This section includes 7 InterviewSolutions, each offering curated multiple-choice questions to sharpen your Current Affairs knowledge and support exam preparation. Choose a topic below to get started.
| 1. |
Compoundof calcium(X)is thecheapestformofalkali, whichcan bedecomposedto giveback X at veryhightemperature.Xis _______. |
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Answer» `CaCO_(3)` |
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| 2. |
Compound of an element A with an alkali metal gave a neutral solution in water. In the periodic table the element A belongs to |
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Answer» SECOND GROUP |
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| 3. |
Compound obtained by passing CO_(2) through BaO_(2) in water is |
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Answer» CO |
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| 4. |
{:("Compound", " Magnetic property") , ("(A) NaCl" , "(p) Ferrimagnetic"),("(B) MnO" , "(q) Paramagnetic"),("(C) CrCl"_(3) , "(r) Ferromagnetic"),("(D) CrO"_(2) , "(s) Diamagnetic"),("(E) MgFe"_(2)O_(4) , "(i) Antiferromagnetic"):} |
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Answer» A-p,B-r,C-q,D-t,E-s MnO - Antiferromagnetic, ` MgFe_(2)O_(4)` - Ferrimagnetic |
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| 5. |
Compound . Find the structure of (X) |
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Answer»
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| 8. |
Compound (D)+I^(-)+H^(+) rarr Gas. Evolved gas is similar to: |
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Answer» Gas-B `I rarr PbCrO_(4) (ACOH` insoluble) `HNO_(2) +I^(-) +H^(+) rarr NO` (Gas H) |
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| 9. |
Compound containing Xe and F having 63.8%of Xe then calculate oxidation number of Xe. |
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Answer» SOLUTION :XE : F `therefore63.8/133:37.2/19` `therefore0.48:1.95` `therefore1:4` `thereforeXe^(+4)` |
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| 11. |
Compound (C) in above sequence of reaction is: |
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Answer»
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| 12. |
Compound 'C' and 'D' are respectively: |
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Answer» `CaO +CaSO_(4)` |
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| 14. |
Compound (A)C_(7)H_(8)O is insoluble in aqueous NaHCO_(3) and dissolves in aqueous NaOH and gives a characteristic colour with neutral FeCl_(3) . When treated with Br_(2)(A) forms compound (B) C_(7)H_(5)O Br_(3). What could be the structure of compound (A) if neither dissolves in aq. NaHCO_(3) nor gives a characteristic colour with FeCl_(3)? |
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Answer»
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| 15. |
Compound (A)C_(7)H_(8)O is insoluble in aqueous NaHCO_(3) and dissolves in aqueous NaOH and gives a characteristic colour with neutral FeCl_(3) . When treated with Br_(2)(A) forms compound (B) C_(7)H_(5)O Br_(3). The most probable structure of compound A is : |
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Answer»
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| 16. |
Compound (A)C_(7)H_(8)O is insoluble in aqueous NaHCO_(3) and dissolves in aqueous NaOH and gives a characteristic colour with neutral FeCl_(3) . When treated with Br_(2)(A) forms compound (B) C_(7)H_(5)O Br_(3). The structure of compound (B) would be : |
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Answer»
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| 17. |
Compound A(C_6H_(12)) does not absorb H_(2) in presence of Ni. It forms two monochloro isomers on photochemical chlorination . Its structure can be |
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Answer»
have two types of CHEMICALS different hydrogen ATOMS so it forms two monochlorol lisomers on photochemical chlornation.
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| 18. |
Compound A(C_(3)H_(5)N) gives preripitate with Tollen's reagent and H_(2) gas is also evolvedon addition on Li metal. Compound A can be |
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Answer» `CH_(3)-CH_(2)-C-=N` |
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| 19. |
Compound A, which is a degradation product of the antibiotic vermiculine has following structure |
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Answer»
It is ALSO obtained by rductive ozonolysis of `C (C_(11)H_(18)O_(2))`. |
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| 20. |
Compound Aon oxidation with OsO_4 // NaIO_4 gives cyclo hexanedial. Structure of compound A will be : |
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Answer»
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| 21. |
Compound A is produced by absorbing dinitrogen trioxide in NA_(2)CO_(3) solution. Compound A is : |
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Answer» `Na_(2)O` |
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| 22. |
Compound 'A' is having water of crystallization by the number of: |
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Answer» 10 |
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| 23. |
Compound 'A' is found to contain 36.5 % Na,25.4 % S and 38.1 % O. Its molecular mass is 126. Calculate the molecular formula of the compound. The compound 'A' is easily oxidised to another compound 'B'. Calculate the percentage composition of 'B'. |
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Answer» `{:("Element","Percentage","Atomic mass","Gram toms (Moles)","Atomic ratio (Molar ratio)","SIMPLEST whole no. ratio"),("Na",36.5,23,(36.5)/(23)=1.59,(1.59)/(0.79)=2,2),("S",25.4,32,(25.4)/(32)=0.79,(0.79)/(0.79)=1,1),("O",38.1,16,(38.1)/(16)=2.38,(2.38)/(0.79)=3,3):}` Empirical formula of the compound `= Na_(2)SO_(3)` Step II. Molecular formula of compound 'A' Empirical formula mass `= 2 xx 23 + 32 + 3 xx 16 = 126 u` Molecular mass = 126 u `n=("Molecular mass")/("Empirical formula mass")=(126)/(126)=1` `:.` Molecular formula of the compound `'A' = n xx` Empirical formula `= 1 xx Na_(2)SO_(3)=Na_(2)SO_(3)` Step III. Percentage composition of compound 'B' `underset((A))(Na_(2)SO_(3))overset([O])(rarr)underset((B))(Na_(2)SO_(4))` Molecular mass of `B = 2 xx 23+32 + 4 xx 16 = 142 u` Percentage of `Na = (46)/(142) xx 100 = 32.4 %` Percentage of `S = (32)/(142) xx 100 = 22.54 %` Percentage of `O = (64)/(142) xx 1000 = 45.07 %`. |
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| 25. |
Compound 'A' is: |
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Answer» `CaSO_(4).2H_(2)O` |
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| 26. |
Compound (A) is: |
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Answer» oxalate SALT (F) `Na_(2)S_(2)O_(3)` (H) `[Bi(S_(2)O_(3))_(3)]^(3-)` (X) `rarr HCOOH (C) H_(2)` (E) `Na_(2)SO_(3)` (G) `Bi_(2)(S_(2)O_(3))_(3)` (I) `Ag_(2)S_(2)O_(3)` (J) `Ag_(2)S` (K) `[Ag(S_(2)O_(3))_(2)]^(3-)` |
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| 27. |
Compound 'A' gives red precipitate with Cu_(2)Cl_(2)//NH_(4)OH solution and decolourises bromine water. The compound 'A' can be |
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Answer» `CH_(2)=CH-UNDERSET(O)underset(||)(C)-CH_(3)` |
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| 28. |
Compound (A) C_(8)H_(9)Br, gives a light yellow precipitate when warmed with alcoholic AgNO_(3) (B) easily form anhydride on heating. Identify the compound (A) |
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(A) is di-substituted `:.` option A is true
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| 29. |
Compound (A) (C_8H_8O) on treatment with NH_2OH.HCI gives (B) and (C) rearrange to give (D) and (E), respectively, on treatment with acid. (B), (C),(D)and (E) are all isomers of molecular formula (C_8H_9NO) . When (D) is boiled with alcoholic KOH, an oil (F) (C_6H_7N) separates out. (F) reacts with CH_3COCI to give back (D). On the other hand. (E) on boiling with alkali followed by acidification gives a white solid (G) (C_7H_6O_2). Identify (A)to (G). |
Answer» SOLUTION :
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| 30. |
Compound (A), C_(6)H_(3)Br, gives a white precipitate when warmed with alcoholic AgNO_(3). Oxidation of (A) gives an acid (B). C_(6)H_(3)O_(4). (B) easily forms anhydride on on heating. Identify the compound (A). |
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| 31. |
Compound (A) C_5H_(10) does not dissolve in cold dil. H_2SO_4. What is (A) ? |
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| 32. |
Components of rectified spirit cannot be separated by distillation because |
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Answer» it FORMS an Azeotropic mixture |
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| 33. |
Compolete the following equations : (i) Na_(2)O_92)+ 2H_(2) O to (W) +H_(2)O_(2) (ii) 2KO_(2)+2H_(2)O to (X) +(Y) +O_(2) (iii) Na_(2) O+ CO_(2)to (Z). |
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Answer» `{:(W, X , Y , Z) , (4Na, K_(2)O , H_(2)O_(2) , Na_(2)CO_(3)):}` `2KO_(2)+ 2H_(2)O to underset((X))(2KOH)+ underset((Y))(H_(2)O_(2))+ O_(2)` `Na_(2) O+CO_(2) to underset((Z))(Na_(2) CO_(3))` |
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| 35. |
Complete the reactions and identify the products. CH_(3) - underset(underset(OH)(|))(CH) - CH_(3) overset(H^(+)//K_(2)Cr_(2)O_(7))rarr A overset((O))rarr B |
Answer» SOLUTION :
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| 36. |
Complete the reactions and identify the products. |
Answer» SOLUTION :
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| 37. |
Complete the reaction: Zn(s)+2H^(+)(aq)to |
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Answer» |
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| 38. |
Complete the reaction: C(s)+H_(2)O(g)overset(Delta)(to) |
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Answer» |
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| 39. |
Complete the reaction: CO(g)+H_(2)O(g)overset(Delta)(to) |
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Answer» |
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| 40. |
Complete the reaction, C CI_(4) |
Answer» SOLUTION :
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| 41. |
Complete the reaction ,C_2H_5NH_2 overset(C_2H_5Br)underset(-HBr)to ? overset(C_2H_5Br)underset(-HBr)to ? overset(C_2H_5Br)underset(-HBr)to? |
| Answer» Solution :`underset(I^(@)-amine)(C_2H_5NH_2)overset(C_2H_5Br)underset(-HBR)to underset(2^(@)-amine)((C_2H_5)NH) overset(C_2H_5Br)underset(-HBr)to underset(3^(@)-amine)((C_2H_5)N)overset(C_2H_5Br)underset(-HBr)tounderset("quarternary AMMONIUM salt")((C_2H_5)_4N^(+)BR)` | |
| 42. |
Complete the reaction as follows. Pyrolysis of kerosene : |
| Answer» Solution :`UNDERSET("kerosene")underset("Dodecane")(C_(12)H_(26)) underset("PD, Pt, Ni")overset("Pyrolysis 973K")rarr underset("Alkane")underset("HEPTANE")(C_(7)H_(16))+underset("Alkene")underset("Pentene")(C_(5)H_(10))+"other products"` | |
| 43. |
Complete the reaction as follows. n-Hexane overset("Aromatization")rarr |
Answer» SOLUTION :
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| 44. |
Complete the reaction as follows. Pyrolysis of hexane : |
Answer» SOLUTION :
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| 45. |
Complete the reaction as follows. Oxidation 2-methylpropane reaction : |
| Answer» Solution :`underset("2-methaylpropane")((CH_(3))_(3)CH) underset(+(O))overset(KMnO_(4))rarr underset("2-methaylpropane-2-ol")((CH_(3))_(3)C-OH)` | |
| 46. |
Complete the reaction as follows. Liberation of dihydrogen gas reaction : |
| Answer» Solution :`underset("Methane")(CH_(4(G))) + underset("STEAM")(H_(2)O_((g))) underset(1273K)OVERSET(NI)rarr underset("monoxide")underset("Carbon")(CO_((g))) + underset("DIHYDROGEN")(3H_(2(g)))` | |
| 47. |
Complete the reaction as follows. n-Heptane overset("Aromatization")rarr |
Answer» SOLUTION :
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| 48. |
Complete the reaction as follows. Incomplete combustion of methane : |
| Answer» Solution :`underset("METHANE")(CH_(4(G))) + O_(2(g)) underset("combustion")OVERSET("INCOMPLETE")rarr C_((s)) + underset("Carbon")(2H_(2)O_((l)))` | |
| 49. |
Complete the reaction as follows. Controlled chlorination of ethane : |
| Answer» Solution :`underset("Ethane")(CH_(3))-CH_(3)+Cl_(2) overset(HV)RARR underset("Chloroethane")(CH_(3)-CH_(2)Cl)+HCl` | |