CHAPTER – 10

HALOALKANES AND HALOARENES

1 Mk Questions:

1) Write the IUPAC name of the following compound :

CH3

H3C – C – CH2Cl

CH3

Ans 1 – Chloro – 2, 2 – dimethylpropane

2) Draw the structure of 2-bromopentane

Ans H3C – CH2 – CH2 – CH – CH3
Br

3) Write a chemical reaction in which iodide ion replaces the diazonium group in a
diazonium salt.
Ans N2+ Cl- + KI(aq) > I + N2 + KCl

4) Out of CH3 CH Cl CH2 CH3 and CH3 CH2 CH2 CH2 Cl which one is hydrolysed more
easily by aq. KOH?
Ans CH3 CH – CH2 CH3 , as it’s a secondary halide
|
Cl

5) How can you convert methylbromide to methylisocyanide in a single step?

Ans CH3Br > CH3NC + Ag Br

2 Mks Questions

1) What are ambident nucleophiles? Explain with an example.

Ans Ambident nucleophiles have two nuclophilic sites through which they can attack.
Eg. [ΘC  N ↔: C = NΘ] linking through C results in alkyl cyanides and through N
results in isocyanides.
2) Write chemical equations when
i) ethylchloride is treated with aq.KOH
ii) chlorobenzene is treated with CH3COCl in presence of anhyd.AlCl3.

Ans i) C2H5Cl > C2H5OH + KCl

COCH3
ii) Cl > Cl + H3COC Cl + HCl
2-chloroacetophenone 4-chloroacetophenone

3) Write the mechanism of the following reaction:

N – BuBr + KCN > n – BuCN
Ans CN- is an ambident nucleophile  it can attack through C and N

C-C bond is stronger than C-N bond, cyanide is formed.

4) Give reasons:
a) The order of reactivity of haloalkanes is RI>RBr>RCl
b) Neopentyl chloride, (CH3)3C – CH3 Cl doesn’t follow SN2 mechanism.
Ans a) Larger the size of halogen atom, weaker the C-X bond,
R group remaining same i.e; bond strength follows the order
R-I <R-Br<R-Cl, hence reactivity is opposite.
b) R – group being bulky, provides steric hindrance to the incoming nucleophile.

5) Why does Wurtz reaction fail in case of tertiary halides?

Ans 3o halides prefer to undergo dehydrohalogenation in presence of a base like Na metal.
CH3 CH3
|
(CH3)3 C-Na+ + H – CH2 – C – Br > (CH3)3 CH + CH2 = C – CH3
|
CH3
3 Mk Questions:

1) Write a chemical test to distinguish between

a) Chlorobenzene and benzyl chloride
b) Chloroform and carbontetrochloride
c) n-propyl bromide and isopropyl bromide

Ans a) Benzyl chloride gives a white ppt with AgNO3 Soln., chlorobenzene does not.
b) Chloroform gives offensive smelling isocyanides, on heating with 1o amine and
KOH, CCl4 doesn’t give this test.
c) Isopropyl bromide, on treating with aq.KOH, gives Propan-2-ol which gives a
yellow ppt. on heating wiith NaOH and I2 n- propyl bromide doesn’t answer this test

2) Complete the following reactions:

i)

ii)

iii)

Ans i)

ii)

iii)

3) Give reasons:
a) p-dichlorobenzene has higher melting point than o- and m- isomers.
b) Haloarenes are less reactive than haloalkanes towards nucleophilic substitution
reactions.
c) Alkyl chloride gives alcohol with aq.KOH, but alkene with alc. KOH.
Ans a) p-isomer has more symmetric structure, so molecules can pack closely.
b) The C-X bond has partial double – bond character due to resonance. Also, in
haloalkanes, X is bonded to sp3 – C while in haloarenes, X is bonded to sp2 –C. sp3-C is less
electronegative, releases electrons to halogen more easily.
c) In aq.solution, KOH is almost completely ionized to give OH- ions, which being a
strong nucleophile, gives a substitution product. An alcoholic soln. of KOH contains alkoxide
ions (RO-), which being a strong base, preferentially eliminates an HCl molecule to form
alkenes.

4) Convert:
a) Ethene to ethanol
b) Chlorobenzene to toluene
c) Chlorobenzene to diphenyl

Ans a) CH2 = CH2 + H2O > CH3CH2OH

b)

c)

5) What are enantiomers? Identify the asymmetric carbons in the following molecule:-
a b c d
HOOC CH (OH) – CH (OH) COOH

Ans Enantiomers are non-superimposable mirror images of an optically active compound.

b and c are asymmetric carbon atoms as they are bonded to 4 different groups.

6) Write short notes on :

a) Gatterman reaction
b) Wurtz reaction
c) Peroxide effect or Kharasch effect

Ans a) Aromatic 1o amines produce benzene diazonium salts with HNO2 (produced in situ) at
273 K. Chloro arenes and bromoarenes can be prepared using Cu/HCl or Cu/HBr from these
diazonium salts.
b) Alkyl halides, when treated with sodium in presence of dry ether, produce an
alkane with even number of C atoms.
2 R-X + Na > R _ R + 2NaX
E.g. 2 CH3 Br + Na > CH3 – CH3 + 2NaBr
If a mix of two different alkyl halides is taken, then a mixture of alkanes is obtained which is
difficult to separate.
E.g. CH3 Br + C2H5Br > CH3-CH3 + C2H5 + CH3-C2H5

c) The addition of Hydrogen bromide to unsymmetrical alkenes in presence of a

peroxide takes place in such a way that H goes to that C which has lesser H atoms and Br goes to
the C with greater number of H atoms.
CH3 – CH = CH2 + H Br > CH3 – CH2 – CH2 Br
This rule doesn’t apply to addition of HCl or HI

7) Explain the following with an example each

a) Swarts reaction
b) Finkelstein reaction
c) Hunsdiecker reaction
Ans a) Flourination of hydrocarbons directly with F2 occurs explosively due to the large
amount of energy released. Hence, they can be conveniently prepared indirectly by halogen
exchange with chloro and bromoalkanes.
CH3Br + AgF → CH3F + AgBr
2 C2H5Cl + .Hg2F2 → 2C2H5F + Hg2Cl2
b) Iodoalkanes can be easily prepared from chloroalkanes or bromoalkanes by heating
with NaI in acetone.
R-Cl + NaI > R – I + NaCl

R –Br + NaI > R – I + NaBr

c) Bromoalkanes can be prepared by refluxing the silver salt of a carboxylic acid

with Bromine in CCl4.

CH3CH2COOAg + Br2 > CH3CH2Br + CO2 + AgBr

The yield of alkyl bromide is 1o>2o>3o
8) Explain why.
a) Vinyl chloride is unreactive in nuceophilic substation reaction
b) 3-Bromocyclohexene is more reactive than 4-Bromocyclohexene in hydrolysis
with aq.NaOH
c) tert-butyl chloride reacts with aq.NaOH by SN1 mechanism, while n-butyl
chloride reacts with aq.NaOH by SN2 mechanism.
Ans a) Vinyl chloride is unreactive in nucleophikic substitution reactions due to
reasanance which results in a partial double bond character of C-Cl bond which is difficult to
break.

b) 3-bromocyclohexene forms allyl carbocation which is more stable than

carbocation formed by 4-Bromocycohexene
c) Tertiary carbocation is stable, so tert-butyl chloride follows SN1 mechanism. N-
butyl chloride would form 1o carbocation which isn’t that stable. Hence it undergoes SN2
mechanism through formation of transition state.

9) Identify the products A and B formed in the following reaction:

CH3CH2CH = CH –CH3 + HCl → A + B
Ans Since both the doubly-bonded C atoms have same number of H atoms, Markonikov’s rule
becomes irrelevant.
So, products will be → CH3 – CH2 – CH – CH2 – CH3 CH3CH2CH2CH CH3
| (A) and | (B)
Cl Cl
3-chloropentane 2-choropentane

10) What happens when:

a) n-butyl chloride is treated with alc.KOH
b) Bromobenzene is treated with Mg in presence of dry ether.
c) Chlorobenze is subjected to hydrolysis.
Ans a) CH3CH2CH2CH2Cl - alc.KOH → CH3-CH2-CH=CH2+KCl + H2O
But – 1 – ene

a) Br + Mg > Mg Br

a) Cl2 + aq.NaOH → no reaction.

CHAPTER – 11
ALCOHOLS, PHENOLS AND ETHERS

1 Mark Questions

1) Write the IUPAC name of CH3 CH= CH – CH- CH2 – CH3

|
OH
A) Hex – 4 –en – 3 –ol

2) Why is the boiling point of C2 H5 OH higher than that of CH3 OH ?

A) Due to more number of C atoms, van der waal’s forces increase.

3) Name the reagent used in bromination of phenol to 2,4, 6 – tribromophenol.

A) Aqueous solution of bromine (Bomine water)

4) Name the alcohol used to prepare the ester CH3 – C OOCH(CH3)CH3

A) Propan-2-ol CH3-CH(OH)-CH3

5) Which is more volatile – o-nitrophenol or p-nitrophenol?

A) o-nitrophenol,, as it has intramolecular H-bonding, whereas p-nitrophenol has
intermolecular H-bonding.

O-Nitrophenol with intra molecular hydrogen bonding

02 MARKS

1) How will you convert:

a) Propene to propan – 2 – ol
b) Ethyl chloride to ethanol
A) a) CH3-CH = CH2 H2O/H+ CH3 – CH – CH3
 |
OH
Propan – 2 – ol

b) CH3 -CH2- Cl aq – NaOH CH3 CH2 OH [o] CH3 - CHO

----------- ------- Ethanal
CrO3/PCC
2) Write the mechanism for the following reaction:
CH3CH2OH CH3CH2Br + H2O

A) 1o alc undergoes the reaction by SN2 mechanism

Protonated Alcohol

3) How would you obtain

i) Picric acid from phenol?
ii) 2- Methylpropan-2-ol from 2- Methylpropene?
A) i)
ii)

4) Give reasons :
a) Boiling points of alcohols decrease with increase in branching of the alkyl chain.
b) Phenol does not give protonation reaction readily
A) a) Because increase in branching of the alkyl chain reduces surface area, so
intermolecular forces of attraction decrease.
b) Because the lone pair on oxygen is delocalized over the benzene ring due to
resonance, hence not available for protonation easily.

5) Explain why cleavage of phenyl alkyl ether with HBr always gives phenol and alkyl
bromide.
A) Due to resonance, the O-C bond in phenyl alkyl ether has a partial double bond character,
hence it is difficult to break.
Also, phenoxide ion is stabilized by resonance, hence we get phenol and alkyl bromide.

03 MARKS

1) Write a short note on Williamson’s Synthesis.

A) An alkl halide, on treating with a suitable sodium alkoxide gives an ether

RONa + RX - R– O – R + NaX
Symmetric and unsymmetric ethers can be prepared by this method
Aryl alkyl ethers can be prepared as shown
But there is no reaction if arylhalide and sodium alkoxide are taken

Best yields of unsymmetrical ethers are obtained when alkyl halides are primary with 2 o
and 3o alkyl halide, dehydrohalogenation occurs to give alkene.

2) Convert:
a) Methyl magnesium chloride --2-methyl propan-2-ol
b) Benzyl chloride --- Benzyl alcohol
c) Phenol -- benzoquinone
A)
a)

propanone

b)

c)

3) Give reasons :

a) The boiling point of ethanol is higher than methoxymethane.

b) Phenol is more acidic than ethanol
c) O- and p-nitrophhenols are more acidic than phenol.
A) a) Ethanol has intermolecular H-bonding while methoxymethane only has dipole-
dipole forces.
b) In phenols, O atom acquires a partial positive charge due to resonance, this
weakens O-H bond, release of H+ is easy. Also, phenoxide ion is stabilised by
resonance. On the other hand, alkoxide ion is destabilized due to the +I effect of
alkyl group.
c) -NO2 group, being electron-withdrawing, stabilizes the o- and p- nitrophenoxide
ions.

4) Describe the mechanism of hydration of ethene to yield ethanol.

A)

Protonation of Alkene

Nucleophilic attack by water on the carbocation

Deprotonation
5) Give equations for Reimer Tiemann reaction and Kolbe’s reaction.
A) Reimer Tiemann reaction – Phenol reacts with chloroform in the presence of alkali to
give o- and p-hydroxy aldehyde.

Kolbe’s reaction – Phenoxide ion generated by treating phenol with NaOH undergoes
electrophilic substitution with CO2

6) Arrange the following compounds in increasing order of their acid strength.

Propan-1-ol, 2, 4, 6-Trinitrophenol, 3 – Nitrophenol,
3, 5- Dinitrophenol, phenol, 4-Methylphenol, 4-Methoxyphenol
A) Propan-1-ol <4-Methoxyphenol<4-Methylphenol<phenol< 3-Nitrophenol
<3, 5 – Dinitrophenol<2, 4, 6 – Trinitro phenol
 Propan – 1 ol has R group, which destabilizes the propoxide ion due to +I effect, hence
weaker than all phenols.
 All e- donating groups reduce acidity of phenols by destabilizing phenoxide ion and e-
withdrawing groups increase acidity.
 Methoxy group is stronger e- - donating groups compared to methyl group.
 Larger the number of e- withdrawing groups, greater the acidity. 2, 4, 6 –
Trinitrophenol is strongest, followed by 3, 5 – Dinitrophenol and 3 – Nitrophenol.

7) Give a simple chemical test to distinguish between:

a) Phenol and cyclohexanol
b) Propan-2-ol and Benzyl alcohol
c) Propan-1-ol and 2-Methylpropan-2-ol
A) a) Phenol produces a deep violet colour with neutral FeCl3 solution., cyclohexanol
doesn’t.
b) Propan-2-ol gives yellow ppt of iodoform with NaOH and I2, benzyl alcohol
doesn’t.
c) On treating with conc. HCl and anhydrous ZnCl2 at room temperature, 2-
methylpropan-2-ol produces turbidity immediately while propan-1-ol doesn’t
produce turbidity at room temperature.

8) Give the mechanism for the reaction: 2C2H5OH C2H5O C2H5

A)

Protonation of Alcohol

Nucleophillic attack by Alcohol

Deprotonation

9) An organic compound A (C6H6O) gives a characteristic colour with aq. FeCl3 Solution.
when (A) is treated with CO2 and NaOH at 410 K under pressure, it gives compound (B) which
on acidification gives compound (C). Compound (C) reacts with acetyl chloride to give (D),
which is a popular pain killer. Deduce the strutures of A,B,C and D and explain all reactions
A) (A) C6H6O must be phenol
Phenol gives sodium salicylate with CO2 which on acidification gives salicylic acid.
Salicylic acid forms aspirin with acetyl chloride.
10) (a) Explain hydroboration-oxidation reaction with an example
A Diborane reacts with alkenes to give trialkyl boranes as addition product. This is
oxidized by H2O2 to alcohol, in the presence of aq.NaOH

(b) Identify A B C in the following reaction.

CH3Br A B C
A CH3CN
B CH3CH2NH2
C CH3CH2N2Cl (Unstable, so forms CH3CH2OH + N2 + HCl with Water
CHAPTER – 12

ALDEHYDES – KETONES AND CARBOXYLIC ACIDS

01 MARK

1) Write the structure of p-methylbenzaldehyde.

A)

2) Complete the reaction :

+ CH3COCl
A)

Acetophenone

3) Arrange the following in increasing order of their acid strength (CH3)2 CHCOOH,
CH3 CH2 CH(Br) COOH, CH3 CH(Br) CH2 COOH.
A) (CH3)2 CHCOOH < CH3 CH(Br)CH2COOH<CH3CH2CH(Br)COOH
4) Write IUPAC name of

A) 5 – Bromo -3- chlorobenzoic acid

5) Give a chemical test to distinguish between acetaldehyde and benzaldehyde.

A) On heating with Na OH and I2, acetaldehyde gives a yellow ppt of iodoform,
benzaldehyde doesn’t

02 MARKS

1) Convert:
a) Ethanol to 1,2 Ethanediol (b) Phenol to acetophenone
A) a) C2H5OH CH2 = CH2 + H2O

Ethane – 1, 2 - diol

b)

3) Give reasons:

a) Monochloroethanoic acid is a weaker acid than dichloroethanoic acid.

b) Benzoic acid is stronger than ethanoic acid

A) a)

Cl has – I effect, making release of protons easier. Also, it stabilises the carboxylate ion.
Monochloroacetic acid has one Cl atom. While dichloroacetic acid has two Cl atoms.
Hence it is a stronger acid.
b) Benzene ring is e- withdrawing, while CH3 group is e- donating. Hence, release of
protons is easier in benzoic acid than ethanoic acid. Also, the benzoate ion is much more
stable than ethanoate ion due to e- - withdrawing benzene ring.

4) Describe Cannizaro’s reaction with example.

A) Aldehydes without α-H undergo self-oxidation and reduction (disproportionation) on
treatment with conc. Alkali. One molecule is reduced to alcohol while the other is oxidized to
salt of corresponding carboxylic acid

5) Complete the equations

a) CH3CHO b) CH3COCH3
A) a) CH3CH2OH b) CH3CH2CH3

03 MARKS

1) Explain Aldol condensation with an example.

A) Aldehydes or ketones having at least one α-H undergo condensation to produce β-
hydroxy aldehyde (aldol) in the presence of a dil. Base.

Eg.2CH3CHO CH3CH(OH)CH2CHO CH3CH=CH-CHO

3-Hydroxybutanal
Eg. If two different molecules of aldehydes and/or ketones undergo aldol
condensation, the reaction is called CROSS ALDOL REACTION.

2) Give reasons
a) There are two –NH2 groups in semicarbazide, but only one is involved in the
formation of semicarbazones:
b) Cyclohexanone forms cyanohydrins in good yield, but 2,2,6-
Trimethylcyclohexanone doesn.t.
c) Aldehydes are more reactive than ketones towards nucleophilic addition.
A) a) One of the NH2 groups is involved in resonance, hence it cannot act as a
nucleophile. Other one is free,  it can act as a nucleophile.

b) CN- can attack easily without any steric hindrance in cyclohexanone.

Lot of CH3 groups offer too much steric hindrance.

c) Aldehydes have one R group and ketones have two. Two R groups cause more steric
hindrance and greater +I effect reduces the electrophilicity of the carbonyl carbon.

3) How will you convert:

a) Propanone to propane
b) Benzoyl chloride to benzaldehyde
c) Ethanal to but-2-enal
A)
a)

b)

c)

4) How will you bring about the following conversions?

a) Benzene to Benzophenone
b) Propyne to acetone
c) p-nitrotoluene to p-nitrobenzaldehyde

Ans 4 a)

b)
c)

5) An organic compound A contains 69.77% carbon, 11.63% hydrogen and rest oxygen.
The molecules mass of the compound is 86. It doesn’t reduce Tollen’s reagent but forms an
addition compound with sodium hydrogen sulphite and gives positive iodoform test. On vigorous
oxidation, it gives ethanoic abd propanoic acids. What is the structure of compound A?

Ans Element % Molar Mass Moles Simple ratio

C 69.77 12 5.81 5
H 11.63 1 11.63 10
O 18.6 16 1.16 1

Empirical formula C5H10O

Empirical formula mass = 5(12) + 10(1) + 1(16) = 86
n= =1
 Moecules formula C5H10O
Since it doesn’t give Tollen’s test but gives positive iodoform test. It is a methyl ketone i.e it has
– C – CH3 group. Since on oxidation it gives ethanoic and propanoic acid, it must be pentan-2-
one.
CH3 CH2 CH2 CO CH3 → CH3COOH + CH3 CH2 COOH
Pentan-2-one

05 MARKS
1) a) Draw the structures of:
i) 5-Chloro-3methyl-pentan-2-one
ii) p-nitropropiophenone

b) Give simple chemical tests to distinguish between:

i) Ethanal and propanal
ii) Phenol and benzoic acid
iii) Benzaldehyde and acepopheone

Ans a) i)

ii)

b) i) CH3 CHO gives a yellow ppt of iodoform with NaOH/I2 (positive iodoform
test) CH3CH2CHO doesn’t answer this test.
ii) Phenol produces deep violet colour with aq-neutral FeCl3 Soln., benzoic acid
doesn’t answer the test.
iii) Acetophenone produces yellow ppt on heating with NaOH+I2, benzaldehyde
doesn’t.

2) Identify A,B,C,D and E in the following sequence:

A B C D+E

A) A → CH4, B → HCOONa, C → C6H5COOOCH,

D → CHO E → C6H5COOH

3) An organic compound A (C3H2O) on treatment with Cu at 573 K gives B. B doesn’t

reduce Fehling’s solution. But gives a yellow ppt. of compound C with I2/NaOH. Deduce the
structures of A, B and C.

A) Since compound B gives iodoform test, it must be having –CO-CH3 group i.e it is a
ketone.
Since B is obtained by dehydrogenation of A,  A is a 2o alcohol
 A is R-CH – CH3
|
OH
Comparing with the given molecules formula, R is –CH3
 A is CH3-CH-CH3
|
OH
Propan-2-ol
The reactions are: O
CH3-CH-CH3 > CH3-C-CH3 > no reactions
OH Acetone
(A) (B)
CH3 COCH3 + 3I2 + 4NaOH → CH3COONa + 3NaI+CHI3 + 3H2O
(C)
So, A = CH3CHCH3 Propan-2-ol
|
OH
B = CH3COCH3 Propan-2-one
C = CHI3 Iodoform

4) a) An organic compound A (C3H6O) is resistant to oxidation but forms a compound

B (C3H8O) on reduction. B reacts with H Br to form a bromide ‘C’ which on treatment with
alcoholic KOH forms an alkene D (C3H6). Deduce the structures A,B,C and D.

b) Carboxylic acids contain a carbonyl group, but do not show the nucleophilic
addition reaction like ketones or aldehydes. Why?

Ans a) CH3-CO-CH3 > CH3-CH-CH3

OH
Acetone Propan-2-ol
‘A’ ‘B’

H Br

CH3-CH=CH2 < CH3-CH-CH3

‘D’ Br
Propene 2-Bromo propane
‘C’
b) This is due to resonance (for structures refer NCERT)

The carboxyl carbon of the resonance hybrid is less positive and hence less
electrophilic than carbonyl ‘C’ of aldehydes and ketones

5) a) Explain the following :

i) Cyanohydrin ii) Acetal iii) 2,4 – DNP derivative

b) Complete the following:

i) CH2CH3 >
COOH
ii) COOH >

iii) C6H5CHO >

Ans a) i) Formed addition of HCN to aldehydes or ketones

C  O  H   CN   C OH
CN

Cyanohydrin

ii) Formed on addition of two moles of alcohol to an aldehyde or ketone.

OR
C = O + 2 R OH DryHC lg as C OR
+ H2O
Acetal

iii) Addition product of aldehydes or ketones with 2,4 – Dinitro phenyl hydrazine in
weakly acidic medium.
NO2 NO2
C = O + H2N NH NO2 C = NNH NO2

b) i)

ii)
iii) C6H5CH = NNHCONH2
Benzaldehyde semicarbazone
CHAPTER – 13

AMINES

01 MARK

1) Draw the structure of prop-2-en-1-amine

Ans H2C = CH – CH2 – NH2

2) Give a chemical test to distinguish between ethylamine and aniline.

Ans They can be distinguished by Azo dye test.
On treating with HNO2 (NaNO2+HCl) followed by alkaline soln. of 2-naphthol (Temp – O-5oC)
Aniline forms an orange dye, while ethylamine only gives ethanol and N2.

3) Arrange the following in increasing order of their solubility in water : C6H5NH2,

(C2H5)2NH, C2H5NH2
Ans C6H5NH2<(C2H5)2NH<C2H5NH2

4) Out of CH3NH2 and (CH3)3 N, which one has higher boiling point?
Ans CH3NH2 due to its ability to form Intermolecular H-bonds (CH3)3N has no H atoms
bonded to N so cannot participate in H bonding.

5) Why is the pkb of aniline greater than methylamine?

Ana In aniline, lone pair of N is delocalized over the benzene ring. reducing basicity. In
CH3NH2, +I effect of –CH3 group increases basicity of CH3NH2.

02 MARKS

1) Explain Gabriel Pthalimide synthesis.

Ans It is used to prepare pure 1o amine. Aromatic 1o amines can’t be prepared by this method
because aryl halides do not undergo nucleophilic substitution with the anion formed by
pthalimide
2) Give reasons:
a) Diazonium salts of aromatic amines are more stable than those of aliphatic amines.

b) Amines are more basic than alcohols of comparable molecular masses.

Ans a) Resonance stabilization of diazonium salts of aromatic amines

b) N is less electronegative than O,  lone pair of electrons are easily available Such
resonance stabilization is not possible in diazonium salts of aliphatic amines.

3) Identify A and B in each of the following:

a) C2H5Cl >A >B

b) C6H5NH2 >A > B

Ans a) A → C2H5CN, B → C2H5CH2NH2

Prppanenitrile propanamine

b) A → C6H5N2+ Cl- B→
Benzene diazonium
Chloride

4) Complete the reactions

a) C6H5N2Cl + H3PO2 + H2O →
b) C6H5NH2 + Br2 (aq) →
Ans a) C6H6. + N2 + H3PO3 + HCl

b)

2, 4, 6 – Tribromoaniline

5) Convert
a) Nitrobenzene to phenol b) aniline to chlorobenzene

Ans a)
b)
03 MARKS

1) Give the structures of A, B, C in the following:

a) CH3Br >A >B >C

b) CH3COOH >A >B >C

Ans a) A → CH3CN, B → CH3CH2NH2, C → CH3CH2OH

b) A → CH3CONH2, B → CH3NH2 C → CH3NC

2) Write short notes on :

a) Coupling reaction
b) Ammonolysis
Ans a) Benzene diazonium salts react with e- rich aromatic compounds such as phenols and
amines to form azo compounds, which are often coloured and are used as dyes.

E.g

b) An alkyl or benzyl halide, on reaction with ethanolic soln. of NH3 undergoes

nucleophilic substitution reaction in which the halogen atom is replaced with –NH2 group. This
cleavage of C-X bond by ammonia molecule is called AMMONOLYSIS.
NH3 + R – X → RN+H3 X-
Substituted ammonium salt
RNH2 > R2NH > R3 N > R4N+X-
Quarternary Ammonium salt
o o o
Disadvantage : Mixture of 1 , 2 , 3 amines and quarternary ammonium salt is obtained.
Order of reactivity of halides with amines is RI > R Br > RCl

3) Write the main products of the following reactions:

a) CH3CH2NH2 >

b) SO2Cl + C2H5NH2

c) CH3CONH2 >

Ans a) CH3CH2OH
b) SO2NH C2H5

d) CH3NH2

4) Give reasons:
a) Amines are basic while amides are neutral.
b) CH3NH2 in water reacts with ferric choride to precipitate Fe (OH)3
c) Reactivity of –NH2 group gets reduced in acetanilide.
Ans a) In amines, R group increase e- density on N due to +I effects, whereas in amides,
O
R – C – group is electron withdrawing.

b) CH3NH2 + H2O → CH3NH3+ + OH-

FeCl3 + 3OH- → Fe(OH)3(↓) + 3Cl-
Reddish - brown
O
c) The lone pair on N is involved in conjugation with R-C-group
O O-
C6H5NH – C – CH3 ↔ C6H5 N+H = C – CH3

5) An aromatic compound ‘A’ on treatment with ammonia followed by heating forms

compound ‘B’, which on heating with Br2 and KOH forms a compound ‘C’ (C6H7N). Give the
structures of A, B and C and write the reactions involved.
Ans ‘A’ must be benzoic acid

A B C

6) Convert
i) Benzene diazonium chloride to nitrobenzene
ii) Nitrobenzene to aniline
iii) Aniline to benzonitrile
NaNO2
Ans i) N 2Cl  HBF4  N 2 BF4  NO2
Cu
Sn
ii) NO2  NH2
HCl

iii)
7) Give reasons
a) Although amine group is O, P- directly in aromatic substitution reaction, aniline on
nitroation gives some amount of m-nitro aniline.
b) Aniline doesn’t undergo Friedel-Craft reaction.

Ans a) Nitration is usually carried out with conc. HNO3+ con.H2SO4 In presence of these
acids, some amount of aniline undergoes protonation to form anilinium ion, so the reaction
mixture consists of aniline and anilinium ion, -NH2 group in aniline is o- and p- directing and
activating while the –NH3 group in anilinium ion is m-directing and deactivating. Nitration of
aniline mainly gives p-nitroaniline (due to steric hindrance at o- position) nitration of anilinium
ion gives m-nitroaniline.

b) Aniline being a lewis base reacts with Lewis acid AlCl3 to form a salt.
C6H5NH2+Al-Cl3. As a result N acquires a positive charge

8) Describe Hinsberg’s test to distinguish between 1o,2o and 3o amines.

Ans The amine is shaken with benzenesulphonyl chloride (Hinsberg reagent) in presence of
aq.KOH soln.
Ans
9) How will you convert 4-Nitrotoluene to 2-Bromobenzoic acid?
Ans

10) a) Predict, with reasons, the order of basicity of the following compounds is gases phase.
(CH3)3 N, (CH3)2 N H, CH3NH2 , NH3
b) Describe Carbylamine reaction.

Ans a) In gaseous phase, solvation effects are missing, Hence, greater the number of alkyl
groups, greater +I effect and stronger the base.
 (CH3)3 N > (CH3)2 NH > CH3NH2 > NH3
b) Aliphatic and aromatic primary amines on heating with CHCl3 and ethanolic KOH
form isocyanides or carbylamines. which are foul-smelling substances. Secondary and tertiary
amines do not show this reaction. Hence this reaction is used as a test for primary amines.
R-NH2 + CHCl3 + 3KOH RNC + 3KCl + 3H2O
Carbylamine
or
Isocyanide
CHAPTER – 14
BIOMOLECULES
01 MARK

1) What are polypepticles?

A) Polymers of amino acids having peptide linkage (– CONH –)

2) Which vitamin’s deficiency causes pernicious anemia?

A) Vitamin B12

3) What is the biological effect of denaturation of proteins?

A) The protein molecule uncoils from an ordered and specific conformation into a
more random conformation. Primary structure remains undisturbed.

4) In what sense are the two strands of DNA not identical but complementary to
each other?

A) If one strand has the bases A T C G, the other strand has T A G C, i.e. A can
only bond with T and C can pair with G. Hence the strands are not identical, but
complementary.

5) Show the reaction of Glucose with Tollen’s reagent.

02 MARKS

Q1. What is meant by

(a) Pyranose structure of glucose

(b) Glycosidic linkage

Ans 1 a) Six-membered cyclic structure of glucose, in analogy with pyran

b) Two monosaccharide units are linked through oxygen atom accompanied

by loss of a water molecule. This linkage is called glycosidic linkage.

Q2) What is the difference between α – form of glucose and β-form of glucose?

Ans These two forms differ from each other in orientation of –OH group at C-1.
α – form is obtained by crystallization from concentrated solution of glucose at 303K while
β – form (melting point 423 K) is obtained by crystallization from hot saturated soln. at 371 K.

Q3) Mention the type of linkages responsible for the formation of the following:
i) Primary structure of proteins
ii) Cross-linking of polypeptide chains
iii) α – helix formation
iv) β – sheet structure.

Ans i) Peptide linkage

ii) H-bond, sulphide linkage, van der waal’s forces
iii) H-bond
iv) Intermolecular H-bonds.

Q4) Why are carbohydrates generally optically active?

Ans Due to presence of chiral or asymmetric carbon atom and absence of plane of symmetry.

Q5) Give reactions characteristic of –CHO group, but not by glucose, as in it, free – CHO
group is absent.
Ans i) No reaction with Schiff’s reagent
CHO
|
(CHOH)4 + Schiff’s reagent → no reaction
|
CH2OH

ii) No reaction with NaHSO3 and NH3

CHO
|
(CHOH)4 + NaHSO3/NH3 → no reaction
|
CH2OH

03 MARKS

Q1) Define :
a) Invert sugar b) Vitamins c) Nucleosides

Ana a) Hydrolysis of sucrose brings about a change in sign of rotation from dextro (+) to
laevo (-), hence it is called invert sugar.

b) Organic compounds which can’t be produced by the body and must be supplied in
small amounts in diet to perform specific biological functions for normal health, growth
and maintenance of body.

c) A unit formed by attachment of a base to I’ position of sugar

Q2) Differentiate between fibrous and globular proteins.

Ans
FIBROUS PROTEINS GLOBULAR PROTEINS

1. Fibre – like structure 1. Polypeptide chains coil around to give a

spherical shape.

2. Water – insoluble e.g. keratin, myosin, 2. Water soluble e.g. insulin,

fibrin etc. haemoglobin, enzymes, hormones.

3. Stable to moderate changes in 3. Very sensitive even to small changes in

temperature and pH. temperature and pH.

Q3) What happens when D-Glucose is treated with

a) HI b) Br2 water c) HNO3

Ans 3
(a) +HI –( 6- (Reduction)
n-Hexane

(b) CHO COOH

Br H O
(CHOH)4 2 2 4 (Mild Oxidation)

OH OH
Glucose Gluconic acid

(c) CHO COOH

(CHOH)4 HNO3 (CHOH)4 (Strong Oxidation)

OH COOH (Saccharic acid)

Q7. (a) Define Zwitter ions with examples?

(b) What is the difference between essential amino acids and non-essential
amino acids?

A7. (a) Amino acids contain - and –COOH groups. These two groups interact
by transferring a proton from carboxyl group to amino group within the molecule.
Hence, a dipolar ion called ZWITTER ION is formed.
+

R CH COOH R CH COO-
(b)
S No Essential Amino Acids Non-Essential Amino Acids

1. Cannot be synthesized by the Can be synthesized by the

body. body.

Therefore should be
supplemented through diet.
Q8. Which
is the sugar 2. Eg Valine, leucine E.g Glycine, alanine
present in
milk? How many monosaccharaides are present it? What are such oligosaccharides
called?

A8. Lactose, two monosaccharaide units (glucose and galactose) such

oligosaccharides are called DISACCHARIDES.

05 MARKS

Q1. Discuss the structure of proteins in detail? What is the difference between α-
helix and β-pleated sheet structures of proteins?

A1. (a) Specific sequence in which various amino acids in a protein are linked to
one-another – primary structures.

(b) The conformation adopted by these polypeptide chains as a result of H-

bonding – SECONDAY STRUCTURES.

(i) α- Helix. Formed by intra molecular H – bonds, causing the

polypeptide chain to coil – up into a spiral structure or right handed helix
Eg . Fibrous protein like keratin and myosin.

(ii) β-pleated sheet structures Polypeptide chains lie side by

side held by intermolecular H-bonds , forming sheets. These sheets can
then be stacked one over the other forming a 3-D structure. This structure
resembles pleated folds of drapery, hence also called β-pleated sheet
structures.

(c) Tertiary Structure. The secondary structure is further arranged, leading

to flowing two possibilities.

(i) FIBROUS PROTEIN. The long linear protein chains form thread
like structure. These are insoluble in water and have β-pleated structure.

(ii) GLOBULAR PROTEINS. Different segments of the protein fold up

to give the entire molecule a spherical shape. The folding involves various
interactions between the side-chains-such as, vander waal’s interactions,
disulphide bridges ,hydrogen bonding etc.

(d) Quaternary Structure. Some proteins exist as assembly of two or

more polypeptide chains called SUBUNITS or PROMOTERS. These subunits
may be identical or different and are held together by H-bonds, electrostatic and
van der waal’s interactions.

The quaternary structure refer to the determination of number of subunits

and their spatial arrangement w.r.t each other in an aggregate protein
molecule.

Primary Secondary Tertiary Quarternary

Structure Structure Structure Structure

Q2. (a) Write important structural and functional differences between DNA and
RNA?

S Structural Differences
No

1. Sugar present is 2 – deoxy –D-(-) Sugar present is D-(-) -

ribose ribose

2. Cytosine and thymine are the Cytosine and Uracil are the
pyrimidine bases pyrimidine bases

3. Double- stranded α- helix Single- stranded α- helix

4. Very large molecules ; molecular Smaller molecules with

mass may vary from six – sixteen molecular mass ranging
million from 20,000- 40,000µ

S No Functional Differences

1. Unique property of replication Usually doesn’t replicate

2. Responsible for transmission of Responsible for protein

hereditary characteristics synthesis

Q2. (b) What deficiency diseases are caused due to lack of vitamins A, , and
K in human diet?

S No Vitamins Deficiency disease

1. A Xerophthalmia , night blindness

2. Beriberi, loss of appetite

3. Anaemia, general weakness

4. K Hemorrhage , slow blood clotting

Q3. (a) An optically active amino acid (A) can exist in three forms depending on
the of the medium. If the molecular formula of (A) is , write

(i) Structure of (A) in aqueous medium. What are such ions called?

(ii) In which medium will the cationic form of (A) exist?

(iii) In alkaline medium, towards which electrode will compound (A)

migrate?

A3. (a) (i) CH COOH In aqueous medium, CH COO-

+
NH2

(A) ZWITTER ION

(ii) In acidic medium, CH COO-+ H+ CH COOH

+ +
(cationic
+ form)
(ii)
In alkaline medium CH COO- + OH- CH COO-

+
NH2

Anionic form

Therefore the compound in alkaline medium will migrate towards anode.

(b) What are reducing sugars ? How are proteins related to amino acids?

A3 (b) Carbohydrates with free aldehyde group that can reduce Fehling’s solution
and Tollen’s reagent are called reducing sugars. All monosaccharaides are
reducing sugars. Also, those disaccharides where the linkage between two
monosaccharaides is not through aldehydic group are also called reducing
sugars.

Q4. (a) Write four characteristics features of enzymes. Name a disease caused by
the deficiency of a particular enzyme?

(b) What is a peptide bond? Explain its formation with an e.g?

A4. (a) (i) Enzymes are specific in their action.

(ii) Work at specific pH & moderate temperature.

(iii) Activity is high.

(iv) Catalyse biochemical reactions and their deficiency can cause

diseases.

Eg Phenylketane urea is caused by deficiency of phenylalanine

hydroxylase and Albinism is caused by deficiency of tyrosinase.

(b) Proteins are polymers of α-amino acids connected to each other by

peptide linkage. Chemically peptide linkage is an amide formed between
–COOH group and –NH2 group.
Q5. (a) Two samples of DNA, A and B have melting points 340K and 350K
respectively. What conclusion can you draw from these data regarding their base
content?

(b) Discuss the composition of starch.

A5. (a) CG base pair has 3 H- bonds and AT base pair has two H – bonds.
Therefore CG base pair is more stable than AT base pair. Since sample B has
higher melting point than sample A, therefore sample B has higher CG content
than sample A.

(b) Starch is made of two components

(i) Amylose (15 – 20%) – Water – soluble, linear polymer of α-D

Glucose in which of one glucose unit is attached to of the other
through α – glycosidic linkage. Aqueous solution of amylose gives blue
colour with iodine solution.

(ii) Amylopectin (30-85%) – Highly branched polymer, large number of

short chains containing 20-25 glucose units joined through α – glycosidic
linkage involving of one glucose unit and of another. The of
terminal glucose unit in each chain is further linked to of some other
glucose unit in the next chain through - α – glycosidic linkage.