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Atomic number of \[\ce{Mn}\], \[\ce{Fe}\] and \[\ce{Co}\] are 25, 26 and 27 respectively. Which of the following inner orbital octahedral complex ions are diamagnetic?
(i) \[\ce{[Co(NH3)6]^{3+}}\]
(ii) \[\ce{[Mn(CN)6]^{3-}}\]
(iii) \[\ce{[Fe(CN)6]^{4-}}\]
(iv) \[\ce{[Fe(CN)6]^{3-}}\]
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Atomic number of \[\ce{Mn, Fe, Co}\] and Ni are 25, 26, 27 and 28 respectively. Which of the following outer orbital octahedral complexes have same number of unpaired electrons?
(i) \[\ce{[MnCl6]^{3-}}\]
(ii) \[\ce{[FeF6]^{3-}}\]
(iii) \[\ce{[CoF6]^{3-}}\]
(iv) \[\ce{[Ni(NH3)6]^{2+}}\]
Concept: undefined >> undefined
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An aqueous pink solution of cobalt (II) chloride changes to deep blue on addition of excess of HCl. This is because:
(i) \[\ce{[Co(H2O)6]^{2+}}\] is transformed into \[\ce{[CoCl6]}^{4-}\]
(ii) \[\ce{[Co(H2O)6]^{2+}}\] is transformed into \[\ce{[CoCl4]}^{2-}\]
(iii) tetrahedral complexes have smaller crystal field splitting than octahedral complexes.
(iv) tetrahedral complexes have larger crystal field splitting than octahedral complex.
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On the basis of crystal field theory explain why Co(III) forms paramagnetic octahedral complex with weak field ligands whereas it forms diamagnetic octahedral complex with strong field ligands.
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Why are low spin tetrahedral complexes not formed?
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Give the electronic configuration of the following complexes on the basis of Crystal Field Splitting theory.
\[\ce{[CoF6]^{3-}, [Fe(CN)6]^{4-} and [Cu(NH3)6]^{2+}}\].
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Arrange following complex ions in increasing order of crystal field splitting energy (∆O):
\[\ce{[Cr(Cl)6]^{3-}, [Cr(CN)6]^{3-}, [Cr(NH3)6]^{3+}}\].
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\[\ce{CuSO4 . 5H2O}\] is blue in colour while \[\ce{CuSO4}\] is colourless. Why?
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Match the complex ions given in Column I with the hybridisation and number of unpaired electrons given in Column II and assign the correct code:
| Column I (Complex ion) | Column II (Hybridisation, number of unpaired electrons) |
| A. \[\ce{[Cr(H2O)6]^{3+}}\] | 1. dsp2, 1 |
| B. \[\ce{[Co(CN)4]^{2-}}\] | 2. sp3d2, 5 |
| C. \[\ce{[Ni(NH3)6]^{2+}}\] | 3. d2sp3, 3 |
| D. \[\ce{[MnF6]^{4-}}\] | 4. sp3, 4 |
| 5. sp3d2, 2 |
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Using crystal field theory, draw energy level diagram, write electronic configuration of the central metal atom/ion and determine the magnetic moment value in the following:
\[\ce{[CoF6]^{3-}, [Co(H2O)6]^{2+}, [Co(Cn)6]^{3-}}\]
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Using crystal field theory, draw energy level diagram, write electronic configuration of the central metal atom/ion and determine the magnetic moment value in the following:
\[\ce{[FeF6]^{3-}, [Fe(H2O)6]^{2+}, [Fe(CN)6]^{4-}}\]
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Why are different colours observed in octahedral and tetrahedral complexes for the same metal and same ligands?
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Toluene reacts with a halogen in the presence of iron (III) chloride giving ortho and para halo compounds. The reaction is ______.
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Assertion: In monohaloarenes, further electrophilic substitution occurs at ortho and para positions.
Reason: Halogen atom is a ring deactivator.
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Phenol is less acidic than ______.
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Phenol can be distinguished from ethanol by the reactions with:
(i) \[\ce{Br2/water}\]
(ii) \[\ce{Na}\]
(iii) Neutral \[\ce{FeCl3}\]
(iv) All the above
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Write the IUPAC name of the following compound.
\[\begin{array}{cc}
\phantom{.}\ce{CH3 - CH - CH - CH - CH - CH3}\phantom{}\\
\phantom{......}|\phantom{......}|\phantom{......}|\phantom{.....}|\phantom{........}\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{C2H5}\phantom{.}\ce{OH}\phantom{...}\end{array}\]
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What is denatured alcohol?
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Out of 2-chloroethanol and ethanol which is more acidic and why?
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Suggest a reagent for conversion of ethanol to ethanal.
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