Concept explainers
Convert each ball-and-stick model to a Fischer projection.
a. b.
(a)
Interpretation: The given ball-and-stick model is to be converted into Fischer projection.
Concept introduction: In Fischer projection formula, the horizontal and vertical line represents the bonds that are present above and below the plane, respectively. The verticals bonds are represented as dashed wedge and horizontal bonds as dark wedge.
Answer to Problem 36P
The Fischer projection of given ball and stick model is shown below.
Figure 1
Explanation of Solution
The ball and stick model of given compound is,
Figure 2
Black colored atoms have four bonds. So, these are the carbon atoms. The grey colored balls have one bond. So, these are the hydrogen atoms. The red colored atoms have two bonds. So, these are oxygen atoms. The molecular structure of given compound is,
Figure 3
The conversion of given compound into Fisher projection is as follows:
The structure
Figure 4
Rotate all the bonds around the carbon atom in such way that all staggered form converted into the eclipsed form in structure
Figure 5
The structure
Figure 6
The Fischer projection of given ball and stick model is shown in Figure 1.
(b)
Interpretation: The products of given reaction are to be drawn.
Concept introduction: In Fischer projection formula, the horizontal and vertical line represents the bonds that are present above and below the plane, respectively. The verticals bonds are represented as dashed wedge and horizontal bonds as dark wedge.
Answer to Problem 36P
The Fischer projection of given ball and stick model is shown below.
Figure 7
Explanation of Solution
The ball and stick model of given compound is,
Figure 8
Black colored atoms have four bonds. So, these are the carbon atoms. The grey colored balls have one bond. So, these are the hydrogen atoms. The red colored atoms have two bonds. So, these are oxygen atoms. The molecular structure of given compound is,
Figure 9
The conversion of given compound into Fisher projection is follow:
The structure
Figure 10
Rotate all the bonds around the carbon atom in such way that all staggered form converts into the eclipsed form in structure
Figure 11
The structure
Figure 12
The Fischer projection of given ball and stick model is shown in Figure 7.
Want to see more full solutions like this?
Chapter 26 Solutions
ORGANIC CHEMISTRY
- Be sure to answer all parts. The Fischer projection of D-glucose is shown below. Draw its mirror image as a Fischer projection. CHO OH HO H. draw structure... H. OH H. OH CH,OHarrow_forwardDraw the eight constitutional isomers having the molecular formula C5H11Cl.a. Give the IUPAC name for each compound (ignoring R and S designations).b. Classify each alkyl halide as 1°, 2°, or 3°.c. Label any stereogenic centers.d. For each constitutional isomer that contains a stereogenic center, draw all possible stereoisomers, and label each stereogenic center as R or S.arrow_forwardDraw the eight constitutional isomers having the molecular formula C5H11Cl. a.Give the IUPAC name for each compound (ignoring R and S designations). b.Classify each alkyl halide as 1°, 2°, or 3°. c.Label any stereogenic centers. d.For each constitutional isomer that contains a stereogenic center, draw all possible stereoisomers, and label each stereogenic center as R or S.arrow_forward
- Label each stereogenic center as R or S.arrow_forwardConvert each compound to a Fischer projection formula.arrow_forwardAnswer each question using the ball-and-stick model of compound A. a. Give the IUPAC name for A, including R,S designations for stereogenic centers. b. Classify A as a 1°, 2°, or 3° alcohol. c. Draw a stereoisomer for A and give its IUPAC name. d. Draw a constitutional isomer that contains an OH group and give its IUPAC name. e. Draw a constitutional isomer that contains an ether and give its IUPAC name. f. Draw the products formed (including stereochemistry) when A is treated with each reagent: [1] NaH; [2] H2SO4; [3] POCI,, pyridine; [4] HCl; [5] SOCI, pyridine; [6] TSCI, pyridine. Aarrow_forward
- Answer each question using the ball-and-stick model of compound A.a.Give the IUPAC name for A, including R,S designations for stereogenic centers. b.Classify A as a 1°, 2°, or 3° alcohol. c.Draw a stereoisomer for A and give its IUPAC name. d.Draw a constitutional isomer that contains an OH group and give its IUPAC name. e.Draw a constitutional isomer that contains an ether and give its IUPAC name. f.Draw the products formed (including stereochemistry) when A is treated with each reagent: [1] NaH; [2] H2SO4; [3] POCl3, pyridine; [4] HCl; [5] SOCl2, pyridine; [6] TsCl, pyridinearrow_forwardConsider the ball-and-stick model of A, and label B and C as either identical to A or an enantiomer of A.arrow_forwardLocate the stereogenic centers in each compound. A molecule may have one or more stereogenic centers. Gabapentin enacarbil [part (d)] is used to treat seizures and certain types of chronic pain.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning