JA DPP No.A1 To A10 For Online

DPPs BOOKLET-1 VIKAAS (JA) | CHEMISTRY
O/I-CHEMISTRY
TARGET : JEE (Main + Advanced) 2022


EST INF ORMA TIO

DPP
DAILY PRACTICE PROBLEMS
Course : VIKAAS(JA) NO. A1

1. Course of the week as per plan:
DPP No. # A1 (JEE-MAIN)
Total Marks: 60 Max. Time: 33 min.
Single choice Objective ('–1' negative marking) Q.1 to Q.12 (3 marks, 2 min.)
Numerical Value Questions ('0' negative marking) Q.13 to Q.15 (3 marks, 3 min.)
1. Which of the following is saturated hydrocarbon?
fuEu esa ls dkSulk larÌr gkbMªksdkcZu gSA
(A) (B) (C) (D*)
2. Carbon has strong tendency to show catenation due to :

(A) Its tetravalency (B) small size
(C) Its high C–C bond energy (D*) All of these
dkcZu esa izcyre Ja`[kyu dk xq.k ik;k tkus dk dkj.k gS %
(A) mldh prqla;kstdrk (B) NksVk vkdkj
(C) bldh vfèkdre C–C caèk ÅtkZ (D*) mijksDr lHkh
3. Which of the following is the empirical formula of C6H6 ?

(A*) CH (B) C2H2 (C) C6H6 (D) none of these
C6H6 dk ewykuqikrh lw=k fuEu esa ls dkSu gS \
(A*) CH (B) C2H2 (C) C6H6 (D) buesa ls dksbZ ugha
4. and are :
(A) Identical (B*) Homologous (C) Alkane (D) Saturated hydrocarbon
rFkk gS %
(A) le:i (B*) letkr (C) ,sYdsu (D) larÌr gkbMªksdkcZu
5. Which of the following is unsaturated hydrocarbon ?
fuEu esa ls dkSu vlarÌr gkbMªksdkcZu gS \
(A) (B) (C) (D*)
6. Which of the following is third member of CnH2n-2 homologous series ?

CnH2n-2 okyh letkr Js.kh dk rhljk lnL; dkSulk gS \
(A) C2H2 (B) C3H4 (C*) C4H6 (D) C4H8
7. Which of the following is molecular formula of ?
dk vkf.od lw=k dkSulk gS \

(A) C7H14 (B) C7H12 (C*) C7H10 (D) C7H8
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PAGE NO.-1
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8. How many  and  bond are present in CH2=CH–CH2–CCH
CH2=CH–CH2–CCH esa fdrus  rFkk  cU/k mifLFkr gSa \
(A*) 10 , 3   (B) 8 , 3   (C) 3 , 10   (D) 12 , 3 
9. How many  and -bonds are there in tetracynoethylene (CN) 2C=C(CN)2 molecule.
VsVªk lk;uks,Fkhyhu (CN2)C=C(CN)2 v.kq esa fdrus  rFkk -cU/k gSA
(A*) 9 , 9  (B) 9 , 7   (C) 5 , 9   (D) 5 , 7 
10. Which of the following alkanes contain primary, secondary, tertiary and quaternary carbon atoms
together?
fuEu esa ls fdl ,Ydsu esa izkFkfed] f}fr;d r`rh;d vkSj prq"d dkcZu ijek.kq mifLFkr gS \
(A) (CH3)3CH (B) (C2H5)3CH
(C*) (CH3)3CCH2CH(CH3)2 (D) (CH3)4C
11. Ketene CH2=C=O has
(A) Only sp2 carbon atom (B) Only sp carbon atom
(C*) sp2 and sp carbon atoms (D) sp3, sp2 and sp carbon atoms
dhVhu CH2=C=O esa gS %
(A) dsoy sp2 dkcZu ijek.kq (B) dsoy sp dkcZu ijek.kq
(C*) sp2 rFkk sp dkcZu ijek.kq (D) sp3, sp2 rFkk sp dkcZu ijek.kqa
12. Number of primary hydrogen is the given compound are
fn;s x;s ;kSfxd esa izkFkfed H dh la[;k gSA
(A) 10 (B*) 18 (C) 14 (D) 16
13. Total number of bonds in HCC–CCH ?

HCC–CCH esa dqy cU/kksa dh la[;k gS \
Ans. 9
14.
How many hydrogen atoms are present in the given structure ?

nh x;h lajpuk esa fdrus gkbMªkstu ijek.kq mifLFkr gSA
Ans. 22
15. Number of secondary halogen in the given compound are
fn;s x;s ;kSfxd esa f}rh;d gSykstu dh la[;k gSA
Ans. 2
PAGE NO.-2
O/I-CHEMISTRY


EST INF ORMA TIO

DPP

1. Course of the week as per plan :
DPP No. # A2 (JEE-ADVANCED)
Multiple choice objective ('–1' negative marking) Q.1 to Q.7 (4 marks, 2 min.)
Match the Following (no negative marking) Q.10 (8 marks, 6 min.)
1. Which of following is/are 3º chloride:
fuEu esa ls dkSuls 3º DyksjkbZM gS@gSa \
(A*) (B) (C) (D*)
2. The alicyclic compound/s is / are :

,fylkbfDyd ;kSfxd gS@gSa %
(A) (B*) (C*) (D*)

O
3. The correct options for a homologous series
(A*) All members have same general formula (B*) All members have same chemical properties
(C) All members have same physical properties (D*) All members have same functional groups
letkrh; Js.kh ds fy, dkSuls fodYi lgh gS\
(A*) lHkh lnL; dk lkekU; lw=k leku gksrk gSA (B*) lHkh lnL;ksa ds jklk;fud xq.k leku gksrs gSaA
(C) lHkh lnL;ksa ds HkkSfrd xq.k leku gksrs gSaA (D*) lHkh lnL;ksa ds fØ;kRed lewg leku gksrs gSaA
4. What is correct about and ?

(A*) both have same empirical formula (B*) both have same general formula
(C*) both have same molecular formula (D) both are homologous
rFkk ds fy, lR; D;k gS?

(A*) nksuks leku ewykuqikrh lw=k j[krs gSA (B*) nksuks leku lkekU; lw=k j[krs gSA
(C*) nksuks leku v.kq lw=k j[krs gSA (D) nksuks letkr gSA
5. How many of the following show general formula CnH2n – 6?

fuEu esa ls fdrus lkekU; lw=k CnH2n – 6 n'kkZrs gSa \
CH3
(A*) H–CC–CC–CH3 (B) CH2=C=C=CH2 (C*) (D) H–CC–H
Sol. (A) C5H10 – 6 = C5H4

(C) C7H14 – 6 = C5H8
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6. Which of the following is/are alicyclic hydrocarbon
fuEu esa ls dkSulk ,fylkbfDyd gkbMªksdkcZu ugha gS &
(A*) (B) (C*) (D*)
Sol. is not an alicyclic hydrocarbon. It is an acyclic hydrocarbon.

,fylkbfDyd gkbMªksdkcZu ugha gSA ;g ,d vpfØ; gkbMªksdkcZu gSA
7. Which molecules have sp3 carbon atom :

fuEu esa ls dkSulk v.kq sp3 ladfjr dkcZu j[krk gSa %
(A*) (B*) (C) HCC–CH=CH2 (D*) H–CC–CH3
8. In the given compounds how many are unsaturated hydrocarbon?

fuEu esa ls fdrus ;kSfxd vlarÌr gkbMªksdkcZu gS\
CH3 OH NH2
, , , , , , , ,
N
Ans. 3
9. How many amines are tertiary amines:

fdrus ,ehu r`rh;d ,ehu gSa \
Ph H
N N
(1) (2) (3) Ph–NH2 (4) Ph3N (5)
Ph NH2
N NH NH
(6) (7) (8) (9)
NH2
Ans. 3
Sol. 1, 4, 6
10. Match the following :

dkWye lqesfyr dhft,A
Column-I Column-II
(Compounds) (Class of compounds)
dkWye-I dkWye-II
¼;kSfxd½ ¼;kSfxd dk oxhZdj.k½
Saturated compound
(A) (p)
(vlarÌr ;kSfxd)
O Heterocyclic compound
(B) (q)
(fo"kepØh; ;kSfxd)
Unsaturated compound
(C) (r)
(vlarÌr ;kSfxd)
(D) OH (s) Hydrocarbon (gkbMªksdkcZu)
Ans. (A  p, s) ; (B  p, q) ; (C  r, s) ; (D p)
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O/I-CHEMISTRY


EST INF ORMA TIO

DPP

1. Course of the week as per plan : 2. Course covered till previous week :
Total Marks: 42 Max. Time : 31 min.
1 2 3 4 5 6
1. In the organic compound CH2  CH – CH2 – CH2 – CH  CH2 , the pair of hybridised orbitals involved in
the formation of C2–C3 bond is :
1 2 3 4 5 6
dkcZfud ;kSfxd CH2  CH – CH2 – CH2 – CH  CH2 esa dkcZu la[;k C2–C3 esa dkSuls ladfjr d{kd lfEefyr
gSa%
(A) sp–sp2 (B) sp–sp3 (C*) sp2–sp3 (D) sp3–sp3
2. Which of the following has correct numbering :
fuEu esa ls fdldk vadu lgh fn;k x;k gS \
4
4 Cl
3 1
2 4
6 3 6
(A) 7 5 3 (B) (C*) 2 (D)
1 5 2
1
2 Br Cl
1
3. In following compound -
fuEu ;kSfxd esa &
CH3 CH3
CH3  CH2  C  CH  CH  CH2  CH3
CH3 CH3
The correct lowest set of locants are :
fuEu esa ls dkSulk LFkkukadks dk U;wure leqPp; lgh gS \
(A*) 3,3,4,5 (B) 3,4,5,5 (C) 4,5,3,3 (D) 5,5,4,3
CH3 CH3
1 2 3
| 4 5| 6 7
Sol. (A) CH3–CH2–C – CH–CH–CH2–CH3
| |
CH3 CH3
Lowest set of Locant (3, 3, 4, 5)
4. Which of the following has longest chain of carbon :
fuEu esa ls fdlesa dkcZu dh lokZf/kd yEch Jà[kyk gS %
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CH2 — CH3
|
(A) CH3 — CH — CH2 — CH — CH3 (B)
|
CH2 — CH3
CH3
|
(C*) (D) CH3 — CH — CH2 — CH2 — CH — CH2 — CH3
|
CH2 — CH3
5. Which of the following is 3º chloride?

fuEu esa ls dkSulk 3º DyksjkbM gS\
(A) CH3–CH2–Cl (B) (CH3)2CHCl (C*) (CH3)3CCl (D) (CH3)3CCH2Cl
6. What is the correct IUPAC name of (C2H5)4C is:

(A) Tetraethyl methane (B*) 3,3-Diethyl pentane
(C) Triethylethane (D) Octane
(C2H5)4C dk lgh IUPAC uke D;k gS \
(A) VsVªk,sfFky esFksu (B*) 3,3-Mkb,sfFky isUVssu (C) Vªkb,sfFky ,sFksu (D) vkWDVsu
7. Which of the following are used as primary suffix :

(A) Bromo (B) Nitro (C) Methoxy (D*) –ene
fuEu esa dkSu çkFkfed vuqyXu ds :i esa iz;qDr gksrk gS %
(A) czkskeksa (B) ukbVªks (C) feFkksDlh (D*) –bZu
CH3 CH3
8. The name of CH3–C—CH2–CH–CH3 is :
CH3
(A) Isohexane (B*) 2,2,4-Trimethylpentane
(C) Neoocatne (D) Isoheptane
CH3 CH3
CH3–C—CH2–CH–CH3 fuEu ;kSfxd dk uke gS %
CH3
(A) vkblksgSDlsu (B*) 2,2,4- VªkbZesfFkyisUVsu (C) fu;ksvkWDVsu (D) vkblksgsIVsu
9.
What is incorrect about the given structure?

nh xbZ lajpuk ds ckjs esa vlR; dFku gS\
(A) It has six D.U. (B) It has ten sp2 hybrid C-atom
(C) It has ten sp2–sp2 C–C  bond (D*) All are incorrect.
(A) bldk D.U. N% gSA (B) ;g nl sp2 ladfjr C-ijek.kq j[krk gSA
(C) ;g nl sp2–sp2 C–C  ca/k j[krk gSA (D*) lHkh dFku xyr gSA
PAGE NO.-6
10. Which of the following groups is attached to the cyclohexane ring in the following compound.
(A) Methyl (B) n-Propyl (C*) Iso-propyl (D) Neo-pentyl

fuEu ;kSfxd esa fuEu esa ls dkSu lk lewg lkbDyksgsDlsu oy; ls tqMk gS &
(A) esfFky (B) n-izksfiy (C*) vkblksizksfiy (D) fu;ksisafVy
11. Which of the following alkyl group are possible from Iso-butane ?
(A) Iso-Butyl & n-butyl (B) Sec. butyl & Ter. butyl
(C) n-butyl & Ter. butyl (D*) Iso-butyl & Ter. butyl
fuEu ls dkSu ls ,fYdy lewg vkblksC;qVsu ls lEHko gaS
(A) vkblksC;wfVy o n-C;wfVy (B) f}rh;d C;wfVy o r`rh;dC;wfVy
(C) n-C;wfVy o r`rh;d C;wfVy (D*) vkblksC;wfVy o r`rh;d C;wfVy
12. Number of sp2 – sp2 C-C -bond in the given compound are :
fn;s x;s ;kSfxd esa gkbMªkstu ijek.kqvksa dh la[;k gSA
Ans. 3
13. How many carbon atoms are present in the principle chain of following compound .
uhps fn;s x;s ;kSfxd dh eq[; Jà[kyk esa fdrus dkcZu ijek.kq ekStqn gSaA
Ans. 11
14. How many 1° hydrogens are present in Iso-octane:
vkblks&vkWDVsu esa fdrus 1° gkbMªkstu mifLFkr gS\
Ans. 15
ChemINFO IUPAC NOMENCLATURE

Daily Self-Study Dosage for mastering Chemistry Allylic / Vinylic / Benzylic
(i) Allylic Compounds: In these compounds monovalent functional group is linked to sp3 – hybridised carbon
atom which is next to carbon-carbon double bond, i.e. to an allylic carbon. These may be further classified as
1°, 2° or 3°.
CH3 I
*
* –Cl
CH2=CH–CH2
1° Allylic chloride 3°-Allylic iodide

Note : * represents allylic carbon.
(ii) Benzylic Compounds : In these compounds, monovalent functional group is attached to a sp 3-hybridized
carbon atom next to an aromatic ring i.e. to a benzylic carbon. These may be further classified as 1°, 2°, 3°.
PAGE NO.-7
(iii) Vinylic Compounds : In these compounds, the monovalent functional group is attached to one of the
carbon atoms of the carbon - carbon double bond.
Note : The compounds which have double bond and OH group on same carbon are unstable hence vinylic
alcohol are unstable.

Daily Self-Study Dosage for mastering Chemistry Allylic / Vinylic / Benzylic
(i),fyfyd ;kSfxd % bu ;kSfxdksa esa ,dy la;ksth fØ;kRed lewg ml sp3– ladfjr dkcZu ijek.kq ls tqM+k gksrk gS tks vkxs
dh vksj dkcZu dkcZu f}caèk vFkkZr~ ,fyfyd dkcZu j[krk gSA bUgsa Hkh 1°, 2° ;k 3° esa oxhZd`r fd;k x;k gSA
uksV : * iznf'kZr ,fyfyd dkcZuA

(ii) csUtkbfyd ;kSfxd % bu ;kSfxdksa esa ,dy la;ksth fØ;kRed lewg ml sp3-ladfjr dkcZu ijek.kq ls tqM+k gksrk gS tks
csUthu ls oy; vFkkZr~ csUtkbfyd dkcZu ls tqM+k gksrk gSA bUgs Hkh 1°, 2°, 3° esa oxhZd`r fd;k x;k gSA
(iii) fouk;fyd ;kSfxd % bu ;kSfxdksa esa ,dy fØ;kRed lewg dkcZu&dkcZu f}caèk ds fdlh ,d dkcZu ls tqM+k gksrk gSA
uksV % ;kSfxd ftuesa leku dkcZu ij f}caèk rFkk OH lewg ik;k tkrk gS] os vLFkk;h gksrk gSA vr% fouk;fyd ,YdksgkWy
vLFkk;h gksrk gSA
Memorize this theory as soon as you get the DPP. Revize it regularly and master this concept by practice.
(i). Which of the following compound is unstable
fuEu esa ls dkSulk ;kSfxd vLFkk;h gS %
(A) CH3–CH=CH–Cl (B) CH2=CH–CH2–OH
(C) CH2=CH–CH2–Cl (D*) CH3–CH=CH–OH
(ii). CH2=CH–Br is a/an

(A) Allylic bromide (B) Benzylic bromide (C*) Vinylic bromide (D) All of these
CH2=CH–Br dk uke gS %
(A) ,fyfyd czksekbM (B) csUtkbfyd czksekbM (C*) fouk;fyd czksekbM (D) mijksDr lHkh
PAGE NO.-8
(iii). Which of the following statement is / are correct for following compound
(A) It is an allylic iodide (B) It is a vinylic iodide

(C) It is 2° benzylic iodide (D*) It is 1° benzylic iodide
fuEu ;kSfxd ds fy, dkSulk dFku lgh gS@gSa
(A) ;g ,d ,fyfyd vk;ksMkbM gSA (B) ;g ,d fouk;fyd vk;ksMkbM gS

(C) ;g ,d 2° csUtkbfyd vk;ksMkbM gSA (D*) ;g ,d 1° csUtkbfyd vk;ksMkbM gSA
PAGE NO.-9
O/I-CHEMISTRY


EST INF ORMA TIO

DPP

Total Marks : 43 Max. Time : 25 min.
Numerical Value Questions ('0' negative marking) Q.9 (3 marks, 3 min.)
1. Which of the following IUPAC names of alkyl radicals is/are correct :
(A*) is 2, 3-dimethylbutyl. (B*) is 1-methylpropyl
(C*) is 1, 2-dimethylpropyl (D*) is 1-methylethyl
fuEu esa ls dkSuls ,fYdy ewyd dk IUPAC uke lgh gSa %
(A*) , 2, 3-MkbesfFkyC;wfVy (B*) , 1-esfFky izksfiy gSA
(C*) , 1, 2-MkbesfFkyizksfiy gSA (D*) , 1-esfFky,sfFky gSA
2. Which of the following IUPAC name is/are correct :
(A*) 1- Ethyl-2-methylcyclopropane
(B*) 4-Ethyl-2-methyl-1-propylcyclohexane
(C*) 1,1,2-Trimethylcyclopentane
(D*) 1,1-Dimethyl-4-propylcyclohexane
PAGE NO.-10
fuEu esa ls dkSulk@dkSuls IUPAC uke lgh gS %
(A*) 1- ,fFky-2-esfFkylkbDyksizksisu
(B*) 4-,fFky-2-esfFky-1-izksfiylkbDyksgsDlsu
(C*) 1,1,2-VªkbesfFkylkbDyksisUVsu
(D*) 1,1-MkbZesfFky-4-çksihylkbDyksgsDlsu
3. The correct structure of 2,3,4-Trimethylhexane is :

2,3,4-VªkbesfFkygsDlsu dh lgh lajpuk gksxh \
(A*) (B*) (C) (D*)
4. In which of the following cyclic ring is a parent chain:

fuEu esa ls fdl dkcZfud ;kSfxd pfØ; oy; iSr`d Ja`[kyk gS %
(A*) (B) (C*) (D*)
5. Which of the following is/are incorrect IUPAC name?

(A*) 1,1,1-Dimethyl ethane (B*) 2- Methyl-3-ethylpentane
(C*) 3- Methyl-4-ethylhexane (D) 3- Ethyl-4-methylhexane
fuEufyf[kr esa dkSulk@dkSuls xyr IUPAC uke gS\
(A*) 1,1,1- MkbZesfFky ,sFksu (B*) 2- esfFky-3-,fFkyisUVsu
(C*) 3-esfFky-4-,fFkygsDlsu (D) 3-,fFky-4-esfFkygsDlsu
6. Which of the following is/are correct ?

Cl Br
(A*) 1-buten-3-yne has 7  & 3 bonds (B) Total number of substituent in OH is 4.

(C*) C2(CN)4 has 9 and 9 bonds. (D*) Cyclohexane has only one type of carbon atoms.
fuEu esa ls dkSulk@dkSuls lgh gS@gSa \
Cl Br
(A*) 1-C;wVhu-3-vkbu 7  rFkk 3 ca/k j[krk gSA (B) OH esa izfrLFkkih dh dqy la[;k 4 gSA

(C*) C2(CN)4 9 rFkk 9 ca/k j[krk gSA (D*) lkbDyksgsDlsu dsoy ,d izdkj dk dkcZu ijek.kq j[krk gSA
PAGE NO.-11
  
Sol. 
(A) H—C C  C—H 7, 3
C
 
H H
Cl Br
(B) OH 3 Substituent (izfrLFkkih)

 
(C) N C   C N 9, 9

C C
   
N C C N
(D) Cyclohexane has only 2º carbon atoms.
(D) lkbDyksgsDlsu dsoy 2º dkcZu ijek.kq j[krk gSA
7. Which of the following is/are correct IUPAC Name ?

fuEufyf[kr esa ls dkSulk@dkSuls lgh IUPAC uke gS\
(A*) CH3–C(CH3)2 – CH2–CH=CH2 4,4-Dimethylpent-1-ene 4, 4-MkbZesfFkyisUV -1-bZu
(B*) CH3CH2C(Br) = CH – Cl 2-Bromo-1-chlorobut-1-ene 2-czkseks-1-DyksjksC;wV-1-bu
(C*) CH3–CH=C–CH2–CH3 3-Ethyl-2-hexene 3-,fFky-2-gSDlhu
CH2–CH2–CH3
(D*) CH2=CH—CH(C2 H5)C=CH2 is ..... 2-Bromo-3-ethylpenta-1,4-diene 2-czksekss-3-,fFkyisUVk-1,4-MkbbZu
Br
8. Which of the following is/are correct IUPAC Name ?

fuEufyf[kr esa ls dkSulk@dkSuls lgh IUPAC uke gS\
(A*) CH3–CH(C2H5)–CH=CH–CH3 4-Methylhex-2-ene 4-esfFkygSDl-2-bZu
(B*) 5,6-Diethyl-3,8-dimethyldec-4-ene
5,6-MkbZ,fFky-3,8-MkbZesfFkyMsd-4-bZu
(C*) Diethenyl pentadiene MkbZ,fFkukby isUVkMkbbZu
(D*) 4-Ethenylhepta-1, 3-dien-6-yne
4-,sfFkukbygsIVk-1, 3-MkbZu-6-vkbu
9. How many of following IUPAC names of given strutures are correct.
fuEu esa ls fdrus IUPAC lajpuk ds uke lgh gSaA
(1) 3,4-Diethyl-2,5-dimethyloctane
3,4-MkbZ,fFky-2,5-MkbZesfFkyvkWDVsu
PAGE NO.-12
(2) 5-Ethyl-1-methyl-2-propylcyclohexane
5-,fFky-1-esfFky-2-izksfiylkbDyksgsDlsu
Br
Cl Br
(3) 1,2,4-Tribromo-3,5,6-trichlorocyclohexane
Br Cl
Cl
1,2,4-VªkbZczkseks-3,5,6-VªkbZDyksjkslkbDyksgsDlsu
Cl Br
| |
(4) CH3—C—CH2—C—CH3 4-Bromo-2-chloro-4-methyl-2-nitrohexane
| |
NO2 Et
4-czkseks-2-Dyksjks-4-esfFky-2-ukbVªksgsDlsu
Ans. 3 (1 , 3 , 4)
10. Match the following : feyku dhft,A

Column I Column II
Compound ;kSfxd Degree of unsaturation vlarÌrrk dh dksfV
(A) (P) 2
CH3
(B) H3C – CH – CH2 – C = CH3 (Q) 5
(C) (R) 4
(D) (S) 3
Sol. (A) (S), (B) (R), (C)  (Q), (D)  (P)

Daily Self-Study Dosage for mastering Chemistry Dienes, or diolefins or alkadienes
Dienes or Diolefins or Alkadienes
Compounds containing two double bonds are called as dienes or diolefins. Dienes may be of three
types.
(i) Cumulative diene : When the two double bonds are present on the adjacent carbon atoms, the diene
is called as cumulative diene. Such sytem is found in allenes.
CH2 = C = CH2 CH3–CH=C=CH–CH3
1, 2-Propadiene 2,3-Pentadiene
(Allene) (Dimethylalleine)
PAGE NO.-13
(ii) Conjugated diene : when the two double bonds are separated by one single bonds, the diene is called
as conjugated diene.
CH2 = CH– CH = CH2

1,3-butadiene
(iii) Isolated diene : When the two double bonds are separated by more than one single bond, the diene is
called isolated diene.
CH2=CH–CH2–CH=CH2 CH2=CH–CH2–CH2–CH=CH2
1,4-pentadiene 1,5-Hexadiene

Daily Self-Study Dosage for mastering Chemistry MkbbZu] ;k MkbvkWfyfQu ;k ,YdkMkbZu
MkbbZu] ;k MkbvkWfyfQu ;k ,YdkMkbZu
,d v.kq esa nks f}cU/k ;qDr ;kSfxd MkbbZu ;k MkbvkWyhu dgykrs gSaA MkbbZu rhu izdkj ds gks ldrs gS &
(i) lap;h MkbbZu % tc nks f}cU/k fudVorhZ dkcZu ijek.kq ij mifLFkr jgrs gS rks bl izdkj ds MkbbZu dk lap;h
MkbbZu dgrs gSA ,slk ra=k ,yhu esa ik;k tkrk gSA
CH2 = C = CH2 CH3–CH=C=CH–CH3
1, 2-izksisMkbu 2,3-isUVkMkbZu
(,yhu) (MkbesfFky ,yhu)
(ii) la;qXeh MkbbZu % tc nks f}cU/k ,d cU/k }kjk i`Fkd gksrs gS],sls MkbbZu dks la;qXeh MkbZu dgrs gSA
(iii) foyfxr MkbbZu % tc nks f}cU/k ,d ls vf/kd ,dy cU/kksa }kjk i`Fkd gksrs gS] ,sls MkbbZu foyfxr MkbZu dgykrs gSA
CH2=CH–CH2–CH=CH2 CH2=CH–CH2–CH2–CH=CH2
1,4-isUVkMkbZu 1,5-gsDlkMkbZu
(i). Which of the following compound is cumulative diene.

fuEu esa ls dkSulk ;kSfxd lap;h MkbbZu ;qDr gSA
(A) (B) (C*) (D)
(ii). Which of the following compound have conjugated diene

fuEu esa ls dkSulk ;kSfxd la;qXeh MkbbZu ;qDr gSA
(A) (B*) (C) (D)
(iii). Which of the following compound does not have isolated diene
fuEu esa ls dkSulk ;kSfxd foyfxr MkbbZu ugha gSA
(A) (B) (C*) (D)
PAGE NO.-14
O/I-CHEMISTRY


EST INF ORMA TIO

DPP

1. Course of the week as per plan : 2. Course covered till previous week :
1. The IUPAC name of is :
(A*) Pent-4-en-2-amine (B) 1-Methylbut-3-en-1- amine

(C) Pent-1-en-4-amine (D) 4-Methylbut-1-en-4-amine
dk IUPAC uke gS %
(A*) isUV-4-bZu-2-,ehu (B) 1-esfFkyC;wV-3-bZu-1- ,ehu

(C) isUV-1-bZu-4-,ehu (D) 4-esfFkyC;wV-1-bZu-4-,ehu
2. The compound 2-Ethylhex-2-ene-1-thiol has the structure :

;kSfxd 2-,fFkygsDl-2-bZu-1-FkkbZvkWy ljapuk j[krk gS %
(A) C2H5CH = CHCH2CH2SH (B)
(C*) (D)
3. The correct IUPAC name for the compound (CH3)3 CSO3H is :

(A) Trimethylmethane-1-sulphonic acid (B) 1,1-Dimethylethane-1-sulphonic acid
(C) Butanesulphonic acid (D*) 2-Methylpropane-2-sulphonic acid
(CH3)3 CSO3H ;kSfxd dk lgh IUPAC uke gS %
(A) VªkbZesfFkyesFksu-1-lYQksfud vEy (B) 1,1-MkbZesfFky,Fksu-1-lYQksfud vEy
(C) C;wVsulYQksfud vEy (D*) 2-esfFkyçksisu-2-lYQksfud vEy
4. IUPAC name of is :
(A) 4-Hydroxy-3-mercaptohexan-2-amine (B*) 5-Amino-4-mercaptohexan-3-ol

(C) 3-Mercapto-2-aminohexan-4-ol (D) 2-Amino-4-hydroxyhexane-3-thiol
dk IUPAC uke gS %
(A) 4-gkbMªkWDlh-3-ejdSIVksgsDlsu-2-,ehu (B*) 5-,ehuks-4-ejdSIVksgsDlsu-3-vkWy

(C) 3-ejdSIVks-2-,ehuksgsDlsu-4-vkWy (D) 2-,ehuks-4-gkbMªkWDlhgsDlsu-3-FkkbZvkWy
PAGE NO.-15
5. The correct IUPAC name of the the compound is :
(A) 1-Ethyl-N-methyl-N-propylpropan-1-amine (B) 3-[N-Methyl-N-propylamino]pentane

(C) N-Methyl-N-propylhexan-3-amine (D*) N-Methyl-N-propylpentan-3-amine
;kSfxd dk IUPAC uke gS%
(A) 1-,fFky-N-esfFky-N-çksfiyçksisu-1-,ehu (B) 3-[N-esfFky-N-çksfiy,ehuks]isUVsu

(C) N-esfFky-N-çksfiygsDlsu-3-,ehu (D*) N-esfFky-N-çksfiyisUVsu-3-,ehu
6. IUPAC name of is :
(A) 1,2,4-Trihydroxycyclopentane (B) Cyclopentane-1,3,4-triol

(C*) Cyclopentane-1,2,4-triol (D) 1,3,4-Trihydroxycyclopentane
dk IUPAC uke gS%
(A) 1,2,4-VªkbZgkbMªkWDlhlkbDyksisUVsUk (B) lkbDyksisUVsUk-1,3,4-VªkbvkWy

(C*) lkbDyksisUVsUk-1,2,4-VªkbvkWy (D) 1,3,4-VªkbZgkbMªkWDlhlkbDyksisUVsUk
7. Which of the following has incorrect IUPAC numbering. fuEu esa ls fdldk xyr IUPAC Øekadu gSA
(A*) (B)
(C) (D)
8. Which is not secondary alcohol

(A) Isopropanol (B) Secondary butanol
(C) 3-methylpentane-2-ol (D*) Pentan-1-ol
fuEu esa ls dkSulk f}rh;d ,YdksgkWy ugha gS &
(A) vkblksizksisuksy (B) f}rh;d C;wVsukWy (C) 3-esfFkyisUVsu-2-vkWy (D*) isUVsu-1-vkWy
9. Which of the following has correct numbering.

fuEu esa ls dkSuls ;kSfxd es lgh vadu gS &
OCH3 SH NH2 OH
3 5 1 1
4 2 4 6 2 6 2
(A) 1 (B*) (C) (D) 3
5 OH 3 1 OH 3 5 OH 5 OH
6 2 4 4
OCH3
5
4 6
Sol. (A) Correct numbering of A is
3
2 1 OH
NH2
5
4 6
(C) Correct numbering of C is
3 1 OH
2
PAGE NO.-16
10. The IUPAC name of the compound CH3CONHBr is :
(A) 1-Bromoacetamide (B*) N-Bromoethanamide
(C) Ethanoyl bromide (D) None of these
CH3CONHBr dk lgh IUPAC uke gSA
(A) 1-czkseks,sflVkekbM (B*) N-czkseks,sFksukekbM (C) ,sFksukWby czksekbM (D) buesa ls dksbZ ugah
11. What is the IUPAC name of :
(A) 3-mercapto-5-amino benzene carboxylic acid.

(B*) 3-amino-5-mercapto benzene carboxylic acid.
(C) 5-amino-3-mercapto benzene carboxylic acid.
(D) 5-mercapto-3-amino benzene carboxylic acid.
dk IUPAC uke D;k gSA
(A) 3-ejdsIVks-5-,ehuks csUthu dkcksZflfyd vEy (B*) 3-,ehuks-5-ejdsIVks csUthu dkcksZflfyd vEy
(C) 5- ,ehuks-3-ejdsIVks csUthu dkcksZflfyd vEy (D) 5-ejdsIVks-3-,ehuks csUthu dkcksZflfyd vEy
12. The correct IUPAC name for the compound is :
(A) 4-Hydroxy-3-methylcyclopentan-1-one (B*) 3-Hydroxy-4-methylcyclopentan-1- one

(C) 5-Methyl -3-oxocyclopentan-1-ol (D) 2-Methyl -4-oxocyclopentan-1-ol
;kSfxd dk lgh IUPAC uke gS %
(A) 4-gkbMªkWDlh-3-esfFkylkbDyksisUVsu-1-vkWu (B*) 3-gkbMªkWDlh-4-esfFkylkbDyksisUVsu-1-vkWu

(C) 5-esfFky-3-vkWDlkslkbDyksisUVsu-1-vkWy (D) 2-esfFky-4-vkWDlkslkbDyksisUVsu-1-vkWy
13. How many carbon atoms are present in parent chain (main chain) of the following compound ?
fuEu ;kSfxd dh tud Ja`[kyk ¼eq[; Jà[kyk½ esa fdrus dkcZu ijek.kq mifLFkr gS \
Ans. 06
Sol.
14. In the given compound IUPAC numbering of –Br is :

fuEufyf[kr ;kSfxd esa] –Br dk lgh IUPAC vadu gS\
PAGE NO.-17
Br
z
y
x
OH
Ans. 4
15. In the given compound how many carbon atoms present in the parent chain.
fuEufyf[kr ;kSfxd dh iSr`d Jaq[kyk esa fdrus dkcZu ijek.kq mifLFkr gS\
COOH
Ans. 7

Daily Self-Study Dosage for mastering Chemistry IUPAC Nomenclature of Aromatic compound in which
Benzene is side chain.
If benzene is used as side chain then phenyl is used as prefix. There are following rule in which benzene is
used as side chain.
Rule -1 : If main chain have any functional group or unsaturation (double or triple bond) then benzene is used
as side chain irrespective of number of carbon in main chain .
CH2 — COOH
OH
i.e,.
2 – Phenyl propanol – 1 1 – Phenyl prop–1-ene Phenyl ethanoic acid
Rule – 2 : If main chain have substitute like halogen , nitro , etc. then benzene is used as side chain.
i.e,
Cl
CH2 — Br
2-chloro-1-phenylpropane Bromophenylmethane
Rule – 3 : If more than one benzene ring attached to same carbon atom then it is consider as side chain.
i.e.,
CH2
Diphenyl methane 2 , 2-Diphenylpentane

Daily Self-Study Dosage for mastering Chemistry ,sjksesfVd ;kSfxd ftues csathu ik'oZ Jà[kyk ds :i esa
iz;qDr gksrh gS dk IUPAC ukedj.kA
;fn csasftu] ik'oZ Jà[kyk esa iz;qDr gksrk gS rks Qsfuy dks iwoZyXu esa iz;qDr djrs gSaA fuEu fu;e }kjk csfUtu dks ik'oZ Jà [kyk
esa iz;qDr djrs gSaA
fu;e-1 : ;fn eq[; Jà[kyk esa dksbZ Hkh fØ;kRed lewg ;k vlarÌrk (f}cU/k ;k f=kcU/k) gks rks csathu dks ik'oZ Jà[kyk ds :i esa
iz;qDr djrs gSa pkgs eq[; Jà[kyk esa fdrus Hkh dkcZu dh la[;k gksA
PAGE NO.-18
CH2 — COOH
OH
mnk-,
2–Qsfuy izksisuksy–1 1–Qsfuy izksi–1-bu Qsfuy ,Fksuksbd vEy
fu;e-2 : ;fn eq[; Jà[kyk esa izfrLFkkih lewg tSls gsykstu] ukbVªks vkfn gS rks csathu dks ik'oZ Jà[kyk esa iz;qDr djrs gSaA
mnk-,
Cl
CH2 — Br
2–Dyksjks–1-Qsfuyizksisu czkseksQsfuyesFksu
fu;e-3 : ;fn ,d gh dkcZu ls ,d ls vf/kd csathu oy; tqM+h gqbZ gks rks csathu dks ik'oZ Jà[kyk ekuk tkrk gSA
CH2
mnk-,
MkbQsfuy esFksu 2 , 2- MkbZQsfuyisUVsu

(i). Correct IUPAC name of the following compound is
Br
Br
(A*) 2,3-Dibromo-1-phenyl pentane (B) 3,4-Dibromo-5-phenyl pentane
(C) 2,3-Dibromophenyl benzene (D) 3,4-Dibromophenyl benzene
fuEu ;kSfxd dk lgh IUPAC uke gS %
Br
Br
(A*) 2,3-Mkbczkseks-1-Qsfuy isUVsu (B) 3,4-Mkbczkseks-5-Qsfuy isUVsu
(C) 2,3-Mkbczkseks Qsfuy csathu (D) 3,4-MkbczkseksQsfuy csathu
(ii). Correct IUPAC name of the following compound is
(A) Ethenyl benzene (B) Ethylbenzene (C*) Phenylethene (D) Ethene benzene
(A) ,fFkfuy csathu (B) ,fFkycsathu (C*) Qsfuy,Fkhu (D) ,Fksucsathu
PAGE NO.-19
(iii). Correct IUPAC name of the following compound is :
(A) Ethyl tribenzene (B*) 1,1,1-Triphenyl ethane

(C) 1-Ethyl-1,1-diphenyl benzene (D) None of these
(A) ,fFkyVªkbcsathu (B*) 1,1,1-VªkbQsfuy ,Fksu

(C) 1-,fFky-1,1-MkbZQsfuycsathu (D) buesa ls dksbZ ugha
PAGE NO.-20
O/I-CHEMISTRY


EST INF ORMA TIO

DPP

Total Marks : 42 Max. Time: 26 min.
1. Which of the following is/are incorrect IUPAC name
(A*) 2-Bromo cyclohex-5-ene carbaldehyde (B*) Ethyl-2-vinyl pentanoate
(C) 5-Bromo-3-chlorohept-3-ene (D*) 2-Ethenylhexa-1,5-diene
fuEu esa ls dkSulk IUPAC uke lgh gSA
(A*) 2-czksekslkbDyksgsDl-5-bZu dkcksZfYMgkbM (B*) ,sfFky-2-foukbZy isUVsuks,V
(C) 5-czkseks-3-DyksjksgsIV-3-bZu (D*) 2-,sfFkfuygsDlk-1,5-MkbbZu
2. In which of the following cyclic ring is parent chain ?

fuEu esa ls fdl dkcZfud ;kSfxd esa pfØ; oy; ewy@iSr`d Ja`[kyk gS \
(A) (B*) (C*) (D*)
3. Which of the following IUPAC names are correct :
(A) CH2—CH—CH2—CH2 3-(Aminomethyl)butanamine
NH2 CH3 NH2

CH2Cl
(B*) CH2—CH—CH2 1,3-Dichloro-2(chloromethyl)propane
Cl Cl
COOH
SO3H
(C*) 4-formyl-2-sulphobenzoic acid
O
HO
(D*) 2-bromo-6-chlorophenol
Br Cl
PAGE NO.-21
fuEu esa ls dkSulk@dkSuls IUPAC uke lgh gS@gSa \
(A) CH2—CH—CH2—CH2 3-( ,ehuksesfFky) C;wVsusekbu

NH2 CH3 NH2
CH2Cl
(B*) CH2—CH—CH2 1,3-MkbZDyksjks -2(DyksjksesfFky) izksisu
Cl Cl
COOH
SO3H
(C*) 4-QkWfeZy-2-lYQkscsUtkWbd vEy
O
HO
(D*) 2-czkseks-6-DyksjksfQuksy
Br Cl
Sol. Correct name of (A) is 2-methylbutane-1,4-diamine.

(A) dk lgh uke 2-esfFkyC;wVsu-1,4-MkbZ,ehu gSA
4. Which of the following has correct IUPAC name ?

CHCl2
(A*) Dicholoro phenylmethane (Benzal chloride)
3 2 1
CH2 – CH2 – CH2 – Br
(B*) 1-Bromo-3-phenylpropane
CH = CH – Cl
(C*) 1-chloro-2-phenyl ethene
(D*) 1-methoxy-2-nitrobenzene
fuEu esa ls fdldk lgh IUPAC uke gS\

CHCl2
(A*) MkbDyksjks QsfuyesFksu (cSUty DyksjkbM)
PAGE NO.-22
3 2 1
CH2 – CH2 – CH2 – Br
(B*) 1-czkseks-3-Qsfuy izksisu
CH = CH – Cl
(C*) 1-Dyksjks-2-Qsfuy ,Fkhu
(D*) 1- esFkkWDlh-2-ukbVªkscsUthu
5. Which of the following is/ are incorrect IUPAC name :

(A*) 2-Methylbutan -3-one
(B) 2-Hydroxypropanoic acid
(C) 5-Ethyl-1-methylcyclohex-1-ene
(D*) 4-Methyl-3-oxopentan-2-ol
fuEu ljpukvksa esa fdldk xyr IUPAC uke gS@gSa

(A*) 2-esfFkyC;wVsu-3-vkWu
(B) 2-gkbMªkWDlhizksisuksbd vEy
(C) 5-,fFky-1-esfFkylkbDyksgsDl-1-bZu
(D*) 4-esfFky-3-vkWDlksisUVsu-2-vkWy
6. Correct structure of 3-Bromo-4-methylcyclohexane-1, 2-dicarboxylic anhydride

3-czkseks-4-esfFkylkbDyksgsDlsu-1, 2-MkbZdkcksfZ Dlfyd ,ugkbMªkbM dh lgh lajpuk gksxh
(A*) (B) (C) (D*)
PAGE NO.-23
7. Which of the following is/are incorrect IUPAC name ?
(A*) 3-Methylenebutanamide (B*) Ethenylcyclohexane
(C*) 1,2,5-tribromo-3,4,6-trichlorocyclohexane (D) Tricyclopropyl methane
fUkEu esa ls dkSulk@dkSuls IUPAC uke lgh ugha gS \
(A*) 3-esfFkyhuC;wVsusekbM (B*) ,fFkuhylkbDyksgsDlsu
(C*) 1,2,5-VªkbZczkseks-3,4,6-VªkbZDyksjkslkbDyksgsDlsu (D) VªkbZlkbDyksizksfiyesFksu
O
3 2
Sol. (A) CH3—CH—CH2—C—NH2 (B)
1 Cyclohexyl ethene
CH2
4 lkbDyksgsfDly ,Fkhu
3-Methyl but-3-enamide
3-esfFkyC;wV-3-busekbM
Br
2
Cl Br
3 2 1 3 1
(C) CH 3 — CH — CH2 — COOH (E) Br 4 6

Cl
5
|4
CH3 — CH Cl
| 1,2,4-Tribromo-3,5,6-trichlorocyclohexane
CH3 1,2,4-VªkbZczkseks-3,5,6-VªkbZDyksjkslkbDyksgsDlsu
5
3, 4– Dimethyl pentanoic acid
3,4-MkbesfFkyisUVsukWbd vEy
8. In how many of the following compound secondary suffix name is used as carboxylic acid ?
fuEu fdrus ;kSfxd esa f}fr;d vuqyXu ds :i esa dkcksZDflfyd vEy uke iz;qDr gqvk gSa \
COOH COOH
OCOCH3 OH
(A) CH3–COOH (B) (C) (D) (E)
Ans. 4
CHO O–CHO
| |
OH
9.
| || NH–CHO
OHC O OH
How many aldehyde (–CHO) groups present in the given compound?
fn;s x;s mijksDr ;kSfxd esa fdrus ,fYMgkbM (–CHO) lewg mifLFkr gksrs gSa\
Ans. 2
10. Match the following compound with their IUPAC name:
Column-I Column-II
Compound IUPAC Name
(P) (W) 3-[2-(2-Oxoethyl)phenyl]propanoic acid
PAGE NO.-24
(Q) (X) 2-[2-(3-Oxopropyl)phenyl]ethanoic acid
(R) (Y) 2-(2-Formylphenyl)ethanoic acid
(S) (Z) 2-Formylbenzenecarboxylic acid
fuEu ;kSfxdksa ds IUPAC uke dk feyku djsaA

dkWye-I dkWye -II
;kSfxd IUPAC uke
(P) (W) 3-[2-(2-vkWDlks,sfFky)Qsfuy]izksisuksbZd vEy
(Q) (X) 2-[2-(3-vkWDlksizksfiy)Qsfuy],sFksuksbZd vEy
(R) (Y) 2-(2-QkWfeZyQsfuy),sFksuksbZd vEy
(S) (Z) 2-QkWfeZycsUthu dkcksZfDlfyd vEy
Ans. (P Z) ; (Q Y) ; (R W) ; (S X)

Daily Self-Study Dosage for mastering Chemistry IUPAC Name of Bicyclo Bridgehead Compounds
Bicyclo Compounds
Compounds with two fused cycloalkane rings are called bicyclo compounds. The carbon atoms common to both
rings are called bridge head atoms. A bond or chain of carbon atoms connecting the bridge heads is called a
bridge.
A bicyclic compound is named by attaching the prefix bicyclo to the name of hydrocarbon corresponding to the
total number of carbon atoms in two rings.
Numbering starts from bridge head to larger ring and then back to smaller ring.
The bracketed number show the number of carbon atoms (except bridge head position carbon atoms) in each
bridge and they cited in decreasing order.
Ex.
PAGE NO.-25

Daily Self-Study Dosage for mastering Chemistry f}pfØ; lsrq'kh"kZ ;kSfxd dk IUPAC uke
f}pfØ; ;kSfxd % pfØ; ;kSfxd ,sls ;kSfxd ftuesa nks lkbDyks ,Ydsu oy; tqM+h gqbZ gksrh gSA f}pfØ; ;kSfxd (ckblkbDyks
;kSfxd) dgykrs gSaA os dkcZu ijek.kq tks nksuks oy; esa mHk;fu"B dks lsrq cfU/kr ijek.kq dgykrs gSaA dkcZu ijek.kqvksa ds cU/k
;k Jà[kyk lsrq
cfU/kr ls tqM+s gksrs gSa bls lsrq dgk tkrk gSA
lsrq cfU/kr
fLFkfr
,d ckblkbDyks ;kSfxd dk ukedj.k nks oy; esa mifLFkr dqy dkcZu ijek.kqvksa ls lEcfU/kr gkbMªksdkcZu ds uke ls iwoZ
ckblkbDyks yxkdj fd;k tkrk gSA
lsrq cfU/kr esa ukedj.k igys cM+h oy; esa djrs gSa vkSj mlds ckn NksVh oy; esa dks"Bd izR;sd lsrq esa dkcZu ijek.kqvksa dh
la[;k ¼lsrqcaf/kr dkcZu ijek.kq ds vykok½ dks ?kVrs Øe esa n'kkZrk gSA
mnkgj.k %
1
2
2 1 10
7
6 lsrq cfU/kr 3 9
3 5 C-ijek.kq 8
4 6
4 5 7
ckblkbDyks [2.2.1]gsIVsu ckblkbDyks[4.4.0]Msdsu
1 5
2 O 6 7
6 4
7 8
5 3 3
1
4 2 9
1,7,7-VªkbesfFkyckblkbDyks[2.2.1]gsIVsu-2-vkWu 7-esfFkyckblkbDyks[4.3.0]ukWusu
(i). The IUPAC name of the compound is
(A*) Bicyclo [2.1.0] pentane (B) 1,2-cyclopropylcyclobutane

(C) Bicyclo [0.1.2] pentane (D) 1-Methylenecyclobutane
;kSfxd dk IUPAC uke gS %

(A*) ckblkbDyks [2.1.0] isUVsu (B) 1,2-lkbDyksizksfiylkbDyksC;wVsu
(C) ckblkbDyks [0.1.2] isUVsu (D) 1-esfFkfyulkbDyksC;wVsu
PAGE NO.-26
(ii). The systematic naming of the following cycloalkane is
(A*) 6-Methylbicyclo [3.2.0] heptane (B) 7-Methylbicyclo [3.2.0] heptane

(C) 2-Methylbicyclo [3.2.0] heptane (D) 3-Methylbicyclo [3.2.0] heptane
fuEufyf[kr lkbDyks,Ydsu dk O;ofLFkr uke gS %
(A*) 6-esfFkyckblkbDyks [3.2.0] gsIVsu (B) 7-esfFkyckblkbDyks [3.2.0] gsIVsu

(C) 2-esfFkyckblkbDyks [3.2.0] gsIVsu (D) 3-esfFkyckblkbDyks [3.2.0] gsIVsu
(iii). IUPAC name of is
(A) Bicyclo [3.2.1] octan-2-oic acid (B) Bicyclo [3.2.1] octan-1-carboxylic acid
(C*) Bicyclo [3.2.1] octan-8-carboxylic acid (D) None of these
dk lgh IUPAC uke D;k gksxk :
(A) ckblkbDyks [3.2.1] vkWDVsu-2-vkWbd vEy (B) ckblkbDyks [3.2.1] vkWDVsu-1-dkcksZfDlfyd vEy
(C*) ckblkbDyks [3.2.1] vkWDVsu-8-dkcksZfDlfyd vEy (D) buesa ls dksbZ ughaA
PAGE NO.-27
O/I-CHEMISTRY


EST INFORM AT IO
DPP

1. The structures (CH3)2CHCH2Br and CH3(CH2)3Br shows :

(A) position isomers (B*) chain isomerism
(C) functional isomerism (D) None of these
lajpuk (CH3)2CHCH2Br rFkk CH3(CH2)3Br fuEu esa ls dkSulh leko;ork n'kkZrs gS %
(A) fLFkfr leko;ork (B*) Jà[kyk leko;ork
(C) fØ;kRed leko;ork (D) buesa ls dksbZ ugha
2. n-Propyl alcohol and isopropyl alcohol are examples of :

(A*) Position isomers (B) Chain isomerism (C) Tautomerism (D) Geometrical isomerism
n-izksfiy ,YdksgkWy rFkk vkblksizksfiy ,YdksgkWy fuEu esa ls dkSulh leko;ork dk mnkgj.k n'kkZrs gS %
(A*) fLFkfr leko;ork (B) Jà[kyk leko;ork (C) pyko;ork (D) T;kferh; leko;ork
3. The compound which is not isomeric with diethyl ether is :

(A) n-Propylmethyl ether (B) Butan-1-ol
(C) 2-Methylpropan-2-ol (D*) Butanone
fuEu esa ls dkSulk ;kSfxd Mkb,fFky bZFkj dk leko;oh ugha gS :
(A) n-izksfiyesfFky bZFkj (B) C;wVsu-1-vkWy (C) 2-esfFkyizksisu-2-vkWy (D*) C;wVsuksu
4. The compound C4H10O can show

(A) Metamerism (B) Functional isomerism (C) Positional isomerism(D*) All types
fuEufyf[kr dkcZfud ;kSfxd C4H10O dkSulh leko;ork n'kkZrk gS %
(A) e/;ko;ork (B) fØ;kRed lek;ork (C) fLFkfr leko;ork (D*) mijksDr lHkh
5. What is the common name of Ethanoic acid?

(A) Formic acid (B*) Acetic acid (C) Acetaldehyde (D) Propionic acid
,sFksukWbd vEy dk lkekU; uke D;k gS \
(A) QkWfeZd vEy (B*) ,flfVd vEy (C) ,flVsfYMgkbM (D) izksisukWbd vEy
6. Which of the following is salicylic acid? fuEu esa ls dkSulk lsfyflfyd vEy gS\
(A) (B) (C) (D*)
PAGE NO.-28
7. Which of the following is not cresol. fuEu esa ls dkSulk fØlkWy ugh gS\
(A) (B) (C) (D*)
8. What is the common name of Ethyl ethanoate?

(A) Methyl formate (B) Acetaldehyde (C) Ethyl formate (D*) Ethyl acetate
,fFky ,sFksuksbV dk lkekU; uke D;k gS \
(A) esfFky QkWesZV (B) ,flVsfYMgkbM (C) ,fFky QkWesZV (D*) ,fFky ,flVsV
9. Which of the following is incorrectly matched?

(A) CH2  CH2 Glycol (B) COOH Oxalic acid
| |
OH OH |
COOH
(C*) Fumaric acid (D) HOOC–CH2–CH2–COOH Succinic acid
fuEu esa ls dkSulk lgh lqesfyr ugha gS \

(A) CH2  CH2 XykbdkWy (B) COOH vkWDlSfyd vEy
| |
OH OH |
COOH
(C*) ¶;wesfjd vEy (D) HOOC–CH2–CH2–COOH lfDlfud vEy
10. Select the incorrect name of the following compound.

OH
O2N NO2
(A) Picric acid

NO2
COOH
OH
(B) Salicyclic acid
OH
(C) Phenol
COOH
(D*) Isophthalic acid
COOH
fuEu ;kSfxdks ds xyr uke dk p;u dhft,A
PAGE NO.-29
OH
O2N NO2
(A) fifØd vEy

NO2
COOH
OH
(B) lsfyflfyd vEy
OH
(C) QhukWy
COOH
(D*) vkblksFkSfyd vEy
COOH
11. Which is Aspirin? fuEu esa ,Lizhu gS\

COOH
OCOCH3
(A) (B*) (C) (D)
12. Which of the following is not benzyl derivative :

fuEu esa ls dkSulk ;kSfxd csfUty O;qRiUu gSa %
CH2–Cl CH2–OH CH2–NH2 OH

(A) (B) (C) (D*)
Sol. In benzyl derivative, any functional group is attached to an sp 3 hybridized C-atom next to benzene ring.
csfUty O;qRiUu esa fØ;kRed lewg csathu oy; ls vxys sp3 ladfjr C–ijek.kq ls tqM+k gksrk gSA
13. What is the possible number of isomers of the aromatic compounds of molecular formula C 7H7Cl.
,sjkseSfVd ;kSfxd v.kqlw=k C7H7Cl ds lHkh lEHkkfor leko;oh fyf[k;sA
Ans. 04
Sol.
14. Number of structurally isomeric carbonyl compounds possible with molecular formula C5H10O ........:
v.kqlw=k C5H10O ds lEHko lajpukRed leko;oh dkcksZfuy ;kSfxdksa dh la[;k gSa %
Ans. 07
Sol. (1) CH3–CH2–CH2–CH2–CHO (2) (3)
PAGE NO.-30
(4) (5) (6)
(7)
15. How many dichlorodiphenyl with molecular formula C12H8Cl2 of each benzene ring containing only one
(–Cl) group are possible
v.kqlw=k C12H8Cl2 MkbZDyksjks MkbZQsfuy ;kSfxd ftlesa ,d (–Cl) lewg ,d csathu oy; ij mifLFkr gks] mlds
fdrus fLFkfr leko;oh lEHko gSaA
Ans. 6
Cl Cl Cl Cl Cl
Sol. Cl
Cl Cl Cl
Cl Cl Cl

Daily Self-Study Dosage for mastering Chemistry IUPAC Name of Spiro Compounds
Spiro are polycyclics that share only one carbon atom. In substituted spiro, the numbering is started next to
the spiro atom in lower membered ring.
Spiro atom
Small ring
The prefix spiro is followed by brackets containing the number of carbon atoms in ascending order, in each
ring attached to common carbon atom and ending with the name of hydrocarbon corresponding to the total
number of carbon atoms in two rings.
Br
5 3
6
4
2
7 1
8
Et
5-Bromo-1-ethylspiro[3.4]octane

Daily Self-Study Dosage for mastering Chemistry Likbjks ;kSfxdks ds IUPAC uke
Likbjks cgqpfØ; gksrs gSa tks fd dsoy ,d dkcZu ijek.kq dk lk>k djrs gSaA izfrLFkkih Likbjks esa] fuEurj lnL;h o;y ds
Øekadu Likbjks ijek.kq ds vkxs ls 'kq: djrs gSaA
Likbjks ijek.kq
NksVh oy;
izR;sd oy; esa leku dkcZu ijek.kq ls tqM+s iwoZyXu Likbjks dks c<+rs Øe esa dkcZu ijek.kq la[;k ;qDr dks"Bdks ds i'pkr~
fy[kk tkrk gS rFkk nks oy; esa dqy dkcZu ijek.kq la[;k vuqlkj gkbMªksdkcZu ds uke ls lekIr fd;k tkrk gSA
PAGE NO.-31
Br O
1 5 3
5 4 6 4 1 7 6 4
4 3
2 5 5
6
3 3 HO 8
7 2
7 8 2 8
Et
1
6 7 9 10 1 2 Me
Likbjks[2.5]vkWDVsu 5-czkseks-1-,fFkyLikbjks[3.4]vkWDVsu Likbjks[2.4]gsIVsu-4-vkWu 2-esfFkyLikbjks[4.5]Mssdsu-8-vkWy
(i). The structure of spiro[3.3]heptane is : Likbjks[3.3]gsIVsu dh lajpuk gS :
(A) (B) (C) (D*)
(ii). The systematic naming of the following compounds is :
(A) 2-Methylspiro[3.4]octane (B) 3-Methylspiro[3.4]octane

(C*) 6-Methylspiro[3.4]octane (D) 7-Methylspiro[3.4]octane
fuEufyf[kr ;kSfxd dk O;ofLFkr uke gS :
(A) 2-esfFkyLikbjks[3.4]vkWDVsu (B) 3-esfFkyLikbjks[3.4]vkWDVsu

(C*) 6-esfFkyLikbjks[3.4]vkWDVsu (D) 7-esfFkyLikbjks[3.4]vkWDVsu
(iii). The correct IUPAC name for the compound
(A) Spiro[3.5]non-1-ene (B*) Spiro[3.5]non-5-ene

(C) Spiro[5.3]dec-5-ene (D) Spiro[3.5]non-2-ene
;kSfxd dk lgh IUPAC uke gS %
(A) Likbjks[3.5]ukWu-1-bZu (B*) Likbjks[3.5]ukWu-5-bZu

(C) Likbjks[5.3]Msd-5-bZu (D) Likbjks[3.5]ukWu-2-bZu
PAGE NO.-32
O/I-CHEMISTRY


EST INF ORMA TIO

DPP

Total Marks : 42 Max. Time: 26 min.
1. have functional isomer relation with
dk fdlls fØ;kRed lewg leko;oh laca/k gSA
(A*) (B*)
(C*) (D*)
2. Which is the correct relationship mentioned in bracket :

(A*) CH3–CN and CH3NC (Functional isomers)
(B*) CH3–O–N=O and CH3 – N  O (Functional isomers)
||
O
(C*) CH3–CH2–CH2–CHO and H3C  CH  CH3 (Chain isomer)
|
CHO
(D*) and (Functional isomers)
fuEu esa ls dkSulk laEcU/k dks"Bd esa fn;k x;k lgh gSaA
(A*) CH3–CN rFkk CH3NC (fØ;kRed leko;oh)
(B*) CH3–O–N=O rFkk CH3 – N  O (fØ;kRed leko;oh)
||
O
(C*) CH3–CH2–CH2–CHO rFkk H3C  CH  CH3 (Jà[kyk leko;oh)
|
CHO
(D*) rFkk (fØ;kRed leko;oh)
Sol. and (rFkk) (Functional isomers)
(fØ;kRed leko;oh)
3. Which of the following alkene can give 3-methylpentane on hydrogenation.
(A*) 3-methylpent-1-ene (B*) 3-methylpent-2-ene
(C) 2-methylpent-1-ene (D*) 2-ethylbut-1-ene
PAGE NO.-33
fuEu esa ls dkSulh ,Ydhu gkbMªkstuhdj.k ij 3-esfFkyisUVsu ns ldrh gSA
(A*) 3-esfFkyisUV-1-bZu (B*) 3-esfFkyisUV-2-bZu (C) 2-esfFkyisUV-1-bZu (D*) 2-,sfFkyC;wV-1-bZu
O O
4. H–C–OC2 H5 and CH 3–C–CH2–OH
Which is/are true about above two structure – (RVP Sir) (IUPAC & Structural Isomers)
(A*) Degree of unsaturation is (1) (B*) Both are functional isomers
(C) Both are metamers (D*) Both have same molecular formula
O O
H–C–OC2 H5 rFkk CH 3–C–CH2–OH
mijksDr nksuksa lajpuk ds lUnHkZ es lgh dFku gS@gSa &
(A*) vlarÌrk dh dksfV (1) gS (B*) nksuksa fØ;kRed leko;oh gS
(C) nksuksa e/;ko;oh gS (D*) nksuksa ds v.kqlw=k leku gSa
O O
Sol. H–C–OC2 H5 and CH 3–C–CH2–OH not a metamers to each other.
O O
H–C–OC2 H5 rFkk CH 3–C–CH2–OH ,d nwljs ds e/;ko;oh ugh gSA
O O O O
5. CH3 –C–O–C CH3 and CH 3–CH2 –C–O–C
Which is/are incorrect about given structure (RVP Sir) (IUPAC & Structural Isomers)
(A*) Both are functional isomers (B*) The degree of unsaturation is 2
(C) Both have same molecular formula (D) Both are metamers to each other
O O O O
CH3 –C–O–C CH3 rFkk CH 3–CH2 –C–O–C
fuEu lajpuk ds fy, dkSulk@dkSulsa dFku lgh gS@gSa &
(A*) nksuksa fØ;kRed leko;oh gSA (B*) vlar‘Ìrrk dh dksfV 2 gSA
(C) nksuksa ds v.kqlw=k leku gSa (D) nksuksa e/;ko;oh gSa
Sol. Both having same functional group so they are not functional isomers the degree of unsaturation is 3.
nksuksa esa leku fØ;kRed lewg ds dkj.k fØ;kRed leko;oh ugha gS rFkk vlar‘Ìrrk dh nj 3 gSA
6. Which of the following relation is correct :
(A*) and are chain iosmers
(B) and are positional isomers
(C*) and are metamers
(D*) and are functional group isomers
PAGE NO.-34
fuEu esa ls dkSulk laca/k lgh gS %
(A*) rFkk Ja`[kyk leko;oh gSAa
(B) rFkk fLFkfr leko;oh gSaA
(C*) rFkk e/;ko;oh gSaA
(D*) rFkk fØ;kRed lewg leko;oh gSaA
Sol. and are identical.
rFkk le:i gSaA
7. Which statement(s) is/are correct.

(A*) Degree of unsaturation tells about H-defficiency from any molecule in the form of multiple bond or
ring.
(B*) Hydrogenation tells about carbon skeleton.
(C*) Monohalogenation tells about type of chemically different hydrogen.
(D*) Ozonolysis tells about position of double or trible bond in molecule.
dkSulk dkSuls dFku lgh gS@gSaA
(A*) vlarÌrrk dh dksfV gesa cgqcU/k ;k oy; ds :i esa fdlh v.kq esa H-U;wurk ds ckjs esa crkrk gSA
(B*) gkbMªkstuhdj.k ges dkcZu <+kWps (skeleton) dh ds ckjs esa crkrk gSA
(C*) eksuksgSykstuhdj.k ges jkl;fud :i ls fHké H ds izdkj ds ckjs esa crkrk gSA
(D*) vkstksuhvi?kVu gesa v.kq esa }cU/k ;k f=kcU/k dh fLFkfr ds ckjs esa crkrk gSA
Sol. Self explanatory.
gy % Lor% le>us ;ksX;A
8. How many monochloro structural isomers will produce when 3-Methylpentane, reacts with chlorine in
presence of sunlight ?
tc 3-esfFkyisUVsu dh vfHkfØ;k lw;Z ds izdk'k dh mifLFkfr esa Dyksjhu ds lkFk dh tkrh gS rks fdrus eksuksDyksjks
lajpuk leko;oh izkIr gksrs gSa\
Ans. 04
Sol.
PAGE NO.-35
9. Number of different products in the given ozonolysis reaction will be :
nh x;h vkstksuhdj.k vfHkfØ;k ls izkIr fHkUu mRiknksa dh laa[;k gksxh%
O3

 Products mRikn
Zn / H2O
Ans. 02
O3
Sol. 
 + CH2 = O
Zn / H2O
4 moles 6 moles
10. Match the Column

Comun–I (Compounds) Column–II (Common Names)
(A) (p) Carbinol
(B) (q) Gycerol
(C) (r) Ethylene glycol
(D) CH3 – OH (s) Phenol

fuEufy[kr dks lqesfyr dhft,
dkWye–I (;kSfxd) dkWye–II (lkekU; uke)
(A) (p) dkchZuksy
(B) (q) Xyhlhjksy
(C) (r) ,FkhyhuXykbdksy
(D) CH3 –OH (s) fQukWy

Ans. A  q, B  r, C  s, D p
PAGE NO.-36
O/I-CHEMISTRY


EST INFORM AT IO
DPP

2. Course covered till previous week :
3. Target of the current week :
4. DPP Syllabus :
O
1. Correct IUPAC name of the compound O is :

Me
O
(A*)2-Methylbutenedioic anhydride (B) 3-Methylbutenedioic anhydride
(C) 2-Methyl-1,4-diketobutene epoxy (D) 2-Methylcyclopentanoxy-1,4-dione
O
;kSfxd dk lgh IUPAC uke gksxk O

Me
O
(A*)2-esfFkyC;wVbZuMkbZvksbd ,ugkbMªkbM (B) 3-esfFkyC;wVbZuMkbZvksbd ,ugkbMªkbM
(C) 2-esfFky-1,4-MkbZdhVksC;wVbZu bikWDlh (D) 2-esfFkylkbDyksisUVuksDlh-1,4-MkbZvkWu
O
CH3
2. The IUPAC name of the compound H – C – N is
CH2 – CH3
(A*) N-Ethyl-N-methylmethanamide (B) N-Methyl-N-ethylmethanamide
(C) N-Ethyl- N-methylformamide (D) N-Ethylmethylmethanamide
O
CH3
;kSfxd dk IUPAC uke gS H – C – N
CH2 – CH3
(A*) N-,fFky-N-esfFkyesFksukekbM (B) N-esfFky-N-,fFkyesFksukekbM
(C) N-,fFky-N-esfFkyQkekZekbM (D) N-,fFkyesfFkyesFksukekbM
3. Which of the following amino acids contains sulfur atom

(A) Serine (B*) Cystein (C) Alanine (D) Proline
fuEu esa ls dkSulk ,sfeuksa vEy lYQj ijek.kq j[krk gSA
(A) lsfju (B*) flLVhu (C) ,sykfuu (D) izksyhu
4. Which of the following contains two-COOH group

(A*) Aspartic acid (B) Tyrosine (C) Histidine (D) Glycine
fuEu esa ls fdl ,sfeuksa vEy esa nks –COOH lewg mifLFkr gSA
(A*) ,sLikfVZd vEy (B) Vk;jksflu (C) fgfLVMhu (D) Xyk;flu
PAGE NO.-37
5. Which of the following give positive test with neutral FeCl3
(A) Leucine (B*) Tyrosine (C) Asparagine (D) Serine
fuEu esa ls dkSu mnklhu FeCl3 ds lkFk èkukRed ijh{k.k nsrk gSA
(A) Y;wflu (B*) Vk;jksflu (C) ,sLIkkftZu (D) lsfju
6. Which of the following will give same product on ozonolysis
I II III
(A) I & II only (B) II & III only (C) I and III only (D*) All
fuEu es ls dkSulk ;kSfxd vkstksuhvi?kVu ij leku mRikn nsrk gSA
I II III
(A) I o II dsoy (B) II o III dsoy (C) I o III dsoy (D*) lHkh
7. can be obtained by ozonolysis of -
fuEu esa ls fdlds vkstksuhvi?kVu }kjk izkIr fd;k tk ldrk gSA
(A) (B) (C) (D*)
8. on reductive ozonolysis [O3/Zn/H2O/] gives :
ds vipk;h vkstksuh vi?kVu [O3/Zn/H2O/] }kjk izkIr mRikn gksaxs&
(A) (CHO)2 + (B*) (CHO)2 + +
(C) + (D) Benzene is stable hence cannot be ozonolysed
csUthu LFkk;h gS] blfy;s bldk vkstksuh vi?kVu ugh gks ldrk
Cl2 / h
X 2  C8H16 
 3 monochloro structural product (3
H / Ni
9. eksuks Dyksjks lajpukRed mRikn½

PAGE NO.-38
Structure of X will be :
X dh lajpuk gksxhA
(A) (B) (C) (D*)
10. Molecular formula C3H9N represents :

(A) Only primary amine (B) Only secondary amine
(C) Three primary amine, two secondary amine and one tertiary amine
(D*) Two primary amine, one secondary amine and one tertiary amine
v.kqlw=k C3H9N iznf'kZr djrk gS %
(A) dsoy izkFkfed ,ehu (B) dsoy f}rh;d ,ehu
(C) rhu izkFkfed ,ehu, nks f}rh;d ,ehu rFkk ,d r`rh;d ,ehu
(D*) nks izkFkfed ,ehu, ,d f}rh;d ,ehu rFkk ,d r`rh;d ,ehu
11. How many ketones with molecular formula C5H10O is possible (structural isomers only).
C5H10O v.kqlw=k ds fdrus dhVksu ¼dsoy lajpukRed leko;oh½ lEHko gS &
(A) 2 (B*) 3 (C) 4 (D) 6
Cl2 / h
12.    'm' monochloro products
Cl2 / h
   'n' dichloro products
The value of m and n are respectively :

(A) 2 and 1 (B*) 2 & 2 (C) 1 & 2 (D) 1 & 1
Cl2 / h
   'm' eksuksDyksjks mRikn
Cl2 / h
   'n' MkbDyksjks mRikn
m vkSj n ds eku Øe'k% gSa :

(A) 2 rFkk 1 (B*) 2 rFkk 2 (C) 1 rFkk 2 (D) 1 rFkk 1
Sol. 'm' no. of product and
'n' no. of product and
PAGE NO.-39
'm' mRikn dh la[;k rFkk
'n' mRikn dh la[;k rFkk
13. How many compounds will give positive iodoform test but negative Tollen’s test ?
fuEu esa fdrus ;kSfxd /kukRed vk;ksMksQkWeZ ijh{k.k rFkk _.kkRed VkWysu vfHkdeZd ijh{k.k nsrs gS \
(a) CH3CHO (b) (c)
(d) (e) (f)
Ans. 3
Sol. (3) b, c, e
14. Consider all possible isomeric amines of molecular weight = 73. How many of them give isocyanide
with CHCl3 and KOH
v.kqHkkj 87 ds lHkh lEHko leko;oh ,ehu ij fopkj dhft,A buesa ls fdrus f}rh;d ,ehu gS \
Ans. 4
15. In how many of the following compound. –OH group directly attached on the benzene ring ?
(1) Glycol (2) Glycerol (3) o-cresol (4) p-cresol
(5) Phenol (6) aniline (7) anisol (8) resorcinol
(9) catechol (10) Hydroquinone
fuEu esa ls fdrus ;kSfxdkas esa –OH lewg csathu oy; ls lh/ks tqM+k gS ?
(1) Xyk;dkWy (2) fXyljkWy (3) o-fØlkWy (4) p-fØlkWy
(5) fQukWy (6) ,fuyhu (7) ,fulkWy (8) jslksflZukWy
(9) dSVsdkWy (10) gkbMªksfDouksu
Ans. 6
PAGE NO.-40
O / I - C H E M I S TR Y


EST INFORM AT IO
DPP

Total Marks : 44 Max. Time : 24 min.
1. Which of the following will decolourise highly diluted KMnO4 solution ?
fuEu esa ls dkSuls ;kSfxd vR;Ur ruq KMnO4 foy;u dks jaxghu dj nsrk gS %
(A) C3H8 (B) CH4 (C*) C2H2 (D*) C2H4
Sol. C2H4 has one C=C while C2H2 has one Carbon-Carbon triple bond.
C2H4 ,d C=C j[krk gSA tcfd C2H2 ,d dkcZu&dkcZu f=kcU/k j[krk gSA
2. and cannot be distinguished by :
(A*) Iodoform test (B*) Tollen's test

(C) Fehling solution test (D*) 2,4-DNP test
rFkk dks fdlds }kjk foHksfnr ugh dj ldrs gS %
(A*) vk;ksMksQkWeZ ijh{k.k (B*) VkWysu ijh{k.k (C) Qsgfyax ijh{k.k (D*) 2,4-DNP ijh{k.k
3. The test that can be used to distinguish between 1-propanol and 2-propanol :
(A*) Lucas test (B*) Iodoform test (C*) Victor mayer test (D) Carbyl amine test
fuEu esa ls fdl ijh{k.k }kjk 1-izksisukWy rFkk 2-izksisukWy ds e/; foHksnu fd;k tk ldrk gS %
(A*) Y;wdkWl ijh{k.k (B*) vk;ksMksQkWeZ ijh{k.k (C*) foDVj&es;j ijh{k.k (D) dkfcZy&,ehu ijh{k.k
Sol. Carbyl amine test is used to distinguish amines.
,ehuksa ds e/; foHksnu djus ds fy, dkfcZy&,ehu ijh{k.k dk mi;ksx fd;k tkrk gSA
4. Test to differentiate between (CH3OH) and (Ph-OH) is/are :
(A*) Victor mayer test (B*) Neutral FeCl3 (C*) Br2/H2O (D) Na metal
fdl ijh{k.k }kjk (CH3OH) rFkk (Ph-OH) ds e/; foHksnu fd;k tk ldrk gS@gSa&
(A*) foDVj&es;j ijh{k.k (B*) mnklhu FeCl3 (C*) Br2/H2O (D) Na /kkrq
5. What is/are the structure of a compound (C3H2D2) which decolourise bromine water.
fuEu esa ls dkSulh lajpuk ;kSfxd (C3H2D2) dh gS tks czksehu ty dks jaxghu djrh gSA
(A*) (B*) (C*) CHD2 – C  CH (D*)
PAGE NO.-41
6. Which of the following compound will give positive test with NaHCO 3?
fuEu es ls dkSuls ;kSfxd NaHCO3 ds lkFk dkSulk ;kSfxd /kukRed ijh{k.k nsrk gS ?
(A*) (B*) (C*) (D)
Sol. Phenol is weaker acid as compare to H2CO3.

gy % fQukWy] H2CO3 ls nqcZy vEy gSA
7. Which of the following test will be given by (squaric acid)
(A*) Br2 water test (B*) 2, 4-DNP test (C*) Neutral FeCl3 (D) Tollen’s test
fuEu esa ls dkSuls ijh{k.k LDosfjd vEy nsrk gSA
(A*) Br2 ty ijh{k.k (B*) 2, 4-DNP ijh{k.k (C*) mnklhu FeCl3 (D) VkWysu ijh{k.k
Sol. Terminal alkyne and –CH=O group gives +ve test with tollens reagent.
vUrLrFk ,YdkbZu rFkk –CH=O lewg VkWysu vfHkdeZd ds lkFk /kukRed ifj{k.k nsrs gSaA
8. Which of the following will give positive iodoform test.
fuEu esa ls dkSu /kukRed vk;MksQkeZ ijh{k.k nsrs gSA
(A) (B*) (C*) (D*)
9. Compound giving offensive smell on heating with chloroform and alkali
,d ;kSfxd tks DyksjksQkWeZ rFkk {kkj ds lkFk xeZ djus ij rhoz vlguh; xa/k ;qDr ;kSfxd nsrk gS] ;kSfxd gSA
(A*) CH3–NH2 (B*) (C) CH3–NO2 (D*) Ph–CH2–NH2
Sol. Aniline and 1° amine on heating with chloroform and alkali gives offensive smell.
Sol. ,fuyhu ,oa 1° ,ehu DyksjksQkeZ rFkk {kkj ds lkFk xeZ djus ij rhoz vlguh; xa/k ;qDr ;kSfxd nsrs gSA
10. Match the given compounds in Column-I with their appropriate descriptions given in Column-II.
Column-I Column-II
CH3 — CH — CH3
(A) | (p) It evolve CO2 gas with NaHCO3
OH
(B) (q) It gives iodoform test
(C) (r) It gives Lucas reagent test .
(D) Reductive ozonolysis products of Benzene (s) It gives Tollen`s test

(t) It gives 2,4 DNP test
PAGE NO.-42
dkWye -I esa fn;s x;s ;kSfxdksa dks dkWye-II ds mfpr fooj.k ls lqesfyr dhft;sA
dkWye-I dkWye-II
CH3 — CH — CH3
(A) | (p) NaHCO3 ds lkFk CO2 xSl fu"dkflr djrk gSA
OH
(B) (q) ;g vk;ksMksQkeZ ijh{k.k nsrk gSA
(C) (r) ;g Y;qdkWl ijh{k.k nsrk gSA
(D) csUthu dk vipf;r vkstksuhdj.k mRikn (s) ;g VkWysu ijh{k.k nsrk gSA
(t) ;g 2,4 DNP ijh{k.k nsrk gSA
Ans. (A) q,r (B) q,t (C) p (D) s , t
PAGE NO.-43

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DPPs BOOKLET-1 VIKAAS (JA) | CHEMISTRY

TARGET : JEE (Main + Advanced) 2022

EST INF ORMA TIO

Course : VIKAAS(JA) NO. A1

(A) (B) (C) (D*)

2. Carbon has strong tendency to show catenation due to :

3. Which of the following is the empirical formula of C6H6 ?

(A) (B) (C) (D*)

6. Which of the following is third member of CnH2n-2 homologous series ?

7. Which of the following is molecular formula of ?

dk vkf.od lw=k dkSulk gS \

(A) 10 (B*) 18 (C) 14 (D) 16

13. Total number of bonds in HCC–CCH ?

How many hydrogen atoms are present in the given structure ?

TARGET : JEE (Main + Advanced) 2022

EST INF ORMA TIO

Course : VIKAAS(JA) NO. A2

2. The alicyclic compound/s is / are :

(A) (B*) (C*) (D*)

4. What is correct about and ?

rFkk ds fy, lR; D;k gS?

5. How many of the following show general formula CnH2n – 6?

Sol. (A) C5H10 – 6 = C5H4

(A*) (B) (C*) (D*)

Sol. is not an alicyclic hydrocarbon. It is an acyclic hydrocarbon.

7. Which molecules have sp3 carbon atom :

8. In the given compounds how many are unsaturated hydrocarbon?

9. How many amines are tertiary amines:

10. Match the following :

(D) OH (s) Hydrocarbon (gkbMªksdkcZu)

TARGET : JEE (Main + Advanced) 2022

EST INF ORMA TIO

Course : VIKAAS(JA) NO. A3

CH3  CH2  C  CH  CH  CH2  CH3

5. Which of the following is 3º chloride?

6. What is the correct IUPAC name of (C2H5)4C is:

7. Which of the following are used as primary suffix :

What is incorrect about the given structure?

(A) Methyl (B) n-Propyl (C*) Iso-propyl (D) Neo-pentyl

(A) esfFky (B) n-izksfiy (C*) vkblksizksfiy (D) fu;ksisafVy

ChemINFO IUPAC NOMENCLATURE

1° Allylic chloride 3°-Allylic iodide

ChemINFO IUPAC NOMENCLATURE

uksV : * iznf'kZr ,fyfyd dkcZuA

(ii). CH2=CH–Br is a/an

(A) It is an allylic iodide (B) It is a vinylic iodide

(A) ;g ,d ,fyfyd vk;ksMkbM gSA (B) ;g ,d fouk;fyd vk;ksMkbM gS

TARGET : JEE (Main + Advanced) 2022

EST INF ORMA TIO

Course : VIKAAS(JA) NO. A4

(A*) is 2, 3-dimethylbutyl. (B*) is 1-methylpropyl

(C*) is 1, 2-dimethylpropyl (D*) is 1-methylethyl

fuEu esa ls dkSuls ,fYdy ewyd dk IUPAC uke lgh gSa %

(A*) , 2, 3-MkbesfFkyC;wfVy (B*) , 1-esfFky izksfiy gSA

(C*) , 1, 2-MkbesfFkyizksfiy gSA (D*) , 1-esfFky,sfFky gSA

2. Which of the following IUPAC name is/are correct :

3. The correct structure of 2,3,4-Trimethylhexane is :

(A*) (B*) (C) (D*)

4. In which of the following cyclic ring is a parent chain:

(A*) (B) (C*) (D*)

5. Which of the following is/are incorrect IUPAC name?

6. Which of the following is/are correct ?

(A) (B) (C) (D*)

(A) (B) (C) (D*)

(A) is 2, 3-dimethylbutyl. (B) is 1-methylpropyl

(C) is 1, 2-dimethylpropyl (D) is 1-methylethyl

(A) , 2, 3-MkbesfFkyC;wfVy (B) , 1-esfFky izksfiy gSA

(C) , 1, 2-MkbesfFkyizksfiy gSA (D) , 1-esfFky,sfFky gSA

(A) (B) (C) (D*)

(A) (B) (C) (D*)

(A) (B) (C) (D*)