Important Questions for Class 11 Chemistry Chapter 8: Chapter 8 of Class 11 Chemistry, "Organic Chemistry: Some Basic Principles and Techniques," introduces the fundamentals of organic chemistry, focusing on the structure, classification, and nomenclature of organic compounds. Key topics include functional groups, types of isomerism (structural and stereoisomerism), and the concept of homologous series.
It also covers the methods of preparation, identification, and analysis of organic compounds, such as distillation, crystallization, and chromatography. The chapter emphasizes the importance of functional groups in determining the properties and reactivity of organic molecules. This foundation is crucial for understanding more advanced topics in organic chemistry.Important Questions for Class 11 Chemistry Chapter 8 PDF
3. Write the bond line formula for
Ans.
4. How are organic compounds classified?
Ans: (i) Acyclic or open chain compounds
(ii) Alicyclic or closed chain or ring compounds.
(iii) Aromatic compounds.
5.Define homologous series?
Ans: A group or a series of organic compounds each containing a characteristic functional group forms a homologous series and the members of the series are called homologous.
6. Write an example of a non-benzenoid compound.
Ans:
Structure of Tropolene
7. What is the cause of geometrical isomerism in alkenes?
Ans: Alkene has a π − bond and the restricted rotation around the π− bond gives rise to geometrical isomerism.
10. Define carbocation.
Ans: A species having a carbon atom possessing a sextet of electrons and a positive charge is called carbocation.
11. What are the nucleophiles?
Ans: The electron rich species are called nucleophiles. A nucleophile has affection for a positively charged centre.
Example- O H − , I − , C N −
12. How can the mixture of kerosene oil and water be separated?
Ans: The mixture of kerosene oil and water can be separated by using a separating funnel.
13. Lassaigne’s test is not shown by diazonium salts. Why?
Ans: Diazonium salts usually leave N 2 on heating much before they have a chance to react with the fused sodium metal. Therefore, diazonium salts do not show positive Lassaigne’s test for nitrogen.
15. Can you use potassium in place of sodium for fusing an organic compound in Lassaigne’s test?
Ans: No, because potassium is more reactive than sodium.
16. Give the reason for the fusion of an organic compound with sodium metal for testing nitrogen, sulphur and halogens.
Ans: The elements present in the compound are converted from covalent form into ionic form by fusing the compound with sodium metal.
18. Write the expanded form of the following condensed formulas into their complete structural formulas.
2. How does hybridization affect electronegativity?
Ans: The greater the s-character of the hybrid orbitals, the greater is the electronegativity. Thus, a carbon atom having a sp-hybrid orbital with 50% s -character is more electronegative than that possessing s p 2 s or sp3 hybridized orbitals.
3. Why is sp hybrid orbital more electronegative than sp2 or s p 3 hybridized orbitals?
Ans: The greater the s-character of the hybrid orbitals, the greater is the electronegativity. Thus, a carbon atom having a sp-hybrid orbital with 50% s -character is more electronegative than that possessing sp2 or sp3 hybridized orbitals.
Example: Hydroxyl group (-OH), Aldehyde group (-CHO), Carboxylic acid group (-COOH), etc.
4. Give two examples of aliphatic compounds.
5. Write an example of an alicyclic compound.
6. For each of the following compounds write a condensed formula and also their bond line formula.