Professional Documents
Culture Documents
PRACTICE TEST 2
Class 12 - Chemistry
Section A
1. (b) hcp and ccp
Explanation: Packing efficiency is the percentage of total filled space by particles i.e.,
Volume occupied by fow spheres inthe unit cell
=
Total volume of unit cell
Since packing efficiency for hcp or ccp is calculated to be 74% which is maximum among all type of
crystals while that of bcc has 68% and scc has 52%
2. (a) Helium
Explanation: Size of Helium is small so does not causes “Bents” to divers when the dive back to surface. As
it is less soluble.
3. (b) Ammonia
Explanation: Urea on reaction with NaOH liberates ammonia.
NH2CONH2 + 2NaOH → Na2CO3 + 2NH3↑
4. (d) b, c
Explanation: Chiral molecules(the object which is non-superimposable on their mirror image) contains
one carbon atom surrounded by four non-identical species. All straight-chain molecules cannot be chiral
because of the presence of two or more identical groups like hydrogens. Even the carbons with double or
triple bonds to a group cannot be considered as a chiral carbon. An asymmetric carbon needs to be
surrounded by four species different from each other through covalent bonds. Hence, the atoms b and c
are asymmetric.
5. (d) o – nitrophenol
Explanation: The nitro-group is an electron-withdrawing group. The presence of this group in the ortho or
para position decreases the electron density in the OH bond. As a result, it is easier to lose a proton. Also,
the o-nitrophenoxide or p-nitrophenoxide ion formed after the loss of protons is stabilized by resonance.
Hence, ortho and para nitrophenols are stronger acids than phenol.
6. (d) α– Aminoacid
Explanation: Proteins are the polymers of α-amino acids. So building unit of a protein is α – Aminoacid.
7. (a) Paramagnetic
Explanation: They will have unpaired electrons so are weakly attracted by a magnetic field.
8. (a) greater for gases with lower solubility.
Explanation: The higher the value of KH at a given temperature, the lower is the solubility of a gas in the
liquid.
9. (a) 3 double bonds; 12 single bonds
Explanation: Cyclotrimetaphosphoric acid contains three double bonds and 12 single bonds as shown
below:
a, b and c are three (double) pi-bonds and numerics 1 to 12 are (single) sigma bonds
10. (d) 2-chloro, 2-methyl propane
Explanation: Longest chain will be of three carbon to which Cl and CH3 will be attached at 2 positions.
1/6
-
11. (b) Chloramphenicol
Explanation: Chlorine containing antibiotics, chloramphenicol, produced by soil microorganisms is very
effective for the treatment of typhoid fever. Chloramphenicol is an antityphoid drug.
12. (a) they are readily excreted in urine
Explanation: B group vitamins and vitamin C are soluble in water so they are grouped together as water
soluble vitamins. These must be supplied regularly in diet because they are readily excreted in urine and
cannot be stored (except vitamin B12) in our body.
2/6
-
22. (a) Mixture of and
Explanation:
The reaction of aromatic arenes with chlorine in the presence of Lewis acid catalysts like iron (III) chloride
gives ortho and para isomers of haloarenes by an electrophilic substitution reaction. Cl2 forms a
coordination complex with FeCl3, forming Cl+FeCl4- complex, which gives a slight positive charge to Cl, and
FeCl4- is negatively charged. This Cl+ then reacts with the aromatic double bonds of the toluene molecule to
form an addition product, followed by deprotonation to form a mixture of o- p- and m- isomers of the
chlorotoluene. The m- isomer is very unstable, so the product form is o-Halotoluene and p-Halotoluene.
23. (d) Cyclopentane
Explanation: Cyclopentane is nearly inert chemically, they react with halogens in the presence of light
through the substitution of one hydrogen atoms. Since the cyclic structure confers a high degree of
symmetry on the molecule, only one monochloro cyclopentane is possible.
3/6
-
2− −
29. (b) CO3 , NO3
2− −
Explanation: CO3 and NO3 are isoelectronic with 32 electrons and sp2 hybridization hence, have
pyramidal structure.
30. (d) Wurtz reaction
Explanation: Alkyl halides react with sodium in dry ether to give hydrocarbons containing double the
number of carbon atoms present in the halide. This reaction is known as the Wurtz reaction.
2RX + 2Na → R-R + 2NaX
So, C6H5CH2CH3 is not prepared by the Wurtz reaction.
Explanation: The higher the value of reduction potential, the higher is its tendency to get reduced Hence,
the order of oxidizing power is
− − −
BrO > IO > ClO
4 4 4
36. (a) Na
Explanation: 2CH3Br + 2Na → CH3CH3 + 2NaBr
37. (a) 4
1
Explanation: 8 corners atoms × atom per unit cell =1 atom
8
4/6
-
41. (d) Br2
′
W illiamso n s synthesis
5/6
-
48. (c) A is true but R is false.
Explanation: Cl2 is an oxidising agent. It bleaches the articles by oxidation permanently in presence of
moisture.
49. (a) Both A and R are true and R is the correct explanation of A.
Explanation: Both A and R are true and R is the correct explanation of A.
Section C
50. (d) water will move from the side (B) to side (A) if a pressure greater than the osmotic pressure is applied
on piston (B).
Explanation: Water will move from the side (B) (concentrated sodium chloride solution) to side (A)
(freshwater) if a pressure greater than the osmotic pressure is applied on piston (B).
51. (a) SN1 mechanism
Explanation:
When benzyl chloride is treated with aqueous sodium hydroxide, where –OH is the nucleophile,
nucleophilic substitution reaction takes place forming benzyl alcohol. Here, the benzene ring is resonance
stabilized and its stability is extended to the methylene group attached, giving a positive charge to –CH2,
making the whole carbocation stable when the bond between benzyl and bromide is broken. This reaction
is SN1 (unimolecular nucleophilic substitution) reaction, it has two steps, and is followed due to the
stability of carbocation. This reaction is concerted and occurs in two steps. First, the halide group leaves
the carbocation, and the nucleophile then attaches itself to the cation, forming alcohol.
52. (a) a mixture of ortho and para nitro phenols
Explanation: Nitration of phenols: Phenols upon treatment with dilute nitric acid undergoes nitration at
low temperature (298 K) to give a mixture of ortho and para nitrophenols. The mixture formed is further
separated into ortho and para nitrophenols by steam distillation on the basis of their volatility. Due to
intramolecular and intermolecular hydrogen bonding, ortho nitrophenols are lesser volatile in comparison
to para nitrophenols which involves only intermolecular hydrogen bonding.
+ −
53. (a) Xe [PtF6 ]
−
Explanation: Xe+ [PtF6 ]
54. (c) All of these
Explanation: Xe has completely filled 5p -orbital. As a result, when it undergoes bonding with an odd
number (1, 3 or 5) of fluorine atoms, it leaves behind one unpaired electron. This causes the molecule to
become unstable. As a result, XeF, XeF3 and XeF5 do not exist.
6/6
-