Drawings Instructor's approval of models L-glyceraldehyde Fischer: L-glyceraldehyde Fischer: D-glyceraldehyde H C Hico OH-c-H D-glyceraldehyde H-6-oh...
Catch Report Sheer - Lab 16 Date Neotion Instructor A. Al Monosaceharides Fischer projections L-glyceraldehyde D-glyceraldehyde How does L-glyceraldehyde differ from D-glyceraldehyde? A.2 Fischer projection of D-glucose Haworth (cyclic) formulas a-D-glucose B-D-glucose Haworth (cyclic) formula for a-D-fructose A.3 Fischer projection of D-fructose
The corresponding structure is: Glyceraldehyde is an aldose monosaccharide. The Fischer projection of D-glyceraldehyde is shown. HO o OH OH HCOH Hпин-Синон HOH CH2OH D-glyceraldehyde H2-OH HCOH O OLHO OH Translate the Fischer projection to show D-glyceraldehyde with wedge and dash bonds. Hi.... C OH HC-OH H₂Ē -oh HO-OH 8 9 RUOP
125 D. Structure and models of amides Compound Condensed structural formula Instructor's approval for models acetic acid ammonia acetamide Write the balanced equation for the reaction of acetic acid and ammonia to form acetamide.
QUESTION 9 In the Fischer projection of Glyceraldehyde shown below, CHO - H-C-OH - CH2OH The molecule is in the D-form The molecule in the L-form The-CHO group is facing forward The H group is facing backward, QUESTION 10 In O-linked and N-linked transmembrane glycoproteins, The side chains of amino acids present on the outside of the membrane are glycosylated The back-bone-NH and Co groups of amino acids present on the inside of the membrane are glycosylated. The side chains...
n 6. The glucose molecules in cellulose are linked together by what type of glycosidic bond (or linkage)? 1. Convert the following D-sugars (shown their chair conformations) into their Haworth formulations & Fischer projections. Н % ОН НО CH2OH но. ОН НО ОН Н Н — НО НО H Haworth МАСА Fischer Н Н HO CH2OH Lo -ОН Н -OH НО НО — H НО он Н Haworth CHCH Fischer
Determine whether each of the following structures is D-glyceraldehyde or L-glyceraldehyde, assuming that the horizontal bonds point toward you and the vertical bonds point away from you. Drag the appropriate structures to their respective bins. Reset Help H H O CHOH С HO -CH2OH -H HOCHZ + oH H O H H O L-glyceraldehyde pglyceraldehyde
The configuration of R-(+)-glyceraldehyde is as follows: o II C-H H-I-OH CH2OH What is the configuration of (-)-lactic acid? COH H-OH CH2OH O R configuration O S configuration d and/configuration O Rand S configuration O configuration
organic chem
11. (a) (6 points) D-tagatose is shown below. Draw the Haworth projection for B-D-tagatopyranose. CH2OH EO HO НО. -OH CH2OH D-tagatose (b) (4 points) Draw Fischer projection for L-tagatose. CH2OH EO HO НО. -OH CH2OH D-tagatose
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?
A D-Glucose B. D-Fructose C. L-Glyceraldehyde 5. What is an epimer? In the following structures indicate the two structures and the specific carbon atoms that are making them epimers. (4 marks) H =0 Н. 1 11 CON HO CHI H. 2 HOCH HC=ON HOSCH 3 H-C-OH CHOH CULOH CHOH