Worksheets Chemistry 1
Worksheets Chemistry 1
Worksheet 3
1. Why formaldehyde cannot be prepared by Rosenmund’s reaction?
2. Benzaldehyde is less reactive towards nucleophilic addition reaction than acetaldehyde. Why/
3. Why aldehydes are more soluble than ketone?
4. Acetaldehyde does not gives Cannizzaro’s reaction, while formaldehyde does.
5. Arrange the following in increasing order of their boiling point- CH3CHO, CH3CH2OH, CH3OCH3,
CH3CH2CH3
6. Out of pentan-2-one and pentan-3-one, which one will give positive iodoform test? Why?
7. Why aromatic carboxylic acids do not undergo friedal craft reaction?
8. pKa value of 4-nitrobenzoic acid is lower than that of benzoic acid.
9. Benzoic acid do not undergo friedal craft reaction. Why?
10. pKa value of chloroacetic acid is lower than pKa of acetic acid. Why?
11. Carboxylic acid has higher boiling point than alcohols. Why?
12. Acetone is soluble in water but benzophenone is not.
13. An organic compound A (C7H6Cl2) on treatment with NaOH solution gives another compound B
(C7H6O). B on oxidation gives an acid C (C7H6O2) which on treatment with a mixture of conc.
HNO3 and H2SO4 gives compound D (C7H5NO4). B on treatment with conc. NaOH gives a
compound E (C7H8O) and C6H5COONa.Deduce the structures of A, B, C,D and E
14. A, B and C are three non cyclic functional isomers of a carbonyl compound with molecular formula
C4H8O. Isomers A and C give positive tollen’s test whereas isomer B does not give Tollen’s test but
gives positive iodoform test. Isomers A and B on reduction with Zn(Hg)/ conc. HCl give same
product D.
15. An organic compound A having molecular formula C3H6O, gives iodoform reaction and forms a
compound B. B on heating with Ag powder, gives compound C. C reacts with dil H2SO4 and
Mercuric sulphate to obtain compound D. Compound D undergoes aldol condensation. Write down
the names and structures of all the compounds starting from A to D with the help of chemical
reaction.
16. Write short notes on-
a. Cyanohydrin
b. Hemiacetals
c. 2,4-DNP derivatives
d. Acetals
e. Oximes
f. Schiff’s base
g. Semicarbazone
h. Ketaks
i. Aldol
j. Imines
17. How will you prepare following compounds from benzene? You may use any inorganic reagent and
any organic reagent having not more than one carbon atom.
a. Methyl benzoate
b. P-nitrobenzoic acid
c. P-nitrobenzaldehyde
d. M-nitrobenzoic acid
e. Phenylacetic acid
18. Although phenoxide ion has more number of resonating structures than carboxylate ions, carboxylic
acid is a stronger acid than phenol. Why?
19. Arrange the following compound in increasing oredre of their reactivity in nucleophilic addition
reactions-
a. Ethanal, propanal, propanone, butanone
b. Benzaldehyde, p-tolualdehyde, p- nitrobenzaldehyde, Acetophenone
20. An organic compound A having molecular formula C4H8O gives orange red ppt with 2,4-DNP reagent.
It does not reduce Tollen’s reagent but gives yellow ppt of iodoform oh heating with NaOH and I2.
compound a on reduction with NaBH4 gives compound B which undergoes dehydration reaction on
heating with conc. H2SO4 to form compound C. Compound C on ozonolysis gives two molecules of
ethanal.
Identify A, B and C and write their structures. Write the reactions of compound A with (a) NaOH/I2 and
B. NaBH4
21. Alpha Hydrogen of aldehydes and ketones are acidic in nature.Explain.
22. Give chemical test to distinguish between-
a. Acetone and acetic acid
b. Phenol and propanoic acid
c. Formic acid and benzoic acid
d. Benzaldehyde and benzoic acid
e. Acetophenone and benzaldehyde
f. Propanal and propanone.
g. Pentan-2-one and pentan-3-one
Worksheet 4- Halolalkanes and haloarenes
1. What happens when benzal chloride is boiled with aqueous sodium hydroxide solution?
2. Haloarenes are less reactive than haloalkanes . Explain.
3. What is meant by chirality of a compound? Give an example.
4. Why is chloroform kept in dark or coloured bottles?
5. Out of CH3CH(CH3)CH2Cl and CH3CH(CH3)Cl which is more reactive towards SN1 mechanism and
why?
6. In the following pairs of halogen compounds, which would undergo SN 2 reaction faster?