Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 25.5, Problem 11P
Interpretation Introduction
Interpretation:
Ribose is an aldopentose (a monosaccharide containing five carbon atoms) that, in its open chain form, has an
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Chapter 25 Solutions
Organic Chemistry
Ch. 25.1 - Prob. 1PCh. 25.2 - Prob. 2PCh. 25.2 - Prob. 3PCh. 25.2 - Prob. 4PCh. 25.2 - Prob. 5PCh. 25.3 - Prob. 6PCh. 25.3 - Prob. 7PCh. 25.4 - Prob. 8PCh. 25.4 - Prob. 9PCh. 25.4 - Prob. 10P
Ch. 25.5 - Prob. 11PCh. 25.5 - Prob. 12PCh. 25.5 - Prob. 13PCh. 25.5 - Prob. 14PCh. 25.5 - Prob. 15PCh. 25.6 - Prob. 16PCh. 25.6 - Prob. 17PCh. 25.6 - Prob. 18PCh. 25.6 - Prob. 19PCh. 25.6 - Prob. 20PCh. 25.6 - Prob. 21PCh. 25.6 - Prob. 22PCh. 25.6 - Prob. 23PCh. 25.7 - Prob. 24PCh. 25.8 - Show the product you would obtain from the...Ch. 25.SE - Prob. 26VCCh. 25.SE - Prob. 27VCCh. 25.SE - Prob. 28VCCh. 25.SE - Prob. 29VCCh. 25.SE - Prob. 30MPCh. 25.SE - Prob. 31MPCh. 25.SE - Glucosamine, one of the eight essential...Ch. 25.SE - D-Glicose reacts with acetone in the presence of...Ch. 25.SE - Prob. 34MPCh. 25.SE - Prob. 35MPCh. 25.SE - Prob. 36APCh. 25.SE - Prob. 37APCh. 25.SE - Prob. 38APCh. 25.SE - Prob. 39APCh. 25.SE - Prob. 40APCh. 25.SE - Assign R or S configuration to each chirality...Ch. 25.SE - Prob. 42APCh. 25.SE - Prob. 43APCh. 25.SE - Prob. 44APCh. 25.SE - Prob. 45APCh. 25.SE - Prob. 46APCh. 25.SE - Prob. 47APCh. 25.SE - Prob. 48APCh. 25.SE - Prob. 49APCh. 25.SE - Prob. 50APCh. 25.SE - Prob. 51APCh. 25.SE - Prob. 52APCh. 25.SE - Prob. 53APCh. 25.SE - Prob. 54APCh. 25.SE - Prob. 55APCh. 25.SE - Prob. 56APCh. 25.SE - Prob. 57APCh. 25.SE - Prob. 58APCh. 25.SE - Prob. 59APCh. 25.SE - Prob. 60APCh. 25.SE - Prob. 61APCh. 25.SE - Prob. 62APCh. 25.SE - Prob. 63APCh. 25.SE - D-Mannose reacts with acetone to give a...Ch. 25.SE - Prob. 65APCh. 25.SE - Prob. 66APCh. 25.SE - Prob. 67APCh. 25.SE - Prob. 68APCh. 25.SE - Prob. 69APCh. 25.SE - Prob. 70APCh. 25.SE - Prob. 71AP
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- Xylulose has the following structural formula. To what carbohydrate class does xylulose belong based on the number of carbons and carbonyl functionality? A) aldotetrose B) aldopentose C) ketotetrose D) ketopentose E) ketohexosearrow_forwardConsider the trisaccharide below and answer the following questions: CH,OH OH CH2 OH OH A но он оня В OH OH HOH,C но CH,OH OH Name of monosaccharide A (Follow this format in typing your answer: ribose): Name the glycosidic linkage between monosaccharides A and B. (strictly follow this format, do not put spaces in between : beta-1,2): Is the trisaccharide a reducing sugar? Type Yes or No:arrow_forwardThe aldonic acid of d-glucose forms a five-membered-ring lactone. Draw its structure.arrow_forward
- 3 On the following molecule indicate (1) what sugar makes up the repeating unit, (2) what type of linkage connects the sugar monomers, and (3) which end is the reducing end and which end is the nonreducing end.arrow_forwardHow do you draw the furanose and pyranose forms of D-ribose (chemical structure)?arrow_forwardThe standard free energy change (ΔG°') for hydrolysis of fructose-l,6-bisphosphate (FBP) to fructose-6-phosphate (F-6-P) and Pi is -16.7 kJ/mol: FBP + H2O → Fructose-6-P + Pi The standard free energy change (ΔG°') for ATP hydrolysis is -30.5 kJ/mol: ATP + H2O → ADP + Pi a What is the standard free energy change for the phosphofructokinase reaction: ATP + Fructose-6-phosphate → ADP + FBP ΔG°' = -13.8 kJ/mol b What is the equilibrium constant for this reaction at 25.0 °C? K'eq =arrow_forward
- Starting with the open-chain form of dribose, write equations for the cyclization reactions that form thepyranose and the furanose forms.arrow_forwardDraw the cyclic forms of beta-1,3'-d-ditalosearrow_forward2. Sucrose is a disaccharide formed from the condensation of glucose and fructose sugars. Draw the structure of sucrose that results from the condensation reaction between the indicated -OH groups. CH2OH 1, CH,OH он 1. OH но CH,OH OH HO H он OHarrow_forward
- Which of the following describes the following monosaccharide: CH;OH H- OH HO- CH,OH aldose and pentose ketose and pentose aldose and tetrose O ketose and tetrose O aldose and hexose O ketose and hexosearrow_forwardOne of the cyclic forms of D-ribose has the structure CH2OH OH ОНОН (a) How many anomeric carbon atoms are present in this structure? (b) How many hemiacetal carbon atoms are present in this structure?arrow_forwardPart 3 of 3 Modify the structure of lactulose to show the monosaccharide products that form from hydrolysis. You may draw the structures in any arrangement that you like, so long as they aren't touching. он H сн, он :☐ Он × 5 H H HO снон Сн, он H Он Н д- Н Н OH Нarrow_forward
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