b) 1. Ho, Lindlar 2. Br₂, DCM (CH₂C₁₂) Skeletal Structure The reaction above produces two enantiomers. Show the Perspective Formulas of each: 1
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- 5. What are the structures of A, B, and C? NBS NaOCH2CH 3 A B hv CH3CH,OH, 4 CHO CH2=CHCO,H 1. 03 2. S(CH3)2 HO2C CHO2. Use the Newman projection to identify the structure shown: (a) as a Fischer projection (b) as a bond-line structure (c) by name Circle your answer for each part. CH2CH3 F+ H CH(CH3)2 CH2CH3 H+ F CH(CH3)2 三F H CH2CH3 H H F no CH(CH3)2 geslaan sam o Y (S)-4-fluoro-2-methylhexane F (R)-4-fluoro-2-methylhexaneAssign the configuration to each asymmetric carbon as R or S. NO2 (b) NO2 (c) (d) OCH3 (a) Br
- (a) Classify each of the following pairs of structures as constitutional isomers, conformational isomers, configurational isomers or identical. Br and Br Br NH, CH, HO но H,C. ii. and CH, CH, Vi. and он Ph CH, он CH, Ph iv. andAa.17.Draw a three-dimensional representation for each molecule. Indicate which ones have a dipole moment and in what direction it is pointing. Q.) (CH3)2C = O
- 5. (a) Identify the relationship of the two compounds below. (b) Write the most stable chair conformation for each. Br CH₂ and A. identical B. constitutional isomers C. stereoisomers D. unrelated Br CH₂Can i get help with this problem6. Newman projections to Lewis structures From the following Newman projections, draw the corresponding Lewis structure in the same conformation. A) B) H. H CH3 H₂C N H OH CI Br CH3 H OH CH3
- I need an explanation on this problem.3.) 2-Methylbutane (isopentane) is used, in conjunction with liquid nitrogen, to freeze tissues for cryosectioning in histology. Below is the potential energy diagram for all the conformers of 2-methylbutane. Provide structures that match structure A, B, and C in the boxes provided. B F IM C A potential energy Conformer A 0° D angle of internal rotation Conformer B E F H 360° (=0°) Conformer C9. The following compound A is less stable than compound B. Using your knowledge on the origin of angle strain and hybridization states of the carbon involved, explain this observation. CH3 less stable than CH₂ A B
