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Chemistry
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Although +3 is the characteristic oxidation state for lanthanoids but cerium also shows +4 oxidation state because:

(i) it has variable ionisation enthalpy

(ii) it has a tendency to attain noble gas configuration

(iii) it has a tendency to attain f 0 configuration

(iv) it resembles Pb4+ 

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

Although Zr belongs to 4d and Hf belongs to 5d transition series but it is quite difficult to separate them. Why?

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

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Although +3 oxidation states is the characteristic oxidation state of lanthanoids but cerium shows +4 oxidation state also. Why?

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

Match the compounds/elements given in Column I with uses given in Column II.

  Column I (Compound/element) Column II (Use)
(i)  Lanthanoid oxide (a) Production of iron alloy
(ii)  Lanthanoid (b) Television screen
(iii)  Misch metal (c) Petroleum cracking
(iv)  Magnesium based alloy is constituent of (d) Lanthanoid metal + iron
(v)  Mixed oxides of lanthanoids are employed (e) Bullets
    (f) In X-ray screen
[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

Match the statements given in Column I with the oxidation states given in Column II.

  Column I Column II
(i) Oxidation state of Mn in MnO2 is (a) + 2
(ii) Most stable oxidation state of Mn is (b) + 3
(iii) Most stable oxidation state of  (c) + 4
  Mn in oxides is (d) + 5
(iv) Characteristic oxidation state of lanthanoids is (e) + 7
[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

Match the property given in Column I with the element given in Column II.

  Column I (Property) Column II (Element)
(i) Lanthanoid which shows
+4 oxidation state
(a) Pm
(ii) Lanthanoid which can show +2
oxidation state
(b) Ce
(iii) Radioactive lanthanoid (c) Lu
(iv) Lanthanoid which has 4f7
electronic configuration in +3
oxidation state
(d) Eu
(v) Lanthanoid which has 4f14
electronic configuration in
+3 oxidation state
(e) Gd
    (f) Dy
[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

On the basis of Lanthanoid contraction, explain the following:

Nature of bonding in \[\ce{La2O3}\] and \[\ce{Lu2O3}\] .

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

On the basis of Lanthanoid contraction, explain the following:

Trends in the stability of oxo salts of lanthanoids from \[\ce{La}\] to \[\ce{Lu}\].

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

On the basis of Lanthanoid contraction, explain the following:

Stability of the complexes of lanthanoids.

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

On the basis of Lanthanoid contraction, explain the following:

Radii of 4d and 5d block elements.

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

On the basis of Lanthanoid contraction, explain the following:

Trends in acidic character of lanthanoid oxides.

[4] d-block and f-block Elements
Chapter: [4] d-block and f-block Elements
Concept: undefined >> undefined

Which of the following reactions will yield phenol?

(i)
(ii)
(iii)
(iv)
[7] Alcohols, Phenols and Ethers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: undefined >> undefined

Name the starting material used in the industrial preparation of phenol.

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

Name the electrophile produced in the reaction of benzene with benzoyl chloride in the presence of anhydrous \[\ce{AlCl3}\]. Name the reaction also.

[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined

Ethylbenzene is generally prepared by acetylation of benzene followed by reduction and not by direct alkylation. Think of a possible reason.

[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined

Can Gatterman-Koch reaction be considered similar to Friedel Craft’s acylation? Discuss.

[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined

Match the common names given in Column I with the IUPAC names given in Column II.

  Column I
(Common names)
  Column II
(IUPAC names)
(i) Cinnamaldehyde (a) Pentanal
(ii) Acetophenone (b) Prop-2-enal
(iii) Valeraldehyde (c) 4-Methylpent-3-en-2-one
(iv) Acrolein (d) 3-Phenylprop-2-enal
(v) Mesityl oxide (e) 1-Phenylethanone
[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined

Match the acids given in Column I with their correct IUPAC names given in Column II.

  Column I
(Acids)
  Column II
(IUPAC names)
(i) Phthalic acid (a) Hexane-1,6-dioic acid
(ii) Oxalic acid (b) Benzene-1,2-dicarboxylic acid
(iii) Succinic acid (c) Pentane-1,5-dioic acid
(iv) Adipic acid (d) Butane-1,4-dioic acid
(v) Glutaric acid (e) Ethane-1,2-dioic acid
[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined

Match the example given in Column I with the name of the reaction in Column II.

  Column I
(Example)
  Column II
(Reaction)
(i) \[\begin{array}{cc}
\phantom{...}\ce{O}\phantom{..............................}\ce{O}\phantom{}\\
\phantom{...}||\phantom{..............................}||\phantom{}\\
\ce{CH3 - C - Cl + H2 ->[Pd - C/BasO4] CH3 - C - H}
\end{array}\]
(a) Friedel Crafts acylation
(ii) (b) HVZ reaction
(iii) (c) Aldol condensation
(iv) \[\begin{array}{cc}
\ce{R - CH2 - COOH ->[Br/Red P] R - CH - COOH}\\
\phantom{.....................}|\\
\phantom{.......................}\ce{Br}
\end{array}\]
(d) Cannizaro’s reaction
(v) \[\ce{CH3 - CN ->[(i) SnCl2/HCl][(ii) H2O/H+] CH3CHO}\] (e) Rosenmund’s reductio
(vi) \[\ce{2CH3CHO ->[NaOH] CH3 - CH = CHCHO}\] (f) Stephen’s reaction
[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined

An alkene ‘A’ (Mol. formula \[\ce{C5H10}\]) on ozonolysis gives a mixture of two compounds ‘B’ and ‘C’. Compound ‘B’ gives positive Fehling’s test and also forms iodoform on treatment with \[\ce{I2}\] and \[\ce{NaOH}\]. Compound ‘C’ does not give Fehling’s test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.

[8] Aldehydes, Ketones and Carboxylic Acids
Chapter: [8] Aldehydes, Ketones and Carboxylic Acids
Concept: undefined >> undefined
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