help with these two questions **Provide the IUPAC name for the structure shown below.**(Note: rather than trying to enter Greek letters required in the name you can use "a" to represent α and "b" to represent β in your answer).**Diagram Explanation:**The structure shown is a cyclic sugar molecule in a Haworth projection, characterized by a six-membered ring. - The ring consists of five carbon atoms and one oxygen atom, forming a pyranose ring.- Each carbon in the ring is bonded to either a hydrogen (H) or a hydroxyl group (OH).- The first carbon (anomeric carbon) has a hydroxyl group attached above the plane of the ring.- The second carbon has a hydroxyl group also above the plane.- The third carbon's hydroxyl group is below the plane.- The fourth carbon has its hydrogen below the plane.- The fifth carbon, connected to a CH2OH group, is above the plane.The molecule represents a β-D-glucopyranose, a common form of glucose. **Provide the IUPAC name for the structure shown below.**(Note: rather than trying to enter Greek letters required in the name you can use a to represent α and b to represent β in your answer).### Diagram ExplanationThe diagram depicts a cyclic organic compound with the following features:- A five-membered ring structure with one oxygen atom integrated, also known as a furanose ring.- There are several hydroxyl (OH) groups attached to the ring: - One hydroxyl group is connected to the carbon next to the oxygen in the ring. - Another hydroxyl group is attached to a carbon opposite the oxygen.- The ring includes: - Two methanol (CH₂OH) groups attached to carbons.- The specific stereochemistry is indicated by the solid and dashed wedges for the hydrogen and hydroxyl group positions. The structure resembles a sugar, possibly a furanose form, given the configuration and presence of hydroxyl groups.

In sugar chemistry, these two isomers are named a different way: alpha and beta. To distinguish these two designations, we need to look at the Haworth projection. In a Haworth projection, the lower edge of the ring is read as being nearer and the upper edge is read as being farther away. However, in a Haworth projection, the hemiacetal carbon is always placed at the right edge of the drawing. In addition, we always keep the oxygen atom on the back edge of the ring (i.e. the upper edge of the drawing). That means the ring oxygen in a Haworth projection is always found in the upper or upper right part of the drawing, with the hemiacetal carbon directly beside it to the right.

Science

Chemistry

Provide the IUPAC name for the structure shown below. (Note: rather than trying to enter greek letters required in the name you can use a to represent a and b to represent B in your answer). H Он H OH OH CH2OH OH H. H.

Provide the IUPAC name for the structure shown below. (Note: rather than trying to enter greek letters required in the name you can use a to represent a and b to represent B in your answer). H Он H OH OH CH2OH OH H. H.

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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