Introduction to General, Organic and Biochemistry
11th Edition
ISBN: 9781285869759
Author: Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher: Cengage Learning
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- When Fructose (shown below) undergoes reduction in the presence of H2 and Pd, two compounds are generated. What is the relationship between the two compounds generated? ОН Но— Н H. OH H OH HO.arrow_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_forward13. The following diagram shows two possible cyclic forms of glucose. H. OH OHOH но но HO- OH OH Structure A alpha-D-glucopyranose In the form on the left, the systematic name of glucose is alpha-D-glucopyranose. What is the systematic name of Structure A? H.arrow_forward
- Q9. Consider the equilibrium for the transesterification reaction. H₂SO4 triacylglycerol + 1-propanol fatty acid propyl ester + glycerol How do you think the amount of 1-propanol affects the amount of product present when the reaction reaches equilibrium? (I.e. What happens to the amount of product if you add more alcohol?) Briefly explain your answer.arrow_forwardIn an aqueous solution, d-glucose exists in equilibrium with two six-membered ring compounds. a.Draw the structures of these compounds. b. Which of the six-membered ring compounds will be the major product?arrow_forward25. Identify the sugars and the glycosidic linkage in the following molecule. HO HƠ OH HO O OH O HO- OH OHarrow_forward
- 1. Simple sugars are defined as polyhydroxy aldehydes/ketones. All carbons except one have an OH group. The remaining carbon has a double bond to oxygen, making it an aldehyde or ketone. For example, the Fisher projection of glucose looks like this: C H- H- -ОН НО -ОН -HO- CH2OH Because a simple sugar has both a carbonyl carbon and built-in nucleophiles, a reaction can occur within the molecule itself to create the hemi-acetal form of the sugar. Propose a mechanism for this reaction when it occurs in an aqueous solution. C -- CH2OH он в CH2OH HO- H H НО H. ОН Н and ОН Н HO- он Он а OH H H- ОН OH H ОН ČH2OHarrow_forwardIdentify the glycosidic bond indicated in the following structure. CH2OH H H. OH H O. но H. OH CH2 H. H H. QH H OH H. O B-1,4-glycosidic bond O a-1,6-glycosidic bond O a-1,4-glycosidic bond O B-1,6-glycosidic bondarrow_forward4. Draw the beta-furanose form of the following carbohydrate CHO H- HO -H 6. OH CH₂OH 5. Draw the alpha-pyranose of the following carbohydrate CHO -H H -OH H -OH HO HO H HO Draw the alpha-pyranose of the following carbohydrate CH₂OH H- CHO -H -OH H -ОН CH₂OHarrow_forward
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