ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Question
Chapter 24.14, Problem 17P
Interpretation Introduction
Interpretation:
The curved arrows are to be added to the given sequence to show the conversion of the conjugate acid of
Concept introduction:
The flow of electrons in the mechanism is shown by curved arrows.
The compound
The product of each step gives ideas about the bonds that break and new bonds that are formed.
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Draw the structure of the expected product when monosaccharide A undergomutarotation upon dissolving in water in the presence of Tollens reagent (AgNO3,NH4OH).
Identify the organic functional group and reaction type for the following reaction.
The reactant is a(n)
- carboxylic acid hexose
- Aldohexose
- aldotetrose
-deoxyhexose
-carboxylic acid tetrose
- ketohexose
The product is a(n)
- carboxylic acid tetrose
- aldotetrose
-alcohol hexose
-aldohexose
-carboxylic acid hexose
- alcohol tetrose
The reaction type is
- hemiacetal formation
-hydrolysis
-oxidation( Benedict’s)
-acetal formation
-reduction( hydrogenation)
- mutarotation
OH
НО
HO
OH
НО
Но
OH
ОН
ОН
OH
What are the monosachharides that make up this trisaccharide?
O a-D-glucopyranose, a-D-galactopyranose, a-D-fructofuranose
a-D-glucopyranose, a-D-galactopyranose, B-D-fructofuranose
a-D-glucopyranose, a-D-glucopyranose, B-D-fructofuranose
a-D-galactopyranose, a-D-glucopyranose, a -D-fructofuranose
Chapter 24 Solutions
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
Ch. 24.2 - Prob. 1PCh. 24.3 - Problem 24.2 Which aldotetrose in the structure...Ch. 24.4 - Prob. 3PCh. 24.4 - Prob. 4PCh. 24.6 - Prob. 5PCh. 24.6 - Prob. 6PCh. 24.7 - Prob. 7PCh. 24.8 - Prob. 8PCh. 24.8 - Prob. 9PCh. 24.9 - Prob. 10P
Ch. 24.10 - Prob. 11PCh. 24.10 - Prob. 12PCh. 24.11 - Prob. 13PCh. 24.12 - Prob. 14PCh. 24.14 - Prob. 15PCh. 24.14 - Prob. 16PCh. 24.14 - Prob. 17PCh. 24.14 - Using Mechanism 24.2 as a guide, write a stepwise...Ch. 24.15 - Prob. 19PCh. 24.17 - Prob. 20PCh. 24.17 - Prob. 21PCh. 24.18 - Prob. 22PCh. 24.18 - Prob. 23PCh. 24.18 - Prob. 24PCh. 24.20 - Prob. 25PCh. 24 - Prob. 26PCh. 24 - Prob. 27PCh. 24 - Prob. 28PCh. 24 - Prob. 29PCh. 24 - Prob. 30PCh. 24 - Prob. 31PCh. 24 - Prob. 32PCh. 24 - Prob. 33PCh. 24 - Prob. 34PCh. 24 - Prob. 35PCh. 24 - Methyl glycosides of 2-deoxy sugars have been...Ch. 24 - Prob. 37PCh. 24 - Prob. 38PCh. 24 - Prob. 39PCh. 24 - Prob. 40PCh. 24 - Treatment of d-mannose with methanol in the...Ch. 24 - Prob. 42PCh. 24 - Prob. 43PCh. 24 - Prob. 44PCh. 24 - Prob. 45DSPCh. 24 - Prob. 46DSPCh. 24 - Prob. 47DSPCh. 24 - Prob. 48DSPCh. 24 - Prob. 49DSP
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- 5)A certain aerobic organism is able to metabolize the followingglycolipid CH,OH H H OH H HO OH A.Draw the 2 resulting structures that would occur upon initial hydrolysis of the O-glycosidic bond.arrow_forwardDraw the following sugar derivatives. 1,3,6-tri-O-methyl-d-fructofuranosearrow_forwardOne pathway for the metabolism of D-glucose 6-phosphate is its enzyme-catalyzed conversion to D-fructose 6-phosphate. Show that this transformation can be accom- plished as two enzyme-catalyzed keto-enol tautomerisms. СНО CH,OH C=0 enzyme catalysis Но Но H OH H H. O- H- -HO- ČH,OPO, ČH,OPO, D-Glucose 6-phosphate D-Fructose 6-phosphatearrow_forward
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