thank you for your help! Draw two related structures in dash/wedge notation of the following for...
12.36 Draw Fischer projections for each of the following dash-wedge structures: a. CHO b. CHO C. CHO с но : Br CH OH Ho : н СН,ОН н : ОН СН,ОН
1. Draw the major product(s) of the following, show wedge dash notation when it is appropriate. I < CH3CH2OH cat. H2SO4 we chama w W.com 0 1. Hg(OAC)2, H20 2. NaBH4 2. The following reaction makes 4 steroisomeric products, draw them and tell how they are related. HCI 7 HCI
DUBU Ugraded 1) Draw the enantiomer and a diastereomer of the following Fischer projection in the boxes below Your answers should be in wedge/dash notation (2 points) Original molecule Enantiomer Diastereomer OOH -OH C-Me SH Merci 2) Provide the full IUPAC name for the following molecule (2 point): undecane 3-bromo 4,5-ethyl 6-methyl 8-ethylene Molecule: 9-11-methylethul) Name 3) Use your knowledge of pka's to rank the following from least basic (1) to most basic (5)? (1 point)
2a. Draw the dash-wedge structures and Fischer projections of the following molecules. R-1-bromoethanol (2S, 3R) - 2-chloro-3-iodobutan-1-ol (HOCH-CHCICHBCH) .. Draw a diastereomer for (2S, 3R) - 2-chloro-3-iodobutan-1-ol.
TV Cyliudiranes an Draw wedge-and-dash bond stereochemical structures - including H atoms at a chirality center and include charges, electrons, and curved arrows. Details count. Draw one enantiomer only for any racemates. Add curved arrows to the first step. - Draw each species (organic and inorganic) resulting from the previous step. . • Include wedge-and-dash bonds. • Include charges and nonbonding electrons. • Add curved arrows for the forward reaction. • Draw the major product. • Include wedge-and-dash bonds. •...
Draw the structures of each compound listed in Table 1 using dash-wedge notation. Compound Drawing Internal Mirror Plane? Chiral? (Y/N) ADsolute Configuration (RAS) cis-1,3- dimethylcyclobutane trans-1,3- dimethylcyclobutane cis-1,2- dimethylcyclobutane trans-1,2- dimethylcyclobutane 2-butanol Meso-2,3 butanediol Glycine (aminoacetic acid) Proline (model both enantiomers) Isoleucine (choose TWO stereoisomers) 1,3 dichloro-allene (CHCI)
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?
Use the Fischer projection below to answer the following questions сн. Br- H H- Br CH,CH, (a) Write the IUPAC name for this molecule using the R/S notation (b) Draw the skeletal structure of the mirror Image, le the enantiomer, of the molecule whose Fischer projection is given above. (Show one wedge bond, one dashed bond, and two sticks attached to the chiral carbon. Show the hydrogen atom bonded to the chiral carbon atom as either a wedge or dash...
Draw the structures, including stereochemistry, of the two intermediates and the final product. Use wedge/dash bonds and hydrogens on chirality centers.
Body Draw the structures, including stereochemistry, of the two intermediates and the final product. Use wedge/dash bonds and hydrogens on chirality centers.