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CBSE Class 12 Chemistry Question Paper 2022 Set 1 Code 5611

(i) The document is the question paper for CBSE Class 12 Chemistry exam with 12 questions divided into 3 sections - A, B and C. (ii) Section A contains 3 very short answer questions carrying 2 marks each. Section B contains 11 short answer questions carrying 3 marks each. Section C contains 1 case-based question carrying 5 marks. (iii) Candidates are instructed to write their roll number, question paper code, and attempt all questions. Calculators and log tables are not allowed.

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100% found this document useful (1 vote)
532 views12 pages

CBSE Class 12 Chemistry Question Paper 2022 Set 1 Code 5611

(i) The document is the question paper for CBSE Class 12 Chemistry exam with 12 questions divided into 3 sections - A, B and C. (ii) Section A contains 3 very short answer questions carrying 2 marks each. Section B contains 11 short answer questions carrying 3 marks each. Section C contains 1 case-based question carrying 5 marks. (iii) Candidates are instructed to write their roll number, question paper code, and attempt all questions. Calculators and log tables are not allowed.

Uploaded by

Sheetal meena
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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CBSE Class 12 Chemistry Question Paper 2022

\ Series : AABB3/1 I lsET-1 I

���=56/1/1
m-t"4. Wawfi m-"IT;f cm ch1 "3ffi:-g� cfiI � � -
Roll No. �l:l\��I

l Candidates must write the Q.P. Code


on the title page of the answer-book.

• <f>tJ�Firfq � � fcf; � m-"IT;f -ij � � 12 ! I


• m-"IT;f 'q � � � 3m: � � w-J-� cm� cf;l ffl3f "3ffi:-g�cfil � �-� l:I\ fffij I
• �"lfFiflq � � fcf; � m-� -ij 12 m ! 1
• �mq;r� �&-11 �cm'"«�, �-3�cfii "qw.fq;J� �fffij I
• �m-"IT;fch1�t� 15 �q;r��11<rrt I m-"IT;fq;f��-ij 10.15 iNf
�� 110.15�-« 10.30��ffl3f�'51"fol-"IT;fch1�����"$R�
�-g�cfil tR � "3ffi: � � I
• Please check that this question paper contains 12 printed pages.
• Q.P. Code number given on the right hand side of the question paper should
be written on the title page of the answer-book by the candidate.
• Please check that this question paper contains 12 questions.
• Please write down the Serial Number of the question in the· answer­
book before attempting it.
• 15 minute time has been allotted to read this question paper. The question
paper will be distributed at 10.15 a.m. From 10.15 a.m. to 10.30 a.m., the
candidates will read the question paper only and will not write any answer
on the answer-book during this period. *
({-114'1 fq�1'1 (�;;s;.iRtct>)
CHEMISTRY (Theory)
f.twftrr'ff11ll:2rrul � Jiq;: 35
Time allowed : 2 hours Maximum Marks : 35

221 A 1 P.T.O.
(i) Pl 'JTR-'R 11jm 12 'JlR ! I Ntft JIR 3/f.Jc11ef ! I

(ii) -
� 'JTR-'R 'fft.r 1i1f 11 � ! '(H � ll r(ti 1f I

(iii) ff 'Iii - 'SIR mJln l # 3 fftfi Jllff ff!J 3'fftt1/ JTcfiT( "$ JlR f I� JlR 2 3F6 q;rt I
(iv) 'ff� - J1R mJln 4 # 11 rre,; ffY 3'fftt1/ JPf;T( "$ JlR f I� JlR 3 JFn q;r' I
(v) ff RN m:J111 l 2 � JrMftrr JlR 8 I � JlR 5 :;fc,; q;r! I
1f -

(vi) "f'ffir rovf �· 4'tt�H2< q;rR11T lifJfrr ! I

C 2 H5 NH2 , (C2 H5 )2 NH, (C2 HJ 3 N

(ii) �-q �cl4dl t��-ij:

(iii) pKb 1{R t � � -q :

lx2=2

2
General Instructions :

Read the following instructions very carefully and strictly follow them.

(i) This question paper contains 12 questions. All questions are


compulsory.
(ii) This question paper is divided into three Sections - Section A, B and C.
(iii) Section - A Q. Nos. 1 to 3 are very short answer type questions
carrying 2 marks each.
(iv) Section - B Q. Nos. 4 to 11 are short answer type questions carrying
3 marks each.
(v) Section - C Q. No. 12 is case based question carrying 5 marks.
(vi) Use of log tables and calculators is NOT allowed.

SECTION-A

1. Define rate of reaction. Write two factors that affect the rate of reaction. 2

2. Arrange the following compounds as directed: (any Two)

(i) In decreasing order of basic strength in aqueous solution :

(ii) In increasing order of solubility in water :

(iii) In decreasing order of their pKb values :

lx2=2

3 a�
Cil"B P.T.O.
3. Pti:if�furn m, � * �� ei:flq;<o, �fu.Q. :

Zn(s) + Cu2+ (aq.) ➔ Zn2+ (aq.) + Cu(s)


Ecellfcna'51q;R�m1TT�
(i) Cu2+ 3IBR1� e1�a1 ��m 3ff"<

(ii) Zn2+ 3mRl � e1�a1 it� m ? lx2=2

�-w
4. 3d-es+,1101 � � Pi£.i�fu.a 3IBR � � � :
Ti4+, V3+, Cr3+ , Mn3+
(q<J.t 1'1 � : Ti= 22, V = 23, Cr = 24, Mn = 25)

� � "3'e' 3IBR 'ch1 q�� 1PtQ,�

(i) � Pcl�4� -ij 3lftf � tI


(ii) � >Ii@ �TcNf1c6l<c6 � I
(iii) � Pcl�4� q � tI.
�*� 3qgq=a q;RUJ� I lx3=3

5. (ch) (i) �R� � � * 3mm 'CR� Llo <Pm oT d4 � � �·��cf�1f.lc6


Pcl�ie �fu.v_ I

(ii) e4l(Jlc6a1 � � cf)l � m � [Ni(CN) 1 2- � � � 1'414?14


4
��'4?1' Slljfcia 4?\�v_ I (q(J.tl'1"sfiJ.tTcfi: Ni= 28)
(iii) IUPAC � � 3mm: "CR Pi"'1f'etfu.a � cf>T � f'etfu.v_ :
1
sl$cffi 1fts1fite �-l,2-sl$�4'l�) ch1i1wl (III) lx3=3
31',lqT

NiCl2 • 6H2O 'ch1 AgNO 3 * � fq�l41 � i "ffi


(11) "(jj'il � 3qe�l-141ZJlcf> �
��lcf> *��*� AgCl*�� 3lcfa)ft@�.� I �fu.Q,:

(i) � 'cf>'I l-1(��I � I


(ii) � -ij 'Ni'� f°aoi4cf> l-141-ilcf>i:tI I
(iii) � cf>T IUPAC � I lx3=3

4 a�
[i]w
3. Write the Nernst equation for the following cell reaction:
Zn(s) + Cu2+ (aq) ➔ Zn2+ (aq) + Cu(s)
How will the Ece11 be affected when concentration of
(i) Cu 2+ ions is increased and
(ii) Zn2+ ions is increased ? lx2=2

SECTION-B
4. Following io�s of 3d-transition series are given:
Ti4+, V3+, Cr3+, Mn3+
(Atomic number: Ti= 22, V= 23, Cr= 24,.Mn = 25)
Identify the ion which is
(i) most stable in aqueous solution.
(i i) a stro_ng oxidising agent.
(iii) colourless in aqueous solution.
Give suitable reason in each. lx3=3

5. (a) (i) On the basis of crystal field theory, write the electronic
configuration for d4 ion if i'.\0 < P.
(ii) Using valence bond theory, predict the hybridization and
magnetic character of [Ni(CN) 4]2-.
(Atomic number of Ni= 28)
(i ii) Write the formula of the following complex using IUPAC norms:
Dichloridobis (ethane-1,2-diamirte) cobalt (III) 1x3=3
OR
(b) When a co-ordination compound NiCl2-6H20 mixed with AgN03, 2
moles of AgCl are precipitated per mole of the compound. Write
(i) Structural formula of the complex.
(ii) Secondary valency of 'Ni' in the complex.
(iii) IUPAC name of the complex. lx3=3

5 g�
[!]� P.T.O.
6. ��q;)fl��t50% ���4oftr-fl.wraf ,����
90%��?
�t: log 2 = 0.3010, log 10 = 1] 3

7. (q;) ����� 3qgcffi 3Gl�(UI ��M �311q;) "'��fa cb)�Q,:


(i) � ��1-1,�s e�(vt�u,
(ii) q,;1f'ii(-ttQff\-1 �
(iii) �Tq;q1-1 "1qq1�s �i:.fiq:;(01 � lx3=3
3lt1qJ
(�) � �311� A, B ctm C 't)e(i;HI �:
LiAlH4 HN0 2
(i) CH 3CH2 Cl KCN A B o oc C

NH3 (a) LiAlH4 C6H5S0 2 �l


(ii) CH3COOH A B C I½ x2=3
Ll (b) H20 )

s. (cf>) �'-1�f&a t � cf>RUT � :


(i) estiqo1 ffii:n 't) q;unqi(Uj cliT �� � � I
(ii) ��tf4�cf>T� ��i I
(iii)
......-...-... � I
cf>TtRt� E0 2+ cf;TlJR' tHj("qqi
M /M 1x3=3

(�) esfil-lUI mg311 "qil" � fl�Q, I d-� t �-ij � ffl � (-isfil-lUI � t �


����? esfiqu, �e,q,�a:.��cflnGR@l� ?· 3

9. � q;,af�q; 4°)fr1q; 'X' �eq:;1 � C5H 100 i 2,4-DNP �t<l"1 lRTa'T t, �


� tf>1 31qi;4�o � "qi«fT i � NaOH 't) � -ij 1 2 t � TJli � 'tR
�,<(lgiq;,4 � � i 1 �'X' � ,jijcflflqi(Ui 'tR � � S!lq-iT�q; � � i 1
�f&Q,:
(i) �fr,q; 'X' c#ft e<i:4-11 I
(ii) 2, 4-DNP�t��'X'c#ft���'SJTCij�'t)e<i:4-11 I
(iii) � 'X' "q;1" NaOH c#ft � -ij 12 "$ � lfll � � � Jt<lit:J � e<i:4-11� I
lx3=3
6 !l.lJJ
iil"M
6. A first order. reaction is 50% complete in 40 minutes. Calculate the time
required for the completion of 90% of reaction.
[Given : log 2 = 0.3010, log 10 = 1] 3

7. (a) Illustrate the following reactions giving suitable example in each


case:
(i) Gabriel phthalimide synthesis.
(ii) Carbylamine reaction.
(iii) Hoffmann bromamide degradation reaction. lx3=3
OR
(b) Write the structures of A, Band C in the following reactions:
LiAlH4 HN02
(i) CH3 CH2 Cl K CN ) A ---- B oc ) C
O
NH3 (a) LiAlH4 C6H5 SO2 Cl
(ii) CH3 COOH, L\ A ) B-------+ C 1 ½ x 2 = 3
(b) H2O

8. (a) Account for the following:


(i) Transition elements have higher enthalpies of atomisation.
(ii) Separation of a mixture of Lanthanoid elements is difficult.
(iii) The E 0M2+/M value for copper is positive. lx3=3
OR
(b) Define transition elements. Which of the d-block elements may not
be regarded as the transition· elements ? Why transition metals
generally form coloured compounds? 3

9. An organic compound 'X' with the molecular formula C 5H 10O forms


2,4-DNP derivative, does not reduce Tollens' reagent but gives positive
iodoform test �n heating with 12.in the presence of NaOH. Compound 'X'
gives ethanoic acid and propanoic acid on vigorous oxidation. Write the
(i ) Structure of the compound 'X'.
(ii) Structure of the product obtained when compound 'X' reacts with
2,4-DNP 'reagent.
(iii) Structures of the products obtained when compound 'X' is heated
with 12 in the presence of NaOH. 1x3=3
f5�11) 7 II P.T.o.
10. (cfl) �-� � <le l4f.lcf>-�$ffl�� 3lm �f&Q, I lx3=3

31trcfl
(�) � �� 34giffl 3c;i�(Oj � f'.1¥..ik-if{gct 1:fGl � "CJftmft@ th)�Q, :

(i) �c:Hl•ft �
'\ "
(l• 1·) 1e!GI�qcf> cf,leftI$s

(iii) � lx3=3

11. (a) f4""1k1ftga�������-300kJmoI-1 l:


+
Zn(s) + 2Ag+ (aq) ➔ Zn2 (aq) + 2Ag(s)
��� E�ell � qf\cf>("f-1 ihl�Q, I

�i: 1 F = 96500 moI-1)


(b) M g Cl 2 �� A::i cf;1 qf\cf>("f.j ihl�Q,m M g2+ m� er m�� A.0 �
2+1=3

�-1J

12. �����G q;)�3fu:�������:

�fc%�1�s, � � cf>i�fcmR;icf> �, cf>l4f.icf> �frli:61 � � qe!-€€t'ff crf � �


cf>i�f.l("f � � � I cf>l�Pi("f �-ij � c#rr �� Jiict�fr-it-1 c#rr � ::6u11("qcf>ai
� � � q;wJf � � � � � i I ��1$ii "cf>T � ��T("ll �
Pct�,$�1-,,.:1-1 � f.14�a �Tcfffiq:;<01 3fu: � �("fl�ii � Pi<if�a �q=q4;:i � Pci<R=fa �
� i 1 4>lil-11 "cf>T fatft4q:; �"1�T("11 � �Tcffftcf><01 3fu: �("q')l$-11 � sJl("f41sJ1-1 � �<R=fa
��ii

�fc%�1$s � � cf>litif.i("f � � � � � � � �
cf>i�fcR.IR-tcf> � �· � � � � � I �e!1$s � 4illl--tl it�
a-e!i$-?lsJ1-1 � � � I J@: q:;q � q:;q � a-�1�-?lsJl-1 � �e!1$s � � �(:'"il("f

��ti
8 ��
(!]�
10. (a) Write any three !"' ences
du1er between physisorption and
chemisorption. 1x3=3
OR
(b) Define the follow·mg terms wit
• h a suitable
• example m each :
(i) Lyophilic sol
(ii) Macromolecular colloid
(iii) Coagulation lx3=3

11. (a) The standard Gibbs energy (�rG0) for the following cell reaction is
-300 kJ mol-1:
Zn(s) + 2Ag+(aq) ➔ Zn2+ (aq) + 2Ag(s)
·Calculate E� ll for the reaction. (Given: lF = 96500 moI- 1)
e
(b) Calculate A::i for MgCl2 if AO values for Mg2+ ion and Cl - ion are
'"
106 S cm 2mol- 1 and 76.3 S cm2mol" 1 respectively. 2 + 1 =3

SECTION-C
12. Read the passage given below and answer the questions that follow :

Aldehydes, ketones and carboxylic acids are some of the important


classes of organic compounds containing carbonyl group. These are highly
-
polar molecules due to higher electro negativity of oxygen relative to
carbon in the carbonyl group. Aldehydes are prepared by dehydrogenation
or controlled oxidation of primary alcohols and controlled reduction of acyl
halides. Ketones are prepared by oxidation of secondary alcohols and
hydration of alkynes.
undergo nucleophilic addition reactions onto
Aldehydes and ketones
xylic acid does not undergo nucleophilic
the carbon yl group but carbo
hydrogens of aldehydes and ketones are
addition reaction. The alpha (a) -
and ketones having at least one a-hydrogen
acidic. Therefore aldehydes
.
undergo Aldo! condensation
9 g!!! P.T.O.
I
[i]ff
� � � � �el4"1 � � � .jilc:R•ficf>(Oj � �61$ID cf>T .3lraf.ft -a
�l<Nftfd � � � I cfiliOfcm�cf> � cf>l � � �161�l, �6i�il �

t mu�� t I �i)�R;cf> cf>i4'f<R:IR-icf> �-"cf>T


�l<mlcti<0,, "11��,��l � �-�4�c"1
�cf>
����et� t �1<N1lcfi<o1 -a �<�a�� s·t I cfi1anfcR.t
� ��61�1 � � -'iRle<et i1.,.,�, -a� amlcf> � � t 1
(a) � "cf>T � � � t -� � Wf�lU�fletal � � � � -ij
1

CH3COCH 3 , CH 3CHO, HCI:IO, C6H5COCH 3


(b) �� si1q-11"1 �������� oe,4Ptcfi qtt�� 1 1

(c) �61�ii � $)i\-11 � � cf>iiOf"cffi�cf> � � � � � �

�-? 1
(d) (i) �61$ID � $)i\11 �� (a) 6t$�-il"1 c€t ����t?

(ii) Pfi:.t�f<sla � 3c<t I� -ct,) ft;tf<siQ. : 1 + 1=2


� NaOH
2 Q-cHO

Pti:.tR-if<sia �31l��� R-if<si.Q.:

(a) KMnO4, KOH


1
(b) H
+

1+1+1+2=5

10
Aldehydes are easily oxidised by mild oxidising agents such as
Tollens' reagent and Fehling's reagent. Carboxylic acids are prepared by
the oxidation of primary alcohols, aldehydes and by hydrolysis of nitriles.
Aromatic carboxy lic acids are prepared by side-chain oxidation of alkyl
benzenes. Carboxylic acids are considerably more acidic than alcohols and
most of simple phenols.
(a) Arrange the following in the increasing order of their reactivity
towards nucleophilic addition reaction. 1
CH3 C0CH3, CH3 CH0, HCH0, C6 H6 C0CH3

( b) Give a ·simple chemi�al test to distinguish between Ethanal and


Propanone. 1
(c) Why carboxylic acid does not give nucleophilic addition reactions like
aldehydes and ketones? 1
(d) (i) Why a-hydrogen of aldehydes and ketones are acidic in nature?
(ii) Write the products in the following: 1 +1=2

Cn a OH
2OCHO-- _9 _ c_•_N_ _ _ _

OR
Write the major products of the following reactions

(a) KMn04, KOH


(i) 1
(b ) H
+

0
II

O
C-Cl
(ii)
I 1

1+1+1+2=5

11
......

221 A 12

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