star each asymmetric carbon atom in the following examples & determine whether it has the R...
6.6 Indicate whether the asymmetric atom in each of the following compounds has the R or S configuration (a) O, C Он (b) он (c) Me PrN CI Et HC NH CH, н CH: но i-Pr alanine OH malic acid
having trouble with R and S configuration, can someone help out with this sheet? 17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
Handout Stereochemistry 1. Designate each of the chirality centers as R or S. Then identify the relationship between the two molecules as enantiomers, diastereomers, identical, or non-related. Bс нс си, сн, H Br H (e) (a) and and сн н" Вr нс н н Br ис, и нс, H and and Br (b) СH Bе Br HT Br н H Br. Br H CH, Br () Нс and and но Br CH Br НаС. H, Br. CH H- (b) (d)...
Indicate whether the asymmetric atom in each of the following compounds has the R or S configuration. Indicate whether the asymmetric atom in each of the following compounds has the R or S configuration.
1. For each of the structure star asymmetric carbon atoms, Lab with R and Sand draw any internal mirror plane of symmetry and label chiral or achiral molecules and meso structures H3C CH2Br OH I Br H -ОН HOH CI Н. TH Br H Br H OH HH CH2Br CH2CH3 a b C Br Br CI CI d СН3 CH3 CH3 ...Н H ОН CHз CHз нас CH3 f е
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
write the majlr elimination products of the following reactions. State whether E1, E2, or E1cB. Write the major elimination product(s) of the following reactions. State whether E1, E2, or Eics II Clearly show all stereochemistry. (CH),co (CH,),COH -сн,сн (сн,,св сH,COH CH, CH (сH,с8 (сH,, COН сн, н-СС. LCHLCH, (сн,,ов (CH)COH H отs (сн,,св (сH,СОН -CH, (CH,,сб (CH),COH (CH,,с8 (CH),COH CH3 (CH,с8 (CH),COH -Br н,с отs - CH3 (CH),C8 (CH3),COH Н,с CH (CH,) Co (CH), CОН Br н H OTs...
Need help with the R and S configurations for the two chair questions numbered 1 and 2 in pink. Assign each of the indicated asymmetric carbons as either (R) or (S). OCH CN СНО СH-ОН н н. OH Н н Br CH3 CH3 СООН С(CH)3 CH=CH2 Br OH CI н- но- H C(CH3)3 CH3 CF2CH3 енз
3. Assign R or S configuration to the chirality centers of the following molecules. ҫн, сн, b) но н H Br COOH c) H CH COOH CH,CH н. сн,Cн он HO d) H Br H Br h) CH CH,о, g) HO Н СООН CH hway.com
Draw the specific reagent(s) necessary to effect the following five (5) transformations. Specify stoichiometric coefficients of reactants, also. A. CH3 Cl B. Cн, CH с, сн, Br н,с. Li D. нс .Li н,с. CuLi E сн, (не. н,с. сн, 2 Draw the specific reagent(s) necessary to effect the following five (5) transformations. Specify stoichiometric coefficients of reactants, also. A. CH3 Cl B. Cн, CH с, сн, Br н,с. Li D. нс .Li н,с. CuLi E сн, (не. н,с. сн, 2