Ncert Chemistry Class 12 intext questions solutions chapter 6 Haloalkanes and Haloarenes

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Haloalkanes and Haloarenes intext questions solutions: Class 12 Chemistry Chapter 6 intext questions solutions

TextbookNcert
ClassClass 12
SubjectChemistry
ChapterChapter 6
Chapter NameHaloalkanes and Haloarenes Class 12 intext questions solutions
CategoryIntext questions
MediumEnglish

Are you looking for Ncert Chemistry Class 12 intext questions solutions chapter 6 Haloalkanes and Haloarenes? Now you can download Haloalkanes and Haloarenes intext questions solutions from here.

Question 6.1: Write structures of the following compounds:

  • (i) 2-Chloro-3-methylpentane
  • (ii) 1-Chloro-4-ethylcyclohexane
  • (iii) 4-tert-Butyl-3-iodoheptane
  • (iv) 1,4-Dibromobut-2-ene
  • (v) 1-Bromo-4-sec. butyl-2-methylbenzene

Solution 6.1: (i) 2-Chloro-3-methylpentane

(ii) 1-Chloro-4-ethylcyclohexane

(iii) 4-tert-Butyl-3-iodoheptane

(iv) 1,4-Dibromobut-2-ene

(v) 1-Bromo-4-sec. butyl-2-methylbenzene

Question 6.2: Why is sulphuric acid not used during the reaction of alcohols with KI?

Solution 6.2: In the presence of sulphuric acid (H2SO4), KI produces HI

2KI + H2SO4 → 2KHSO4 + 2HI

Since H2SO4 is an oxidizing agent, it oxidizes HI (produced in the reaction to I2).

2HI + H2SO4 → I2 + SO2 + H2O

As a result, the reaction between alcohol and HI to produce alkyl iodide cannot occur. Therefore, sulphuric acid is not used during the reaction of alcohols with KI. Instead, a non-oxidizing acid such as H3POis used.

Question 6.3: Write structures of different dihalogen derivatives of propane.

Solution 6.3: There are four different dihalogen derivatives of propane. The structures of these derivatives are shown below.

(i) 1, 1-Dibromopropane

(ii) 2, 2-Dibromopropane

(iii) 1, 2-Dibromopropane

(iv) 1, 3-Dibromopropane

Br-CH2-CH2-CH2-Br

Question 6.4: Among the isomeric alkanes of molecular formula C5H12, identify the one that on photochemical chlorination yields

  • (i) A single monochloride.
  • (ii) Three isomeric monochlorides.
  • (iii) Four isomeric monochlorides.

Solution 6.4: (i) To have a single monochloride, there should be only one type of H-atom in the isomer of the alkane of the molecular formula C5H12. This is because, replacement of any H-atom leads to the formation of the same product. The isomer is neopentane.

Neopentane

(ii) To have three isomeric monochlorides, the isomer of the alkane of the molecular formula C5H12 should contain three different types of H-atoms.

Therefore, the isomer is n-pentane. It can be observed that there are three types of H atoms labelled as a, b and c in n-pentane.

(iii) To have four isomeric monochlorides, the isomer of the alkane of the molecular formula C5H12 should contain four different types of H-atoms. Therefore, the isomer is 2-methylbutane. It can be observed that there are four types of H-atoms labelled as a, b, c, and d in 2-methylbutane.

Question 6.5: Draw the structures of major monohalo products in each of the following reactions:

Solution 6.5:

Question 6.6: Arrange each set of compounds in order of increasing boiling points

  • (i) Bromomethane, Bromoform, Chloromethane, Dibromomethane.
  • (ii) 1-Chloropropane, Isopropyl chloride, 1-Chlorobutane.

Solution 6.6: (i)

For alkyl halides containing the same alkyl group, the boiling point increases with an increase in the atomic mass of the halogen atom.

Since the atomic mass of Br is greater than that of Cl, the boiling point of bromomethane is higher than that of chloromethane.

Further, for alkyl halides containing the same alkyl group, the boiling point increases with an increase in the number of halides. Therefore, the boiling point of Dibromomethane is higher than that of chloromethane and bromomethane, but lower than that of bromoform.

Hence, the given set of compounds can be arranged in the order of their increasing boiling points as:

Chloromethane < Bromomethane < Dibromomethane < Bromoform.

(ii)

For alkyl halides containing the same halide, the boiling point increases with an increase in the size of the alkyl group. Thus, the boiling point of 1-chlorobutane is higher than that of isopropyl chloride and 1-chloropropane.

Further, the boiling point decreases with an increase in branching in the chain. Thus, the boiling point of isopropyl alcohol is lower than that of 1-chloropropane.

Hence, the given set of compounds can be arranged in the increasing order of their boiling points as:

Isopropyl chloride < 1-Chloropropane < 1-Chlorobutane

Question 6.7: Which alkyl halide from the following pairs would you expect to react more rapidly by an SN2 mechanism? Explain your answer.

Solution 6.7: (i)

2-bromobutane is a 2° alkylhalide whereas 1-bromobutane is a 1° alkyl halide. The approaching of nucleophile is more hindered in 2-bromobutane than in 1-bromobutane. Therefore, 1-bromobutane reacts more rapidly than 2-bromobutane by an SN2 mechanism.

(ii)

2-Bromobutane is 2° alkylhalide whereas 2-bromo-2-methylpropane is 3° alkyl halide. Therefore, greater numbers of substituents are present in 3o alkyl halide than in 2° alkyl halide to hinder the approaching nucleophile. Hence, 2-bromobutane reacts more rapidly than 2-bromo-2-methylpropane by an SN2 mechanism.

(iii)

Both the alkyl halides are primary. However, the substituent -CH3 is at a greater distance to the carbon atom linked to Br in 1-bromo-3-methylbutane than in 1-bromo- 2methylbutane. Therefore, the approaching nucleophile is less hindered in case of the former than in case of the latter. Hence, the former reacts faster than the latter by SN2 mechanism.

Question 6.8: In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?

(i) 

(ii) 

Solution 6.8: (i)

SN1 reaction proceeds via the formation of carbocation. The alkyl halide (I) is 3° while (II) is 2°. Therefore, (I) forms 3° carbocation while (II) forms 2° carbocation. Greater the stability of the carbocation, faster is the rate of SN1 reaction. Since 3° carbocation is more stable than 2° carbocation. (I), i.e. 2−chloro-2-methylpropane, undergoes faster SN1 reaction than (II) i.e., 3-chloropentane.

(ii)

The alkyl halide (I) is 2° while (II) is 1°. 2° carbocation is more stable than 1° carbocation. Therefore, (I), 2−chloroheptane, undergoes faster SN1 reaction than (II), 1-chlorohexane.

Question 6.9: Identify A, B, C, D, E, R and R1 in the following:

Solution 6.9:

Since D of D2O gets attached to the carbon atom to which MgBr is attached, C is

Therefore, the compound R − Br is

When an alkyl halide is treated with Na in the presence of ether, a hydrocarbon containing double the number of carbon atoms as present in the original halide is obtained as product. This is known as Wurtz reaction. Therefore, the halide, R1−X, is

Therefore, compound D is

And, compound E is

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