Chemistry Chapter 11 Short Questions for Class 11

Chemistry Chapter 11 Short Questions for Class 11

Last Updated on June 10, 2026 by Ahsa.Pk

These are the most important Chemistry chapter 11 short questions for Class 11. The 1st-year chapter 11 of Chemistry is related to reaction kinetics. These questions are for the Punjab Textbook Board and can be used within all of Punjab where this syllabus is taught.

Students are advised to prepare these questions in order to perform the best in the board examination.

Chemistry Chapter 11 Short Questions for Class 11

  1. Define the following:
    i) Cycloalkanes    ii) Isomerism    iii) Conjugated dienes    iv) Inductive effect
  2. Differentiate between:i) Aliphatic and Aromatic hydrocarbons    ii) Homolytic and Heterolytic Fission    iii) Electrophile and Nucleophile
  3. Explain why alkanes do not undergo addition reactions.
  4. How is elimination reaction considered the opposite of an addition reaction?
  5. Compare the carbocation stability in propene and 2-butene.
  6. Given the molecular formula C₅H₁₀, list all possible structural isomers that are alkenes.
  7. When propene (C₃H₆) undergoes electrophilic addition with HBr, it forms 2-bromopropane as the major product. Explain why 2-bromopropane is favored over 1-bromopropane, using the concept of carbocation stability.
  8. Explain why conjugated alkenes may show different reactivity compared to isolated alkenes.
  9. Explain how inductive effects from alkyl groups stabilize carbocations in alkenes.
  10. Write the equation for each reaction:
    i) CH₃CH₂CH=CH₂ with H₂ (Ni catalyst)    ii) CH₃CH=CH₂ with Cl₂    iii) CH₃CH₂CH=CHCH₂CH₃ with H₂O (H₂SO₄ catalyst)
  11. Write structural formulas for each of the following compounds:
    i) Isobutylene   ii) 2,3,4,4-Tetramethyl-2-pentene   iii) 2,5-Heptadiene   iv) 4,5-Dimethyl-2-hexene   v) Vinyl acetylene   vi) 1,3-Pentadiene   vii) 1-Butyne   viii) 3-n-Propyl-1,4-pentadiene   ix) Vinyl bromide   x) But-1-en-3-yne   xi) 4-Methyl-2-pentyne   xii) Isopentane
  12. Write down IUPAC names of the following compounds:
    i) H₃C–CH=CH(CH₂)₂CH₃   ii) (CH₃)₂C=CH₂   iii) CH₃–CH₂–CH₂–C=CH₂ (with CH(CH₃)₂ branch)   iv) CH₂=CH–CH=CH₂   v) CH₂=C–CH₂CH₂CH₃ (with C₂H₅)   vi) (CH₃CH₂)₃CH   vii) CH₃CH₂C(CH₃)₂CH(CH₂CH₃)CH₃   viii) CH₂=CH–C≡C–CH=CH₂   ix) (CH₃)₃C–CH₂–C(CH₃)₃   x) CH₂=CH–C≡CH   xi) CH₃C(CH₃)₂(CH₂)CH₃ (and structures a, b, c)
  13. Differentiate between alicyclic and aromatic compounds.
  14. Define the term isomerism. Give examples.
  15. How does functional group isomerism differ from metamerism? Give examples.
  16. Define tautomerism with an example.
  17. Justify that in alkanes sigma bonds are inert.
  18. Why are alkanes called paraffins?
  19. Differentiate between hydrogenolysis and hydrogenation.
  20. Give the general mechanism of electrophilic addition reactions of alkenes.
  21. What is Markovnikov’s rule? Give an example.
  22. How would you convert ethene into ethyl alcohol?
  23. Convert ethene to (a) Halohydrin (b) Ethylene oxide.
  24. How is ethylene glycol prepared from ethene?
  25. What is ozonolysis? Describe it giving an example. Also give its mechanism.

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