(a)
Interpretation:
Fischer projection structure of the given molecule is to be drawn.
Concept introduction:
The two-dimensional projection of a three-dimensional organic molecule is nothing but Fischer projection. Fischer projections are generally drawn with the longest carbon chain vertical. The two groups attached to each carbon except the first and last are shown on horizontal bonds. The carbon atoms in the middle of the chain are represented by the intersections of vertical and horizontal lines. The vertical lines show bonds that aligned away from the observer, while the horizontal bonds are aligned towards the observer.
Interpretation:
(b)
Fischer projection of the given molecule is to be drawn.
Concept introduction:
The two-dimensional projection of a three-dimensional organic molecule is nothing but Fischer projection. Fischer projections are generally drawn with the longest carbon chain vertical. The two groups attached to each carbon except the first and last are shown on horizontal bonds. The carbon atoms in the middle of the chain are represented by the intersections of vertical and horizontal lines. The vertical lines show bonds that aligned away from the observer, while the horizontal bonds are aligned towards the observer.
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ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
- Label each Haworth projection as an α or β anomer and convert the Haworth projection to a sixmembered ring with wedges and dashed wedges.arrow_forwardPlease draw the expanded structure of D-tagatose and its Fischer Projection (chiral C represented as a cross).arrow_forwardDraw the two possible Haworth structures for each the following sugars in their cyclized form. Be sure to label each as an ? or a ? anomer.arrow_forward
- Please draw the expanded structure of D-altrose and its Fischer Projection (chiral C represented as a cross).arrow_forwardHi i wanna know what the Fischer projection for this one is. What i want to know is how do i know which oh is left and right ? Ik horizontal is towarda us and vertical is away but is there any trick that might help am confused thank uarrow_forwardmy question : Draw a three-dimensional line structure of the Fischer projection (a) using the template (c) fischer projection a is the monosaccharide but just in a different format which doesnt really matter. please just use template to show me the fischer projection of the monosaccharidearrow_forward
- Draw a Fischer projection of the monosaccharide from which each of thefollowing glycosides was prepared.arrow_forwardNeed help on B and C Stereogenic centers are supposed to have 4 different molecules connected to them?arrow_forwardA Fischer projection of a monosaccharide is shown below:arrow_forward
- a. Draw the Fischer projection of monosaccharide A below. Hint: Place the carbonyl group close to the top of the drawing. Name monosaccharide A. b. Use the given template to draw the most stable conformation of monosaccharide A.arrow_forwardPlace an asterisk (*) next to any chiral (stereogenic) carbon atoms in the following molecule:arrow_forwardConsider the following Fischer Projections:arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning