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- Q1Q4 R and S Configurations For each of the labelled chirality centers, determine the R or S configuration. Br H3C CH2CH3 C(CH3)3 B D E CH,OH F CH2BR F CI SCH3 G OH I H 4-CEC ОНYou may draw the structures in either Kekule, condensed, or mixed format initially. In the tables draw them as skeletal structures. Attach the sheet of paper with your DEPT spectra at the end of this packet before turning your packet in.
- Choose the correct answer. Choose.. Choose... An alkyne with molecular formula C5H10 A ketone with molecular formula C4H8O A ketone with molecular formula C3H8O An alkene with molecular formula C5H8 An alkene with molecular formula C5H10 An aldehyde with molecular formula C2H40 An aldehyde with molecular formula CH4O H. A saturated hydrocarbon with molecular formula C6H14 Choose..Figure 1.9: The structure of this acid (C5H10O2) is: 4 singlet triplet 3 doublet 3 n=8 Figure 3: ¹H-NMR of unknown ether C (molecular formula C5H12O). Figure 1.10: The structure of this ether (C5H10O2) is: Figure 1.11: The structure of this compound (C7H16) is: мий doublet n=8 ми ми doublet triplet 1CH2=CH-C-O-CH3 C3 C2 C1 Cme Which order indicates the correct order of carbon chemical shift of the four carbons of the compound ○ A. C₂ < C3 C1 < Cme ○ C₁< B. C3 < C2 Cme О с. Cme V C3 < C1 C2 V
- How many signals would be in a CNMR AND HNMR for this product? Please explain in depth. H3C OH Z10. Fill the blanks. Name Methoxyethane Ethyl acetate Dime 2-Bromopropane 1,4-Dibromobutane Acetone 3-Methylpentane 1,2- Dichloeopropane Ethanol 2-Chloro-2- methylbutane Structure År Xu Br Possible chemical shift for each unique peak Integral Ratio between (among) peaksis this S or R configuration? explain how please?
