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
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**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
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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