Chemistry MCQs for NEET — Practice Questions with Answers

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IUPAC name of H2[PtCl6] is:

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Explanation

 


H2[PtCl6] is an acid, not salt hence its name : hexachloroplatinic (IV) acid

 

whenever HYDROGEN is present as cation , it is called as acid rather than salt.

ie 

KNO2 is known as POT nitrite

but HNO2 is not known as HYDROGEN NITRITE, its known as  NITROUS ACID.

Which of the following ligand does not as π-acid ligand?

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Explanation

(d) Due to absence of vacant atomic orbital as well as π* molecular orbital O22- does not as π acid ligand .

[Mn(CO)4NO] is diamagnetic because:

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Explanation

 [Mn+1(CO)4(NO-)] : Paramagnetic due to presence of unpaired e- in NO- [Mn-1(CO)4(NO+)] : No. of unpaired e- either on ligands or on Mn-1 hence it is diamagnetic

If CO ligands are substituted by NO in respective neutral carbonyl compounds then which of the following will not be correct formula ?

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Explanation

(d) Ligand NO is 3e- donar hence three CO ligands can be substituted by two NO ligands.

Which of the following species can act as reducing agent ?

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Explanation

(b) Mn(CO)6 can act as reducing agent because the metal carbonyl is stable when EAN is equal to nearest noble gas configuration.

[Mn(CO)6]-e- [Mn(CO)6]+EAN =37              EAN=36(less stable)           (more stable)

What is electronic arranegment of metal atom/ionin octahedral complex with d4 configuration , if 0< pairing energy ?

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Which of the following statement is not correct ?

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Explanation

(c) [Ni(CN)4]4- ; sp3;Tetrahedral complex.

Give the correct of initial or F for following statements. Use is statement is true and if it is false

(I) Co(III) is stabilised in presence of weak ligands , while Co(II) is stabilised in presence of strong field ligand.

(II) Four coordinated complexes of Pd(II) and Pt(II) are diamagnetic and square planar.

(III) [Ni(CN)4]4- ion and [Ni(CO)4] are diamagnetic tetrahedral and square planar.

(IV) Ni2+ ion does not inner orbital octahedral complexes.

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Match List-I with List-II and select the correct answer using the codes given below :

                      List-I                                              List-II

(I) [FeF6]3-                                                   (A) 1.73 BM

(II) [Ti(H2O)6]3+                                             (B) 5.93 BM

(III) [Cr(NH3)6]3+                                            (C) 0.00 BM

(IV) [Ni(H2O)6]2+                                             (D) 2.83 BM

(V)  [Fe(CN)6]4-                                               (E) 3.88 BM

          (I)    (II)   (III)   (IV)   (V)                       (I)    (II)   (III)   (IV)   (V) 

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Explanation

The correct matching is: (I) [FeF₆]³⁻ - (B) 5.93 BM (high spin d⁵ configuration), (II) [Ti(H₂O)₆]³⁻ - (A) 1.73 BM (d¹ configuration), (III) [Cr(NH₃)₆]³⁺ - (E) 3.88 BM (d³ configuration), (IV) [Ni(H₂O)₆]²⁺ - (D) 2.83 BM (d⁸ configuration), (V) [Fe(CN)₆]⁴⁻ - (C) 0.00 BM (diamagnetic, low spin d⁶ configuration).

Set of d-orbitals which is used by central metal during formation of MnO4-?

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Explanation

The central metal atom manganese (Mn) in the MnO4- ion has an oxidation state of +7. According to the aufbau principle, the five 3d orbitals (dxy, dyz, dxz, dx2-y2, dz2) are progressively filled. In the +7 oxidation state, Mn has a d0 configuration, meaning all 3d orbitals are vacant. Therefore, the set of d-orbitals used by the central metal during the formation of MnO4- is dxy, dyz, and dxz.

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