. Yes it contains chiral center which I have marked in the above structure
And there is 2 substituent at atom 2 that is chloride and methyl substituent
1 Determine the R/S orientation of the indicated chiral center(s) in the following molecules. If there...
CHE CHE CH3 HC CH3 Br CH3 Br Brs H CH3 2,3-dibromobutane The wedge-dash representation of 2,3-dibromobutane is shown. What is the orientation of the chiral center(s)? 25 Write the orientation as in the following examples, (25) or (2,3S), not 2s or 2,35. Je sure to include the parentheses and the number, and comma as necessar Which of the Newman structures is equivalent to the wedge-dash structure? - D Note that the equivalent Newman structure will not necessarily have the...
4. Put an asterisk (*) next to each chiral center in the structure of erythronolide B, a metabone precursor to the commercial antibiotic, erythromycin. H3C .CH OH CH3 нс, Toi Erythronolide R Нас Анас OH 5. Determine whether the chirality centers in the following molecules have Rors configuration. (a) H (b) OCH2CH3 (c) OH NO-C-OH HC-CH3 H₃C-C-CH₂OH (a) HOH (b) c) HOCHZ HOCH2 CO2H 6. Are the following molecules chiral or achiral? If they are chiral, put an asterisk next...
Need help with these Orgo Chem problems. mostly with the naming part. thank you Draw the most stable chair conformation of cis-1,2-dimethylcyclohexane 1) Draw the ring flip of the structure in question #1 2) Draw all contributing resonance structures for the following molecules. Make sure to show all arrows showing 3) movement of electrons. :c: Name the following molecules 4) 5) Assign R/S configuration to the molecule, 2-bromobutane, shown Br H H H HyC CH3 2-bromobutane Which of the following...
1. Draw the dash-wedge structure that corresponds to the following Newman proje OH Htci CH CH3 4 Label each stereocenter in the following molecule with an asterisk (*) and identity it as na configuration. molecule with an asterisk (*) and identify it as having an R or an S NH2 3. Draw the most stable chair conformation for the following molecule. 4. Draw 3-ethoxypentane. 5. Assign the priority of the substituents around the asymmetric carbon. Br H I BY BE
I have the answer to this problem but I do not understand for R and S how to determine which atom gets a wedge or dash. Please explain Ciastereomer 2. Draw (2R)-2-chloro-2-butanol and (2S)-2-chloro-2-butanol in 3D format (wedge and dashes shown clearly) CI, OH Ev & DH 2-chloro-2-butanol
Indicate whether each of the following molecules R, S, Z or E. Label the substituents according to priority. The third molecule is a Fischer projection. Cl H2C SH H CH3 CH3 Label each pair of molecules as enantiomers, diasteromers, identical molecules constitutional isomers, or not isomers at all. No partial credit. H3C SH CH3 CH(CH3)2 H3C CH2CH2F CH(CH3)2 H3C CH2CH3 and H CH3 and H SH Cl HOH OH and CH3
6.(14) Determine the absolute configuration (R or S) for each chiral center in the following pairs of molecules. Also determine if the pairs are identical, enantiomers or diastereomers. CH3 ŅH uta ÇO2H a) b) & 11 CO2H & HO OH NH CH3 CH2 Cl -H CH3 CH3
3. (4 pts) Complete the Fischer projection drawn below by adding the four substituents to the chiral carbon of (s)-2-methyl-3-bromo-hexane. 4. (4 pts) Draw a wedge and dash structure representing (1R 2R,3S)-1,2- dichloro3-ethylcyclohexane. 5. (4pts) 2-bromobutane is shown below. Is this (R)-2-bromobutane or (S)-2 bromobutane? 6. (6 pts) For each chiral carbon in ascorbic acid (vitamin C), shown below, assign Ror S to each stereocenter. How many stereoisomers of ascorbic acid are possible? OH HO ОН 7. (9 pts) (Are...
1. (23 pts.) Label each stereocenter (chiral center) as Ror S. Label each molecule as chiral or achiral. CH ен-он H- CH3 . Он CH2OH Сн,он h) н он В ньон нон НО-Б-н ен,он но- н H-LOH CH OH
3. R, S Configurations Assign R, S configurations to each indicated chirality center in the molecules below. 14. OH 15. COOH ---H CH NH2 HỌN H -CH3 HO alanine norepinephrine - 18. 16. HOC / OHH HV CH; НС . H7 HO COH CH2 dihydrocarvone tartaric acid