If the following monosaccharide underwent cyclization to form a furanose, which of the following is one of the possible structures that would be seen? Н HO CH₂OH Н ОН CH₂OH :0 A -OH -Н OH CH₂OH ОН ОН CH₂OH CH₂OH ОН -0. В ОН ОН CH₂OH OH CH₂OH OH с ОН OH ОН CH₂OH OH D OH ОН
If the following monosaccharide underwent cyclization to form a furanose, which of the following is one of the possible structures that would be seen? Н HO CH₂OH Н ОН CH₂OH :0 A -OH -Н OH CH₂OH ОН ОН CH₂OH CH₂OH ОН -0. В ОН ОН CH₂OH OH CH₂OH OH с ОН OH ОН CH₂OH OH D OH ОН
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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
Transcribed Image Text:**Question:**
If the following monosaccharide underwent cyclization to form a furanose, which of the following is one of the possible structures that would be seen?
**Image Description:**
Above the options is a linear monosaccharide structure:
1. **Linear Structure:**
- Vertical structure with five carbon atoms.
- Contains hydroxyl (OH) groups attached to the second, third, and fourth carbon, a hydrogen atom attached to the first and fifth carbon, and a carbonyl group (C=O) attached to the first carbon.
- A CH₂OH group is attached at both ends, to the first and the fifth carbon.
Below this structure are four cyclized structures labeled A, B, C, and D.
2. **Cyclized Structures:**
- **Option A:**
- Five-membered ring (furanose) with an oxygen atom in the ring.
- Hydroxyl groups are attached to the second, third, fourth, and fifth carbon.
- CH₂OH group is above the ring on the fifth carbon.
- **Option B:**
- Five-membered ring (furanose) with an oxygen in the ring.
- Hydroxyl groups are attached to the first, second, and third carbon.
- CH₂OH group is above the ring on the first carbon.
- **Option C:**
- Six-membered ring with an oxygen atom in the ring.
- Hydroxyl groups are attached to the second, third, fourth, and fifth carbon.
- CH₂OH group is above the ring on the fifth carbon.
- **Option D:**
- Six-membered ring with an oxygen atom in the ring.
- Hydroxyl groups are attached to the first, second, third, and fourth carbon.
- CH₂OH group is above the ring on the first carbon.
**Options:**
- A
- B
- C
- D
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