Draw the step-by-step procedure of linear form (Fischer Projection) of a- D Glucose andB- D Glucose to Haworth. Paste the picture of your drawing below this imageanomeric carbonH-č-OHHO-C-HH-C-OHH-C-OHanomersofglucoseHO-C-Hно-с—нH-C-OHH-Ċ-OHH-C-0-H-C-0-CH,OHCH,OHa-D-glucoseB-D-glucose

The Fischer projection is a two-dimensional representation of a three-dimensional organic molecule.…

Answered: Draw the step-by-step procedure of…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Draw the step-by-step procedure of linear form (Fischer Projection) of a- D Glucose and B- D Glucose to Haworth. anomeric carbon H-C-OH HO-C-H H-C-OH H-Č-OH anomers of glucose HO-C-H но-с—н H Č-OH H-C-OH H-ċ-o H-C-0- CH,OH ČH,OH a-D-glucose В-D-glucose
What is the complete name of the following sugar? но он носн он Write out the words alpha and beta. This question is case-sensitive. Capitalize only the configuration designation, D or L, example: beta-D-glucopyranose.
Following are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers. CHO сно H-C- OH H-C-OH H-C- OH но-с — н н-с—он но- ČHOH ČH,OH сно CHO Н-с—он но—с— н H-C- OH H-C-OH но—с—н Н-с—он ČHOH ČH,OH сно сно н-с—он но—с —н но—с— н но -с — н H-C- OH но- C-H ČH,OH ČH,OH
Write the name for the trisaccharide depicted below (for example, of the form a - D - xylofuranose). Be sure to include if the sugars are in the pyranose or furanose conformations in the name and include the linkages between sugars (for example, (2 - - > 4)). CH₂OH ОН OH н ОН -CH₂ H\H ОН н н ОН CH2OH н ОН но н н ОН
In the space provided, draw a Haworth projection for the beta anomer of the following monosaccharide Fischer projection. CHO HO-C-H HO-C-H HO-C-H H-C-OH CH,OH
Following are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers and the pairs that are epimers СНО СНО СНО H-C-OH H-C-OH H-C-OH H-C-OH Но-С—н H-C-OH H-C-OH Но-ҫ—н Но—с—н CHOH CHĻOH ČH,OH СНО СНО СНО Но —С— н H-C-OH HO-C-H Н—С—он Но -С—н HO-C-H H-c-OH H-C-OH HO-C-H CH̟OH ČHĻOH ČHĻOH Pairs of Enantiomers Pairs of Epimers
Draw the Fischer projection formula for each sugar and give the importance/use of each. D- deoxyribose D- glucose D- galactose D- fructose D- ribulose
Catch the KILLER DNA message #1: GTA-CGA-TGT-ATT-ACT-ATC-ATT Transcription to mRNA: CAU GCU ACA UAA UGA UAG UAA Translation of codons to Amino Acids: What is the Clue?
Complete the following table by providing the Fischer and Haworth Projections of the given sugars. (Please be careful with the alpha and beta, and the complete and abbreviated) (not a graded question) Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer L-Galactose L-Fructose
Raffinose (see prev. question for structure) is not digestible by humans yet is found in foods we eat all the time like beans, cabbage, brussels sprouts etc. What 2 human digestible compounds can Raffinose be broken down into? Just as a side note, Raff is NOT digestible by us, but our helpful gut bacteria break it down for us into the 2 compounds that are the answer to this question. O a-D-glucose O B-D-fructose sucrose a-D-galactose Lactose maltose
Draw the Gentiobiose: 2 Glucose, beta-(1,6)
Which of the following is an anomer of B-D-gulopyranose? O O го ОН H ОН H ОН H H ОН CH₂OH -II- H H ОН ОН CH2OH H ОН ОН CH2OH О 0. H CH2OH то Н H H ОН H H - о H ОН ОН H ОН H ОН ОН H О ОН ОН H N

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