CHM 211 STEREOCHEMISTRY Chapter 5 Write the IUPAC name for the following compounds and including the Rors configuration...
11. Draw a dash-wedge structure for the following? (1 pt each) (a) (1R)-1-bromo-1,3,3trimethylcyclohexane (b) (2S, 4S)- 2-bromo-4-methylhexane 12. Draw fisher projection formula of (2S, 3R, 4S)- 2,4-dichloro-3-methylhexane? (1 pt)
2. Draw the flowing substances. a. bond-line with dash-wedges to indicate appropriate stereochemistry (1R 4R)-1,4-dibromo-1-chloro-1-fluoropentane b. Fisher projection formula: (3R)-6-bromo-1-hexen-3-ol 3. Write the IUPAC name of the following compounds including stereochemical details. QUA CH3 b. HODC- H₃C
2. Draw the flowing substances. a. bond-line with dash-wedges to indicate appropriate stereochemistry: (IR,4R)-1,4-dibromo-1-chloro-1-fluoropentane b. Fisher projection formula: (3R)-6-bromo-1-hexen-3-ol 3. Write the IUPAC name of the following compounds including stereochemical details. a. OH CH, b. HO -Br Hас" H
CHM 211 STEREOCHEMISTRY Chapter 5 3. Hexane and 3-methylpentane are examples of: (a) Enantiomers (6) Constitutional isomers (c) Diasercomers (d) Conformers 4. Which of the following is a meso compound? CH CHE CH Htci (a) CH (b) " (d) WH+ CH.CH H- CH.CH Htc CH H 5. Which of the following is NOT true about enantiomer? (a) The have the same boiling point (b) The have the same melting poing (c) The have the same density (d) The have the...
CH201 Ch4 In-class quiz Name: 1. Provide the IUPAC name of the following two compounds. M 2. Draw the new man projection of the following compound if viewed from C2-C3. 3. Two stereoisomers of trimethylcyclohexane are shown below (compounds A and B). Compare cyclohexane chair conformations to determine which isomer has a lower energy. Explain your reasoning. сна ICH₃ Bonus: 4. a-D-Glucose is shown below. Draw its two chair forms. Which conformation is more stable? Explain. I recommend using the...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...