logging in or signing up cyclic structure of glucose poonampanhal Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 768 Category: Education License: All Rights Reserved Like it (1) Dislike it (0) Added: December 02, 2009 This Presentation is Public Favorites: 0 Presentation Description explains the cyclic structure of glucose and fructose Comments Posting comment... Premium member Presentation Transcript CYCLIC STRUCTURE OF GLUCOSE : CYCLIC STRUCTURE OF GLUCOSE How we come to know of its cyclic nature?? Poonam Panchal REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE : REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE 2,4- DNP TEST (FOR ALDEHYDE GROUP)– NEGATIVE SCHIFF’S TEST(FOR ALDEHYDE GROUP)– NEGATIVE REACTION WITH HYDROXYLAMINE (NH2OH)— CONFIRMS PRESENCE OF CARBONYL GROUP FURTHER REACTION OF PENTAACETATE OF GLUCOSE WITH HYDROXYLAMINE– NEGATIVE INDICATING ABSENCE OF FREE –CHO GROUP REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE : REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE -Form of glucose-------crystallization from conc. Solution of glucose at 303K ß-form of glucose--------crystallization from hot and saturated aqueous solution at 371K. Problem solved : Problem solved BY CYCLIC HEMIACETAL STRUCTURE Compare Alpha and Beta Glucose : Compare Alpha and Beta Glucose The position of the -OH group on the anomeric carbon (#1) is an important distinction for carbohydrate chemistry. The Beta position is defined as the -OH being on the same side of the ring as the C # 6. In the chair structure this results in a horizontal projection. The Alpha position is defined as the -OH being on the opposite side of the ring as the C # 6. In the chair structure this results in a downward projection. The alpha and beta label is not applied to any other carbon - only the anomeric carbon, in this case # 1. fructose : fructose Structure Open chain structure of fructose : Open chain structure of fructose Ring structure of fructose : Ring structure of fructose Furan and pyran rings : Furan and pyran rings FURAN PYRAN CLASSIFICATION OF CARBOHYDRATES : CLASSIFICATION OF CARBOHYDRATES ON THE BASIS OF HYDROLYSIS : ON THE BASIS OF HYDROLYSIS MONOSACCHARIDES Can not be hydrolysed further to give simpler unit of polyhydroxy aldehyde or ketone e.g. glucose,fructose,ribose OLIGOSACCHARIDES Yield 2 to 10 monosaccharide units, on hydrolysis. Disaccharides, trisaccharides, tetrasaccharides POLYSACCHARIES Called Non-Sugars Yield a large number of monosaccharide units e.g. Starch, cellulose,glycogen On the basis of reactions : On the basis of reactions REDUCING SUGARS All those carbohydrates which reduce Fehling’s solution and Tollen’s reagent are referred to as reducing sugars. e.g. all monosaccharides NONREDUCING SUGARS Do not have free carboxyl group. e.g. sucrose You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.
cyclic structure of glucose poonampanhal Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 768 Category: Education License: All Rights Reserved Like it (1) Dislike it (0) Added: December 02, 2009 This Presentation is Public Favorites: 0 Presentation Description explains the cyclic structure of glucose and fructose Comments Posting comment... Premium member Presentation Transcript CYCLIC STRUCTURE OF GLUCOSE : CYCLIC STRUCTURE OF GLUCOSE How we come to know of its cyclic nature?? Poonam Panchal REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE : REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE 2,4- DNP TEST (FOR ALDEHYDE GROUP)– NEGATIVE SCHIFF’S TEST(FOR ALDEHYDE GROUP)– NEGATIVE REACTION WITH HYDROXYLAMINE (NH2OH)— CONFIRMS PRESENCE OF CARBONYL GROUP FURTHER REACTION OF PENTAACETATE OF GLUCOSE WITH HYDROXYLAMINE– NEGATIVE INDICATING ABSENCE OF FREE –CHO GROUP REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE : REACTIONS THAT CAN NOT BE EXPLAINED BY OPEN CHAIN STRUCTURE -Form of glucose-------crystallization from conc. Solution of glucose at 303K ß-form of glucose--------crystallization from hot and saturated aqueous solution at 371K. Problem solved : Problem solved BY CYCLIC HEMIACETAL STRUCTURE Compare Alpha and Beta Glucose : Compare Alpha and Beta Glucose The position of the -OH group on the anomeric carbon (#1) is an important distinction for carbohydrate chemistry. The Beta position is defined as the -OH being on the same side of the ring as the C # 6. In the chair structure this results in a horizontal projection. The Alpha position is defined as the -OH being on the opposite side of the ring as the C # 6. In the chair structure this results in a downward projection. The alpha and beta label is not applied to any other carbon - only the anomeric carbon, in this case # 1. fructose : fructose Structure Open chain structure of fructose : Open chain structure of fructose Ring structure of fructose : Ring structure of fructose Furan and pyran rings : Furan and pyran rings FURAN PYRAN CLASSIFICATION OF CARBOHYDRATES : CLASSIFICATION OF CARBOHYDRATES ON THE BASIS OF HYDROLYSIS : ON THE BASIS OF HYDROLYSIS MONOSACCHARIDES Can not be hydrolysed further to give simpler unit of polyhydroxy aldehyde or ketone e.g. glucose,fructose,ribose OLIGOSACCHARIDES Yield 2 to 10 monosaccharide units, on hydrolysis. Disaccharides, trisaccharides, tetrasaccharides POLYSACCHARIES Called Non-Sugars Yield a large number of monosaccharide units e.g. Starch, cellulose,glycogen On the basis of reactions : On the basis of reactions REDUCING SUGARS All those carbohydrates which reduce Fehling’s solution and Tollen’s reagent are referred to as reducing sugars. e.g. all monosaccharides NONREDUCING SUGARS Do not have free carboxyl group. e.g. sucrose