NEB question archive / Class 12 / Chemistry

Class 12 Chemistry NEB Past Questions

Revise chemistry using questions organised by chapter and the year recorded in the MeroMentor question bank.

Years and sets follow imported records and have not been independently checked against original papers. This is a study archive, not an official NEB publication. Class 11 records may include school-level exams; older records may follow the former HSEB syllabus.

Chapter-wise questions

1888 questions
Aldehydes & Ketones2082 BSshort1 marks

1. Why do these compounds give positive iodoform test?

Aldehydes & Ketones2082 BSshort1 marks

2. How would you convert compound (Y) into pseudonitrol?

Aldehydes & Ketones2082 BSmcq1 marks

3. A sequence of reactions is represented as: Benzene $\xrightarrow{CH_3Cl/Anhy. AlCl_3} (A) \xrightarrow{CeO_2/H^+, [O]} (B) \xrightarrow{alc. KCN, Reflux} (C)$ Predict the name of reaction that converts (B) to (C).

  1. A. Benzoin condensation
  2. B. Perkin's condensation
  3. C. Aldol condensation
  4. D. Claisen condensation
Aldehydes & Ketones2082 BSshort1 marks

4. Write the chemical equations to illustrate the following reaction: 2, 4-DNP test

Aldehydes & Ketones2082 BSshort2 marks

5. Write any two methods for the preparation of compound (Z).

Aldehydes & Ketones2082 BSshort1 marks

6. Write any two methods for the preparation of compound (Z).

Aldehydes & Ketones2082 BSlong8 marks

7. An organic compound (X) reacts with Grignard's reagent to give (Y), which on oxidation gives (Z). All of the compounds (X), (Y) and (Z) give positive iodoform test. a. Identify the compounds (X), (Y) and (Z) with reactions and conditions involved. b. Why do these compounds give positive iodoform test? c. How would you convert compound (Y) into pseudonitrol? d. Write any two methods for the preparation of compound (Z).

Aldehydes & Ketones2082 BSlong5 marks

8. An organic compound (X) reacts with Grignard's reagent to give (Y), which on oxidation gives (Z). All of the compounds (X), (Y) and (Z) give positive iodoform test. a. Identify the compounds (X), (Y) and (Z) with reactions and conditions involved. b. Why do these compounds give positive iodoform test? c. How would you convert compound (Y) into pseudonitrol? d. Write any two methods for the preparation of compound (Z).

Aldehydes & Ketones2082 BSshort2 marks

9. How would you convert compound (Y) into pseudonitrol?

Aldehydes & Ketones2082 BSshort1 marks

10. Why do these compounds give positive iodoform test?

Aldehydes & Ketones2082 BSshort1 marks

11. Write the chemical equations to illustrate the following reaction: 2, 4-DNP test

Aldehydes & Ketones2082 BSshort3 marksSub-question (a)

12. Identify the compounds (X), (Y) and (Z) with reactions and conditions involved.

Aldehydes & Ketones2082 BSshort2 marksSub-question (a)

13. Identify the compounds (X), (Y) and (Z) with reactions and conditions involved.

Amino Compounds2082 BSmcq1 marks

14. Which of the following compounds gives positive carbylamine reaction?

  1. A. (CH3)2NH
  2. B. (CH3)3N
  3. C. (CH3)4N+
  4. D. CH3NH2
Amino Compounds2082 BSlong5 marks

15. You are given the mixture of two compounds A and B. $A=CH_{3}CH_{2}CH_{2}-NH_{2}$ and $B=CH_{3}CH_{2}NHCH_{3}$. How would you separate their mixture by applying Hoffmann's method? Give the nitrous acid test to distinguish between compounds A and B.

Amino Compounds2082 BSshort2 marks

16. How will you carry out the following conversions? Aniline into chlorobenzene

Amino Compounds2082 BSlong5 marks

17. A list of compounds is given as follows: p-aminoazobenzene, Benzenediazonium chloride, Aniline, Nitrobenzene, Phenol and Benzene. From the above list of compounds, prepare a sequence of reaction chain with suitable conditions and reagents.

Amino Compounds2082 BSshort2 marksSub-question (b)

18. Give the nitrous acid test to distinguish between compounds A and B.

Carboxylic Acids2082 BSlong5 marks

19. An aliphatic compound (A) reacts with SOCl2 to give (B). The compound (B) is heated with ammonia to produce (C). The compound (C) is further heated with Br2/KOH to yield (D). The compound (D) gives (E) when treated with NaNO2/HCl at low temperature. The compound (E) is a primary alcohol which gives positive iodoform test. Identify compound (A) to (E) with the reactions involved.

Carboxylic Acids2082 BSmcq1 marks

20. A compound 'Z' with molecular formula $C_3H_4O_4$ is heated to produce compound 'Y' and $CO_2$ gas. Heating of compound 'Y' with $P_2O_5$ forms compound 'X' and water molecule. Identify the compound 'X'.

  1. A. Ethanoic acid
  2. B. Ethanoic anhydirde
  3. C. Methanoic anhydride
  4. D. Ethanal
Cement2082 BSshort3 marks

21. Answer the following questions: Draw the flowsheet diagram for the manufacture of Portland cement.

Chemical Kinetics2082 BSlong5 marks

22. Define instantaneous rate of reaction. Write down the rate expressions of the following reaction. $2N_2O_5(g) \rightarrow 4NO_2(g) + O_2(g)$ If 2.24 litres of $O_2$ at NTP is produced in 30 minutes, what is the rate of disappearance of $N_2O_5(g)$?

Chemical Kinetics2082 BSmcq1 marks

23. The half-life of a certain reaction is 50 seconds and it remains constant even if the initial concentration of the reactant is doubled. What is the order of the reaction?

  1. A. Zero order reaction
  2. B. First order reaction
  3. C. Second order reaction
  4. D. Pseudo-first order reaction
Chemistry in Service to Mankind2082 BSlong2 marks

24. How are addition and condensation polymers formed? Write an example of each.

Electrochemistry2082 BSshort2 marks

25. Construct the galvanic cell notation for the given electrodes indicating anode and cathode.

Electrochemistry2082 BSshort1 marks

26. Calculate the cell potential for the given cell at 25°C.

Electrochemistry2082 BSlong5 marks

27. You are given the standard reduction potentials, $E^{\circ}_{Zn^{2+}/Zn} = -0.76 V$, $E^{\circ}_{Mg^{2+}/Mg} = -2.38 V$. Answer the following questions: a. What is standard electrode potential? b. Construct the galvanic cell notation for the given electrodes indicating anode and cathode. c. Write the complete cell reaction for the given cell. d. Calculate the cell potential for the given cell at 25°C.

Electrochemistry2082 BSshort1 marks

28. Write the complete cell reaction for the given cell.

Electrochemistry2082 BSmcq1 marks

29. Standard reduction potential values for P, Q, R and S are +0.34V, -0.76V, +0.0V and -3.05V, respectively. What is the correct order of their reducing power?

  1. A. P > R > Q > S
  2. B. S > R > Q > P
  3. C. Q > P > S > R
  4. D. S > Q > R > P
Electrochemistry2082 BSshort1 marksSub-question (a)

30. What is standard electrode potential?

Ethers2082 BSshort1 marks

31. Write the chemical equations to illustrate the following reaction: Williamson's reaction

Ethers2082 BSshort2 marks

32. How will you carry out the following conversions? c. Ethoxyethane into methoxymethane

Haloalkanes2082 BSshort2 marks

33. How will you carry out the following conversions? a. Ethanol into chloroform

Haloalkanes2082 BSlong5 marks

34. A chemical reaction occurs as follows: CH₃CH₂CH₂Br + aq. KOH → B + KBr (A). a. Identify the compound 'B' in the above reaction. b. Which substitution reaction mechanism occurs in the above reaction and why? c. What is the product formed when alc. KOH solution is used instead of aq. KOH in the above reaction? d. How can you obtain nitropropane from compound 'A'?

Haloalkanes2082 BSshort2 marks

35. Which substitution reaction mechanism occurs in the above reaction and why?

Haloalkanes2082 BSshort2 marks

36. Which substitution reaction mechanism occurs in the reaction of 1-bromopropane with aqueous KOH and why?

Haloalkanes2082 BSshort1 marks

37. Write the chemical equations to illustrate the following reaction: Reimer-Tiemann reaction

Haloalkanes2082 BSshort1 marks

38. What is the product formed when alc. KOH solution is used instead of aq. KOH in the above reaction?

Haloalkanes2082 BSshort1 marks

39. How can you obtain nitropropane from compound 'A'?

Haloalkanes2082 BSshort1 marksSub-question (a)

40. Identify the compound 'B' in the above reaction.

1 / 48

Continue your Chemistry revision

Chapter practice and explanations are available through your enrolled MeroMentor course.

Go to my courses