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- what is the structure and jvalues? (c10H14O).d) Molecular relationships; identify whether the compounds in each group are const. isomers, conformers, enantiomers, diastereomers, identical, meso or none of the above. ОН ОН H3C Br H3C LF H Br CH3 HO CI Br Br CI NH NHb) a) b) Identify the functional group for each organic compound below and give the IUPAC name the compound. 0 CH3CH₂CH₂CH₂C-O-CH₂CH3 CH3-C=CH2 CH₂ CH3 mature Functional group_ Name: Functional group_ Name:
- 1. Identify the configuration of each chiral center in the following compounds. Draw the enantiomer for each of the following compounds. a) b) c) ОН ΘΗ OH H CH₂CH₂OH 1FO 23: Identify and draw conformers. NH₂ NH2 NH2 NH2 NH2 NH2 1 NH2 NH2 4 2 3 (a) List any two structures that are related as conformers. Answer by listing exactly two numbers. (b) Draw one conformer of the new structure shown here: 1 and 3 (b) OH HO OH13. Identify the functional group present in each compound. Then give the IUPAC name for each of the following: a) b) OH CH₂CH3
- Name the following structures CH3 CH3 F CH3 Br H3C H CH3 H CH3CH₂CH₂CH₂OHQ1: Give the IUPAC names for the following compounds (d) CH3 CH3CCN CH3 (g) Br (h) -CN BrCH2CHCH2CH2CO2HWhich of the following line drawings represents the correct stereochemistry o molecule shown in the Newman projection below? E + Н. H I CH₂CH3 LOH H CH3 OH OH || IV OH 5.... OH A) I B) II C) III D) IV K
- Which of the following structures are identical? (Green = Cl.)Following is a structural formula for cortisol (hydrocortisone). Draw a stereo-representation of this molecule showing the conformations of the five- and six-membered rings.Determine the type of structural isomerism exhibited by the pairs of compounds below, if any? Η Η Η Η Η H-CEC-C-C-C-C-H H H H-C-C-CEC-C-C-H H H нн and H HHHH H H
