Which is the correct name for the structure below?CH;OHНОOHFuttonationsriveO a-D-arabinofuranoseebookO a-D-arabinopyranoseTeamsO B-D-arabinofuranoseOB-D-arabinopyranose

The answer is Alpha D arabinofuranose is a dextrorotated arabinofuranose with an alpha…

Answered: Which is the correct name for the…

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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Aldose monosaccharides can be oxidized when treated with a mild oxidizing agent. In this reaction, the aldehyde group of the open-chain aldose is oxidized to a carboxylic acid group. In basic solution, ketose monosaccharides can also be oxidized, forming carboxylic acids because they can undergo a rearrangement to an aldose form. Monosaccharides (cyclic hemiacetals) can also react with an alcohol to form acetals, called glycosides, and water. In this reaction, the OH of the anomeric carbon is replaced by the OR group of the alcohol. D-ribose (Figure 1) is treated with a mild oxidizing agent. Edit the structure for D-ribose to show the product of this reaction. M Edit the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Include all hydrogen atoms. ► View Available Hint(s) [1] A H 12D H H H H 7 L EXP. CONT.i L 1 -O-H O H ew -O-H enodic Table -O-H H C N O S CI Br I P F
Name the nitrogenous bases that are bonded
The following hexoses are....
12.
What is this lipid? What test wll identify this?
Which of the following represents a pair of epimers? A с OH OH -OH OH НО-С-Н НО-С-Н OH O C-H OH O C-H H-C-OH НО-С-Н H-C-OH H-C-OH H-C-OH НО-С-Н H-C-OH НО-С-н CH.OH CH.OH В н 0 Н- C-OH H-C-OH H-C-OH H-C-OH CH, OH D Н 20 НО -H но- -Н FO H+H H-C=O но-с-н H-C-OH CH,OH Н-С=0 но он H-C=0 HO-OH O= н-н H-C=O
1- Please refer to the Fisher representation of the 5 monosaccharides below: ÇH2OH CHO CHO CHO CHO H- H- он H- OH OH HO HO но- H- OH HO Но- H- -OH H- H- -OH HO- OH HO H- -OH H- -OH HO HO H- OH ČH2OH ČH2CH ČH2CH ČH2CH ČH2CH D-Fructose D-Glucose L-Glucose L-Idose D-Galactose 1a- Which one(s) of the above molecules belong(s) to the subcategory of aldohexoses? and which one(s) of these molecules belong(s) to the subcategory of ketohexoses? Briefly explain your response. 1b- Which one of the above molecules is an enantiomer of D-Glucose? and which one is an epimer of L-Ildose? Briefly explain your response.
Is this saponifiable or not what is this lipid
why does A2-B3 structure is active (contain the antibiotic) and the (A2- B2,A1-B1,A1-B2,A1-B3,A3-B1,A3-B2,A3- B3) are nonactive help please! atorial proce below. A1 A2 A3 N=0 H 2-nitrobenzaldehyde 5-nitro-2-furaldehyde 3-nitrobenzaldehyde B1 B2 NH₂ HN. 4-bromophenylhydrazine hydrochloride B3 NH₂ Br HN. 4-cyanophenylhydrazine hydrochloride NH₂ HN CẠNH NH₂ aminoguanidine bicarbonate
From the image indicate which ones are pentoses:
Below is Gulose in the open chain form: CHO H C-OH H C-OH HO C-H H- OH CH2OH Which of the following shows B-D-Gulose? A) B) CH2OH CH2OH OH ОН OH OH H H. OH OH H OH C) D) E) CH2OH H OH OH OH OH H CH2OH ČH2OH H H H. H. OH H. H. OH OH ÓH ОН H. -T -T I-
Convert the Fischer projection to the Haworth projection of the a-furanose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. CH₂OH -H Cyclization -OH -OH CH₂OH Answer Bank CH₂OH HO- -H H- OH

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Which is the correct name for the structure below? CH,OH HỌ OH on OH O a-D-arabinofuranose ok O a-D-arabinopyranose ms O B-D-arabinofuranose OB-D-arabinopyranose