{"id":4699,"date":"2016-05-17T11:49:00","date_gmt":"2016-05-17T06:19:00","guid":{"rendered":"http:\/\/mycbseguide.com\/blog\/ncert-solutions-class-11-chemistry-organic-chemistry-some-basic-principles-part-1\/"},"modified":"2018-10-22T18:18:39","modified_gmt":"2018-10-22T12:48:39","slug":"ncert-solutions-class-11-chemistry-organic-chemistry-some-basic-principles-part-1","status":"publish","type":"post","link":"https:\/\/mycbseguide.com\/blog\/ncert-solutions-class-11-chemistry-organic-chemistry-some-basic-principles-part-1\/","title":{"rendered":"NCERT Solutions class-11 Chemistry Organic Chemistry Some Basic Principles Part-1"},"content":{"rendered":"

ORGANIC CHEMISTRY \u2013 SOME BASIC PRINCIPLES AND TECHNIQUES<\/strong><\/center> <\/p>\n

1. What are hybridisation states of each carbon atom in the following compounds?<\/p>\n

<\/p>\n

2. Indicate the bonds in the following molecules:<\/p>\n


\n3. Write bond line formulas for: Isopropyl alcohol, 2,3-Dimethyl butanal, Heptan-4-one.<\/p>\n

4. Give the IUPAC names of the following compounds:<\/p>\n

(a)<\/p>\n

\"14360839068514.jpg\"<\/p>\n

(b)<\/p>\n

\"1436083909108.jpg\"<\/p>\n

(c)<\/p>\n

\"1436083909891.jpg\"<\/p>\n

(d)<\/p>\n

\"14360839108358.jpg\"<\/p>\n

(e)<\/p>\n

\"14360839116053.jpg\"<\/p>\n

(f) <\/p>\n

5. Which of the following represents the correct IUPAC name for the compounds concerned?<\/p>\n

(a) 2,2-Dimethylpentane or 2-Dimethylpentane<\/p>\n

(b) 2,4,7-Trimethyloctane or 2,5,7-Trimethyloctane<\/p>\n

(c) 2-Chloro-4-methylpentane or 4-Chloro-2-methylpentane<\/p>\n

(d) But-3-yn-1-ol or But-4-ol-1-yne<\/p>\n

6. Draw formulas for the first five members of each homologous series beginning with the following compounds.<\/p>\n

(a) H-COOH<\/p>\n

(b)<\/p>\n

(c) <\/p>\n

7. Give condensed and bond line structural formulas and identify the functional group(s) present, if any, for:<\/p>\n

(a) 2,2,4-Trimethylpentane<\/p>\n

(b) 2-Hydroxy-1,2,3-propanetricarboxylic acid<\/p>\n

(c) Hexanedial<\/p>\n

8. Identify the functional groups in the following compounds<\/p>\n

(a)<\/p>\n

\"14360839585072.jpg\"<\/p>\n

(b)<\/p>\n

\"14360839591179.jpg\"<\/p>\n

(c)<\/p>\n

\"14360839601215.jpg\"<\/p>\n

9. Which of the two: is expected to be more stable and why?<\/p>\n

10. Explain why alkyl groups act as electron donors when attached to a system.<\/p>\n

11. Draw the resonance structures for the following compounds. Show the electron shift using curved-arrow notation.<\/p>\n

(a) <\/p>\n

(b) <\/p>\n

(c) <\/p>\n

(d) <\/p>\n

(e)<\/p>\n

(f) <\/p>\n

12. What are electrophiles and nucleophiles? Explain with examples.<\/p>\n

13. Identify the reagents shown in bold in the following equations as nucleophiles or electrophiles:<\/p>\n

<\/p>\n

14. Classify the following reactions in one of the reaction type studied in this unit.<\/p>\n

(a) <\/p>\n

(b)<\/p>\n

(c) <\/p>\n

(d) <\/p>\n

15. What is the relationship between the members of following pairs of structures? Are they structural or geometrical isomers or resonance contributors?<\/p>\n

(a)<\/p>\n

\"14360840410024.jpg\"<\/p>\n

(b)<\/p>\n

\"14360840417539.jpg\"<\/p>\n

(c)<\/p>\n

<\/p>\n

16. For the following bond cleavages, use curved-arrows to show the electron flow and classify each as homolysis or heterolysis. Identify reactive intermediate produced as free radical, carbocation and carbanion.<\/p>\n

(a)<\/p>\n

<\/p>\n

(b)<\/p>\n

\"14360840695144.jpg\"<\/p>\n

(c)<\/p>\n

\"14360840702569.jpg\"<\/p>\n

(d)<\/p>\n

\"14360840711734.jpg\"<\/p>\n

17. Explain the terms Inductive and Electromeric effects. Which electron displacement effect explains the following correct orders of acidity of the carboxylic acids?<\/p>\n

(a) <\/p>\n

(b) <\/p>\n

18. Give a brief description of the principles of the following techniques taking an example in each case.<\/p>\n

(a) Crystallisation<\/p>\n

(b) Distillation<\/p>\n

(c) Chromatography<\/p>\n

19. Describe the method, which can be used to separate two compounds with different solubilities in a solvent S.<\/p>\n

20. What is the difference between distillation, distillation under reduced pressure and steam distillation?<\/p>\n","protected":false},"excerpt":{"rendered":"

ORGANIC CHEMISTRY \u2013 SOME BASIC PRINCIPLES AND TECHNIQUES  1. What are hybridisation states of each carbon atom in the following compounds? 2. Indicate the bonds in the following molecules: 3. Write bond line formulas for: Isopropyl alcohol, 2,3-Dimethyl butanal, Heptan-4-one. 4. Give the IUPAC names of the following compounds: (a) (b) (c) (d) (e) (f) … Read more<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[47,281],"tags":[],"class_list":["post-4699","post","type-post","status-publish","format-standard","hentry","category-cbse-class-11","category-ncert-solutions"],"yoast_head":"\nNCERT Solutions class-11 Chemistry Organic Chemistry Some Basic Principles Part-1 | myCBSEguide<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/mycbseguide.com\/blog\/ncert-solutions-class-11-chemistry-organic-chemistry-some-basic-principles-part-1\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"NCERT Solutions class-11 Chemistry Organic Chemistry Some Basic Principles Part-1 | myCBSEguide\" \/>\n<meta property=\"og:description\" content=\"ORGANIC CHEMISTRY \u2013 SOME BASIC PRINCIPLES AND TECHNIQUES  1. What are hybridisation states of each carbon atom in the following compounds? 2. Indicate the bonds in the following molecules: 3. Write bond line formulas for: Isopropyl alcohol, 2,3-Dimethyl butanal, Heptan-4-one. 4. Give the IUPAC names of the following compounds: (a) (b) (c) (d) (e) (f) ... 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