Class : 12 CHAPTER 6 HALOALAKNES AND HALOARENES ASSIGNMENT -2
1. Which one of the two compounds, CH3Br and CH3I will react faster in an SN2 1
reaction withOH-?
2. Write the structure of the following compound 1
i) 1-Bromo-4-sec-butyl-2-methylbenzene ii)4-tert. Butyl-3-iodoheptane
3. Which one of these compounds is more easily hydrolysed by KOH solution and 1
why? CH3CHClCH2CH3 or CH3CH2CH2CH2Cl
4. An alkyl halide with molecular formula C4H9Br is optically active. What is its structure? 1
5. Out of Chlorobenzene and benzyl chloride, which one gets easily hydrolysed by 1
aqueous NaOH and Why?
6. Give a chemical test to distinguish between the following pairs of compounds. 1
i)Benzyl chloride and chlorobenzene. ii)C2H5Br and C6H5Br.
7. Which has higher boiling point and why?1-Chloropentane or 2-methyl-2-chlorobutane 1
8. What are ambidentnucleophiles ? Explain with an example. 1
9. Give reason : p-nitrochlorobenzene undergoes nucleophilic substitution faster 1
than chlorobenzene. Explain giving structures as well.
10. Give the IUPAC name of 2
CH3
i) CH3CH═CH- C- CH3 ii) C6H5CH2CH2Cl
Br
11. Write the structures of the major products in the following reactions: 2
i ) CH3CH=C(CH3) 2 + HBr→
ii) C6H5ONa + C2H5Cl→
12. What are enantiomers? Give the structural formula of the alkane with minimum number 2
of
Carbon atoms capable of showing chirality.
13. An optically active compound having molecular formula C7H15Br reacts with aqueous 2
KOH to give a racemic mixture of products. Write the mechanism involved for this
reaction.
14. Propose mechanism of the reaction taking place when 2-Bromo pentane is 2
heated with alcoholic KOH to form alkenes.
Out of 2-bromopentane, 2-Bromo-2-methylbutane and 1-bromopentane, which
compound is most reactive towards elimination reaction and why?
15. Write the mechanism of the following reaction: 2
16. Give reasons: 1
Allyl chloride is more reactive than n-propyl chloride towards nucleophilic mar
substitution reaction. k
Haloalkanes react with KCN to give alkyl cyanide as main product while AgCN each
they form isocyanide as main product.
Use of DDT was banned in United States in 1973
iv)Benzylic halides show high reactivity towards SN1
reaction.
v)Grignard reagents should be prepared under anhydrous condition.
vi)C6H5CHClCH3 is hydrolysed more easily with KOH than C6H5CH2Cl.
vii)Aryl halides are less reactive towards nucleophilic substitution reaction.
viii)Chloroform is stored in closed dark coloured bottles.
ix) Although Chlorine is an electron withdrawing group, yet it is ortho- para
directing in electrophilic substitution reaction.
x) Sulphuric acid is not used in the reaction of alochols with KI.
xi) The dipole moment of Chlorobenzene is lower than that of cyclohexyl chloride.
xii) Alkyl chloride with aqueous KOH leads to the formation of alcohols but in the
presence of alcoholic KOH alkenes are major products.
xiii) p-Dichlorobenzene has higher melting point and lower solubility than those of
o- and m-isomers.
xiv) Electrophilic reactions in haloarenes occur slowly.
17. Define the following: 1
i) Racemisation ii) Retention iii) Chirality mar
k
each
18. Write the structural formulae of the organic compounds A,B, C and D in the 2
following sequence of reaction.
[Link]
CH3CH(Br)CH2CH3 >A
[Link] H2O, Hg2+, H2SO4
A > B >C >D
19. Write the formula of main product formed in the following chemical reactions 3
Na, dry ether
i ) (CH3)2CHCl >
Δ
ii) CH3Br + AgF >
Dry acetone
i i i) CH3CH2Br + NaI >
20. Answer the following: 3
i) Identify chiral C in CH3CHOHCH2CH3 and CH3CHOHCH3
ii) Which of these will react faster in SN2 displacement
and why? 1-bromopentane or 2-bromopentane
iii) Which one of the following has the highest dipole moment?
CH2Cl2 ii) CHCl3 iii) CCl4
21. Starting from methyl bromide, how will you prepare 3
i) Nitromethane and methyl nitrite?
ii) Methyl cyanide and methyl
isocyanide. Write the complete reaction
involved.
22. Identify the Chiral molecule in the following pair. 3
Write the structures of the product when chlorobenzene is treated with methyl
chloride in the presence of sodium metal and dry ether.
C) Write the structures of the alkene formed by dehydrohalogenation of
1-Bromo-1-methyl cyclohexane with alcoholic KOH.
23. How are the following conversions carried out? 1
i)Ethanol to propanenitrile ii) Toluene to Benzyl alcohol each
iii) Benzene to 4-Bromonitrobenzene iv) But-1-ene to n-Butyliodide.
v)Chlorobenzene to p-nitrophenol vi) 1-Chlorobutane to
n-Butyliodide.
24. Explain with an example: 1
i)Sandmeyer’ s reaction ii)Finkelstein reaction iii)Swarts reaction iv) Wurtz reaction each
v) Fittig reaction vi)Wurtz-Fittig reaction vii) Diazotisation
25. Give the uses of Freon, DDT, Carbontetrachloride and Iodoform. 1
each
