Compound B
Since mCPBA is a Stereospecific epoxidation reagent.
E- epoxide is major.
what is the product? please draw CI o-OH (a) (b) Compound A Compound B Mixture of...
What is the total number of stereoisomers possible for the compound shown above? ci OH ci O 6 O 8 O 4 O 16 O 3
What is the most likely product of the following reaction? OH PCIE CI ylyl my 1 II OI II O III O IV a racemic mixture of I and II
By using Nucleophilic aromatic substitution predict the final
product. Please explain, thank you.
O OH CI FeCl3 OME
What is(are) the major Organic product(s) in the following reaction? "CH HCI CI CH,OH (b) CH,OH CH; 0- CH,CI CI H ci (e ( 1) CHỊCH CH,OH ci C1
12. What is the major product in the following reaction? Cl2/CHCl3 -60 C Cl CI Cl OH OH CI
12. What is the major product in the following reaction? Cl2/CHCl3 -60 C Cl CI Cl OH OH CI
Question 33 The correct structure for ethyl 2-chloropentanoyl chloride is: o OH CI CI ОН OH I II III "CI CI CI IV V A. II B. I C. IV D.V E. III Question 34 A compound with the molecular formula Cg4 gBro gave the following H NMR spectrum: triplet, 5 1.4 quartet, 8 3.9 multiplet, 5 7.0 (4H) There was no evidence of an -OH band in the IR spectrum. A possible structure for the compound is: Br Br...
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OH OH CI CI Select one: O a. enantiomers O b. conformations c. constitutional isomers d. diastereomers
What is the product of the following reaction? 12, KOH of CI OH 5. IV Select one: a. 11 O b. IV O c. 1 O d. III What is the starting material for the following reaction? Brz Br HOA O OH OH all IV Select one: a. O c.V
What is the major Organic product expected from the following reaction? OH оно ci CH3CH2OH OH OCH.CH H2CH.CO Ci (b) OH (d (e (1)
Please write neatly.
3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI 0 SOCl OH heat NH 1) CH3MgBr excess CH, CH, -OCH,C 2) H2O COOMe LIAIH OH Ci 0
3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI
0...