Identify the Haworth structure showing the ẞ-isomer of the following Fischer projection.H(Hint: Draw it using the 3-step method provided in your textbook to figure out.)ΟCH.OHHO OHHOHOHHOHHHCH.OHHO OHHOHHHOHHOHCH,OHHHOHHHOOHHOHCH.OHHHOHOHHOOH0HO HHO1HOHHOHCH₂OH

Beta form -OH group is above the plane, here there are two form in which OH is above the palne . A…

Answered: Identify the Haworth structure showing…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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2. Provide a general name for the sugars and say whether they are D or L sugars. Draw the mirror image of each isomer. Fischer projection CH₂OH C=O HO -H H- OH H- -ОН CH₂OH Classification: Other isomer Fischer projection CHO HOH H- -OH H-OH HOH CH₂OH Classification: Classification: Other isomer Classification:
Check the box under each ketose. If there are none, check the None of the above box under the table. H Н I НО н ОН ОН н ОН CH2OH НО H None of the above. CH₂OH Н -ОН CH₂OH H Но H Н ОН ОН ОН CH2OH Н. НО I НО Н -Н I ОН Т ОН CH2OH НО H Н CH₂OH C=0 н -ОН ОН CH₂OH
Which Fischer projection corresponds to D-glucose? CHO CHO H- -OH но- -H HO H. H- H- -ОН Но H- -ОН но- ČH2OH ČH2OH CH2OH CHO но Но Но H- HO- H- HO- H- -ОН H- OH ČH2OH ČH2OH
ОН 2. the Fischer projection that corresponds to the monosaccharide shown in the box. О н HO OH но- OH НО 0 OH OH OH H-OH -ОН 3. the Haworth projection that corresponds to the structure shown in the box. OCH, НО OH athul algasida О Н H-OH H-OH но-н но- HO -O OCH, OH O H H-OH НО-Н H-OH H-OH OH ОН НО НО OOCH, HO H-OH но-н но-н OH H-OH OH НО OH OCH, OH OH О н H-OH H-OH H НО но-н ОН НО -oOCH, ОН он он
Translate the wedge-and-hashed structure to its Fischer projection. OH OH H. OH Select the Fischer projection that matches the structure. CHO CHO Но- H- -HO- H- HO- HO но H- HO ČH2OH CH,OH CH,OH CHO CHO но- H- HO. HO Но HO- CH2OH CH2OH
4. Classify each pair of compounds as either enantiomers, diastereomers, identical, constitutional isomers, or not isomers. x HO OH NH OH H. H HN HO Me H HO n-Pr Me -OH
Group 3: Convert this Haworth projection to its Fischer projection: CH,OH он CH2OH он он Group 4: Convert this Fischer projection to its Haworth projection: сно H- OH но H- но -H- CH;OH
What is the reduction of D-erythrose? OH H. CH2OH Select the correct answer below: CH,OH OH H. OH H- OH CH2OH
The image shows Fischer projections for the structures of four isomers of a ketopentose. CH₂OH CH₂OH CH₂OH ПА пс C=O D HOEC H HOECH CH,OH A C=O H➡ COH но-с-н CH₂OH Which of the structures are stereoisomers of B? B Which of the structures are diastereomers of D? C=O HOI-C-H HOI-C-H CH₂OH с 000 ΤΑ B HO D CH₂OH O Which of the structures are enantiomers of C? H HI COH D CH₂OH
4. Circle and label hemiacetal and acetal in each of the following molecules. OH CH OH ОН CH₂OH OH OH Lactose 0. OH OH ОН CH OH OH 0. OH OH О CH₂OH Sucrose CH2OH OH
Draw Haworth projection formulas for the a-anomer of monosaccharides with each of the following Fischer projection formulas. a. CHO HOH H- HO- H -ОН -Η OH CH₂OH b. CHO H -OH H -ОН HO H CH₂OH
Which of the following sugars is the enantiomer of structure A? H- -HO- но- H- Но- ČH2OH A Н. H. H. H. H- OH но- -H H- ОН но- H. но- H ОН H- HO- H- но -H но- H- H- - HO- H- ОН H- OH H- ОН CH2OH ČH2OH CH2OH ČH2OH 1 2 3 4 Select one: а. 4 b. 2 С. None of the above d. 1 е. 3 I I エエ

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