There are following rules to assign the R and configuration and draw the structure.
1)
When priority order is clockwise and the lowest priority group is behind the plane then we call it as R configuration.
And
When priority order is anticlockwise and the lowest priority group is behind the plane then we call it as S configuration.
2)
When priority order is clockwise and the lowest priority group is not behind the plane then we call it as S configuration.
When priority order is anticlockwise and the lowest priority group is not behind the plane then we call it as R configuration.
We use these rules to predict the structure.

Redraw (4S, 5R)-4-ethyl-5-propylnonane using wedges and dashes to show the correct stereochemistry
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)
(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?...
Draw the structure for the following compound using wedges and dashes. trans−1−ethyl−2−methylcyclopentane
Draw the structure of each of the following compounds. Using wedges and dashes, indicate the stereochemistry. (R)-2-Ethoxy-1, 1-dimethylcyclobutane Cyclopropyl isopropyl ether
please write out answers, thank you.
Stereochemistry 5. Using dashes and wedges, Draw all the structures for the following molecules. F₃C нсусн, Он (Indicate the steochemistry) b. 6. a. Circle the stereochemistry in the following compound. Он о HO ТОН 0 OH b. What is maximum number of stereoisomers in the above compounds. Label each as diastereomer and enantiomer) c. Label each stereochemistry with Ror S configuration?
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)
4. Convert the following structures to bond-line notation, using wedges and dashes to convey the correct absolute configuration (i.e. R or S). Et OH CH3 OH CH3 Me
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
Please find A,B,C and D, as well as indicate stereochemistry
using wedges and dashes.
Question 6 The following sequence of reactions was employed during synthetic studies on reidispongiolide A, a cytotoxic marine natural product (7 Ph 1) CHCHMgBr 1) NaH B 2) CH cat Oso A C+ D Ph 2) H O Ph NMO
Chem 266 Kritik Assignment 11 Where it states stereochemistry, dashes and wedges must be used to show stereochemistry. Note: for some reaction enantiomers are formed. 15 Marks. One mark for each correct product. Must show stereochemistry and all products for full mark. LIAIHA P 1. CHCCNA 2. Ho a 1. (CH),CHMgr 2. H,0" 1.0, 2. H,02 R and two product v any order 1. CHỊCH MgBr 2. HO" H2SO4 1.0, 2. (CH), т w and two product any order х...