
СО,Н сО-СН-СH, a. СО-Н "CО,Н Н,СО BI H3CO Cl b. H3CO Н,СО ОСН) ОСН, СО,Н Ph "СО-Н -Br Н,СО- Br d H3CO Н,СО OCH3...
11. Indicate the order of stability CH н сн. Br CH сH, На н н. Br H H н н" Br н H н н н' Br н A В C D 12. Which of the following structures does NOT have tetrahedral geometry around any of its central central atoms. Use resonance to help explain A. В. с. D. = NH2 13. Is it theoretically possible to separate the pair of compounds below by distillation? Explain briefly CH CHs Br...
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...
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...
size Ion 0.01 0.05 0.001 0.005 0.1 a,pm) Charge +/-1 Activity coefficient (y) H+ 900 0.967 0.933 0.914 0.86 0.83 |(C,HS2СHCO, (С,Н, ) (02N)3CH20-(CH,)NH+, CH30gH4CO2- 800 0.966 0.931 0.912 0.82 0.85 700 0.965 0.930 0.909 0.845 0.81 u+,CgHgco,, носдH, со,, CIC, H,Cо,, CsH,CH,со2, сH,-снсH,со,-, (CH3)2CHCH2CO2-, (CH3CH2)4N+, (C3H7)2NH2+ 600 0.907 0.965 0.929 0.835 0.80 C,CHCO ,, Cl, cco (CH,CH2),NH+, (с,н, NH,+ |Na+, CdCi+, cIo,, 10;, нсо,, н,РОд, HSO,, H,As0, Co(NH3)4(NO2)2, CH3C02, CICH2C02, (CH3)4N*, (CH3CH2)2NH2+, H2NCH2CO2 |+н,NCH,CO, H, (Cн,), NH. сH, сH,NH3+...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...