Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN: 9780618974122
Author: Andrei Straumanis
Publisher: Cengage Learning
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- 2. Provide the stereochemical assignments for the chiral centers as they would be reported in IUPAC naming. (ie. # letter, # letter) You don't need to name the entire molecule. Brarrow_forward2. Determine the geometrical isomerism (E or Z) for the following molecules. a. CH3 F, Br H3C H. B b. What is the correct name for this molecule? CH3 C1 H. Br" H. CH3 c.Assign a R or S configuration for each stereo-center: H3C OH Et CH3 d. For the structure below, Assign (R) and (S) for each chiral carbon? CH3 O. CH3 OCH3 e. Determine the double bond stereochemistry (E or Z) for the following molecules. A Barrow_forwardDo not give handwriting solution.arrow_forward
- How many stereoisomers estuary for this molecule? Show how you know. A. 8 B. 3 C. 4 D. 6arrow_forwardOrganic Chemistry 1. Please draw out the three structures ? Please explain why one and two have meso stereoisomers, and III does not ? Thank youarrow_forwardplease help with these homework questions.arrow_forward
- 5. Draw the structure of (S)-1-bromo-1-chloropropane. Take care to indicate the three- dimensional stereochemistry properly. 6. How many chiral centers does the following compound contain? CH3 7. Label each chiral carbon in the molecule below as having R or S configuration. HO₂C H F. H3C H CH₂CH3arrow_forwardNonearrow_forward6. Indicate whether the circled carbon in each of these is chiral a. CH3-CH-CH2-CH3 b. CH3-CH2-C-CH3 Cl c. CH3-CH2-CH-OH d. Br CH2 ©H H,C CH2 CH3 HC. CH2 Br CHarrow_forward
- (1) Determine the isometric relationship, constitutional, enantiomers, distereomers, geometric (cis/trans), or meso, between each pair of organic compounds. Please explain further than "identical" (ii) circle all structures that are not optically active. d. e. f.g. d. g. SH ļ SH SH SH Br 11 OH OH or or 3 SH z Br SHarrow_forward3. Circle all meso compounds ( H. CH3 H3C- HO- CH3 OH CH3 H. CH3 но CI- CH3 HO,arrow_forwardUse the skeletal structure provided. CI OH HO .. A. provide the Fischer projections of the skeletal structure shown B. provide the structure (Fischer or skeletal) of a constitutional isomer C. provide the structure (Fischer or skeletal) of the enantiomer isomer H3C CH3 D. provide the structure (Fischer or skeletal) of a diastereomer isomer indicate if the structure can be classified as a meso compound. O Yes, meso O No, not mesoarrow_forward
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