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Chemistry
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Explain the following reaction:

Wolff-Kishner reduction

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

Observe the graph shown in figure and answer the following questions:


Write the relationship between k and t1/2 (half-life period)

[3] Chemical Kinetics
Chapter: [3] Chemical Kinetics
Concept: undefined >> undefined

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Account for the following:

Arrange the following compounds in the increasing order of their basic strength in aqueous solution: CH3NH2,(CH3)3N,(CH3)2NH

[9] Amines
Chapter: [9] Amines
Concept: undefined >> undefined

Explain the following reactions:

Clemmensen reaction

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

Write the main product in the following reaction:

\[\ce{CH3CH2CHO ->[Zn(Hg)/Conc. HCl]}\]

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

Arrange the following compounds in increasing order of their boiling points:

CH3CH2OH, CH3−CHO, CH3−COOH

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

Which isomer of C5H10 gives a single monochloro compound C5H9Cl in bright sunlight?

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

A first-order reaction is 50% complete in 30 minutes at 300 K and in 10 minutes at 320 K. Calculate activation energy (Ea) for the reaction. [R = 8.314 J K−1 mol−1]

[Given: log 2 = 0.3010, log 3 = 0.4771, log 4 = 0.6021]

[3] Chemical Kinetics
Chapter: [3] Chemical Kinetics
Concept: undefined >> undefined

Calculate the ΔrG0 and log Kc, for the given reaction at 298 K:

\[\ce{Ni_{(s)} + 2Ag^+_{( aq)} <=> Ni^{2+}_{( aq)} + 2Ag_{(s)}}\]

Given: `"E"_("Ni"^(2+)//"Ni")^0` = −0.25 V, `"E"_("Ag"^+//"Ag")^0` = +0.80 V, 1F = 96500 C mol−1.

[2] Electrochemistry
Chapter: [2] Electrochemistry
Concept: undefined >> undefined

Among the following, which has the highest value of pKb?

[9] Amines
Chapter: [9] Amines
Concept: undefined >> undefined

What happens to the rate constant k and activation energy Ea as the temperature of a chemical reaction is increased? Justify.

[3] Chemical Kinetics
Chapter: [3] Chemical Kinetics
Concept: undefined >> undefined

The complex [Co(NH3)5(NO2)]Cl2 is red in colour. Give IUPAC the name of its linkage isomer.

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

Why is the boiling point of o-dichlorobenzene higher than p-dichlorobenzene, but the melting point of para-isomer is higher than ortho-isomer?

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

Assertion (A): The half-life of a reaction is the time in which the concentration of the reactant is reduced to one-half of its initial concentration.

Reason (R): In first-order kinetics, when the concentration of reactant is doubled, its half-life is doubled.

[3] Chemical Kinetics
Chapter: [3] Chemical Kinetics
Concept: undefined >> undefined

Arrange the isomeric dichlorobenzene in the increasing order of their boiling point and melting points.

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

Arrange the decreasing order of pKb values.

\[\ce{C6H5NH2, C6H5NHCH3, C6H5CH2NH2, CH3NH2, NH3}\]

[9] Amines
Chapter: [9] Amines
Concept: undefined >> undefined

Write the structure of the following organic halogen compound.

1,4-Dibromobut-2-ene

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

Indicate the types of isomerism exhibited by the following complexes and draw the structures for this isomer:

Pt(NH3)(H2O)Cl2

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

What is the basicity of H3PO4?

[7] P - Block Elements
Chapter: [7] P - Block Elements
Concept: undefined >> undefined

Write the structure of the following organic halogen compound.

4-tert-Butyl-3-iodoheptane

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