$13.62 Identify the chiral carbons, if any, in each of the following compounds: (13.2) 0-CH, ОН О | | a. CH, CH-CH...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...
Identify the labeled chiral carbons as Ror Sin the molecule shown below. HO. ОН Br Br IIIIII H 2) H' 1) CH3 CH, A 15.25 OB 15.2 O C 1R.25 Fullscre
Examine the following compounds. CH3-CH2-CH2-CH)-CH2-CH3 НО-СН-СН-CH--CH--CH-ОН С A ОН Но-СН--СH-CH-CH--CH-ОН CH--CH-CH-СH--CH-ОН D would be the most soluble in water Structure O A В O C O D
12.32 Identify each dentify each of the following structures as chiral or achiral. If chiral, indicate the chiral carbon. DE COCINA 12.37 I a. CH2-C 2. CH3 -C-CH2CH=CH3 100CH, D Br SSL b. CH3-C=CH-CH3 St OH OH bon d oc. CH3-C-CH-CH3 Listen Clone d. Br-CH-CH-CH3
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
in the following molecules identify the chiral atom(s) if any: CI CH Br i. HOOC iv. CHCIF-CF O-CF2H 5b.6pts. Draw the following structures and label any chirality centers a. 2,4-dimethyl heptane b. 1,3-dichlorocyclohexane 5e.3pts. Draw an alcohol which is chiral and has four carbons. 5d. 4pts. convert the following structure to Fisher projection CH3 Cl
write condensed structures fore each of the following compounds Homework Problems 7.1 Write condensed structures for each of the following compounds: a. 2,2,4-trimethylpentane b. 5-isopropyl-2-methyloctane c. 1,1,3,3-tetrabromopropane d. 1,1-dichlorocyclopentane e. 1,4-diethylcyclohexane f. 1-bromo-2-methylcyclobutane What are the IUPAC names of the following compounds? 7.2 CH2CH, CH3 a) CH, C CH, CH, CH СH,CH, сн, CH2CH, b) CH2CH d) (CH),CCH2CH e) F Br Br Write the structural formulas and names for FOUR isomers of cycloalkane, CSH10. 7.3 7.4 Propose structures for molecules...
1. Mark the chiral carbon atoms of the following compounds with “* сі он (2) Сн, сненсH, CICI (1) сн, —сн—сн—сн, Сн, он (3) сH, CH CH-CH, (4) сH, CH-CHCHCH.
Examine the following molecules, and circle any that are chiral. Then, draw a box around any meso compounds. 4. CH3 он H2N H3 Br CH он CI он H O NH 5. Assign the absolute configuration (Ror S) to each stereogenic center in the following chiral molecules using the Cahn-Ingold-Prelog priority rules
1.) How many chiral carbons are present in the compound below? Place an asterisk next to the chiral carbons. (CH3)2N CH, OH N ICE CCH 2.) Assign priorities to the substituents in the following set: (Lowest priority is 4.) - -NH2 -Br -COOH -CHO 3.) Label each chiral carbon in the compound below as Ror S. * COH Br H 1. Hoci TH H CH3 4) Predict the product and show the complete electron-pushing mechanism for the reaction below: O=C...