structure of D would be


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35.

The major organic product formed from the following reaction (ii) LiAlH4 (iii) H2O(i) CH3NH2 ... is


36.

The monomer of the polymer

 

  • H2C = C(CH3)2

  • (CH3)2C = C(CH3)2

  • CH3CH = CH CH3

  • CH3CH = CH2


37.

Electrolytic reduction of nitrobenzene in weakly acidic medium gives

  • aniline

  • nitrosobenzene

  • N-phenylhydroxylamine

  • p-hydroxyaniline


38.

Which of the following undergoes nucleophilic substitution exclusively by SN1 mechanism?

  • Benzyl chloride

  • Ethyl chloride

  • Chlorobenzene

  • lsopropyl chloride


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39.

Which functional group participates in disulphide bond formation in proteins?

  • Thiolactone

  • Thiol

  • Thioether

  • Thioester


40.

The chirality of the compound

  • R

  • S

  • Z

  • E


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