Assign E or Z designations to each of the following if appropriate: (2) H₃C H (b)...
3. Assign R or S configuration to the following molecules: Br F Н. F H- Br CH, Br CHECH, H CH2CH3 CH2CH3 CH, CH, -CHE OH H CH=CH2 H3CH2 HY CH(CH3)2 CH 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers Identical d Meso Compounds
3. Assign R or S configuration to the following molecules: Br I F H F H F Br Br -CHE CH=CH2 CH2CH3 CH2CH3 out from H₂C... -CH3 OH CH3CH, -CH=CH2 CH3 CH(CH3)2 H
Give the IUPAC stereochemical designation (E or Z) for each of the following. Give the IUPAC stereochemical designation (E or Z) for each of the following. CH3 CH2-CH-CH2-CH3 D CH2-OH H CH2 H3C - H3Ca 12)-3-chloro-5-methylhept-2-e (Z)-2-dueteromethylenebut-3- H3 C CH3 сHз C. H3C-CH2 D. H₃C H₃C CH₂ Home ECHO RE)-4-secbutyl-3-isopropyl-2,2 CH3 (E)-3-methylpent-2-ene
9.4 Draw a structural formula for each of the following esters: a. cyclohexyl propanoate b. methyl formate e, ethyl benzoate d. isopropyl acetate e. butyl butanoate f. propyl pentanoate 9.5 Assign names to each of the following amines: NH b. CH, -NH-CH2-CH c. (CH-CH2),N 4. NH - CHE 6, CHỊCH,CH, NH, 9.6 Complete the following equations: a. CH CH NH2 + HCI NH b. + HCI C. CHỊCHÚNH - CHI + HBr + d. N(CH)2 + HBr - 9.7 Draw...
Give the IUPAC name of each of the following compounds aromate D) amine E) ketone 2. Give the IUPAC name of each of the following compounds: H OH HC (a) Hoc (b) CHE (c) Hoc HO (d) CH3 CHE HC (e) Ho-o (1) na CH₂ H CH₂ HyC N. CH3 HC N ( g ) сн.
assign the R** he R or S designation to each enter by number in The follawing projechone 1CH2 1CH3 F ce CH3 di stinguish thellowing paunds, using imple lal test? 940-0 H H H2 OH tr 4CH Br 20 H Cl H CH3 How to 4CH3 H-CH-CH,OH CH-CH-CH3 CH-CH OHCH3-CH-CH-CH3 FH3 CH3-CHIC-C w CH2-CH2-CH-CH OH CHe H-CICHICH H-CH2-CH2-CH CH2-CH t Ok 2 CH3CH-CHCy CH2-CH-CH3 20 ОH OH
Assign R, S configurations to each indicated chirality center in the molecules below. A. OH B. COOH НО. ---H co CHANH CH; HAN HO H norepinephrine alaine 0 D. C. H E. HOC OH moje H н. CH3 H2C H НО CO H CH2 tartaric acid dihydrocaryone
Assign R, S configurations to each indicated che e se A. OH! HO TTCH NH, merupp hale HOC / OH H HO HC COZH acid tarber CH, 1. The configuration of this carbon atom (A) is 2. The configuration of this carbon atom (B) is 3. The configuration of this carbon atom (E) is Consider the structure of streptimidone to answer the following question(s). OH OH strep timidone H3C H 4. Assign R or S configuration to each chirality center...
5. Which of the following structures is an isomer of the compound in the box? CHE Chu-Chi-CH-CH-CH, A CH:CH-CH2 - CH2 B. CH, CH CH үн. CH-CH-CH-CHECK to the CH сна C. 8_5-8 CH-CH2CH сна D. CHECH-CH2-CH-CH3 1 CHE CHE 6. Determine the following pairs whether they are conformational isomers, structural (constitutional) isomers, optical isomers, geometric isomers, or not isomers. A. B. OH c. D. E F. H G. H. HO I J. K. L.
CH3 6. Assign IUPAC names for each of the following compounds: d) CHS-C-CH3 CH₂CH3 CH2CH2 C H2CH2CH3 CH3-CH2-CH2-C-CH2-CH2-C-CH3 H2 CH₂ CH₂ H CH2CH3