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Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC chapter 10 - Haloalkanes and Haloarenes [Latest edition]

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Chapters

Physical Chemistry

    1: Solid State

    2: Solutions

    3: Electrochemistry

    4: Chemical Kinetics

    5: Surface Chemistry

Inorganic Chemistry

    6: General Principles and Processes of Isolation of Elements

    7: p-Block Elements

    8: d-and ƒ-Block Elements

    9: Coordination Compounds

Organic Chemistry

▶ 10: Haloalkanes and Haloarenes

   Chapter 11: Alcohols, Phenols and Ethers

   Chapter 12: Aldehydes, Ketones and Carboxylic Acids

   Chapter 13: Organic Compounds containing Nitrogen

   Chapter 14: Biomolecules

    15: Polymers

   Chapter 16: Chemistry in Everyday Life

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC chapter 10 - Haloalkanes and Haloarenes - Shaalaa.com
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Solutions for Chapter 10: Haloalkanes and Haloarenes

Below listed, you can find solutions for Chapter 10 of CISCE Nootan for Chemistry Part 1 and 2 [English] Class 12 ISC.


REVIEW EXERCISESVERY SHORT ANSWER TYPE QUESTIONSSHORT ANSWER TYPE QUESTIONSLONG ANSWER TYPE QUESTIONSOBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONSFILL IN THE BLANKS TYPE QUESTIONS
REVIEW EXERCISES [Pages 567 - 604]

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC 10 Haloalkanes and Haloarenes REVIEW EXERCISES [Pages 567 - 604]

REVIEW EXERCISES | Q 10.1 (i) | Page 567

What are haloalkanes?

REVIEW EXERCISES | Q 10.1 (ii) | Page 567

How are haloalkanes classified?

REVIEW EXERCISES | Q 10.2 (i) | Page 567

What do you understand by a 3° alkyl halide?

REVIEW EXERCISES | Q 10.2 (ii) | Page 567

Give an example of a 3° alkyl halide.

REVIEW EXERCISES | Q 10.3 | Page 567

What is the main structural difference between 1° and 2° alkyl halides?

REVIEW EXERCISES | Q 10.4 (i) | Page 567

Write the structure of the following:

Vinyl chloride

REVIEW EXERCISES | Q 10.4 (ii) | Page 567

Write the structure of the following:

Allyl chloride

REVIEW EXERCISES | Q 10.5 (i) | Page 567

Write the structure of a chloroalkene.

REVIEW EXERCISES | Q 10.5 (ii) | Page 567

Write the structure of a chloroalkyne.

REVIEW EXERCISES | Q 10.6 (i) (a) | Page 570

Write the structural formula of the following compound.

n-propyl chloride

REVIEW EXERCISES | Q 10.6 (i) (b) | Page 570

Write the IUPAC name of the following compound.

n-propyl chloride

REVIEW EXERCISES | Q 10.6 (ii) (a) | Page 570

Write the structural formula of the following compound. 

iso-butyl chloride

REVIEW EXERCISES | Q 10.6 (ii) (b) | Page 570

Write the IUPAC name of the following compound.

iso-butyl chloride

REVIEW EXERCISES | Q 10.6 (iii) (a) | Page 570

Write the structural formula of the following compound.

sec-butyl chloride

REVIEW EXERCISES | Q 10.6 (iii) (b) | Page 570

Write the IUPAC name of the following compound.

sec-butyl chloride

REVIEW EXERCISES | Q 10.6 (iv) (a) | Page 570

Write the structural formula of the following compound. 

iso-amyl chloride

REVIEW EXERCISES | Q 10.6 (iv) (b) | Page 570

Write the IUPAC name of the following compound. 

iso-amyl chloride

REVIEW EXERCISES | Q 10.6 (v) (a) | Page 570

Write the structural formula of the following compound. 

neo-pentyl chloride

REVIEW EXERCISES | Q 10.6 (v) (b) | Page 570

Write the IUPAC name of the following compound.

neo-pentyl chloride

REVIEW EXERCISES | Q 10.7 (i) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{\phantom{.}F\phantom{..........}Cl}\\
|\phantom{...........}|\\
\ce{CH3 - C - CH2 - C - CH3}\\
|\phantom{...........}|\\
\ce{\phantom{....}C2H5\phantom{......}C2H5}\\
\end{array}\]

REVIEW EXERCISES | Q 10.7 (ii) | Page 570

Give the IUPAC name of the following compound.

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

REVIEW EXERCISES | Q 10.7 (iii) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{\phantom{......}CH3}\\
\phantom{...}|\\
\ce{CH3 - C - Cl}\\
\phantom{...}|\\
\ce{\phantom{......}CH3}\\
\end{array}\]

REVIEW EXERCISES | Q 10.7 (iv) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{CH3 - CH - CH2Cl}\\
\phantom{}|\phantom{....}\\
\ce{C2H5}\\
\end{array}\]

REVIEW EXERCISES | Q 10.7 (v) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{\phantom{...}CH3}\\
|\\
\ce{\phantom{...}CH2}\\
|\\
\ce{CH2 = CH - CH - C = CH2}\\
\phantom{.............}|\\
\ce{\phantom{.............}Cl}\\
\end{array}\]

REVIEW EXERCISES | Q 10.7 (vi) | Page 570

Give the IUPAC name of the following compound.

(CH3)3C·CH2·CH2Cl

REVIEW EXERCISES | Q 10.7 (vii) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{CH3\phantom{.......}}\\
|\phantom{..........}\\
\ce{CH3 - C - CH2 - CH2Cl}\\
|\phantom{..........}\\
\ce{CH3\phantom{.......}}\\
\end{array}\]

REVIEW EXERCISES | Q 10.7 (viii) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{\phantom{.......................}CH3\phantom{.}}\\
\phantom{....................}|\\
\ce{CH3 - CH2 - CH - CH - C - CH3}\\
\phantom{........}|\phantom{......}|\phantom{......}|\phantom{.}\\
\ce{\phantom{..........}Br\phantom{....}CH3\phantom{..}CH3\phantom{}}\\
\end{array}\]

REVIEW EXERCISES | Q 10.7 (ix) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{CH3 - CO - CH - CH2 - CH2Cl}\\
|\phantom{.....}\\
\ce{CH3\phantom{..}}
\end{array}\]

REVIEW EXERCISES | Q 10.7 (x) | Page 570

Give the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{CH3 - CO - CH - CH2 - CH2Cl}\\
|\phantom{.....}\\
\ce{C2H5\phantom{.}}
\end{array}\]

REVIEW EXERCISES | Q 10.8 (i) | Page 570

Write the structure of the following compound and identify it as a 1°, 2° or 3° halide.

2-chloro-2-methylbutane

REVIEW EXERCISES | Q 10.8 (ii) | Page 570

Write the structure of the following compound and identify it as a 1°, 2° or 3° halide. 

2-iodobutane

REVIEW EXERCISES | Q 10.8 (iii) | Page 570

Write the structure of the following compound and identify it as a 1°, 2°, or 3° halide. 

1-bromo-2-methylpropane

REVIEW EXERCISES | Q 10.8 (iv) | Page 570

Write the structure of the following compound and identify it as a 1°, 2° or 3° halide. 

1-chloro-2, 2-dimethylpropane

REVIEW EXERCISES | Q 10.8 (v) | Page 570

Write the structure of the following compound and identify it as a 1°, 2° or 3° halide.

chloroethane

REVIEW EXERCISES | Q 10.9 | Page 570

Write all the possible chain and position isomers of the compounds having formula C5H11Cl. Write their IUPAC names and identify them as 1°, 2° and 3° halides.

REVIEW EXERCISES | Q 10.10 (i) | Page 570

Name the following compound in the IUPAC system:

\[\begin{array}{cc}
\ce{CH3 - CH - CH2 - CH2Br}\\
|\phantom{............}\\
\ce{Cl\phantom{...........}}
\end{array}\]

REVIEW EXERCISES | Q 10.10 (ii) | Page 570

Name the following compound in the IUPAC system:

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

REVIEW EXERCISES | Q 10.10 (iii) | Page 570

Name the following compound in the IUPAC system:

\[\begin{array}{cc}
\ce{CH2Cl}\\
|\phantom{.....}\\
\ce{CH2Cl}
\end{array}\]

REVIEW EXERCISES | Q 10.10 (iv) | Page 570

Name the following compound in the IUPAC system:

CH3CHCl2

REVIEW EXERCISES | Q 10.10 (v) | Page 570

Name the following compound in the IUPAC system:

CHCl3

REVIEW EXERCISES | Q 10.10 (vi) | Page 570

Name the following compound in the IUPAC system:

CCl4

REVIEW EXERCISES | Q 10.11 | Page 584

Write the names and possible structures for the compounds having molecular formula, C3H7Cl.

REVIEW EXERCISES | Q 10.12 | Page 584

Write the structural formula and IUPAC names of two optically active halides containing five carbon atoms each in their molecules.

REVIEW EXERCISES | Q 10.13 (i) | Page 584

How is bromoethane prepared from ethane?

REVIEW EXERCISES | Q 10.13 (ii) | Page 584

How is bromoethane prepared from ethanol?

REVIEW EXERCISES | Q 10.13 (iii) | Page 584

How is bromoethane prepared from ethene?

REVIEW EXERCISES | Q 10.13 (iv) | Page 584

How will you prepare iodoethane from bromoethane?

REVIEW EXERCISES | Q 10.14 (i) | Page 584

How will you prepare iodoethane from bromoethane?

REVIEW EXERCISES | Q 10.14 (ii) | Page 584

How will you prepare bromopropane from butanoic acid?

REVIEW EXERCISES | Q 10.14 (iii) | Page 584

How will you prepare chloroethane from ethanol?

REVIEW EXERCISES | Q 10.14 (iv) | Page 584

How will you prepare 1-bromopropane from propene?

REVIEW EXERCISES | Q 10.15 (i) | Page 584

Explain the following briefly:

Although haloalkanes are polar in character, yet they are insoluble in water.

REVIEW EXERCISES | Q 10.15 (ii) | Page 584

Explain the following briefly:

The boiling point of bromoethane is higher than that of chloroethane.

REVIEW EXERCISES | Q 10.15 (iii) | Page 584

Explain the following briefly:

t-butyl bromide has a lower boiling point than n-butyl bromide.

REVIEW EXERCISES | Q 10.15 (iv) | Page 584

Explain the following briefly:

Alkyl iodides usually become brown on standing.

REVIEW EXERCISES | Q 10.16 | Page 584

Why do alkyl halides show nucleophilic substitution reactions?

REVIEW EXERCISES | Q 10.17 | Page 584

Rearrange the following in the order of increasing ease of dehydrohalogenation:

CH3CH2Cl, CH3CHClCH3 and CH3CCl(CH3)2.

Give reasons.

REVIEW EXERCISES | Q 10.18 | Page 584

The treatment of alkyl chlorides with aqueous KOH leads to the formation of alcohols but in the presence of alcoholic KOH, alkenes are major products. Explain.

REVIEW EXERCISES | Q 10.19 | Page 584

Arrange the following in the order of their increasing reactivity in nucleophilic substitution reactions.

CH3F, CH3I, CH3Br, CH3Cl

REVIEW EXERCISES | Q 10.20 (i) | Page 585

How will you convert methyl bromide (bromomethane) to acetic acid (ethanoic acid)?

REVIEW EXERCISES | Q 10.20 (ii) | Page 585

How will you convert prop-1-ene to 1-bromopropane?

REVIEW EXERCISES | Q 10.20 (iii) | Page 585

How will you convert propan-2-ol to 1-bromopropane?

REVIEW EXERCISES | Q 10.20 (iv) | Page 585

How will you convert n-propyl bromide to isopropyl bromide?

REVIEW EXERCISES | Q 10.20 (v) | Page 585

How will you convert bromoethane to ethoxyethane?

REVIEW EXERCISES | Q 10.20 (vi) | Page 585

How will you convert propan-1-ol to 2-bromopropane?

REVIEW EXERCISES | Q 10.21 | Page 585

Explain why do haloalkanes give alkyl cyanides when treated with KCN but give alkyl isocyanides with silver cyanide?

REVIEW EXERCISES | Q 10.22 (i) | Page 585

What is peroxide effect?

REVIEW EXERCISES | Q 10.22 (ii) | Page 585

Explain with a suitable example of the peroxide effect.

REVIEW EXERCISES | Q 10.23 (i) | Page 585

What happens when propene is treated with hydrobromic acid?

REVIEW EXERCISES | Q 10.23 (ii) | Page 585

What happens when ethanol is treated with thionyl chloride?

REVIEW EXERCISES | Q 10.23 (iii) | Page 585

What happens when ethanol is treated with phosphorus tribromide?

REVIEW EXERCISES | Q 10.23 (iv) | Page 585

What happens when bromoethane is treated with alcoholic silver cyanide?

REVIEW EXERCISES | Q 10.23 (iv) | Page 585

What happens when 1-chloropropane is heated at 573 K?

REVIEW EXERCISES | Q 10.24 | Page 585

Which isomer of C4H9Cl will have the lowest boiling point and why?

REVIEW EXERCISES | Q 10.25 (i) | Page 585

Complete the following reaction.

\[\ce{CH3 - CH = CH2 + HBr ->[Peroxide]}\]

REVIEW EXERCISES | Q 10.25 (ii) | Page 585

Complete the following reaction.

\[\ce{CH3CH2CH2Cl ->[Alcoholic KOH][Δ]}\]

REVIEW EXERCISES | Q 10.25 (iii) | Page 585

Complete the following reaction.

\[\ce{C2H5Cl + Na ->}\]

REVIEW EXERCISES | Q 10.25 (iv) | Page 585

Complete the following reaction.

\[\ce{CH3Br + KCN -> A ->[H2O/H^+][] B}\]

REVIEW EXERCISES | Q 10.25 (iv) | Page 585

Complete the following reaction.

\[\ce{(CH3)2CHBr  + (alc.)KOH ->[Δ][]}\]

REVIEW EXERCISES | Q 10.26 | Page 585

Which is most reactive towards SN1 reaction?

CH3CH2Br, (CH3)2CHBr, (CH3)3C.Br

REVIEW EXERCISES | Q 10.27 | Page 585

Which of the following is most reactive for its reaction with HCI?

CH3CH2CH2CH2OH,  \[\begin{array}{cc}
\phantom{.........}\ce{OH}\\
\phantom{........}|\\
\ce{CH3 - CH2 - CH - CH3}
\end{array}\], (CH3)2CH-CH2OH, (CH3)3C.OH

REVIEW EXERCISES | Q 10.28 (i) | Page 585

Which one among the following pairs does have higher boiling point?

1-bromopropane or 1-iodopropane

REVIEW EXERCISES | Q 10.28 (ii) | Page 585

Which one among the following pairs does have higher boiling point?

1-bromopropane or 1-bromobutane

REVIEW EXERCISES | Q 10.28 (iii) | Page 585

Which one among the following pairs does have higher boiling point?

isobutyl bromide or t-butyl bromidec

REVIEW EXERCISES | Q 10.29 (i) | Page 585

Identify the compound X, Y and Z in the following sequence of reaction.

\[\ce{C2H5Br ->[alc. KOH][]X->[Br2][]Y->[alc. KOH][]Z}\]

REVIEW EXERCISES | Q 10.29 (ii) | Page 585

Identify the compound X, Y and Z in the following sequence of reaction.

\[\ce{CH2 = CH2 ->[HBr][]X->[KCN][]Y->[H2O][Dil.acid]Z}\]

REVIEW EXERCISES | Q 10.29 (iii) | Page 585

Identify the compound X, Y and Z in the following sequence of reaction.

\[\ce{CH3OH ->[HBr][]X->[H2/Ni][525]Y->[Cl2][hv]Z}\]

REVIEW EXERCISES | Q 10.30 | Page 585

What is Saytzeff’s rule? Explain with an example.

REVIEW EXERCISES | Q 10.31 (i) | Page 593

What are polyhalogen compounds?

REVIEW EXERCISES | Q 10.31 (ii) | Page 593

Write the structures of three commercially important polyhalogen compounds.

REVIEW EXERCISES | Q 10.32 (i) | Page 593

How will you prepare chloroform from acetone (give equations)?

REVIEW EXERCISES | Q 10.32 (ii) | Page 393

How will you prepare chloroform from ethanol (give equations)?

REVIEW EXERCISES | Q 10.33 | Page 593

How will you prepare chloroform from acetone (give equations)?

REVIEW EXERCISES | Q 10.34 | Page 593

How is iodoform prepared from acetone?

REVIEW EXERCISES | Q 10.35 | Page 593

Show with the help of chemical equations, what happens when chloroform is exposed to sunlight and air for a long time?

REVIEW EXERCISES | Q 10.36 | Page 593

Chloroform is a chlorine compound, but it does not give white precipitate with silver nitrate solution. Give reasons.

REVIEW EXERCISES | Q 10.37 (i) | Page 593

What happens when chloroform is treated with phenol in the presence of alcoholic KOH at 340 K?

REVIEW EXERCISES | Q 10.37 (ii) | Page 593

What happens when chloroform is boiled with aqueous KOH?

REVIEW EXERCISES | Q 10.37 (iii) | Page 593

What happens when chloroform is heated with silver powder?

REVIEW EXERCISES | Q 10.37 (iv) | Page 593

What happens when reaction:

Aniline reacts with chloroform in the presence of alcoholic potassium hydroxide

REVIEW EXERCISES | Q 10.38 | Page 593

What precautions are necessary to be taken for the safe storage of chloroform?

REVIEW EXERCISES | Q 10.39 (i) | Page 593

How would you distinguish the following pair of compounds?

Methanol and Ethanol

REVIEW EXERCISES | Q 10.39 (ii) | Page 593

How would you distinguish the following pair of compounds?

n-propyl alcohol and iso-propyl alcohol

REVIEW EXERCISES | Q 10.40 (i) | Page 593

What happens when iodoform is heated with caustic potash?

REVIEW EXERCISES | Q 10.40 (ii) | Page 593

What happens when chloroform is treated with acetone?

REVIEW EXERCISES | Q 10.40 (iii) | Page 593

What happens when carbon tetrachloride is heated with dry hydrogen fluoride in the presence of antimony pentachloride?

REVIEW EXERCISES | Q 10.41 (i) | Page 593

Explain the following:

The use of carbon tetrachloride as fire extinguisher is not very safe.

REVIEW EXERCISES | Q 10.41 (ii) | Page 593

Explain the following:

Chloroform is not used as an anaesthetic nowadays.

REVIEW EXERCISES | Q 10.41 (iii) | Page 593

Explain the following:

A small amount of ethanol should be added to chloroform before its packaging.

REVIEW EXERCISES | Q 10.42 (i) | Page 593

Complete the following reaction:

\[\ce{C2H5NH2 + CHCl3 + KOH (alc{.}) ->[Warm]}\]

REVIEW EXERCISES | Q 10.42 (ii) | Page 593

Complete the following reaction.

\[\ce{CHCl3 + HNO3 ->[\Delta]}\]

REVIEW EXERCISES | Q 10.42 (iii) | Page 593

Complete the following reaction:

\[\ce{CHI3 + C2H5NH2 + KOH(alc.) ->}\]

REVIEW EXERCISES | Q 10.42 (iv) | Page 593

Complete the following reaction:

\[\ce{CHCl3 + Cl2 ->[hv][]}\]

REVIEW EXERCISES | Q 10.42 (v) | Page 593

Complete the following reaction:

\[\ce{CHCl3 + Ag ->[Heat][]}\]

REVIEW EXERCISES | Q 10.43 (i) | Page 593

How would you convert iodoform to acetylene?

REVIEW EXERCISES | Q 10.43 (ii) | Page 593

How would you convert carbon tetrachloride to chloroform?

REVIEW EXERCISES | Q 10.43 (iii) | Page 593

How will you prepare chloroform from acetone (give equations)?

REVIEW EXERCISES | Q 10.43 (iv) | Page 593

How would you convert chloroform to diethyl carbonate?

REVIEW EXERCISES | Q 10.43 (v) | Page 593

How would you convert propanone to iodoform?

REVIEW EXERCISES | Q 10.44 (i) | Page 593

What is the iodoform test?

REVIEW EXERCISES | Q 10.44 (ii) | Page 593

How is the iodoform test carried out?

REVIEW EXERCISES | Q 10.44 (iii) | Page 593

What is iodoform test significance in organic chemistry?

REVIEW EXERCISES | Q 10.45 | Page 593

Write the reactions involved in the preparation of iodoform from propan-2-ol.

REVIEW EXERCISES | Q 10.46 (i) | Page 593

What are Freons?

REVIEW EXERCISES | Q 10.46 (ii) | Page 593

How is feron prepared?

REVIEW EXERCISES | Q 10.46 (iii) | Page 593
What are the limitations of freon use as a refrigerant?
REVIEW EXERCISES | Q 10.47 (i) | Page 593

Starting from chloroform how would you prepare acetylene?

REVIEW EXERCISES | Q 10.47 (ii) | Page 593

Starting from chloroform how would you prepare propyne?

REVIEW EXERCISES | Q 10.47 (iii) | Page 593

Starting from chloroform how would you prepare chloropicrin?

REVIEW EXERCISES | Q 10.48 | Page 593

A sweet smelling organic compound (A) is slowly oxidised by air in the presence of light to a highly poisonous gas. On warming with silver powder, it forms a gaseous substance (B) which is also formed by the action of calcium carbide on water. Identify (A) and (B), and write the chemical equations of the reactions involved.

REVIEW EXERCISES | Q 10.49 (i) | Page 593

How is pure chloroform prepared?

REVIEW EXERCISES | Q 10.49 (ii) | Page 593

How is pure chloroform stored?

REVIEW EXERCISES | Q 10.50 (i) | Page 593

How is ethyl bromide prepared in the laboratory?

REVIEW EXERCISES | Q 10.50 (ii) | Page 593

Describe ethyl bromide important synthetic applications.

REVIEW EXERCISES | Q 10.51 (i) | Page 603

Write the IUPAC name of the following compound.

REVIEW EXERCISES | Q 10.51 (ii) | Page 603

Write the IUPAC name of the following compound.

REVIEW EXERCISES | Q 10.51 (iii) | Page 603

Write the IUPAC name of the following compound.

REVIEW EXERCISES | Q 10.51 (iv) | Page 603

Write the IUPAC name of the following compound. 

REVIEW EXERCISES | Q 10.51 (v) | Page 603

Write the IUPAC name of the following compound.

REVIEW EXERCISES | Q 10.51 (vi) | Page 603

Write the IUPAC name of the following compound.

REVIEW EXERCISES | Q 10.52 (i) | Page 603

Write the structural formula and give the IUPAC name of the following: 

o-bromotoluene

REVIEW EXERCISES | Q 10.52 (ii) | Page 603

Write the structural formula and give the IUPAC name of the following:

Benzyl chloride

REVIEW EXERCISES | Q 10.52 (iii) | Page 603

Write the structural formula and give the IUPAC name of the following:

Benzotrichloride

REVIEW EXERCISES | Q 10.52 (iv) | Page 603

Write the structural formula and give the IUPAC name of the following:

o-chlorobenzene sulphonic acid

REVIEW EXERCISES | Q 10.53 | Page 603

Describe a method for the preparation of haloarenes from diazonium salts.

REVIEW EXERCISES | Q 10.54 | Page 603

Describe a method for the preparation of haloarenes from benzene.

REVIEW EXERCISES | Q 10.55 | Page 603

How many isomers are possible for the compound C7H7Cl? Write their structures and give their IUPAC names.

REVIEW EXERCISES | Q 10.56 | Page 603

Why do alkyl halides (haloalkanes) undergo hydrolysis more easily than aryl halides (haloarenes)?

REVIEW EXERCISES | Q 10.57 | Page 603

Account for the fact that halogen in chlorobenzene is less reactive than in methyl chloride.

REVIEW EXERCISES | Q 10.58 | Page 603

Why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides?

REVIEW EXERCISES | Q 10.59 | Page 603

Arrange the following compounds in the order of increasing reactivity towards nucleophilic substitution reactions:

  1. Chlorobenzene
  2. 2, 4-dinitrochlorobenzene
  3. 4-nitrochlorobenzene
  4. 2, 4, 6-trinitrochlorobenzene
REVIEW EXERCISES | Q 10.60 (i) | Page 603

Explain the following briefly.

In chlorobenzene, the electrophilic substitution takes place at o- and p-positions.

REVIEW EXERCISES | Q 10.60 (ii) | Page 603

Explain the following briefly. 

Allyl chloride is hydrolysed readily as compared to 1-chloropropane.

REVIEW EXERCISES | Q 10.60 (iii) | Page 603

Explain the following briefly.

Vinyl chloride is less reactive than ethyl chloride.

REVIEW EXERCISES | Q 10.60 (iv) | Page 603

Explain the following briefly.

The electrophilic substitution reactions in haloarenes occur slowly as compared to those in benzene.

REVIEW EXERCISES | Q 10.61 (i) | Page 603

What happens when chlorobenzene is treated with ethyl chloride in the presence of sodium in dry ether?

REVIEW EXERCISES | Q 10.61 (ii) | Page 603

What happens when chlorobenzene is heated with aqueous ammonia in the presence of cuprous oxide at 475 K and under high pressure?

REVIEW EXERCISES | Q 10.61 (iii) | Page 603

What happens when iodobenzene is heated with copper powder in a sealed tube?

REVIEW EXERCISES | Q 10.61 (iv) | Page 603

What happens when benzene diazonium chloride is treated with an aqueous solution of potassium iodide?

REVIEW EXERCISES | Q 10.61 (v) | Page 603

What happens when chlorine is passed in boiling toluene in the presence of sunlight?

REVIEW EXERCISES | Q 10.62 (i) | Page 604

Write the resonance structures of chlorobenzene and explain.

REVIEW EXERCISES | Q 10.62 (ii) | Page 604

Why is chlorobenzene less reactive than chloroethane towards nucleophiles?

REVIEW EXERCISES | Q 10.62 (iii) | Page 604

Explain whether chloroethene should be more or less reactive than chloroethane towards nucleophiles.

REVIEW EXERCISES | Q 10.63 (i) | Page 604

Account for the following: 

Haloalkanes are more reactive than haloarenes.

REVIEW EXERCISES | Q 10.63 (ii) | Page 604

Account for the following:

Haloalkanes undergo nucleophilic substitution, whereas haloarenes undergo electrophilic substitution.

REVIEW EXERCISES | Q 10.64 (i) | Page 604

Give the structure and name of the product in the following reaction.

Chlorination of toluene in the presence of anhydrous AlCl3.

REVIEW EXERCISES | Q 10.64 (ii) | Page 604

Give the structure and name of the product in the following reaction.

Sulphonation of chlorobenzene.

REVIEW EXERCISES | Q 10.64 (iii) | Page 604

Give the structure and name of the product in the following reaction.

Nitration of bromobenzene.

REVIEW EXERCISES | Q 10.64 (iv) | Page 604

Give the structure and name of the product in the following reaction.

Friedel-Crafts methylation of chlorobenzene.

REVIEW EXERCISES | Q 10.65 | Page 604

How will you distinguish C2H5Br from C6H4Br?

REVIEW EXERCISES | Q 10.66 (i) | Page 604

What is Sandmeyer’s reaction?

REVIEW EXERCISES | Q 10.66 (ii) | Page 604

Illustrate with a suitable example of Sandmeyer’s reaction?

REVIEW EXERCISES | Q 10.67 (i) | Page 604

How is the following conversion carried out?

Chlorobenzene to benzoic acid

REVIEW EXERCISES | Q 10.67 (ii) | Page 604

How is the following conversion carried out?

Chlorobenzene to benzene

REVIEW EXERCISES | Q 10.67 (iii) | Page 604

How the following conversion can be carried out?

Aniline to chlorobenzene

REVIEW EXERCISES | Q 10.67 (iv) | Page 604

How can the following conversion be brought about?

Chlorobenzene to phenol

REVIEW EXERCISES | Q 10.67 (v) | Page 604

How is the following conversion carried out?

Chlorobenzene to benzylamine

REVIEW EXERCISES | Q 10.67 (vi) | Page 604

How is the following conversion carried out?

Chlorobenzene to aniline

REVIEW EXERCISES | Q 10.68 (i) | Page 604

Complete the following chemical equation.

\[\ce{C6H5N2Cl + HCl ->[CuCl][]?}\]

REVIEW EXERCISES | Q 10.68 (ii) | Page 604

Complete the following chemical equation. 

\[\ce{C6H5N2Cl + Conc{.}HNO3 ->[H2SO4(Conc{.})][]?}\]

REVIEW EXERCISES | Q 10.68 (iii) | Page 604

Complete the following chemical equation.

REVIEW EXERCISES | Q 10.68 (iv) | Page 604

Complete the following chemical equation. 

\[\begin{array}{cc}
\ce{\phantom{.....}O}\\
\phantom{.....}||\\
\ce{C6H5Cl + CH3-C-Cl ->[AlCl3][]?}
\end{array}\]

REVIEW EXERCISES | Q 10.68 (v) | Page 604

Complete the following chemical equation.

\[\ce{C6H5Br + 2Na + CH3Br ->[dry ether][]?}\]

REVIEW EXERCISES | Q 10.68 (vi) | Page 604

Complete the following chemical equation. 

\[\ce{2C6H5Cl + 2Na ->[Dry ether][]?}\]

REVIEW EXERCISES | Q 10.69 (i) | Page 604

Identify X, Y and Z in the following sequence of reactions:

\[\ce{C6H6 ->[Cl2,FeCl3][]X->[NaOH_{(aq)}][263K, 300atm] Y ->[Dil{.}HCl][]Z}\]

REVIEW EXERCISES | Q 10.69 (ii) | Page 604

Identify X, Y and Z in the following sequence of reactions:

\[\ce{C5H5NH2 ->[Na NO2, HCl][273K]X->[CuBr, HBr][]Y->[CH3Cl][AlCl3]Z}\]

REVIEW EXERCISES | Q 10.69 (iii) | Page 604

Identify X, Y and Z in the following sequence of reactions:

\[\ce{C6H5Cl->[CuCl, HCl][]X->[CuCn][Pyridine, Δ]Y->[Dil{.}HCl][]Z}\]

REVIEW EXERCISES | Q 10.70 (i) | Page 604

How will you distinguish between the following pair of compounds? 

Chlorobenzene and benzyl chloride

REVIEW EXERCISES | Q 10.70 (ii) | Page 604

How will you distinguish between the following pair of compounds?

o-chlorotoluene and benzyl chloride

REVIEW EXERCISES | Q 10.70 (iii) | Page 604

How will you distinguish between the following pair of compounds?

Bromobenzene and benzyl bromide

REVIEW EXERCISES | Q 10.70 (iv) | Page 604

How will you distinguish C2H5Br from C6H4Br?

REVIEW EXERCISES | Q 10.71 (i) | Page 604

Give one example of the following reaction: 

Wurtz Reaction

REVIEW EXERCISES | Q 10.71 (ii) | Page 604

Give one example of the following reaction:

Wurtz-Fittig Reaction

VERY SHORT ANSWER TYPE QUESTIONS [Pages 608 - 609]

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC 10 Haloalkanes and Haloarenes VERY SHORT ANSWER TYPE QUESTIONS [Pages 608 - 609]

VERY SHORT ANSWER TYPE QUESTIONS | Q 1. (i) | Page 608

Give one example of a 1° haloalkane.

VERY SHORT ANSWER TYPE QUESTIONS | Q 1. (ii) | Page 608

Give one example of a 2° haloalkane.

VERY SHORT ANSWER TYPE QUESTIONS | Q 1. (iii) | Page 608

Give an example of a 3° alkyl halide.

VERY SHORT ANSWER TYPE QUESTIONS | Q 2. | Page 608

Which of the following are nuclear halogen derivatives?

VERY SHORT ANSWER TYPE QUESTIONS | Q 3. (i) | Page 608

Give one example of a primary alcohol.

VERY SHORT ANSWER TYPE QUESTIONS | Q 3. (ii) | Page 608

Give one example of a secondary alcohol.

VERY SHORT ANSWER TYPE QUESTIONS | Q 3. (iii) | Page 608

Give one example of tertiary alcohol.

VERY SHORT ANSWER TYPE QUESTIONS | Q 4. (a) | Page 608

Write the IUPAC name of the following compound.

\[\begin{array}{cc}
\ce{Br\phantom{...}Br\phantom{.......}}\\
|\phantom{.....}|\phantom{........}\\
\ce{CH3-CH-CH-COOC2H5}
\end{array}\]

VERY SHORT ANSWER TYPE QUESTIONS | Q 4. (b) | Page 608

Write the IUPAC name of the following compound.

(CH3)3C.CH2.CH2Cl

VERY SHORT ANSWER TYPE QUESTIONS | Q 4. (c) | Page 608

Write the IUPAC name of the following compound. 

\[\begin{array}{cc}
\ce{\phantom{...................}CH3}\\
\phantom{.................}|\\
\ce{CH3-CH2-CH-CH-C-CH3}\\
\phantom{.......}|\phantom{.....}|\phantom{.....}|\phantom{.}\\
\ce{\phantom{.........}Br\phantom{...}CH3\phantom{..}CH3\phantom{.}}\\
\end{array}\]

VERY SHORT ANSWER TYPE QUESTIONS | Q 4. (d) | Page 608

Write the IUPAC name of the following compound. 

\[\begin{array}{cc}
\ce{\phantom{...........}CH3}\\
\phantom{.........}|\\
\ce{CH3-CH2-CH-C-CH2Cl}\\
\phantom{....}|\phantom{.....}|\\
\ce{\phantom{......}Br\phantom{...}CH3}
\end{array}\]

VERY SHORT ANSWER TYPE QUESTIONS | Q 5. (a) | Page 608

Write the IUPAC name of the following:

n-butyl bromide

VERY SHORT ANSWER TYPE QUESTIONS | Q 5. (b) | Page 608

Write the IUPAC name of the following:

tert-butyl bromide

VERY SHORT ANSWER TYPE QUESTIONS | Q 5. (c) | Page 608

Write the IUPAC name of the following:

sec-pentyl bromide

VERY SHORT ANSWER TYPE QUESTIONS | Q 6. | Page 608

Write the position isomers of C4H9Br.

VERY SHORT ANSWER TYPE QUESTIONS | Q 7. | Page 608

What is the order of the ease of replacement of different types of H atoms by halogen atoms in alkanes?

VERY SHORT ANSWER TYPE QUESTIONS | Q 8. | Page 608

Among PCl5 and SOCl5, which reagent is preferred for the preparation of chloroalkanes from alcohols?

VERY SHORT ANSWER TYPE QUESTIONS | Q 9. | Page 608

Arrange 1-bromobutane, 1-bromo-2-methylpropane and 2-bromo-2-methylpropane in the order of their increasing boiling points.

VERY SHORT ANSWER TYPE QUESTIONS | Q 10. | Page 608

Inspite of being polar, why are haloalkanes insoluble in water?

VERY SHORT ANSWER TYPE QUESTIONS | Q 11. | Page 608

Why do alkyl iodides become brown or violet on standing?

VERY SHORT ANSWER TYPE QUESTIONS | Q 12. | Page 608

Arrange 1°, 2° and 3° haloalkanes in the decreasing order of their reactivity towards nucleophilic substitution reactions.

VERY SHORT ANSWER TYPE QUESTIONS | Q 13. (a) | Page 608

Name the reagent used to convert a haloalkane into an alcohol.

VERY SHORT ANSWER TYPE QUESTIONS | Q 13. (b) | Page 608

Name the reagent used to convert a haloalkane into an ether.

VERY SHORT ANSWER TYPE QUESTIONS | Q 13. (c) | Page 608

Name the reagent used to convert a haloalkane into an amine.

VERY SHORT ANSWER TYPE QUESTIONS | Q 13. (d) | Page 608

Name the reagent used to convert a haloalkane into an alkene.

VERY SHORT ANSWER TYPE QUESTIONS | Q 14. | Page 608

Arrange primary, secondary and tertiary haloalkanes in the decreasing order of the ease of dehydrohalogenation.

VERY SHORT ANSWER TYPE QUESTIONS | Q 15. | Page 608

What happens when an alkyl iodide is heated with hydroiodic acid in the presence of red phosphorus?

VERY SHORT ANSWER TYPE QUESTIONS | Q 16. (i) | Page 608

How will you convert ethyl bromide into ethyl alcohol?

VERY SHORT ANSWER TYPE QUESTIONS | Q 16. (ii) | Page 608

How will you convert methyl bromide (bromomethane) to acetic acid (ethanoic acid)?

VERY SHORT ANSWER TYPE QUESTIONS | Q 16. (iii) | Page 608

How will you convert ethyl bromide into diethyl ether?

VERY SHORT ANSWER TYPE QUESTIONS | Q 17. (i) | Page 608

What are arenes?

VERY SHORT ANSWER TYPE QUESTIONS | Q 17. (ii) | Page 608

Give two examples of arenes.

VERY SHORT ANSWER TYPE QUESTIONS | Q 18. | Page 608

Sort out o-, p- and m-directing groups among the following:

-OH, -NO2, -CONH2, -CN, -Cl, -CH3, -COOH, -OCH3

VERY SHORT ANSWER TYPE QUESTIONS | Q 19 | Page 608

p-Dichlorobenzene has higher m.p. and lower solubility than those of o- and m-isomers. Discuss.

VERY SHORT ANSWER TYPE QUESTIONS | Q 20. (a) | Page 609

How can the following conversion be brought about?

Chlorobenzene to phenol

VERY SHORT ANSWER TYPE QUESTIONS | Q 20. (b) | Page 609

How is the following conversion carried out?

Chlorobenzene to aniline

VERY SHORT ANSWER TYPE QUESTIONS | Q 20. (c) | Page 609

How is the following conversion carried out?

Chlorobenzene to benzoic acid

VERY SHORT ANSWER TYPE QUESTIONS | Q 21. | Page 609

How is chlorobenzene converted into diphenyl/biphenyl?

VERY SHORT ANSWER TYPE QUESTIONS | Q 22. | Page 609

How is chlorobenzene converted into diphenyl/biphenyl?

VERY SHORT ANSWER TYPE QUESTIONS | Q 23. | Page 609

How would you obtain pure chloroform in the laboratory?

VERY SHORT ANSWER TYPE QUESTIONS | Q 24. | Page 609

Why is chloroform stored in brown bottles?

VERY SHORT ANSWER TYPE QUESTIONS | Q 25. (a) | Page 609

What happens when chloroform is subjected to nitration?

VERY SHORT ANSWER TYPE QUESTIONS | Q 25. (b) | Page 609

What happens when chloroform is subjected to hydrolysis?

VERY SHORT ANSWER TYPE QUESTIONS | Q 25. (c) | Page 609

What happens when chloroform is subjected to dehalogenation?

VERY SHORT ANSWER TYPE QUESTIONS | Q 26. (a) | Page 609

Which of the following pair of compounds can be distinguished by iodoform test? 

Methanol and ethanol

VERY SHORT ANSWER TYPE QUESTIONS | Q 26. (b) | Page 609

Which of the following pair of compounds can be distinguished by iodoform test?

Methanol and butan-1-ol

VERY SHORT ANSWER TYPE QUESTIONS | Q 26. (c) | Page 609

Which of the following pair of compounds can be distinguished by iodoform test? 

Butan-1-ol and butan-2-ol

VERY SHORT ANSWER TYPE QUESTIONS | Q 27. (i) | Page 609

What is pyrene?

VERY SHORT ANSWER TYPE QUESTIONS | Q 27. (ii) | Page 609

What is pyrene used for?

VERY SHORT ANSWER TYPE QUESTIONS | Q 28. (i) (a) | Page 609

Draw structure of DDT.

VERY SHORT ANSWER TYPE QUESTIONS | Q 28. (i) (b) | Page 609

Write the IUPAC name of the following:

DDT

VERY SHORT ANSWER TYPE QUESTIONS | Q 28. (ii) (a) | Page 609

Write the structure of the following:

Gammaxene

VERY SHORT ANSWER TYPE QUESTIONS | Q 28. (ii) (b) | Page 609

Write the IUPAC name of the following: 

Gammaxene

VERY SHORT ANSWER TYPE QUESTIONS | Q 29. (a) | Page 609

What happens when (write chemical equations only) silver acetate is heated with bromine in the presence of CCl4?

VERY SHORT ANSWER TYPE QUESTIONS | Q 29. (b) | Page 609

What happens when (write chemical equations only) n-propyl bromide is treated with sodium ethoxide?

VERY SHORT ANSWER TYPE QUESTIONS | Q 29. (c) | Page 609

What happens when (write chemical equations only) iso-propyl chloride is treated with silver nitrite?

VERY SHORT ANSWER TYPE QUESTIONS | Q 29. (d) | Page 609

What happens when (write chemical equations only) benzene is heated with iodine in the presence of iodic acid?

VERY SHORT ANSWER TYPE QUESTIONS | Q 29. (e) | Page 609

What happens when (write chemical equations only) benzenediazonium chloride is heated with hydrobromic acid in the presence of cuprous bromide?

VERY SHORT ANSWER TYPE QUESTIONS | Q 30. | Page 609

Complete the following chemical equation

\[\ce{CHCl3 + C2H5NH2 + 3KOH -> {.....}}\]

VERY SHORT ANSWER TYPE QUESTIONS | Q 31. (i) | Page 609

How the following conversion can be carried out?

1-Bromopropane to 2-bromopropane

VERY SHORT ANSWER TYPE QUESTIONS | Q 31. (ii) | Page 609

How would you convert propanone to iodoform?

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (a) | Page 609

Give the IUPAC name of the following compound:

CH3CH(Cl)CH(Br)CH3

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (b) | Page 609

Give the IUPAC name of the following compound:

CHF2CBrClF

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (c) | Page 609

Give the IUPAC name of the following compound:

ClCH2C≡CCH2Br

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (d) | Page 609

Give the IUPAC name of the following compound:

(CCl3)3CCl

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (e) | Page 609

Give the IUPAC name of the following compound:

CH3C(p-ClC6H4)2CH(Br)CH3

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (f) | Page 609

Give the IUPAC name of the following compound:

(CH3)3CCH=CClC6H4I-p

VERY SHORT ANSWER TYPE QUESTIONS | Q 32. (g) | Page 609

Give the IUPAC name of the following compound:

CH3CHCl(CH2)2CCl2C2H5

VERY SHORT ANSWER TYPE QUESTIONS | Q 33. (a) | Page 609

Which compound in the following pair will react faster in SN2 reaction with OH?

CH3Br or CH3I

VERY SHORT ANSWER TYPE QUESTIONS | Q 33. (b) | Page 609

Which compound in the following pair will react faster in SN2 reaction with OH?

(CH3)3CCl or CH3Cl

VERY SHORT ANSWER TYPE QUESTIONS | Q 33. (c) | Page 609

Which compound in the following pair will react faster in SN2 reaction with OH?

CH2=CHBr or CH2=CH-CH2Br

VERY SHORT ANSWER TYPE QUESTIONS | Q 34. (a) | Page 609

Arrange the following compounds in increasing order of SN1 reactivity.

ClCH2CH = CHCH2CH3, CH3C(Cl) = CHCH2CH3, CH3CH = CHCH2CH2Cl.

VERY SHORT ANSWER TYPE QUESTIONS | Q 34. (b) | Page 609

Arrange the following compounds in increasing order of SN1 reactivity.

CH3CH2Br, CH2 = CHCH(Br)CH3, CH2 = CHBr, CH3CH(Br)CH3.

VERY SHORT ANSWER TYPE QUESTIONS | Q 34. (c) | Page 609

Arrange the following compounds in increasing order of SN1 reactivity.

(CH3)CCl, C6H5C(CH3)2Cl, (CH3)2CHCl, CH3CH2CH2Cl.

VERY SHORT ANSWER TYPE QUESTIONS | Q 35. (a) | Page 609

Predict the order of reactivity of the following compounds in dehydrohalogenation:

CH3CH2CH2CH2Cl, (CH3)2CHCH2Cl, (CH3)2CH-CH2Br, CH3CH(Br)CH2CH3, (CH3)3C-Br

VERY SHORT ANSWER TYPE QUESTIONS | Q 35. (b) | Page 609

Predict the order of reactivity of the following compounds in dehydrohalogenation:

CH3CH(Br)CH3, CH3CH2CH2Br, (CH3)2CH-CH2Br, (CH3)3C-CH2Br

VERY SHORT ANSWER TYPE QUESTIONS | Q 36. pen | Page 609

Which of the following compounds will give positive iodoform test? 

Butan-1-ol, Butan-2-ol, Tert-butyl alcohol, Ethanol, Propanol, Propanone, Butan-2-one, Pentan-3-one, Cyclohexanone, 1-methylcyclohexanol, 1-phenylethanol, 2- phenylethanol?

SHORT ANSWER TYPE QUESTIONS [Pages 611 - 612]

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC 10 Haloalkanes and Haloarenes SHORT ANSWER TYPE QUESTIONS [Pages 611 - 612]

SHORT ANSWER TYPE QUESTIONS | Q 1. | Page 611

How are haloalkanes classified?

SHORT ANSWER TYPE QUESTIONS | Q 2. | Page 611

Among aromatic halogen compounds, how are nuclear derivatives different from side chain derivatives? Explain with examples.

SHORT ANSWER TYPE QUESTIONS | Q 3. (a) | Page 611

How is bromoethane prepared from ethene?

SHORT ANSWER TYPE QUESTIONS | Q 3. (b) | Page 611

How is bromoethane prepared from ethanol?

SHORT ANSWER TYPE QUESTIONS | Q 4. | Page 611

How would you obtain bromoethane from silver propanoate?

SHORT ANSWER TYPE QUESTIONS | Q 4. (a) | Page 611

Explain with an example of the following reaction:

Finkelstein reaction

SHORT ANSWER TYPE QUESTIONS | Q 4. (b) | Page 611

Explain with an example of the following reaction:

Hunsdiecker reaction

SHORT ANSWER TYPE QUESTIONS | Q 5. | Page 611

Why are the melting points and boiling points of haloalkanes much higher than those of the parent alkanes?

SHORT ANSWER TYPE QUESTIONS | Q 6. | Page 611

Why do the boiling points of isomeric haloalkanes decrease with increase in branching?

SHORT ANSWER TYPE QUESTIONS | Q 7. | Page 611

Explain the following briefly:

Although haloalkanes are polar in character, yet they are insoluble in water.

SHORT ANSWER TYPE QUESTIONS | Q 8. | Page 611

Why are haloalkanes more reactive than haloarenes?

SHORT ANSWER TYPE QUESTIONS | Q 9. | Page 611

Why do 3° alkyl halides undergo substitution by SN1 mechanism, whereas 1° alkyl halides by SN2 mechanism?

SHORT ANSWER TYPE QUESTIONS | Q 10. (a) | Page 611

How will you carry out the following conversion?

2-bromopropane to propan-2-ol

SHORT ANSWER TYPE QUESTIONS | Q 10. (b) | Page 611

How will you carry out the following conversion?

Bromoethane to methoxyethane

SHORT ANSWER TYPE QUESTIONS | Q 10. (c) | Page 611

How will you carry out the following conversion?

Iodomethane to dimethylamine

SHORT ANSWER TYPE QUESTIONS | Q 10. (d) | Page 611

How will you carry out the following conversion?

1-bromobutane to but-1-ene

SHORT ANSWER TYPE QUESTIONS | Q 10. (e) | Page 611

How will you carry out the following conversions?

1-chloropropane to 2-chloropropane

SHORT ANSWER TYPE QUESTIONS | Q 11. (a) | Page 611

What is an ambident group?

SHORT ANSWER TYPE QUESTIONS | Q 11. (b) | Page 611

Why does potassium cyanide give a nitrile while silver cyanide an isonitrile when treated with an alkyl halide?

SHORT ANSWER TYPE QUESTIONS | Q 12. | Page 611

What is Saytzeff’s rule? Explain with an example.

SHORT ANSWER TYPE QUESTIONS | Q 13. (a) | Page 611

What are haloarenes?

SHORT ANSWER TYPE QUESTIONS | Q 13. (b) | Page 611

Give two examples of haloarenes.

SHORT ANSWER TYPE QUESTIONS | Q 14. (a) | Page 611

How will you obtain chlorobenzene from benzene?

SHORT ANSWER TYPE QUESTIONS | Q 14. (b) | Page 611

How will you obtain iodobenzene from benzene?

SHORT ANSWER TYPE QUESTIONS | Q 14. (c) | Page 611

How will you obtain bromobenzene from benzene diazonium chloride?

SHORT ANSWER TYPE QUESTIONS | Q 14. (d) | Page 611

How the following conversion can be carried out?

Aniline to chlorobenzene

SHORT ANSWER TYPE QUESTIONS | Q 15. | Page 611

Discuss the mechanism of nuclear halogenation of benzene and explain the role of halogen carrier.

SHORT ANSWER TYPE QUESTIONS | Q 16. | Page 611

Why do isomeric (o-, m- and p-) dihalobenzenes possess almost similar boiling points?

SHORT ANSWER TYPE QUESTIONS | Q 17. | Page 611

p-Dichlorobenzene has higher m.p. and lower solubility than those of o- and m-isomers. Discuss.

SHORT ANSWER TYPE QUESTIONS | Q 18. | Page 611

Explain the low reactivity of haloarenes as compared to haloalkanes on the basis of resonance.

SHORT ANSWER TYPE QUESTIONS | Q 19. | Page 611

Why is the C-Cl bond length in chlorobenzene shorter as compared to that in chloromethane?

SHORT ANSWER TYPE QUESTIONS | Q 20. | Page 611

Why is the C-Cl bond in chlorobenzene less polar as compared to that in chloromethane?

SHORT ANSWER TYPE QUESTIONS | Q 21. | Page 611

Why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides?

SHORT ANSWER TYPE QUESTIONS | Q 22. (a) | Page 611

How can the following conversion be brought about?

Chlorobenzene to phenol

SHORT ANSWER TYPE QUESTIONS | Q 22. (b) | Page 611

How is the following conversion carried out?

Chlorobenzene to aniline

SHORT ANSWER TYPE QUESTIONS | Q 22. (c) | Page 611

How would you convert chlorobenzene to p-chloroacetophenone?

SHORT ANSWER TYPE QUESTIONS | Q 22. (d) | Page 611

How is chlorobenzene converted into diphenyl/biphenyl?

SHORT ANSWER TYPE QUESTIONS | Q 22. (e) | Page 611

How would you convert chlorobenzene to toluene?

SHORT ANSWER TYPE QUESTIONS | Q 22. (f) | Page 611

How is the following conversion carried out?

Chlorobenzene to benzene

SHORT ANSWER TYPE QUESTIONS | Q 23. | Page 611

Among chlorobenzene and 4-nitrochlorobenzene, which is more reactive towards nucleophilic substitution reactions and why?

SHORT ANSWER TYPE QUESTIONS | Q 24. | Page 611

Why do haloarenes undergo electrophilic substitutions at o- and p-positions?

SHORT ANSWER TYPE QUESTIONS | Q 25. | Page 611

During electrophilic substitution reactions of haloarenes, the p-isomer usually dominates. Explain, why?

SHORT ANSWER TYPE QUESTIONS | Q 26. (a) | Page 611

How will you prepare chloroform from ethanol (give equations)?

SHORT ANSWER TYPE QUESTIONS | Q 26. (b) | Page 611

How would you obtain chloroform from propanone?

SHORT ANSWER TYPE QUESTIONS | Q 27. pen | Page 611

Why is it necessary to take extra precautions for the safe storage of chloroform and what are the precautions?

SHORT ANSWER TYPE QUESTIONS | Q 28. (a) | Page 611

What happens when chloroform is treated with zinc and hydrochloric acid?

SHORT ANSWER TYPE QUESTIONS | Q 28. (b) | Page 611

What happens when chloroform is boiled with aqueous KOH?

SHORT ANSWER TYPE QUESTIONS | Q 28. (c) | Page 611

How would you convert iodoform to acetylene?

SHORT ANSWER TYPE QUESTIONS | Q 28. (d) | Page 611

Write a chemical reaction useful to prepare the following:

Carbon tetrachloride from carbon disulphide.

SHORT ANSWER TYPE QUESTIONS | Q 28. (e) | Page 611

What happens when carbon tetrachloride is treated with steam at high temperatures?

SHORT ANSWER TYPE QUESTIONS | Q 28. (f) | Page 611

What happens when carbon tetrachloride is treated with moist iron filings?

SHORT ANSWER TYPE QUESTIONS | Q 29. (a) | Page 611

What is carbylamine reaction?

SHORT ANSWER TYPE QUESTIONS | Q 29. (b) | Page 611

What is carbylamine reaction significance?

SHORT ANSWER TYPE QUESTIONS | Q 30. | Page 611

How is iodoform prepared from acetone?

SHORT ANSWER TYPE QUESTIONS | Q 31. (a) | Page 611

What is the iodoform test?

SHORT ANSWER TYPE QUESTIONS | Q 31. (b) | Page 611

What type of compounds respond to the iodoform test?

SHORT ANSWER TYPE QUESTIONS | Q 31. (c) | Page 611

Give a simple chemical test to distinguish between the following pair of compounds:

Pentan-2-one and Pentan-3-one

SHORT ANSWER TYPE QUESTIONS | Q 32. (a) | Page 611

What are Freons?

SHORT ANSWER TYPE QUESTIONS | Q 32. (b) | Page 611

How is feron prepared?

SHORT ANSWER TYPE QUESTIONS | Q 32. (c) | Page 611

Discuss uses of freons.

SHORT ANSWER TYPE QUESTIONS | Q 33. (a) | Page 611

What is DDT?

SHORT ANSWER TYPE QUESTIONS | Q 33. (b) | Page 611

Explain the preparation of the following compound.

DDT

SHORT ANSWER TYPE QUESTIONS | Q 34. (a) | Page 611

Write the structure of the following:

Gammaxene

SHORT ANSWER TYPE QUESTIONS | Q 34. (b) | Page 611

Write the preparation of benzene hexachloride.

SHORT ANSWER TYPE QUESTIONS | Q 34. (c) | Page 611

Write the uses of benzene hexachloride.

SHORT ANSWER TYPE QUESTIONS | Q 35. (i) | Page 611

Account for the following: 

Haloalkanes are more reactive than haloarenes.

SHORT ANSWER TYPE QUESTIONS | Q 35. (ii) | Page 611

Account for the following:

Haloalkanes undergo nucleophilic substitution, whereas haloarenes undergo electrophilic substitution.

SHORT ANSWER TYPE QUESTIONS | Q 36. | Page 611

Describe with chemical equation what happens when chloromethane is reacted with toluene in the presence of anhydrous aluminium chloride?

SHORT ANSWER TYPE QUESTIONS | Q 37. (ii) | Page 612

Account for the following:

Haloarenes are insoluble in water but are soluble in benzene.

SHORT ANSWER TYPE QUESTIONS | Q 37. (ii) | Page 612

Account for the following: 

Haloalkanes are more reactive than haloarenes.

SHORT ANSWER TYPE QUESTIONS | Q 37. (iii) | Page 612

Account for the following:

Haloalkanes undergo nucleophilic substitution reactions.

SHORT ANSWER TYPE QUESTIONS | Q 38. (a) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

(CH3)2CHCH(Cl)CH3

SHORT ANSWER TYPE QUESTIONS | Q 38. (b) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3CH2CH(CH3)CH(C2H5)Cl

SHORT ANSWER TYPE QUESTIONS | Q 38. (c) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3CH2C(CH3)2CH2I

SHORT ANSWER TYPE QUESTIONS | Q 38. (d) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

(CH3)3CCH2CH(Br)C6H5

SHORT ANSWER TYPE QUESTIONS | Q 38. (e) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3CH(CH3)CH(Br)CH3

SHORT ANSWER TYPE QUESTIONS | Q 38. (f) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3C(Cl)(C2H5)CH2CH3

SHORT ANSWER TYPE QUESTIONS | Q 38. (g) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3C(C2H5)2CH2Br

SHORT ANSWER TYPE QUESTIONS | Q 38. (h) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3CH = C(Cl)CH2CH(CH3)2

SHORT ANSWER TYPE QUESTIONS | Q 38. (i) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3CH = CHC(Br)(CH3)2

SHORT ANSWER TYPE QUESTIONS | Q 38. (j) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

p-ClC6H4CH2CH(CH3)2

SHORT ANSWER TYPE QUESTIONS | Q 38. (k) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

m-ClCH2C6H4CH2C(CH3)3

SHORT ANSWER TYPE QUESTIONS | Q 38. (l) | Page 612

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:

o-Br-C6H4CH(CH3)CH2CH3

SHORT ANSWER TYPE QUESTIONS | Q 39. (a) | Page 612

Write the structure of the following compound:

2-Chloro-3-methylpentane

SHORT ANSWER TYPE QUESTIONS | Q 39. (b) | Page 612

Write the structure of the following organic halogen compound.

p-Bromochlorobenzene

SHORT ANSWER TYPE QUESTIONS | Q 39. (c) | Page 612

Write the structure of the following compound:

1-Chloro-4-ethylcyclohexane

SHORT ANSWER TYPE QUESTIONS | Q 39. (d) | Page 612

Write the structure of the following organic halogen compound.

2-(2-Chlorophenyl)-1-iodooctane

SHORT ANSWER TYPE QUESTIONS | Q 39. (e) | Page 612

Write the structure of the following organic halogen compound:

Perfluorobenzene

SHORT ANSWER TYPE QUESTIONS | Q 39. (f) | Page 612

Write the structure of the following compound:

4-tert. Butyl-3-iodoheptane

SHORT ANSWER TYPE QUESTIONS | Q 39. (g) | Page 612

Write the structure of the following compound:

1-Bromo-4-sec. butyl-2-methylbenzene

SHORT ANSWER TYPE QUESTIONS | Q 39. (h) | Page 612

Write the structure of the following compound:

1,4-Dibromobut-2-ene

SHORT ANSWER TYPE QUESTIONS | Q 40. | Page 612

A hydrocarbon C5H10 does not react with chlorine in dark but gives a single monochloro compound C5H9Cl in bright sunlight. Identify the hydrocarbon.

SHORT ANSWER TYPE QUESTIONS | Q 41. | Page 612

A hydrocarbon C5H12 gives only one monochlorination product. Identify the hydrocarbon.

SHORT ANSWER TYPE QUESTIONS | Q 42. | Page 612

What are ambident nucleophiles? Explain with an example.

SHORT ANSWER TYPE QUESTIONS | Q 43. (a) | Page 612

Write the equation for the preparation of 1-iodobutane from 1-butanol.

SHORT ANSWER TYPE QUESTIONS | Q 43. (b) | Page 612

Write the equation for the preparation of 1-iodobutane from 1-chlorobutane.

SHORT ANSWER TYPE QUESTIONS | Q 43. (c) | Page 612

Write the equation for the preparation of 1-iodobutane from but-1-ene.

SHORT ANSWER TYPE QUESTIONS | Q 44. (a) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

CH3OC(CH3)2

SHORT ANSWER TYPE QUESTIONS | Q 44. (b) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

CH3C ≡ CCH2CH3

SHORT ANSWER TYPE QUESTIONS | Q 44. (c) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

CH3CH2CH2N(CH3)2

SHORT ANSWER TYPE QUESTIONS | Q 44. (d) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

C6H5 - CH2OCOCH3

SHORT ANSWER TYPE QUESTIONS | Q 44. (e) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

CH3CH2CH2CH2NO2

SHORT ANSWER TYPE QUESTIONS | Q 44. (f) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

CH3CH2CH2CN

SHORT ANSWER TYPE QUESTIONS | Q 44. (g) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

C6H5CH2N+ ≡ C

SHORT ANSWER TYPE QUESTIONS | Q 44. (h) | Page 612

How would you prepare following compound using a nucleophilic substitution reaction? Mention the equations only.

CH3CH2 − O − N = O

SHORT ANSWER TYPE QUESTIONS | Q 45. (a) | Page 612

Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:

1-Bromo-1-methylcyclohexane

SHORT ANSWER TYPE QUESTIONS | Q 45. (b) | Page 612

Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:

Cyclohexylmethylbromide

SHORT ANSWER TYPE QUESTIONS | Q 45. (c) | Page 612

Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:

2-Chloro-2-methylbutane

SHORT ANSWER TYPE QUESTIONS | Q 45. (d) | Page 612

Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene.

3-bromopent-1-ene

SHORT ANSWER TYPE QUESTIONS | Q 45. (e) | Page 612

Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:

2, 2, 3-Trimethyl-3-bromopentane

SHORT ANSWER TYPE QUESTIONS | Q 47. | Page 612

The nucleophilic substitution of primary alkyl chlorides with sodium acetate is catalysed by sodium iodide. Explain why.

SHORT ANSWER TYPE QUESTIONS | Q 48. (a) | Page 612

In the following reaction, a new ring is formed. Use curved arrow notation to explain the formation of the new ring.

1, 4-dibromobutane (0.1 mol) is treated with sodium sulphide (0.1 mol) in aqueous ethanol.

SHORT ANSWER TYPE QUESTIONS | Q 48. (b) | Page 612

In the following reaction, a new ring is formed. Use curved arrow notation to explain the formation of the new ring.

1-chloro-2-(2-hydroxyphenyl) ethane is treated with aqueous sodium hydroxide.

SHORT ANSWER TYPE QUESTIONS | Q 49. | Page 612

Why does p-methoxybenzyl bromide react faster than p-nitrobenzyl bromide with ethanol to form an ether product?

SHORT ANSWER TYPE QUESTIONS | Q 50. | Page 612

Explain the formation of the product in the following reaction:

\[\ce{CH3CH = CHCH2Cl + H2O->CH3CH = CHCH2OH + CH3CH(OH)CH = CH2}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (i) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH2CH2Cl + NaI ->[acetone][heat]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (ii) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (iii) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH(Br)CH2CH3 + NaOH ->[water]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (iv) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH2Br + KCN ->[aq.ethanol]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (v) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{(CH3)3 CBr + H2O ->[Heat][]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (vi) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{(CH3)2CH - CH(Br) CH2CH3->[C2H5ONa][Ethanol/Heat]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (vii) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH2Cl + SbF3->[Heat]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (viii) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{CH2 = CHCH2Br + CH3C ≡ CNa ->[Liq{.} NH3]}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (ix) | Page 612

Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH = C(CH3)2 + HBr ->}\]

SHORT ANSWER TYPE QUESTIONS | Q 51. (x) | Page 612

Write the structure of the major organic product in the following reaction:

SHORT ANSWER TYPE QUESTIONS | Q 51. (xi) | Page 612

Write the structure of the major organic product in the following reaction:

SHORT ANSWER TYPE QUESTIONS | Q 51. (xii) | Page 612

Write the structure of the major organic product in the following reaction:

SHORT ANSWER TYPE QUESTIONS | Q 52. | Page 612

In the following monobromination reaction, the number of possible chiral products is

LONG ANSWER TYPE QUESTIONS [Page 615]

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC 10 Haloalkanes and Haloarenes LONG ANSWER TYPE QUESTIONS [Page 615]

LONG ANSWER TYPE QUESTIONS | Q 1. (i) | Page 615

What are haloalkanes?

LONG ANSWER TYPE QUESTIONS | Q 1. (ii) | Page 615

What are haloarenes?

LONG ANSWER TYPE QUESTIONS | Q 1. (iii) | Page 615

How are haloalkanes classified?

LONG ANSWER TYPE QUESTIONS | Q 1. (iv) | Page 615

How are haloarenes classified? Give suitable examples.

LONG ANSWER TYPE QUESTIONS | Q 2. (a) | Page 615

Write short notes on Markownikoff ’s rule.

LONG ANSWER TYPE QUESTIONS | Q 2. (b) | Page 615

Explain with a suitable example of the peroxide effect.

LONG ANSWER TYPE QUESTIONS | Q 2. (c) | Page 615

Write a short note on the allylic substitution.

LONG ANSWER TYPE QUESTIONS | Q 3. (a) | Page 615

Mention any three methods of preparation of haloalkanes from alcohols.

LONG ANSWER TYPE QUESTIONS | Q 3. (b) | Page 615

What is halide exchange method for the preparation of iodoalkanes?

LONG ANSWER TYPE QUESTIONS | Q 4. (a) | Page 615

Discuss the relative stability of different types of haloalkanes.

LONG ANSWER TYPE QUESTIONS | Q 4. (b) | Page 615

Why do alkyl iodides become brown or violet on standing?

LONG ANSWER TYPE QUESTIONS | Q 5. (a) | Page 615

Why do alkyl halides show nucleophilic substitution reactions?

LONG ANSWER TYPE QUESTIONS | Q 5. (b) | Page 615

Discuss the mechanisms of SN1 and SN2 reactions shown by nucleophilic substitution reactions.

LONG ANSWER TYPE QUESTIONS | Q 6. (a) | Page 615

Explain why do haloalkanes give alkyl cyanides when treated with KCN but give alkyl isocyanides with silver cyanide?

LONG ANSWER TYPE QUESTIONS | Q 6. (b) | Page 615

Explain why:

Alkyl halides form nitroalkanes on treatment with silver nitrite but form alkyl nitrites on treatment with potassium nitrite.

LONG ANSWER TYPE QUESTIONS | Q 7. (a) | Page 615

What is Saytzeff’s rule? Explain with an example.

LONG ANSWER TYPE QUESTIONS | Q 7. (b) | Page 615

On the basis of Saytzeff’s rule, explain the ease of dehydrohalogenation of different types of haloalkanes.

LONG ANSWER TYPE QUESTIONS | Q 8. (a) | Page 615

Discuss some important methods of preparation of haloarenes.

LONG ANSWER TYPE QUESTIONS | Q 8. (b) | Page 615

How are aralalkyl halides prepared?

LONG ANSWER TYPE QUESTIONS | Q 9. pen | Page 615

Explain the lower reactivity of haloarenes as compared to haloalkanes on the basis of hybridisation state of carbon of C−X bond.

LONG ANSWER TYPE QUESTIONS | Q 10. | Page 615

What is the effect of substituents on the reactivity of haloarenes? Explain with suitable examples.

LONG ANSWER TYPE QUESTIONS | Q 11. (a) | Page 615

Explain why the electrophilic substitution reactions in haloarenes occur slowly and require more drastic conditions as compared to those in benzene.

LONG ANSWER TYPE QUESTIONS | Q 11. (b) | Page 615

Explain why:

Haloarenes undergo electrophilic substitution at o- and p-positions and not at m-positions.

LONG ANSWER TYPE QUESTIONS | Q 12. (a) | Page 615

Write a short note on Fittig reaction.

LONG ANSWER TYPE QUESTIONS | Q 12. (b) | Page 615

Write a short note on Wurtz-Fittig reaction.

LONG ANSWER TYPE QUESTIONS | Q 12. (c) | Page 615

Write a short note on Ullmann reaction.

LONG ANSWER TYPE QUESTIONS | Q 13. (a) | Page 615

How is iodoform prepared from ethanol? Give balanced equation.

LONG ANSWER TYPE QUESTIONS | Q 13. (b) | Page 615

How is iodoform prepared from acetone?

LONG ANSWER TYPE QUESTIONS | Q 14. (a) | Page 615

What is the iodoform test?

LONG ANSWER TYPE QUESTIONS | Q 14. (b) | Page 615

How is the iodoform test carried out?

LONG ANSWER TYPE QUESTIONS | Q 14. (c) | Page 615

Discuss some important applications of the iodoform test.

LONG ANSWER TYPE QUESTIONS | Q 15. (a) | Page 615

What are polyhalogen compounds?

LONG ANSWER TYPE QUESTIONS | Q 15. (b) (i) | Page 615

Explain the preparation of the following compound.

DDT

LONG ANSWER TYPE QUESTIONS | Q 15. (b) (ii) | Page 615

Write the preparation of benzene hexachloride.

LONG ANSWER TYPE QUESTIONS | Q 15. (b) (iii) | Page 615

How is feron prepared?

LONG ANSWER TYPE QUESTIONS | Q 15. (c) (i) | Page 615

Give the uses of DDT.

LONG ANSWER TYPE QUESTIONS | Q 15. (c) (ii) | Page 615

Write the uses of benzene hexachloride.

LONG ANSWER TYPE QUESTIONS | Q 15. (c) (iii) | Page 615

Discuss uses of freons.

LONG ANSWER TYPE QUESTIONS | Q 16. (i) | Page 615

How will you bring about the following conversion in not more than two steps?

Ethanol to But-1-yne

LONG ANSWER TYPE QUESTIONS | Q 16. (ii) | Page 615

How will you bring about the following conversion in not more than two steps?

Ethene to Bromoethene

LONG ANSWER TYPE QUESTIONS | Q 16. (iii) | Page 615

How will you bring about the following conversion?

Propene to 1-nitropropane

LONG ANSWER TYPE QUESTIONS | Q 16. (iv) | Page 615

How will you bring about the following conversion?

Toluene to benzyl alcohol

LONG ANSWER TYPE QUESTIONS | Q 16. (v) | Page 615

How will you bring about the following conversion?

Propene to propyne

LONG ANSWER TYPE QUESTIONS | Q 16. (vi) | Page 615

How will you bring about the following conversion?

Ethanol to ethyl fluoride

LONG ANSWER TYPE QUESTIONS | Q 16. (vii) | Page 615

How will you bring about the following conversion?

Bromomethane to propanone

LONG ANSWER TYPE QUESTIONS | Q 16. (viii) | Page 615

How will you bring about the following conversion?

But-1-ene to but-2-ene

LONG ANSWER TYPE QUESTIONS | Q 16. (ix) | Page 615

How will you bring about the following conversion?

1-Chlorobutane to n-octane

LONG ANSWER TYPE QUESTIONS | Q 16. (x) | Page 615

How will you bring about the following conversion in not more than two steps?

Bromoethane to cis-Hex-3-ene

LONG ANSWER TYPE QUESTIONS | Q 16. (xi) | Page 615

How will you bring about the following conversion in not more than two steps?

Benzyl alcohol to Phenylethanenitrile

LONG ANSWER TYPE QUESTIONS | Q 16. (xii) | Page 615

How are the following conversions carried out?

benzene to biphenyl

LONG ANSWER TYPE QUESTIONS | Q 16. (xiii) | Page 615

How will you bring about the following conversion in not more than two steps?

Cyclopentene to Cyclopenta-1, 3-diene

LONG ANSWER TYPE QUESTIONS | Q 16. (xiv) | Page 615

How will you bring about the following conversion in not more than two steps?

Aniline to Phenyl isocyanide

LONG ANSWER TYPE QUESTIONS | Q 17. (a) | Page 615

How would you distinguish the following pair of compounds?

Methanol and Ethanol

LONG ANSWER TYPE QUESTIONS | Q 17. (b) | Page 615

How will you distinguish between propan-1-ol and propan-2-ol?

LONG ANSWER TYPE QUESTIONS | Q 17. (c) | Page 615

How will you distinguish between the following pair of compounds? 

Chlorobenzene and benzyl chloride

LONG ANSWER TYPE QUESTIONS | Q 17. (d) | Page 615

How will you distinguish between n-Butylamine and diethylamine?

LONG ANSWER TYPE QUESTIONS | Q 18. (i) | Page 615

Give reasons:

The dipole moment of chlorobenzene is lower than that of cyclohexyl chloride.

LONG ANSWER TYPE QUESTIONS | Q 18. (ii) | Page 615

Explain why alkyl halides, though polar, are immiscible with water?

LONG ANSWER TYPE QUESTIONS | Q 18. (iii) | Page 615

Explain why vinyl chloride is unreactive in nucleophilic substitution reactions.

LONG ANSWER TYPE QUESTIONS | Q 18. (iv) | Page 615

Explain why neopentylbromide undergoes nucleophilic substitution reactions very slowly.

LONG ANSWER TYPE QUESTIONS | Q 18. (v) | Page 615

Explain why 3-bromocyclohexene is more reactive than 4-bromocyclohexene in hydrolysis with aqueous NaOH.

LONG ANSWER TYPE QUESTIONS | Q 18. (vi) | Page 615

Explain why tert-butyl bromide reacts with aqueous sodium hydroxide by SNl mechanism while n-butyl chloride reacts by SN2 mechanism.

LONG ANSWER TYPE QUESTIONS | Q 18. (vii) | Page 615

Explain why Grignard reagents should be prepared under anhydrous conditions?

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS [Pages 616 - 617]

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC 10 Haloalkanes and Haloarenes OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS [Pages 616 - 617]

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 1. | Page 616

The decreasing order of reactivity of alkyl halides is ______.

  • RI > RCl > RBr

  • RBr > RCl > RI

  • RI > RBr > RCl

  • Cl > RBr > Rl

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 2. | Page 616

A sample of chloroform, before using as an anaesthetic, is tested ______.

  • by Fehling solution

  • by ammonical cuprous chloride

  • by ammonical silver nitrate

  • after boiling with alc. KOH, with silver nitrate

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 3. | Page 616

In the reaction \[\ce{Primary amine + CHCl3 + alc{.} KOH -> Products}\], the main product is ______.

  • cyanide

  • isocyanide

  • acid

  • aldehyde

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 4. | Page 617

When propene is heated at 400°C in the presence of chlorine, it gives ______.

  • polyvinyl chloride

  • no reaction

  • 1, 2-dichloropropane

  • allyl chloride

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 5. | Page 617

Which process does not occur during the formation of CHCl3 from C2H5OH and bleaching powder?

  • Hydrolysis

  • Oxidation

  • Elimination

  • Chlorination

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 6. | Page 617

Chlorine reacts with ethanol to give ______.

  • diethyl chloride

  • chloroform

  • acetaldehyde

  • chloral

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 7. | Page 617

The compound with the highest boiling point is ______.

  • CH4

  • CH3OH

  • CH3Cl

  • CH3OCH3

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 8. | Page 617

Haloform reaction does not take place with ______.

  • acetone

  • 2-chloropropane

  • ethanol

  • methanol

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 9. | Page 617

The number of possible isomers for the compound C2H3Cl2Br is ______.

  • 2

  • 3

  • 4

  • 5

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 10. | Page 617

Which of the following is a 2° alkyl halide?

  • CH3CH2Br

  • \[\begin{array}{cc}
    \ce{Cl\phantom{.........}}\\
    |\phantom{.........}\\
    \ce{CH3 - CH - CH2CH3}
    \end{array}\]

  • (CH3)3C.Cl

  • CH3Br

OBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONS | Q 11. | Page 617

The IUPAC name of sec-butyl bromide is ______.

  • 1-bromobutane

  • 2-bromobutane

  • 1-bromo-2-methylpropane

  • 2-bromo-2-methylpropane

FILL IN THE BLANKS TYPE QUESTIONS

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC 10 Haloalkanes and Haloarenes FILL IN THE BLANKS TYPE QUESTIONS

Solutions for 10: Haloalkanes and Haloarenes

REVIEW EXERCISESVERY SHORT ANSWER TYPE QUESTIONSSHORT ANSWER TYPE QUESTIONSLONG ANSWER TYPE QUESTIONSOBJECTIVE (MULTIPLE CHOICE) TYPE QUESTIONSFILL IN THE BLANKS TYPE QUESTIONS
Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC chapter 10 - Haloalkanes and Haloarenes - Shaalaa.com

Nootan solutions for Chemistry Part 1 and 2 [English] Class 12 ISC chapter 10 - Haloalkanes and Haloarenes

Shaalaa.com has the CISCE Mathematics Chemistry Part 1 and 2 [English] Class 12 ISC CISCE solutions in a manner that help students grasp basic concepts better and faster. The detailed, step-by-step solutions will help you understand the concepts better and clarify any confusion. Nootan solutions for Mathematics Chemistry Part 1 and 2 [English] Class 12 ISC CISCE 10 (Haloalkanes and Haloarenes) include all questions with answers and detailed explanations. This will clear students' doubts about questions and improve their application skills while preparing for board exams.

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Concepts covered in Chemistry Part 1 and 2 [English] Class 12 ISC chapter 10 Haloalkanes and Haloarenes are Overview of Haloalkanes and Haloarenes.

Using Nootan Chemistry Part 1 and 2 [English] Class 12 ISC solutions Haloalkanes and Haloarenes exercise by students is an easy way to prepare for the exams, as they involve solutions arranged chapter-wise and also page-wise. The questions involved in Nootan Solutions are essential questions that can be asked in the final exam. Maximum CISCE Chemistry Part 1 and 2 [English] Class 12 ISC students prefer Nootan Textbook Solutions to score more in exams.

Get the free view of Chapter 10, Haloalkanes and Haloarenes Chemistry Part 1 and 2 [English] Class 12 ISC additional questions for Mathematics Chemistry Part 1 and 2 [English] Class 12 ISC CISCE, and you can use Shaalaa.com to keep it handy for your exam preparation.

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