Chemistry-74.Phase-3 - 4-Objective
FACULTY TRAINING TEST
PHASE – III & IV
CHEMISTRY
SCREENING PAPER
Time: 1 Hour Maximum Marks: 90
Instructions:
1. This paper consists of 30 QUESTIONS only.
2. Attempt ALL questions.
3. Each correct answer carries 3 marks and each incorrect answer carries –1 mark.
4. Use of Calculator is NOT PERMITTED
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1. Acetone is easily oxidised with
(A) Tollen’s reagent (B) Fehling’s solution
(C) Acidic dichromate solution (D) Benedict’s solution
2. CH3CO2NH4 Identify C
(A) CH3CH2CONH¬2 (B) CH3CN
(C) Ac2O (D) AcOH
3. The refluxing of Me2NCOMe with acid gives
(A) 2MeNH2 + HOAc (B) 2MeOH + MeCONH2
(C) Me2NH + HOAc (D) Me2NCO2H + CH4
4. Alkaline hydrolysis of urea with dil. NaOH gives
(A) Biuret and ammonia (B) Ammonia and sodium carbonate
(C) Nitrogen and sodium carbonate (D) Ammonia and cyanuric acid
5. An organic compound X on treatment with acidified K2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodometyhane. The compound X can be
(A) CH3OH (B) CH3COCH3
(C) CH3CHO (D) CH3CH(OH)CH3
6. Concentrated sodium hydroxide and benzaldehyde react to produce
(A) Benzyl alcohol (B) Hydrobenzamide
(C) Cinnamic acid (D) Benzophenon
7. Which of the following reactions cannot be used for the reduction of
R2CO R2CH2
(A) Clemmenson’s reduction (B) Wölff Kishner reduction
(C) Wurtz reaction (D) HI/Red P at 200°C
8. Which salt can be produced by the reaction of CO and caustic soda
(A) CH3CO2Na (B) C2H2O4
(C) HCO2Na (D) CH2O
9. From the following values of dissociation constants of four acids which value represents the strong acid?
(A) 2 10–2 (B) 0.02 10–1
(C) 3 10–4 (D) 2 10–4
10. Formalin is an aqueous solution of
(A) Furfural (B) Fluorescein
(C) Formaldehyde (B) Formic acid
11. Which of the following compounds on treatment with LiAlH4 will give a product that will give a positive iodoform test
(A) CH3CH¬2CHO (B) CH3CH2CO2CH3
(C) CH3CH2OCH2CH3 (D) CH3COCH3
12. Electrolysis of an aqueous solution of CH3CO2K gives
(A) CH4 (B) C2H4
(C) C2H6 (D) C2H2
13. Fehling’s solution is a mixture of two solutions. While one contains CuSO4, the other contains.
(A) Potassium tartarate (B) Sodium oxalate
(C) Sodium potassium oxalate (D) Sodium potassium tartarate
14. Reductive ozonolysis of benzene produces
(A) Acetone (B) Maleic anhydride
(C) Phthalic acid (D) Glyoxal
15. Under Wölff Kishner reduction conditions, the conversion which may be brought about is
(A)
(B)
(C)
(D)
16. Ethanol vapours are passed over heated copper at 300°C and product is treated with aq. NaOH. The final product is
(A) aldol (B) -hydroxybutyraldehyde
(C) both (A) and (B) (D) None
17. Which of the following reactions does not yield an amine?
(A) R – X + NH3 (B) R – CH = NOH
(C) R – CN (D) R – CONH2
18. Beckmann rearrangement is not effected by
(A) Sulphuric acid (B) Carbonic acid
(C) Palmitic acid (D) PCl5
19. The end product of the following reaction is
(A) Ethyl cyanide (B) Ethylamine
(C) Methyl amine (D) Actamide
20. A compound A having the molecular formula C7H7NO on treatment with Br2/NaOH gives an amine B. B upon diazotisation and coupling with phenol gives an azodye. A can be
(A) PhCONHCH3 (B) PhCONH2
(C) PhNO (D) o, m-(or) p-C6H4(NH2)CHO
21. The amine forming an alcohol with NaNO2/H+ followed by hydrolysis is
(A) 1° (B) 2°
(C) 3° (D) 4°
22. HO – CH2 – CH2 – – Ph A. A is
(A) Primary alcohol (B) Secondary alcohol
(C) Tertiary alcohol (D) Diol
23. The alkyl halide that does not under go any substitution reaction is
(A)
(B)
(C)
(D)
24.
(A)
(B)
(C)
(D)
25. The optically active compound that shows positive idoform test is
(A)
(B)
(C)
(D)
26.
The above structures (A) and (B) represent
(A) Resonance structures (B) Tautomers
(C) Enantiomers (D) Anomers
27.
(A)
(B)
(C)
(D)
28.
(A) CH2 = CH2 (B) CH CH
(C)
(D)
29.
The above conversion can be done by
(A) CO + HCl/AlCl3 (B) HCN + HCl/AlCl3
(B) CHCl3/NaOH (D) All the above
30. The compound having the most acidic proton is
(A)
(B)
(C)
(D)
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FACULTY TRAINING TEST
PHASE – III & IV
CHEMISTRY
SCREENING PAPER
ANSWERS
1. C 2. D 3. C 4. B
5. D 6. A 7. C 8. C
9. A 10. C 11. D 12. C
13. D 14. D 15. D 16. C
17. C 18. C 19. B 20. B
21. A 22. A 23. C 24. B
25. C 26. B 27. A 28. A
29. D 30. D
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