Draw a planar structure for the following compound using dashed or solid wedges to show the...
(1R,2S,3R)-2-chloro-1-ethyl-3-methylcyclohexane
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Draw a planar structure for the following compound using dashed or solid wedges to show the...
Draw one planar structure each for the following compounds using dashed or solid wedges to show...
Draw one planar structure each for the following compounds using dashed or solid wedges to show the stereochemistry of the substituent groups. To be graded properly, include the hydrogen atoms on the chirality centers (asymmetric carbons). cis-1,3-dimethylcyclohexane trans-1,3-dimethylcyclohexane
Draw one planar structure each for the following compounds using dashed or solid wedges to show...
Draw one planar structure each for the following compounds using dashed or solid wedges to show the stereochemistry of the substituent groups. To be graded properly, include the hydrogen atoms on the chi centers (asymmetric carbons) cis-1,3-dimethylcyclohexane trans-1,3-dimethylcyclohexane
A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the planar...
A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the corresponding planar (overhead) representation, using wedges and hashed bonds to indicate the substituent positions. To be graded properly, include the hydrogen atoms on the chirality centers (asymmetric carbons). Be sure that both wedges/hashed bonds are drawn on the outside of the ring, or else the stereochemistry may be interpreted as square planar.
5. (a) Draw the structure of (1 S,2S,5R)-5-ethyl-2-isobutylcyclohexanol. Use solid and dashed wedges to show the...
5. (a) Draw the structure of (1 S,2S,5R)-5-ethyl-2-isobutylcyclohexanol. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) io noto gos owenA.msxo bnoooe orlt lo veb odt no oub al toomngla batgoo ( 0)emmyalo onelo a of bup (b) Draw both chair conformations for this structure. (0.4 pts) (c) Draw a box around the most stable chair conformation. (0.2 pts)
6. (a) Draw the structure of (18,25,5R)-5-ethyl-2-isobutylcyclohexanol. Use solid and dashed wedges to show the proper...
6. (a) Draw the structure of (18,25,5R)-5-ethyl-2-isobutylcyclohexanol. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) (b) Draw both chair conformations for this structure. (0.4 pts) OG (c) Draw a box around the most stable chair conformation. (0.2 pts)
8. (a) Draw the structure of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane. Use solid and dashed wedges to show the...
8. (a) Draw the structure of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) (b) Now draw a Newman projection for the most stable conformation of the C(4)-C(5) bond. (0.4 pts) H (c) Draw a diastereomer of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane (0.2 pts)
Draw the structure of 2R 3R)-2,3-dichloropentane. Use bold or hashed wedges to indicate the configuration at...
Draw the structure of 2R 3R)-2,3-dichloropentane. Use bold or hashed wedges to indicate the configuration at asymmetric C atoms. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas. 2 . H: 1200 mAh 31.+07 Marvin JS ChemAxon LADDODOOD
consider the molecule with two chiral centers. draw all remaining possible stereoisomers using solid and dashed...
consider the molecule with two chiral centers. draw all remaining
possible stereoisomers using solid and dashed wedges
label each chiral center as R or S
5. Consider the molecule 1-chloro-3-tertbutylcyclohexane with two chiral centers: a. Using COMPOUND A (below) as a starting molecule, draw all remaining possible stereoisomers using solid and dashed wedges (no chairs). Compound B Compound A Compound C Compound D 6. On BOTH COMPOUND A and COMPOUND D (above), clearly label each chiral center as either R...
(a) Draw the structure of (4R,5R)-4-ethyl-5-luoro-2-methytheptane. Use solid and dashed wedges to show the proper configurations...
(a) Draw the structure of (4R,5R)-4-ethyl-5-luoro-2-methytheptane. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) . (b) Now draw a Newman projection for the most stable conformation of the C(4)-C(5) bond. (0.4 pts) (c) Draw a diastereomer of (4R,5R)-4-ethyl-5-fluoro-2-methylheptane (0.2 pts) The specific rotation [a] of pure quinine is-165. A solution containing 9. both quinine and its enantiomer has a specific rotation of -63 Calculate the percentage of quinine present in the mixture?...
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to...
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to show R and S. (2S, 4S, 6S)-2-bromo-4, 6-diethyloctane (1R, 3R, 5S)-1-bromo-3-chloro-5-isobutylcycloheptane
Draw one planar structure each for the following compounds using dashed or solid wedges to show the stereochemistry of the substituent groups. To be graded properly, include the hydrogen atoms on the chirality centers (asymmetric carbons). cis-1,3-dimethylcyclohexane trans-1,3-dimethylcyclohexane
Draw one planar structure each for the following compounds using dashed or solid wedges to show the stereochemistry of the substituent groups. To be graded properly, include the hydrogen atoms on the chi centers (asymmetric carbons) cis-1,3-dimethylcyclohexane trans-1,3-dimethylcyclohexane
5. (a) Draw the structure of (1 S,2S,5R)-5-ethyl-2-isobutylcyclohexanol. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) io noto gos owenA.msxo bnoooe orlt lo veb odt no oub al toomngla batgoo ( 0)emmyalo onelo a of bup (b) Draw both chair conformations for this structure. (0.4 pts) (c) Draw a box around the most stable chair conformation. (0.2 pts)
6. (a) Draw the structure of (18,25,5R)-5-ethyl-2-isobutylcyclohexanol. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) (b) Draw both chair conformations for this structure. (0.4 pts) OG (c) Draw a box around the most stable chair conformation. (0.2 pts)
8. (a) Draw the structure of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) (b) Now draw a Newman projection for the most stable conformation of the C(4)-C(5) bond. (0.4 pts) H (c) Draw a diastereomer of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane (0.2 pts)
Draw the structure of 2R 3R)-2,3-dichloropentane. Use bold or hashed wedges to indicate the configuration at asymmetric C atoms. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas. 2 . H: 1200 mAh 31.+07 Marvin JS ChemAxon LADDODOOD
consider the molecule with two chiral centers. draw all remaining
possible stereoisomers using solid and dashed wedges
label each chiral center as R or S
5. Consider the molecule 1-chloro-3-tertbutylcyclohexane with two chiral centers: a. Using COMPOUND A (below) as a starting molecule, draw all remaining possible stereoisomers using solid and dashed wedges (no chairs). Compound B Compound A Compound C Compound D 6. On BOTH COMPOUND A and COMPOUND D (above), clearly label each chiral center as either R...
(a) Draw the structure of (4R,5R)-4-ethyl-5-luoro-2-methytheptane. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) . (b) Now draw a Newman projection for the most stable conformation of the C(4)-C(5) bond. (0.4 pts) (c) Draw a diastereomer of (4R,5R)-4-ethyl-5-fluoro-2-methylheptane (0.2 pts) The specific rotation [a] of pure quinine is-165. A solution containing 9. both quinine and its enantiomer has a specific rotation of -63 Calculate the percentage of quinine present in the mixture?...
Provide the structure for the following compounds given the IUPAC names. Use dashes and wedges to show R and S. (2S, 4S, 6S)-2-bromo-4, 6-diethyloctane (1R, 3R, 5S)-1-bromo-3-chloro-5-isobutylcycloheptane
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