4) Take a look at these structures of monosaccharides (3 pts) *CHOH CHOH CH,OH OH CH,OH SH HOM HO OH OH H H OH OH H . H OH GLUCOSE HOH GALACTOSE OH FRUCTOSE What is the molecular formula for the the following monosaccharides? a. glucose: C b. fructose: C c. galactose: C 5) A. Show the anomeric carbon. (1 pts) B. Draw B-D-Fructopyranose (2 pts) Fructose Isomers 6) Identify monosaccharide (M), disaccharide (D) or Polysaccharide (P) (3 pts) a....
Help!!!! keloletrose aldotriose O ketotriose O aldopentose O ketopentose O aldotetrose CHO H-OH CH OH O aldotetrose O ketohexose O ketotetrose O ketopentose O aldopentose O aldohexose CH-OH OH 0 OH OH OH O aldohexose kelotetrose O ketohexose O ketopentose O aldotetrose O aldopentose fructose Previous Give Up & View s
8. Use the image to answer the questions that follow HO-CH HO-CH2 HO-CH2 CHO H₂o OH CHO CHO OCH CHOICH CH-OH CHCc CHOICH CH 10 | | CH-CH HỒ CH-CH CH-CH CH-CH CH-CH но он но HO он но OH OH HO A B C D Do not e How many carbons does each of the above sugars contain? Name to E n ipo Which sugars are aldoses and which are ketoses? Identify each sugar. Name the linkage for each...
CHO 1. NH2OH 2. Ac2o 3. CH,O CHO OH H- HO H HO H HCN H OH OH H- OH H- -OH H- CH2OH CH2OH The Wohl degradation is a series of reactions that shorten an aldose chain by one carbon, it is almost the exact opposite of the Kiliani In this reaction the aldose aldehyde carbonyl group is converted into a nitrile. The resulting cyanohydrin loses HCN under basic cone Conversion of the aldehyde to a nitrile is accomplished...
Br a. OCH CHO OH H o Br O o OH SH Using IUPAC rules, name the followng six organic compounds(just click on the link). You may wish to complete your work and a separate piece of paper, then scan/take a picture of your work and e-mail it to me. Sum2020T2Nom.pdf Minimize File Preview ZOOM + Br OCH,CH OH H H o BI
Part I (15pts). Carbohydrates CH2OH H-C-OH H-C OH HO-C-H HO H-C-OH H-C-OH CH2OH H-C-OH H-C-OH CH2OH CH2OH Simple sugars have a molecular formula of Cn(120)n, what is the molecular formula for each sugar above. What is the name of each compound above-write it under the compound. Circle each chiral carbon in the molecules above. In what ways are the structures of D-glucose and D-galactose the same?
CH3 H2SO4 н,с. OH сH, 2. OTs SH NaSH н, с сH, OTs No reaction H,с. Cн, o CH3 HBr Br HO H,с CH Provide the reagents necessary to carry out the following conversions. Br SH NadH NasH
draw fisher projections for both the D and L isomers of the following 12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O он HOH HOH но CH,OH CH,OH 3 Draw Fischer projections for both the D and L isomers of the following a. 2,3-dihydroxypropanoic acid b. 2-chloro-3-hydroxypropanoic acid Draw Fischer projections for both the D and L somers of the following amino acids:...
ta 2.0 L. O .O. HC-CC- 24 d. HC OH 1 2 CH,CHỊU. 2.H,0 c. CH CH 1. SOCH OH 2. LIAHOT-Bus CH,CHE 1. SOCI OH 2 CH CHO Php C ake h. CH CH, NaBH CH,CH, OH 1. AH,THE 2 HOHO I CHOCHEM 1. CH CH CH.CH 3. SO.
For each of the disaccharides or polysaccharides select from the response list the correct hydrolysis products. Responses may be used more than once or need not be used at all. a) glucose only b) glucose and galactose c) glucose and fructose d) glucose and ribose 35. Sucrose 36. Lactose 37. Cellulose 38. Starch 39. Glycogen For each of the disaccharides or polysaccharides select from the response list the correct characterization of the type of glycosidic linkages present in the compound....