Concept explainers
(a)
Interpretation : The given names needs to be matched with the given structures.
Concept Introduction : Based on number of carbon atoms and
(b)
Interpretation : The given names needs to be matched with the given structures.
Concept Introduction : Based on number of carbon atoms and functional group, monosaccharides can be classified as aldo and keto sugar. Similarly, based on number of carbon atoms monosaccharides can be classify as tetrose, pentose, and hexose sugar.
(c)
Interpretation : The given names needs to be matched with the given structures.
Concept Introduction : Based on number of carbon atoms and functional group, monosaccharides can be classified as aldo and keto sugar. Similarly, based on number of carbon atoms monosaccharides can be classify as tetrose, pentose, and hexose sugar.
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Basic Chemistry
- What type of bond holds these two monosaccharides together in this structure? HO- H. -O H H. OH A H HO 3. 12 HO. HB HO 3 1 HO OH ) B(1,4) glycosidic bond 2 a (1,4) glycosidic bond 3 aB (1.4) glycosidic bond 4) a (1,6) glycosidic bond INarrow_forward(19, 9) Draw a structural formula for the major organic product of the reactions shown below. You do not have to consider stereochemistry.arrow_forward15.6 Stearic acid and linoleic acid each have 18 carbon atoms. Why does stearic acid melt at 69 °C but linoleic acid melts at -5 °C? 15.7 Draw the line-angle formula for each of the following fatty acids: a. palmitic acid b. oleic acid 15.8 Draw the line-angle formula for each of the following fatty acids: a. stearic acid b. linoleic acidarrow_forward
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- 13.42 For each of the following, give the monosaccharide units produced by hydrolysis, the type of glycosidic bond, and the name of the disaccharide including a or B: a. CH2OH CH₂OH Н HO Н ОН Н Н ОН Н ____Н Н ОН Н Н ОН ОН Нarrow_forward4. 5. 6. 3. 1. What is Monosaccharaide? 2. Н - OH HO-H HO Н Н Н, Н HO-H Н -ОН -ОН CH₂OH H + OH H-OH ОН CH₂OH онтн D-glucose CHO H+OH H+ OH H-OH CH2OH OH CH₂OH -D-glucose OH (H-C-OH)4 CH₂OH Carbohydrates +Cu2+ -Cu20 [0]HNO3 ОН H₂ / Ni, LiAlH4 2Cu(OH)2 +CH OH, [HCI] gas A glucocidic bond formation +fructose V-2arrow_forwardWhich functional group on furosemide's structure below is most likely to be negatively charged at physiological pH (7.4)? CI HN- NH2 ОНarrow_forward
- Illustrate with equation,indicating how the following substrate or reactant would be converted to their final products. A.cyclopentane and tert-butoxypentene B.7-oxabicyclo(4.1.0)heptane C.oxirane and 1,2 diphenoxyethanearrow_forward(19, 5) Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol or enone below. You do not have to consider stereochemistry. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. FOR E/Z stoichiometry one: Consider E/Z stereochemistry of alkenes. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.arrow_forwardWhich functional group on furosemide’s structure below is most likely to be negatively charged at physiological pH (7.4)?arrow_forward
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