From the given data, it is observed that compound A and C, compound B and D are identical
8) Identify all identical compounds. А с D E H CICL CI HCl H CI уу...
Q7.1 6 Points Br OH OH CI Br F А D E OH ОН. H2N- F G H J Which of these rings is OPTICALLY ACTIVE? (select all that apply) Compound A Compound B Compound C Compound D Compound E Compound F Compound G Compound H Compound Compound J None of these Q7.2 3 Points Br OH OH CI Br F А B с D E OH OH xazk HN F G H Which of these rings is MESO? (select...
Consider compounds A, B, C, and D, shown in the image CH3 CI CI H- A D Which compound, either B, C, or D, is identical to A? Which compound is an enantiomer of A? compound C none compound D compound B compound C compound B compound D none m
2- Consider the AON network illustrated below: M E H Activity А B с D E F Duration 5 3 7 2 3 4 5 H a) Calculate the project completion time b) What is the critical path? c) Calculate the slack time for each activity.
Which represents a gauche conformation? A B C D E CI Н. CI CI CI H H CBr Br H H Н. H I H H Br H HY H H H Br Br H H HH B?
C А B QUESTION 7 8 9 E 5 C T Y E R H G D F S A B N. N V Х C @ QUESTION 1 Which of the following will be least reactive toward addition of water to the carbonyl? oi H С B А 0 0 0 0 B QUESTION 2 Click Save and Submit to save and submit. Click Save All Answers to save all answers.
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...
answer all parts Identify compounds A, C, D and E in the following synthetic sequence: OCH, Bri Mg PCC но он D- - E FeBr ether 2. Ho CH, CI, H,0° cat. Hint: For the first reaction, remember you have two ortho/para directors for the electrophilic bromination of the ring, but the methoxy group dominates (stronger electron-donating effect). Identify the structures of compounds A to D in the following synthetic sequence: dilute H K.C. MBO MESO, no nec KH,H,O, KOH,...
7. What is the relationship between these two compounds? CHO CH OH H HH HE A. The compounds are identical. B. The compounds are enantiomers. C. The compounds are diastereomers. D. The compounds are structural isomers. нонс OHC 8 What is the relationship between these two compounds? соон COOH H- ci CH A. The compounds are identical. B. The compounds are enantiomers. C. The compounds are diastereomers. D. The compounds are structural isomers. CH CH3 CH,OH CH, OH 9. What...
2. (3 points) Consider molecules shown below: CH3 CHs CH CHs CHs CI CCI CH CI CH CI- H-CCI H-CCI Н-с—н HCH H-CH H--CH H-CH H-CH HCCI CI H H Н-С—СI CI Cн, CHs CH CHs CH3 E D. C. A (a) Identify all pairs of diastereomers. CAACBE (b) Identify all meso compounds. (c) Identify all pairs of enantiomers. (A (810le AOLBO
What is the major product of the following reaction? HCl(9) ? (excess) H (b) (d) H CI H H H CICI HCI HH C