Critical Thinking Questions: 12. Label one box in Model 4 with the name "dis-1,2-dimethylcyclobutane" and the...
This is the best copy I have. This is exactly what I received Model 3: Representations of methylcyclobutane H Skeletal Ball-and-stick Wedee and Wedge and dash Perspective ("stick") Cash with explicit hydrogens Model 4: 1.2-dimethylcyclobutane, shown with ring carbons numbered 1-4 (b) LACH 2CH SCH Name (9) Are the molecules in boxes (a) and (b) of Model 4 constitutional womers of each other? Explain 10. Pher than bonds to cartons within the ring, what we aroups are bonded to 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...
3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules prevents full rotation of the ring atoms. For this reason, stereoisomerism may also occur in cyclic molecules. a) Prepare a model of cyclohexane, C6H12. Draw the condensed formula. b) Build a model of methylcyclohexane (C7H14) by replacing one of the hydrogens of cyclohexane with a methyl group. Draw the skeletal formula for methylcyclohexane. 2 c) How many different isomers exist for methylcyclohexane (CyH34)? d)...