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Science (English Medium) Class 12 - CBSE Important Questions for Chemistry

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The following questions are case-based questions. Read the passage carefully and answer the questions that follow:

Nucleophilic Substitution:
Nucleophilic substitution reaction of haloalkane can be conducted according to both SN1 and SN2 mechanisms. SN1 is a two-step reaction, while SN2 is a single-step reaction. For any haloalkane, which mechanism is followed depends on factors such as the structure of haloalkane, properties of leaving group, nucleophilic reagent and solvent.

Influences of solvent polarity:
In SN1 reaction, the polarity of the system increases from the reactant to the transition state, because a polar solvent has a greater effect on the transition state than the reactant, thereby reducing activation energy and accelerating the reaction. In SN2 reaction, the polarity of the system generally does not change from the reactant to the transition state, and only charge dispersion occurs. At this time, the polar solvent has a great stabilizing effect on Nu than the transition state, thereby increasing activation energy and slow down the reaction rate. For example, the decomposition rate (SN1) of tertiary chlorobutane at 25°C in water (dielectric constant 79) is 300000 times faster than in ethanol (dielectric constant 24).

The reaction rate (SN2) of 2-bromopropane and NaOH in ethanol containing 40% water is twice slower than in absolute ethanol. Hence the level of solvent polarity has an influence on both SN1 and SN2 reactions but with different results. Generally speaking, a weak polar solvent is favourable for SN2 reaction, while a strong polar solvent is favourable for SN1. Generally speaking, the substitution reaction of tertiary haloalkane is based on SN1 mechanism in solvents with a strong polarity (for example ethanol containing water).

Answer the following questions:

(a) Why racemisation occurs in SN1? (1)

(b) Why is ethanol less polar than water? (1)

(c) Which one of, the following in each pair is more reactive towards SN2 reaction? (2)

(i) CH3 – CH2 – I or CH3CH2 – Cl

(ii)

OR

(c) Arrange the following in the increasing order of their reactivity towards SN1 reactions: (2)

(i) 2-Bromo-2-methylbutane, 1-Bromo-pentane, 2-Bromo-pentane

(ii) 1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 2-Bromo-3- methylbutane

Appears in 3 question papers
Chapter: [6] Haloalkanes and Haloarenes
Concept: Hydrocarbons: Alkanes >> Reactions of Haloalkanes - Nucleophilic Substitution Reactions

Account for the following:

Helium is used in diving apparatus.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: P - Block Group 18 Elements >> Concept of Group 18 Elements

Draw the structures of the following molecules: XeF2

 

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: P - Block Group 18 Elements >> Concept of Group 18 Elements

Account for the following:

N2 is less reactive at room temperature.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: Concept of Group 15 Elements

Draw the structures of the following: H4P2O7 (Pyrophosphoric acid)

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: p-Block elements of Group 15 Elements >> Oxoacids of Phosphorus

What happens when 

H3PO3 is heated ?

Write the reactions involved.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: p-Block elements of Group 15 Elements >> Phosphine

Write the mechanism of the following reaction:

Appears in 3 question papers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: Chemical Reactions of Alcohols and Phenols >> Reactions Involving Cleavage of Carbon–Oxygen (C–O) Bond in Alcohols

Write the main product(s) in each of the following reactions:

Appears in 3 question papers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: Chemical Reaction of Ethers - Cleavege of C-O Bonds

Write the main product(s) in each of the following reactions:

Appears in 3 question papers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: Methods of Preparation of Alcohols

Write the main product(s) in each of the following reactions:

Appears in 3 question papers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: Chemical Properties of Phenol

Account for the following :

Ozone is thermodynamically unstable.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: P - Block Group 16 Elements >> Ozone

Account for the following : Solid PCl5 is ionic in nature.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: p-Block elements of Group 15 Elements >> Phosphorus Halides

Account for the following:

Fluorine forms only one oxoacid HOF.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: P - Block Group 17 Elements >> Oxoacids of Halogens

Draw the structure of BrF5

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: P - Block Group 17 Elements >> Interhalogen Compounds

Compare the oxidizing action of F2 and Cl2 by considering parameters such as bond dissociation enthalpy, electron gain enthalpy and hydration enthalpy.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: Concept of Group 17 Elements

Write the conditions to maximize the yield of H2SO4 by contact process.

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: P - Block Group 16 Elements >> Sulphuric Acid

Arrange the following in the increasing order of property mentioned :

H3PO3, H3PO4, H3PO2 (Reducing character)

 

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: Concept of Group 15 Elements

Write the structures of A, B, C, D and E in the following reactions:

Appears in 3 question papers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: Chemical Properties of Phenol

What is the basicity of H3PO4?

Appears in 3 question papers
Chapter: [7] P - Block Elements
Concept: p-Block elements of Group 15 Elements >> Oxoacids of Phosphorus

Name the reagents used in the following reactions:

Appears in 3 question papers
Chapter: [7] Alcohols, Phenols and Ethers
Concept: Methods of Preparation of Alcohols
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