Did I draw the wedge/dash drawing correctly? Da Convert the following Fischer projection into a to...
oints): Draw a correct wedge/dash drawing of the following Fischer projection І ОН -он І І он І -он
2.Draw a Newman projection, a wedge-dash structure and a Fischer projection for all four stereoisomers of 2-bromo-3-chlorobutane. The wedge dash structure is given for part a – all you need to do is finish the Newman projection and the Fischer projection. a.2R, 3R. On each structure show how you determined where each group goes. (part a only) b.2S,3S c.2S, 3R d.2R, 3S CH3 Brci CH CH3
Select the wedge/dash drawing of the following Fischer projection. ОН ОН ОН н+он нон т ОН ОН ОН
Select the wedge/dash drawing of the following Fischer projection. ОН ОН ОН н+он нон т ОН ОН ОН
Given the following perspective drawing: H " HSH OH HỌC CHỊ Choose the Fischer projection, from the choices below, that is identical in constitution, configuration and conformation CH3 HO- Hs—+ エエーー H3C4H Нас # ### CH CH3 CH3 H HO— SH H CH3 Submit Answer Tries 0/1 Given the following perspective drawing: t-Bu If a Cr14年 QH Choose the Fischer projection, from the choices below, that is identical in constitution, configuration and conformation -Bu H1-CI HO— Br 一二 十 一F-Bu...
7. Draw a wedge and dash structure of the following Newman projection GHz ви HBr CH3 t Br 8. Which of the following is a gauche conformation for butane? Which is the least stable conformation? The most stable? What is the dihedral angle for conformation ? нсна н CH... HOC CH3 сна нен нан, нен нен н" нэн IV 9. What is the IUPAC name of the following compound?
8. Draw stereochemical drawings of the product(s) of each of the following reactions (use the wedge dash drawings provided). In the provided circles, assign configuration RS for the indicated chiral carbons and determine the stercochemical relationship between the final two products. 2-butyne - Na NII, O 1. MCPBA 2. H,0,H,O Stereochemical drawing of product(s) of I. MCPBA
can you make sure i did these correctly 8. (3 pts) Draw the structure of 4,4-diethyl-6-Isopropyinonane. 9. Draw the following: a. ( pts) Newman projection from the perspective of the arrow. = H tt (H) BO Use alkyl group abbreviations (Me, Etipr, etc. See table given in class on naming!) b. (4 pts) Newman projection from the perspective of the arrow. SH Use alkyl group abbreviations! Te C. (4 pts) The straight-chain drawing of the following Newman projection. Draw out...
Did I do this correctly? 21. Name and draw the product of the following reaction: H NO2 O Tupac Name: 1- (2.4 -Dinitroprenyl)- isopropyli denenud razia ch3 NO2 + HEN H3C "CH3 .C NO2 "N-N CH3 "NO2 Acetone 2,4-Dinitrophenyl- hydrazine Acetone 2,4- Ginitropnery) hydrazine 22. Draw the product of the following reaction: Connor name CH3 CHE CH3C=CHCCHE H2NNH2 CH3-ċ=CH-CH₂-CH3 KOH at CH3 23. Draw the product of the following reaction: 1. CH_MBt, ether 2.H30* 24. What is the order of...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...