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Arrange following complex ions in increasing order of crystal field splitting energy (∆O):

\[\ce{[Cr(Cl)6]^{3-}, [Cr(CN)6]^{3-}, [Cr(NH3)6]^{3+}}\].

[5] Coordination Compounds
Chapter: [5] Coordination Compounds
Concept: undefined >> undefined

\[\ce{CuSO4 . 5H2O}\] is blue in colour while \[\ce{CuSO4}\] is colourless. Why?

[5] Coordination Compounds
Chapter: [5] Coordination Compounds
Concept: undefined >> undefined

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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
[5] Coordination Compounds
Chapter: [5] Coordination Compounds
Concept: undefined >> undefined

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:

\[\ce{[CoF6]^{3-}, [Co(H2O)6]^{2+}, [Co(Cn)6]^{3-}}\]

[5] Coordination Compounds
Chapter: [5] Coordination Compounds
Concept: undefined >> undefined

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:

\[\ce{[FeF6]^{3-}, [Fe(H2O)6]^{2+}, [Fe(CN)6]^{4-}}\]

[5] Coordination Compounds
Chapter: [5] Coordination Compounds
Concept: undefined >> undefined

Why are different colours observed in octahedral and tetrahedral complexes for the same metal and same ligands?

[5] Coordination Compounds
Chapter: [5] Coordination Compounds
Concept: undefined >> undefined

Toluene reacts with a halogen in the presence of iron (III) chloride giving ortho and para halo compounds. The reaction is ______.

[6] Haloalkanes and Haloarenes
Chapter: [6] Haloalkanes and Haloarenes
Concept: undefined >> undefined

Assertion: In monohaloarenes, further electrophilic substitution occurs at ortho and para positions.

Reason: Halogen atom is a ring deactivator.

[6] Haloalkanes and Haloarenes
Chapter: [6] Haloalkanes and Haloarenes
Concept: undefined >> undefined

Phenol is less acidic than ______.

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

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

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Write the IUPAC name of the following compound.

\[\begin{array}{cc}
\phantom{.}\ce{CH3 - CH - CH - CH - CH - CH3}\phantom{}\\
\phantom{......}|\phantom{......}|\phantom{......}|\phantom{.....}|\phantom{........}\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{C2H5}\phantom{.}\ce{OH}\phantom{...}\end{array}\]

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

What is denatured alcohol?

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Out of 2-chloroethanol and ethanol which is more acidic and why?

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Suggest a reagent for conversion of ethanol to ethanal.

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Suggest a reagent for conversion of ethanol to ethanoic acid.

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Arrange the following compounds in increasing order of acidity and give a suitable explanation.

Phenol, o-nitrophenol, o-cresol

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Name the enzymes and write the reactions involved in the preparation of ethanol from sucrose by fermentation.

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Dipole moment of phenol is smaller than that of methanol. Why?

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

The carbon-oxygen bond in phenol is slightly stronger than that in methanol. Why?

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Arrange water, ethanol and phenol in increasing order of acidity and give reason for your answer.

[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined
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