Homework Help is Here – Start Your Trial Now!
Science
Chemistry
(i) Draw the cyclic beta form of structure II. (i) Draw the cyclic alpha form of structure II.

(i) Draw the cyclic beta form of structure II. (i) Draw the cyclic alpha form of structure II.

Organic Chemistry
Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter25: Biomolecules: Carbohydrates
Section25.6: Reactions Of Monosaccharides
Problem 17P
See similar textbooks
icon
Related questions
Question
Refer to the structures in the box to answer the questions
(i) Draw the cyclic beta form of structure II. (j) Draw the cyclic alpha form of structure II. (k) Draw the aldonic acid that results when structure VI is treated with Br2 and H₂O. (1) Draw the aldaric acid that results when structure VI is treated with HNO3. (m) Is the aldaric acid from the preceding question optically active? Explain. (n) Draw structural formula for one of the monosaccharides that results when Structure Vis treated successively with NaBH4 and H₂O.
Transcribed Image Text:(i) Draw the cyclic beta form of structure II. (j) Draw the cyclic alpha form of structure II. (k) Draw the aldonic acid that results when structure VI is treated with Br2 and H₂O. (1) Draw the aldaric acid that results when structure VI is treated with HNO3. (m) Is the aldaric acid from the preceding question optically active? Explain. (n) Draw structural formula for one of the monosaccharides that results when Structure Vis treated successively with NaBH4 and H₂O.
Box 1 OH H CH₂OH OH О I OH OCH3 CHO H -OH H-OH НО H H OH CH₂OH II H CHO OH но- HO-H HO-H H-OH НО CH₂OH III (a) What is the relative configuration of Structure I? (b) What is the relative configuration of Structure III? (d) Identify one nonreducing sugar from the list. но-+ (e) Identify one reducing sugar from the list. (f) Identify a pair of epimers from the list. CH₂OH H H-OH H-OH (g) Identify a pair of enantiomers from the list. (c) Which monosaccharide is an optically inactive meso compound? -H CH2OH IV CH₂OH =0 H OH НО- но-т H но- -Н CH₂OH V (h) Draw the enol that is produced when structure V is dissolved in water. HO Н H Н- НО CHO -H OH OH H CH2OH VI
Transcribed Image Text:Box 1 OH H CH₂OH OH О I OH OCH3 CHO H -OH H-OH НО H H OH CH₂OH II H CHO OH но- HO-H HO-H H-OH НО CH₂OH III (a) What is the relative configuration of Structure I? (b) What is the relative configuration of Structure III? (d) Identify one nonreducing sugar from the list. но-+ (e) Identify one reducing sugar from the list. (f) Identify a pair of epimers from the list. CH₂OH H H-OH H-OH (g) Identify a pair of enantiomers from the list. (c) Which monosaccharide is an optically inactive meso compound? -H CH2OH IV CH₂OH =0 H OH НО- но-т H но- -Н CH₂OH V (h) Draw the enol that is produced when structure V is dissolved in water. HO Н H Н- НО CHO -H OH OH H CH2OH VI
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 2 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Discovery of Radioactivity
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning
SEE MORE TEXTBOOKS