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TEST IN FORMATI ON
Syllabus : Organic Reaction Mechanisms-I & Organic Reaction Mechanisms-II and Reduction,
Oxidation & Hydrolysis, Cheminfo (Till date)
Single choice Objective ('–1' negative marking) Q.1 to Q.20 (3 marks, 2 min.) [60, 40]
(A) it has six carbon atoms (B*) it's molecular formula is C6H12
(C) it's empirical formula is CH (D) it has six sp 2 hybridised carbon atoms
(A) ;g N% dkcZu ijek.kq j[krk gSA (B*) bldk v.kqlw=k C6H12 gSA
(C) bldk ewykuqikrh lw=k CH gSA (D) ;g N% sp 2 ladfjr dkcZu ijek.kq j[krk gSA
3. When Acetaldehyde is heated with Fehling solution, a red precipitate is formed Red Precipitate is due to ?
tc ,lhVsfYMgkbM dks Qsgfyax foy;u ds lkFk xeZ djrs gS rc yky vo{ksi curk gSA yky vo{ksi fuEu ds dkj.k curk
gS \
(A*) Cu2O (B) Cu (C) CuO (D) CuSO4
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5. The correct decreasing order of electron density in aromatic ring of following compounds is :
fuEufyf[kr ;kSfxdkas esa ,sjkseSfVd oy; ij bysDVªkWu ?kuRo dk lgh ?kVrk gqvk Øe gksxk %
(A) (II) > (III) > (IV) > (I) (B*) (III) > (II) > (IV) > (I)
(C) (IV) > (I) > (III) > (II) (D) (III) > (II) > (I) > (IV)
Sol. + m group increases electron density and – m group decreases electron density in aromatic ring.
,sjkseSfVd oy; esa + m lewg bysDVªkWu ?kuRo c<+k nsrk gS rFkk – m lewg bysDVªkWu ?kuRo esa deh dj nsrk gSA
9. Which is Aspirin ?
fuEu esa ,Lizhu gS \
10. An unknown compound A has a molecular formula C 4H6. When A is treated with an excess of Br 2 a new
substance B with formula C4H6Br4 is formed. A forms a white precipitate with ammoniacal silver nitrate
solution. A may be
(A*) But-1-yne (B) But-2-yne (C) But-1-ene (D) But-2-ene
,d vKkr ;kSfxd dk v.kqlw=k C4H6 gSA tc A dks Br2 ds vkf/kD; ds lkFk mipkfjr djrs gS] rks v.kqlw=k C4H6Br4 dk ,d
u;k inkFkZ B curk gSA A veksfu;ke; flYoj ukbVªsV foy;u lkFk 'osr vo{ksi cukrk gSA A gks ldrk gS &
(A) C;wV-1-vkbu (B) C;wV-2-vkbu (C) C;wV-1-bu (D) C;wV-2-bu
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11. Choose the correct reaction to obtain the given product ¼fn;s x;s izkIr mRikn ds ckjs esa lgh vfHkfØ;k dks pqfu;sA½
(A*) D / Pd (B) D / Pt
2 2
(C) D / Ni (D) D / Ni
2 2
Sol. D / Pd
2
Product
mRikn
Sol.
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x y
13. Ph—CC—Ph
x y
Ph—CC—Ph
X Br
Sol. Ph – C C – Ph 2
Na(NH3 ( )) CCl4
14. product is :
mRikn gS &
LiAlH4
15. H2N–(CH2)4–COOH ?
Sol. H2N CH2)4 – COOH LiAlH
4
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16. The products A and B in the reactions given below are :
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17. Product of given reaction is :
H / Pd(CaCO ) Quinoline
2 3
H / Ni PHI
18. A 2
B ,
A and B can be :
(A) Both are n-Butane (B) Both are Butane-1,2,3,4 -tetraol
(C) A is n-Butane & B is Butane-1,2,3,4 -tetraol (D*) A is Butane-1,2,3,4 -tetraol & B is n-Butane
H / Ni PHI
A 2
B ,
19. Which reducing agent, would you use to carry out the following transformation.
fuEu :ikUrj.k ds fy, vki dkSulk vipk;d dke esa ysxsa \
LiAlH4
20. product is mRikn gS &
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